Positie invoeren

Het overzicht van de statistiek van de lonen bij het beroep "QC Scientist in Belgium"

Ontvang statistische informatie per mail

Het overzicht van de statistiek van de lonen bij het beroep "QC Scientist in Belgium"

1 600 € Gemiddeld maandsalaris

Niveau van het gemiddelde loon tijdens de laatste 12 maanden: "QC Scientist in Belgium"

Valuta: EUR USD Jaar: 2021
Op de staafdiagram is de verandering van het gimiddelde loon van het beroep QC Scientist in Belgium getoond.

Indeling van de "QC Scientist" vacatures in de regionen Belgium

Valuta: EUR
Volgens het diagraam zijn er in Belgium het grootste aantal vakatures van de beroep QC Scientist in geopend. Op de tweede plaats staat {regionPName2} en op de derde {regionPName3}.

Top provincies Belgium volgens niveau van het loon voor de beroep "QC Scientist"

Valuta: EUR
Volgens het diagraam zijn er in Belgium het grootste aantal vakatures van de beroep QC Scientist in geopend. Op de tweede plaats staat {regionPName2} en op de derde {regionPName3}.

Top van de gelijkaardige vacatures volgens niveau van het loon in Belgium

Valuta: EUR
Onder de gelijkaardige beroepen in Belgium met het meest hoge loon is Data scientist. Volgens de gegevens van onze site het niveau van het loon bedraagt 6385 eur. Op de tweede plaats staat Lab medewerker met het loon van 2800 eur en op de derde plaats staat Onderzoek uitvoerend met het loon van 1600 eur.

Aanbevolen vacatures

QC/Equipment Engineer
Alten, Flanders
The function ALTEN ontwikkelt en levert Life Sciences expertise aan toonaangevende bedrijven in de wereld. Vandaag de dag is ALTEN België een belangrijke speler in de Life Sciences (Pharmaceutical, Medical Devices…) met 30 klanten. Als wereldspeler met een lokale aanwezigheid zijn we flexibel en in staat om ons aan te passen aan de behoeften van elke klant. Daarom zijn we op zoek naar QC/Equipment Engineers om het team te versterken. Als QC/Equipment Engineer heb je volgende taken: het selecteren en aankopen van nieuw equiptment het bepalen van een kwalificatiestrategie het opvolgen van systeemkwalificatie (IQ, PQ, OQ) en het leveren van de bijhorende documentatie (regulatory & compliance-gewijs) het toelichten van processen/procedures bij audits technisch support bieden indien er vragen, problemen of defecten zijn het deelnemen aan QMS systeem team Your profile Industrieel/Bio-ingenieur of gelijkwaardig door ervaring Communicatief sterk in het Engels Ervaring in het kwalificeren van labotoestellen Ervaring in een GMP omgeving Flexibiliteit (planningsgewijs) Analytisch denkvermogen Stressbestendig What we offer Waarom ALTEN BELGIUM? Bij ALTEN geloven we in samen groeien: Werken binnen een Business Unit met een ambitieuze groei waardoor u beroep kan doen op een groot netwerk Menselijk kapitaal is onze prioriteit; we ondersteunen de carrièreontwikkeling van onze consultants met regelmatige follow-ups in een team waar communicatie centraal staat Samenwerken met toonaangevende bedrijven binnen hoogtechnologische omgevingen- Naast een aantrekkelijk salarispakket biedt ALTEN Academy u een portfolio van trainingen aan
Business Development Manager, Health Science R&D/QC (BE)
SGS Group Belgium, Waver, Nijvel, Wavre
SGS is the world’s leading inspection, verification, testing and certification company. We’re also the benchmark worldwide for quality and integrity. And that makes us very proud. This can only happen thanks to almost 100 000 colleagues worldwide, with more than 1750 employees in Belgium only. Our employees give 110% of themselves every day, divided over all expertises, branches and cultures. Our coworkers build their own way inside the company, the services and the expertise. To strengthen our sales and business development organization for our laboratory in Wavre, we are currently looking for a Business Development Manager, Health Science R&D/QC Prospect new customers and develop new opportunities with existing clients in Europe Lead important new/strategic projects and act as the “reference person” Establish, monitor and coordinate timely action plans, taking into consideration positive and negative deviations from target Lead the process to establish a mid-term strategy and a yearly budget Represent the SGS Health Sciences R&D/QC in conventions, exhibitions, professional associations (etc.) Scientific educational background Languages: Very good level in French, Dutch and English About 5 years sales experience in the Life Science Industry for Small and/or large molecules Very good knowledge of the activities of a chemistry laboratory and/or the pharmaceutical industry Good understanding of the regulatory QC requirements (GMP, FDA) Good ability to communicate and create contacts Permanent contract Full-time We are looking Originele vacature is te vinden op StepStone.be – Maak nu een Jobagent aan op StepStone en vind je droombaan https://bit.ly/2jPYsZC Vind gelijkaardige jobs, informatie over werkgevers en carrièretips op StepStone.be
Scientist Method Validation
Eurofins Scientific, Gent
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 48,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing. In 2019, Eurofins generated total revenues of EUR € 4.56 billion, and has been among the best performing stocks in Europe over the past 20 years. Eurofins CDMO is one of the leading CDMOs in Europe providing high-quality, customized drug development solutions for specialty and biopharma clients. Our focus is to support clients on the earliest phases of their development pathway (from API to the clinical packaging). Its Belgian subsidiary, Eurofins Amatsigroup NV, is based in Ghent, offering a complete drug development package for new drug entities (biological and chemical) up to early clinical phases to third parties to help them in speeding up the development and manufacturing of their drugs. Job Description We are looking for a person that reports to the QC Manager of Eurofins Amatsigroup NV. His/her main responsibilities Key responsibility: you are responsible for the validation of analytical methods to support the quality control testing of Drug Products used in clinical trials. You interact with Analytical Development, Project management and the Sponsor in preparation of validating the different analytical methods needed for the Drug Product Release and stability testing. You write Validation Protocols in accordance with international recognized guidelines (ICH, FDA, Ph. Eur., USP). You execute and follow-up the execution of the Validation Protocol in compliance with the GMP principles and the procedures of the Eurofins Quality Management System. You calculate, review and summarize the analytical test results in Validation Reports. Qualifications Education and experience Master Degree with a scientific orientation (Analytical Chemistry or Pharmaceutical sciences) with a first profound professional experience, preferably in a pharmaceutical setting. Key scientific knowledge: in-depth knowledge of Liquid Chromatography is a must (Waters U(H)PLC systems; UV/ELSD detectors and Empower CDS). Proven record of accomplishment in analytical method validation. Experience within a GMP environment is a major asset. Experience with Karl Fischer, Dissolution, UV spectroscopy and Laser diffraction techniques provide added value. Competences Able to work independently after training in matters entrusted to you. Team player with strong organizational and communication skills. Problem solving, flexible mindset whilst being punctual and quality driven. Professionally fluent in English and Dutch (written and spoken). MS office adapted. Additional Information Work in a fast growing organization. A position with responsibility within a dynamic company. Personal development through learning on the job and additional external trainings. Other jobs at Eurofins Belgium BioPharma Services
Senior Validation Engineer (Laboratory), Belgium
Sanofi, Gent
Join Ablynx, a Sanofi company as a Senior Validation Engineer (Laboratory) responsible for the coordination and implementation of qualification, validation and system operational life cycle activities in a GxP environment. Part of your role will be to write and execute the validation deliverables for laboratory equipment and computerized systems as a member of the Validation team (part of the GMP Unit). This full-time permanent position will be based in Ghent, Belgium. About Ablynx Ablynx, a Sanofi company, is engaged in the development of Nanobodies®, proprietary therapeutic proteins based on single-domain antibody fragments, which combine the advantages of conventional antibody drugs with some of the features of small-molecule drugs. Nanobodies have potential uses in the treatment of a range of serious and life-threatening human diseases. Ablynx advances a portfolio of Nanobody-based therapeutic programs in several major disease areas, including inflammation, haematology, immuno-oncology and oncology. About growing with us In this role you will…. Perform activities in a GxP environment in close contact with the Good Manufacturing Practice (GMP) Quality Control (QC) Lab Manage multiple and complex computerized systems validation and equipment qualification projects. The planning is discussed and aligned within the Validation team and involved stakeholders Write, review and finalize the validation documentation (URS, RA, protocols, reports, trace matrix, requalification, periodic review, non-conformities) for new or existing systems (lab equipment, computerized systems) used in the GxP environment Perform and review (re)qualification and calibration of systems used in the GxP environment. Initiate, review and follow-up on Quality Events to ensure completion within due date Interact with external and internal suppliers in function of design, validation, implementation, maintenance and calibration of systems Optimize and maintain operational procedures on validation, calibration and the life cycle of systems based on regulations and guidance documents Organize training sessions on the operating instructions for personnel working with the system. Coach, motivate and support your Validation team members in all of the above tasks About you Qualifications/ Education & work experience Master in a relevant field of sciences Experience with GMP guidelines and a GMP working environment 3 years of experience in (computerized) systems validation and/or in lab equipment qualification Knowledge of Data Integrity, 21 CFR Part 11, USP and GAMP guidelines Experience in project management of validation projects – advantageous Software and IT affinity – advantageous Excellent communication, collaboration skills and ability to work cross-functionally Team player, enthusiastic, independent and self-motivated Practical hands-on mentality Sense for problem solving, initiative, quality, accuracy and detail Oral and written fluency in Dutch and English Inspire your Journey: what Sanofi can offer you: An international work environment, in which you can develop your talent and realize ideas and innovations within a competent team. An attractive, market-oriented salary aligned with your qualifications and including social benefits above average (e.g. company pension plans, health management). An individual and well-structured introduction and training when you onboard. You can create your own career path within Sanofi. Your professional and personal development will be supported purposefully. As a globally successful and constantly growing company, Sanofi provides international career paths as well. This is our Sanofi. Discover yours. If you feel you have the required experience please apply, alternatively contact Sandra.Rombisanofi.com directly for more details. We are proud to have been awarded Global Top Employer 2021 LI-EUR At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all. Sanofi is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions. With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Sanofi, Empowering Life Suggested Jobs (Senior) Associate Scientist Mass Spectrometry Follow Us Global Terms & Conditions and Data Privacy Statement
Scientist - Assay Production Support
The Binding Site Group, België, BE
Would you like to be part of an organisation which is committed to improving patient lives worldwide through education, collaboration and innovation? Do you want to make a difference? If the answer is ‘yes’ then you’re just the kind of person we’re looking for We have a fantastic new opportunity for a Scientist who is passionate and enthusiastic to work in in the Production Support - Assay department. The successful candidate will be expected to maintain specialist knowledge relevant to manufacture and the use of assays and will be responsible for the completion of projects, investigations and experiments. You will be responsible for carrying out any required improvements and correction in the in-process testing of kits manufactured at The Binding Site ensuring that the product has been provided promptly and meeting specification. Principal Duties and Responsibilities. Completion of investigation and experimental reports. To carry out such initial validation as is appropriate to ensure successful performance once projects are handed across. To ensure that any improvements initiatives are carried out in a timely manner. To critically assess raw materials and generate raw material specifications including QC limits if required. To assess new materials and equipment where necessary and give feedback on suitability for use. To develop specialist experience and knowledge with respect to immunoassays and so contribute to the specification and design of future products. To carry out design changes to existing products or processes when required and assist in the investigation of complaints. To critically evaluate analytical methods and equipment to maintain highest possible standards. To develop/contribute to new techniques/scientific understanding to improve upon existing and future products. A relevant Scientific Degree in a biological sciences or chemistry discipline or relevant practical experience in immunoassay development Experience of laboratory work, eg. Final year project or previous employment. Good knowledge of immunology. Good knowledge of immunodiagnostics. Excellent working knowledge of Microsoft Excel and Word Experience or knowledge of operating automated analysers Excellent verbal and written communication skills. To be friendly and approachable. To be flexible to the needs of the business Working for us: Founded in 1986 by a group of former researchers based at the University of Birmingham, The Binding Site is today recognised as a market leader in the development of products for the investigation of a range of disorders involving immunodeficiency. The Company is built on the success of its people and provides the ideal environment to meet a wide range of career aspirations. It recognises the value of its employees and looks to provide development and support opportunities to maximise the potential of its 1,100 staff. Working at Binding Site means being part of a global community that delivers innovative solutions with shared ideas and a collective dedication to improving patient lives, worldwide. Location: Birmingham Hours: 40 hrs Necessary (always active) Analytics
Laboratory Scientist - Biology
QUALITY ASSISTANCE, België, BE
To face our constant growth, we are currently actively looking for a Laboratory Scientist - Biology You will be requested to work on projects for the characterisation and quality control of Biomolecules YOUR MISSION You will report to the Technical leader and you will be part of a team of 5/6 people composed of Laboratory Technicians, Analysts and/or Scientists According to the client’s projects and your level of expertise, you may be required to ensure different tasks such as Performing daily laboratory activities related to method application, development, validation and transfer Performing analyses Processing data Writing reports and associated supporting documents Presenting/discussing results Validating raw data Validating experimental results and ensuring protocols are respected Applying methods for QC and stability studies Communicating with clients Training team members and others on technical skills if needed PROFILE You have a scientific background with knowledge of biologics (Antibody, peptide, protein, ADC…) You are have a strong technical expertise in at least two of these following techniques Surface Plasmon Resonance Cell-based assays Electrophoresis testing on proteins Ligand binding assays You have working experience in a regulated environment ideally in the pharmaceutical industry You have good knowledge of Working with Cell lines and/or proteins using at least one the following techniques: Cytotoxicity testing (Antibody-Dependent Cell-Mediated Cytotoxicity (ADCC), Complement Dependent Cytotoxicity (CDC), …), Reporter gene assays, Cell death, Proliferation, SDS-PAGE, Western Blot, IEF, ELISA, biacore, octet and protein dosage Development, validation and/or application of analytical methods Pharmaceutical guidances Working experience with antibodies or antibody fragments is a plus You have good communication skills both in French and English (B2 Level) - writing scientific documents, reports, protocols and mails, phone conferences, contacts with clients. About Quality Assistance Quality Assistance is a leading European Contract Research Organisation providing the pharmaceutical industry with all the analytical services required by EMA and FDA regulations for the development and marketing of innovative human medicinal products. We assist our clients from candidate selection, through non-clinical and clinical studies, to marketing authorisation, using our state-of-the-art, product-dedicated expertise in analytical sciences. For each customer and each project, we design customised solutions, define analytical protocols, develop and validate specific new analytical methods and perform characterisation, stability, pharmacokinetic, biomarker and immunogenicity studies as well as batch release testing, in order to evaluate the Quality, Safety and Efficacy of the given drugs. The company holds a unique position on the market with all its laboratories on one site, 190 highly qualified professionals and over 35 years’ expertise at the forefront of analytical sciences. The Quality Assistance environment is GMP, GLP and GCLP/GCP compliant. Why join Quality Assistance ? We are a true career partner. We accelerate people’s access to new medicines. We offer an inspiring work-life balance in a human scale environment. We care about mutual respect, assistance and communication. We listen to your needs and your suggestions. We offer a market-competitive remuneration package including numerous fringe benefits. You will also be provided with a company car.
Sr Scientist (Extracellular Vesicles),Visa offered, Belgium
NonStop Recruitment Schweiz AG, België, BE
Sr Scientist (Extracellular Vesicles),Visa offered, Belgium Belgium €75K to €80K per Year March 19, 2021 Ref: OK 1528_1616165320 Permanent Another great opportunity within an up-and-coming area of Extracellular Vesicles, use your experience within a growing company and have a HUGE impact on their business. You will be able to have a real impact and develop together. My client, an ambitious start up within the field of Exosomes is looking for an experienced Researcher who wants to use his experience and make an impact within the business. Even though they are relatively new on the market, they are backed by an experienced R&D team that has been operational for over 10 years. You will manage the R&D pipeline, offer training and oversee execution according to QMS, develop and validate protocols/procedures related to the EVs production, isolation, purification, characterization, quantification, activity, mode of action; follow the requirements of the GMP and QC departments, supervise project timelines, tech transfer to CDMO, etc. The company focuses on a very niche area of Extracellular Vesicles I would love to hear from you if you match the below requirements: PhD in the field of extracellular vesicles Strong lab technics: ELISA, PCR, WB, FACS, nanoparticle counting, cell culture Nanoparticle isolation, quantification and characterization Microscopy: light, fluorescent Fluent English (Dutch or French would be a bonus) Interested? Share your CV to discuss this opportunity further Location of the company is Antwerp area so please make sure it's convenient for you to commute there. There is potentially some flexibility to work some days from home. Also they will be moving the site to Liege in 2 years so again please make sure it will be sustainable for you in the future. Please forward your CV in the Word format to o.kolesnichenkononstopconsulting.com or recommend this role to someone who would be suitable. Tbey are looking for quite niche skills in the area of EXTRACELLULAR VESCICLES so VISA SPONSORSHIP will be offered if you have a strong experience in the field. The job market changes very quickly so do not forget to connect with me on Linked in, check other roles that I am hiring for at the moment and follow for any future relevant roles. NonStop is dedicated to raising the standard of ethical recruitment and comprises a number of brands, each having their own niche sector focus. Find out how NonStop Recruitment can help you today. Download our app for on-the-go job search and apply. Find out more
Analytical Product Development Scientist
CTI Education Group, Elsene, Brussel Hoofdstad, Ixelles
Analytical Product Development Scientist Adres Catalent Pharma Solutions is the leading global provider of advanced delivery technologies and development solutions for drugs, biologics and consumer health products. For our growing production site located in Brussels (Neder-Over-Heembeek) specializing in sterile technologies, we are currently looking for an Analytical Product Development Scientist . The main role of the Analytical Product Development Scientist is to act as link between the departments of New Product Introduction (NPI), the Analytical Product Development and QC labs, and Catalent’s customers/suppliers. In order to better satisfy the demands of our clients, our APD Scientist ensures the development of NPI analytical projects within the lab. This position offers a wide variety of tasks, daily challenges and a real opportunity to learn. The Role Manage laboratory projects with the client, the suppliers and the Catalent departments involved, from a technical, documentary, scientific and quality standpoint Ensure the logistics, regulatory, technical, scientific and documentary aspects of methodology transfer projects Ensure communication and follow-up on development, validation and stability activities. Deliver necessary documents to clients and present them in case of client audits and regulatory inspections. Act as scientific Subject Matter Expert Analyze samples according to specifications and ensure traceability of every analysis Follow all safety rules and use adequate equipment in order to ensure your colleagues’ safety as well as your own. The Candidate PhD in Chemistry, biochemistry or Master in Chemistry/bio chemistry with project management experience At least 2 years’ experience in the pharma industry or performing analysis in a laboratory Fluent in English and French MS Office (advance knowledge) Rigorous, able to adapt to change, stress resistant and resilient Knowledge of cGMP and regulatory affairs is a plus Defined career path and annual performance review and feedback process Competitive contributory pension and benefits package all offered from day one of employment
NPI Coordinator NBE
UCB S.A., België, BE, Braine-l'Alleud
Let's push the boundaries together and make the most of your talents Location: Braine L'alleud, Walloon Brabant, Belgium Job Function: Production Job ID: 72914 At UCB, we put our heart, soul, and skills into making a difference for people living with severe disease. Working together to push the boundaries, we blend the best of our talents to unlock innovation. Will you join us in our pioneering adventure? To strengthen our Internal Manufacturing Department , based in our hub in Braine-l’Alleud , Belgium , we are looking for a talented individual to fill the position of Quality Control Biologics New Product Integration Lead. As Quality Control Biologics NPI Lead , you will: Participate to all meetings with stakeholders (Development analytical lead, Industrial analytical lead, supply, Manufacturing NPI, stability lead, etc) in term of planning and samples follow-up (i.e., shipment and reception). Coordinate all studies (release, stability studies, process validation, etc through lims or requests of analysis) asked by the stakeholders, ensure the follow-up and communicate the results. Facilitate the analytical transfer of the new products to the Quality Control laboratory (i.e. plan the activities with SME analysts and team lead, review protocol, data and reports of the analytical transfer, escalade issues or roadblocks, equipment needs to the Scientist). Smoothly communicate internally within the Quality Control lab team urgencies and priorities asked by different stakeholders to adjust the planning with the Team leads. Work in close collaboration with SME for local specification creation or update. Handle actions, deviations and realize investigations based on QBD within the laboratory in close collaboration with team leads and QA team member (with Trackwise and LIMS systems). The QC NBE NPI Lead will report to the Head of laboratory. He/she will work in close collaboration with Team leaders, scientist and technicians of the laboratory (transversal matrix). You will also contribute by: HSE Apply the company's Health and Safety policy within the laboratory. Ensure a safe working environment to meet site safety objectives. Management Motivate, recognize team members performance, behaviors and compliance of rules whilst firmly supporting teamwork and spirit. Manage conflicts. Increase team’s competency by ensuring adequate training, coaching and development of technicians in function of the team and people potentials in alignment with the Team leads. Define and communicate openly the objectives of individuals and of the team in accordance with the company’s strategy and formally assess the results with the adequate KPI (Key Performance Indicators) covering HSE, quality and overall performance both for the individuals and the team. Ensure continuous feedback: technicians, peers, management, and stakeholders. Operations Ensure the day-to-day operational planning and coordination to satisfy the stakeholder/client needs based on a monthly forecast in close collaboration with the team leaders. Organize daily meetings with team (Tier 1) to follow-up on the planning and collect and give informations. Ensure that each one contribution is done in due time. Ensure required corrective actions are taken and put in force. Implement, follow-up and communicate on KPI with its related corrective actions. Inform stakeholders and responsible of the lab if deviations from the day-to-day-planning occur. Be prepared and participate actively to weekly/monthly planning meetings, propose solutions, demonstrate creativity and pro-activity to ensure adherence to plan and performance. Ensure that continuous improvement is part of day-to-day activities of the laboratory. Ensure that the lab infrastructure including facilities, utilities and equipment are well maintained. Maximize the utilization of departments budget within given budget limits. Be accountable for a pro-active collaboration with different stakeholders. Quality Ensure follow-up and compliance of procedures and instructions, and update if needed. Ensure follow-up of corrective actions and preventive actions. Ensure audit readiness, participate to the preparation, the follow-up and the realization of audits. Ensure the follow-up of OOS and take actions to reduce the number of laboratories OOS. Ensure adequate training/coaching of technicians linked to the analytical activities requested and performed . I nterested? For this position you’ll need the following education, experience and skills : Education PhD or Master’s degree required in bioengineering, analytical chemistry applied to biological products, biochemistry, biology or equivalent. Experience Min 8-10 years of expertise in the pharmaceutical analysis of, preferably, New Biological Entities and more specifically monoclonal antibodies. Areas of expertise on specific technologies applied to biological products are Electrophoresis, ELISA, Cell based assay, SDS Page, qPCR, aseptic working environment, HPLC/UPLC, CE, Compendial, etc. Proven experience in GMP environment. Proven experience on the use of LIMS software for sample management is an asset. Proven experience on the use of Trackwise software for deviation management is an asset. Proven project leadership skills including planning, monitoring, issue resolution, investigations (DMAIC, 5M, etc), decision making and reporting. Proven experience of 2-3 years in analytical transfer between development to QC is a requirement. Strong organization skills with proven records. Green belt ownership is an asset or training in in Root cause analysis. Understanding of all analytical disciplines related to CMC for late stage development and commercial products (analytical development, stability testing and quality control of drug substance, drug product, raw material and intermediate). Implementation and maintenance of 5S mind set and environment is an asset. “Green” mindset is a requirement. About us. UCB- Inspired by Patients. Driven by Science. Everything we do starts with a simple question: “How will this create value for people living with severe diseases?” By putting patients at the heart of what we do, our approach – from discovery to development to delivery – is continuously transformed and designed around patient needs and their journey. With a team of approximately 7,500 employees and operations in more than 40 countries, we are a global biopharmaceutical company investing more than a quarter of our revenue in cutting-edge scientific research. We are focused on addressing chronic, neurological, immunological, and bone diseases. Curious to know more? Please visit our website www.ucb.com . UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer.
Analytical Product Development Scientist
Alverno Laboratories, Sint-Joost-ten-Node, Brussel Hoofdstad, Saint-Joss ...
Analytical Product Development Scientist Adresse Fonction PhD Langues Catalent Pharma Solutions is the leading global provider of advanced delivery technologies and development solutions for drugs, biologics and consumer health products. For our growing production site located in Brussels (Neder-Over-Heembeek) specializing in sterile technologies, we are currently looking for an Analytical Product Development Scientist . The main role of the Analytical Product Development Scientist is to act as link between the departments of New Product Introduction (NPI), the Analytical Product Development and QC labs, and Catalent’s customers/suppliers. In order to better satisfy the demands of our clients, our APD Scientist ensures the development of NPI analytical projects within the lab. This position offers a wide variety of tasks, daily challenges and a real opportunity to learn. The Role Manage laboratory projects with the client, the suppliers and the Catalent departments involved, from a technical, documentary, scientific and quality standpoint Ensure the logistics, regulatory, technical, scientific and documentary aspects of methodology transfer projects Ensure communication and follow-up on development, validation and stability activities. Deliver necessary documents to clients and present them in case of client audits and regulatory inspections. Act as scientific Subject Matter Expert Analyze samples according to specifications and ensure traceability of every analysis Follow all safety rules and use adequate equipment in order to ensure your colleagues’ safety as well as your own. The Candidate PhD in Chemistry, biochemistry or Master in Chemistry/bio chemistry with project management experience At least 2 years’ experience in the pharma industry or performing analysis in a laboratory Fluent in English and French MS Office (advance knowledge) Rigorous, able to adapt to change, stress resistant and resilient Knowledge of cGMP and regulatory affairs is a plus Defined career path and annual performance review and feedback process Competitive contributory pension and benefits package all offered from day one of employment
Analytical Product Development Scientist
Catalent Pharma Solutions, België, BE
Analytical Product Development Scientist Creation: 16/03/2021 Address Function Experienced Job domain Phd Languages Contract type 01 - Long term Final date of submission of applications Catalent Pharma Solutions is the leading global provider of advanced delivery technologies and development solutions for drugs, biologics and consumer health products. For our growing production site located in Brussels (Neder-Over-Heembeek) specializing in sterile technologies, we are currently looking for an Analytical Product Development Scientist . The main role of the Analytical Product Development Scientist is to act as link between the departments of New Product Introduction (NPI), the Analytical Product Development and QC labs, and Catalent’s customers/suppliers. In order to better satisfy the demands of our clients, our APD Scientist ensures the development of NPI analytical projects within the lab. This position offers a wide variety of tasks, daily challenges and a real opportunity to learn. The Role Manage laboratory projects with the client, the suppliers and the Catalent departments involved, from a technical, documentary, scientific and quality standpoint Ensure the logistics, regulatory, technical, scientific and documentary aspects of methodology transfer projects Ensure communication and follow-up on development, validation and stability activities. Deliver necessary documents to clients and present them in case of client audits and regulatory inspections. Act as scientific Subject Matter Expert Analyze samples according to specifications and ensure traceability of every analysis Follow all safety rules and use adequate equipment in order to ensure your colleagues’ safety as well as your own. The Candidate PhD in Chemistry, biochemistry or Master in Chemistry/bio chemistry with project management experience At least 2 years’ experience in the pharma industry or performing analysis in a laboratory Fluent in English and French MS Office (advance knowledge) Rigorous, able to adapt to change, stress resistant and resilient Knowledge of cGMP and regulatory affairs is a plus Defined career path and annual performance review and feedback process Competitive contributory pension and benefits package all offered from day one of employment
Molecular R&D Scientist
DiaSorin, Asse, Halle-Vilvoorde
Responsible for initiating & executing scientific research and/or development strategies for the company in collaboration with the team. Investigates the feasibility of applying scientific principles & concepts to potential inventions, products & problems. Executes laboratory research. Maintains broad knowledge of state-of-the-art principles & theories. May act as spokesperson on corporate research & development. Main Responsibilities Your Contributions • Investigates the feasibility of applying scientific principles & concepts to potential inventions, products & problems. Executes and may to plan laboratory research as for a project or projects. Has the ability to serve as an independent investigator. Produces & analyzes data for publication & presentation at scientific meetings. Maintains broad knowledge of state-of-the-art principles & theories. May act as in-house consultant & advise management on scientific decisions. Able to interface with internal & external scientists & other departments. May serve as a technical representative, core team or extended team member during the product development process. Authors various manufacturing & raw material specifications & QC documents required for transfer of products to manufacturing. Authors other documents & reports required during the product development process. Uses professional concepts & relationships to contribute to the development & completion of company goals & objectives in creative & effective ways. May direct 1–3 Research Associates Qualifications Experience Personal Strengths Mobility You Education Bachelor’s, Master’s or Ph.D. in a scientific discipline or equivalent with a minimum of 4 years of experience in a research and development environment. Biology, Chemistry, Biotechnology, Engineering or equivalent Experience Molecular experience is a must Experience designing primers and probes for molecular assays Worked independently on projects • Demonstrates potential for technical proficiency, scientific creativity, collaboration with others and independent thought. Ability to work with statistical concepts. DNA/RNA extraction. DNA/RNA amplification assay development (e.g. RT-PCR, sequencing) Primers/probes design for molecular assay development Skills • Demonstrates ability to exercise independent judgment within defined procedures to determine appropriate action. Normally receives general instruction on routine work and detailed instruction on new assignments Ability to read, analyze, and interpret pertinent scientific and technical journals, financial reports, and legal documents Ability to respond to common and scientific inquiries or complaints from customers, regulatory agencies, or members of the business community Ability to write speeches and articles for publication that conform to prescribed style and format. Ability to prepare presentations and manuscripts that effectively present information. Experience with product development or design control highly desirable Technical writing skills / experience Well-organized, ability to work well independently as well as part of a team High commitment and self-motivation DiaSorin S.p.A. - Share Capital € 55.948.257 R.E.A. 180729 Fiscal Code and Subscription to Vercelli Companies Register no 13144290155
method expert, principal scientist, principal expert (BE)
Randstad Group Belgium, Gent
Are you the Principal Scientist CAR-T we are looking for? Are you an expert on CAR-T and looking for a new challenge? Say no more We got the perfect job for you Johnson & Johnson is looking for a Principal Scientist Method Expert CAR-T for their CAR-T facility in Gent (Belgium). Are you interested or do you want more information? Feel free to contact me by phone at: 32 2 472 78 22 . CAR-T (chimeric antigen receptor T-cell therapy) is an innovative approach to eliminate cancer cells, which work by harnessing the power of a patient’s own immune system. They are created from the patients’ own T cells and are engineered to eliminate cancer cells expressing a specific antigen. The Principal Scientist Method Expert, CAR-T Manufacturing manages the method transfer and validation activities, in support of the Malvern Analytical Development team and Raritan Janssen Supply Chain (JSC) site, in full compliance with established cGMP and JSC requirements. The role develops and implements long-term strategies, and execution of Quality Control programs and manages the knowledge development of technical professionals within the QC department. Quality Leadership: The Principal Scientist Method Expert will be a member of the QC CAR-T leadership team that partners with analytical development and chemistry, manufacture and control scientists and is accountable for the method transfer/validation of the CAR-T testing methods. The Principal Scientist Method Expert provides dedicated experienced support and is responsible for the knowledge development programs within the QC CAR-T facilities in EMEA. Operational Quality performance: The Principal CAR-T Scientist Method Expert is responsible for setting up the protocols and reports for the CAR-T method transfer/validation programs. The Principal CAR-T Scientist Method Expert will lead complex laboratory investigation issues by demonstrating strong reasoning skills Proactively and continuously challenge the status quo and implement QC method improvements. Maintains detailed knowledge of industry guidelines/trends, regulatory requirements, and applicable pharmacopeia while remaining current in on-the-job training requirements. Collaborates with Analytical Development, Quality Assurance, Manufacturing, Technical Operations, Engineering and Maintenance to support business needs. Contributes to global strategies related to the QC laboratories which align with compliance and business objects as well as the overall J&J vision. Makes adjustments to roles and responsibilities of department to meet business needs. Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements. What do we expect from you? A Doctoral level degree (PhD, MD or equivalent) with a concentration in cell therapy or related field and at least 5 years of pharmaceutical/biotech proven experience. Candidates with BS/MS degrees will also be considered if accompanied by appropriate additional years of experience. Strong communication and interpersonal skills, a high level of organizational ability, attention to detail, and ability to work effectively in a collaborative environment globally (US and EU) is required. Experience negotiating and influencing decision-making processes, and the ability to reason and lead issues through to resolution is preferred. The candidate must be highly organized and capable of working in a team environment with a positive attitude under some supervision. Knowledge of cGMP regulations and FDA/EU guidance is required. Comfortable with speaking and interacting with inspectors. Good written and verbal communication skills are required. What does J&J have to offer you? A high salary Company car and fuel card 39 Holidays Annual performance bonus Meal vouchers of 8€/day worked Hospita Originele vacature is te vinden op StepStone.be – Maak nu een Jobagent aan op StepStone en vind je droombaan https://bit.ly/2jPYsZC Vind gelijkaardige jobs, informatie over werkgevers en carrièretips op StepStone.be
Principal Scientist Method Expert CAR-T (BE)
Randstad Group Belgium, Gent
Are you the Principal Scientist CAR-T we are looking for? Are you an expert on CAR-T and looking for a new challenge? Say no more We got the perfect job for you Johnson & Johnson is looking for a Principal Scientist Method Expert CAR-T for their CAR-T facility in Gent (Belgium). Are you interested or do you want more information? Feel free to contact me by phone at: 32 2 472 78 22 . CAR-T (chimeric antigen receptor T-cell therapy) is an innovative approach to eliminate cancer cells, which work by harnessing the power of a patient’s own immune system. They are created from the patients’ own T cells and are engineered to eliminate cancer cells expressing a specific antigen. The Principal Scientist Method Expert, CAR-T Manufacturing manages the method transfer and validation activities, in support of the Malvern Analytical Development team and Raritan Janssen Supply Chain (JSC) site, in full compliance with established cGMP and JSC requirements. The role develops and implements long-term strategies, and execution of Quality Control programs and manages the knowledge development of technical professionals within the QC department. Quality Leadership: The Principal Scientist Method Expert will be a member of the QC CAR-T leadership team that partners with analytical development and chemistry, manufacture and control scientists and is accountable for the method transfer/validation of the CAR-T testing methods. The Principal Scientist Method Expert provides dedicated experienced support and is responsible for the knowledge development programs within the QC CAR-T facilities in EMEA. Operational Quality performance: The Principal CAR-T Scientist Method Expert is responsible for setting up the protocols and reports for the CAR-T method transfer/validation programs. The Principal CAR-T Scientist Method Expert will lead complex laboratory investigation issues by demonstrating strong reasoning skills Proactively and continuously challenge the status quo and implement QC method improvements. Maintains detailed knowledge of industry guidelines/trends, regulatory requirements, and applicable pharmacopeia while remaining current in on-the-job training requirements. Collaborates with Analytical Development, Quality Assurance, Manufacturing, Technical Operations, Engineering and Maintenance to support business needs. Contributes to global strategies related to the QC laboratories which align with compliance and business objects as well as the overall J&J vision. Makes adjustments to roles and responsibilities of department to meet business needs. Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements. What do we expect from you? A Doctoral level degree (PhD, MD or equivalent) with a concentration in cell therapy or related field and at least 5 years of pharmaceutical/biotech proven experience. Candidates with BS/MS degrees will also be considered if accompanied by appropriate additional years of experience. Strong communication and interpersonal skills, a high level of organizational ability, attention to detail, and ability to work effectively in a collaborative environment globally (US and EU) is required. Experience negotiating and influencing decision-making processes, and the ability to reason and lead issues through to resolution is preferred. The candidate must be highly organized and capable of working in a team environment with a positive attitude under some supervision. Knowledge of cGMP regulations and FDA/EU guidance is required. Comfortable with speaking and interacting with inspectors. Good written and verbal communication skills are required. What does J&J have to offer you? A high salary Company car and fuel card 39 Holidays Annual performance bonus Meal vouchers of 8€/day worked Hospita Originele vacature is te vinden op StepStone.be – Maak nu een Jobagent aan op StepStone en vind je droombaan https://bit.ly/2jPYsZC Vind gelijkaardige jobs, informatie over werkgevers en carrièretips op StepStone.be
Process Development Scientist
Corden Pharma, Brussel, Brussel Hoofdstad, Bruxelles
CordenPharma est un partenaire de premier plan en matière de développement et de fabrication sous contrat (CDMO) avec environ 2000 employés à travers l’Europe et les États-Unis et un chiffre d’affaires annuel > 500 M€, permettant aux entreprises pharmaceutiques et biotechnologiques de lier leurs exigences en matière de succès des produits à la vie plus saine de leurs patients. Fondé en 1987, CordenPharma Brussels (précédemment connu sous le nom de Peptisyntha Brussels) faisait partie du groupe Solvay jusqu’à son acquisition par CordenPharma en octobre 2013. CordenPharma Brussels a accumulé plus de 30 ans de succès dans la fourniture aux entreprises pharmaceutiques et biotechnologiques de la fabrication d’API peptidiques cGMP à petite et grande échelle. Grâce à son expertise et à ses capacités dans toutes les technologies de fabrication synthétique, CordenPharma Brussels évalue et personnalise son approche pour obtenir le processus de fabrication le plus efficace pour ses clients. Nous recherchons un QC Technicien pour rejoindre notre département Quality Control. Le QC Technician travaille au sein du laboratoire Contrôle de Qualité. Son rôle consiste à s’assurer, par diverses analyses, que les produits soient fabriqués, conservés et conditionnés dans le respect des cGMP. Il applique et respecte les règles de sécurité, les procédures internes, les cGMP et les délais qui lui sont donnés. Tâches et responsabilités >> Assure et interprète des analyses (matières premières, contrôle en cours de fabrication (IPC), intermédiaires, produits finis, échantillons de stabilité) >> Assure le double-check des analyses de ses collègues et réalise des maintenance d’appareil lorsque cela est nécessaire. >> Réalise des études d’applicabilité pour la teneur en eau par Karl-Fisher sur des matières premières, intermédiaires ou produits finis. >> Participe ou Dirige des projets d’amélioration continue au sein du laboratoire QC afin d’améliorer la performance et/ou l’efficacité des techniciens Profil et compétences >> Graduat en chimie/biochimie (baccalauréat) >> Expérience professionnelle confirmée dans une fonction similaire de minimum 3 ans >> Connaissance pratique des techniques d’analyse physico-chimiques (HPLC, UHPLC, IC, GC, potentiométrie, titration, UV, IR entre autres) >> Expérience (c)GMP indispensable avec connaissance approfondie des (c)GMP applicables au QC. >> Rigueur et souci du détail >> Excellentes capacités d’organisation, d’analyse et de coordination >> Esprit d’équipe et capacité à travailler dans un environnement interdisciplinaire et international. >> Excellentes aptitudes à la communication orale et écrite (anglais et français) et à la collaboration transversale. >> Connaissance pratique des applications Microsoft (Word, Excel et PowerPoint) et des logiciels chromatographiques (Empower, ou Openlab). La connaissance de LIMS et Trackwise sont considérés comme atouts. Notre offre Nous offrons un contrat permanent, un salaire compétitif et des responsabilités variées et motivantes. Horaire en shift : 6h – 14h & 14h – 22h (5j/7) Dans ce cas, nous devrions absolument faire connaissance. Nous nous réjouissons de recevoir votre candidature via le lien ci-dessous ou sur jobs.brusselscordenpharma.com
Process Development Scientist – Downstream
Corden Pharma, Brussel, Brussel Hoofdstad, Bruxelles
CordenPharma est un partenaire de premier plan en matière de développement et de fabrication sous contrat (CDMO) avec environ 2000 employés à travers l’Europe et les États-Unis et un chiffre d’affaires annuel > 500 M€, permettant aux entreprises pharmaceutiques et biotechnologiques de lier leurs exigences en matière de succès des produits à la vie plus saine de leurs patients. Fondé en 1987, CordenPharma Brussels (précédemment connu sous le nom de Peptisyntha Brussels) faisait partie du groupe Solvay jusqu’à son acquisition par CordenPharma en octobre 2013. CordenPharma Brussels a accumulé plus de 30 ans de succès dans la fourniture aux entreprises pharmaceutiques et biotechnologiques de la fabrication d’API peptidiques cGMP à petite et grande échelle. Grâce à son expertise et à ses capacités dans toutes les technologies de fabrication synthétique, CordenPharma Brussels évalue et personnalise son approche pour obtenir le processus de fabrication le plus efficace pour ses clients. Nous recherchons un QC Technicien pour rejoindre notre département Quality Control. Le QC Technician travaille au sein du laboratoire Contrôle de Qualité. Son rôle consiste à s’assurer, par diverses analyses, que les produits soient fabriqués, conservés et conditionnés dans le respect des cGMP. Il applique et respecte les règles de sécurité, les procédures internes, les cGMP et les délais qui lui sont donnés. Tâches et responsabilités >> Assure et interprète des analyses (matières premières, contrôle en cours de fabrication (IPC), intermédiaires, produits finis, échantillons de stabilité) >> Assure le double-check des analyses de ses collègues et réalise des maintenance d’appareil lorsque cela est nécessaire. >> Réalise des études d’applicabilité pour la teneur en eau par Karl-Fisher sur des matières premières, intermédiaires ou produits finis. >> Participe ou Dirige des projets d’amélioration continue au sein du laboratoire QC afin d’améliorer la performance et/ou l’efficacité des techniciens Profil et compétences >> Graduat en chimie/biochimie (baccalauréat) >> Expérience professionnelle confirmée dans une fonction similaire de minimum 3 ans >> Connaissance pratique des techniques d’analyse physico-chimiques (HPLC, UHPLC, IC, GC, potentiométrie, titration, UV, IR entre autres) >> Expérience (c)GMP indispensable avec connaissance approfondie des (c)GMP applicables au QC. >> Rigueur et souci du détail >> Excellentes capacités d’organisation, d’analyse et de coordination >> Esprit d’équipe et capacité à travailler dans un environnement interdisciplinaire et international. >> Excellentes aptitudes à la communication orale et écrite (anglais et français) et à la collaboration transversale. >> Connaissance pratique des applications Microsoft (Word, Excel et PowerPoint) et des logiciels chromatographiques (Empower, ou Openlab). La connaissance de LIMS et Trackwise sont considérés comme atouts. Notre offre Nous offrons un contrat permanent, un salaire compétitif et des responsabilités variées et motivantes. Horaire en shift : 6h – 14h & 14h – 22h (5j/7) Dans ce cas, nous devrions absolument faire connaissance. Nous nous réjouissons de recevoir votre candidature via le lien ci-dessous ou sur jobs.brusselscordenpharma.com
Application Development Scientist Coatings
, zwijnaarde, BE
ResponsibilitiesThis role is responsible for developing new products or new applications for existing products enabling industrial coatings formulators to differentiate performance, reduce cost and increase efficiency. The position reports to the EMEA coatings group leader and supports customers in the region but also operates within a global industrial team. Job Responsibilities:Safety:- Comply with all corporate, division, and group safety requirements- Demonstrate commitment to continuous safety improvement and model good safety behaviorsTechnical:- Following the stage gate process apply deep understanding of coatings and regulatory requirements to develop new products or new applications for existing products that enable coatings formulators to differentiate performance, reduce cost and increase efficiency- Engage with customers to discover needs, match fitness for use characteristics with product offerings, and support the engagements through final commercialization.- Determine fitness:for:use criteria for specific industrial coatings applications and reduce these to formulation characteristics using knowledge of coatings structure:process:property relationships- Select raw materials for starting point formulations to test developmental resins, pigments, solvents, additives and other ingredients- Provide technical support to manufacturing and QC organizations during product scale up and commercialization.- Develop new technical literature to support new products, applications or techniques- Establish peer level connect with universities, research institutes, co:suppliers and customers to identify potential opportunities for synergies and joint development.- Provide regular insights on new technologies, applications and competitive solutions in the architectural coatings segment and play a key role in development of Eastman's intellectual property strategy.- Oversee testing of coatings to industry standards- Support quality, health, and safety initiatives as they relate to formulation, material safety, and technical data sheets.- Mentor and support development of technicians.- Works closely with the European technical service team and Eastman's customers to support them on new product launches.Communication:- Assess and communicate customer needs and project results to marketing, manufacturing, technology, and business partners, tailoring the communication to the audience- Attend trade shows / technical conferences to align with market trends and establish/strengthen market connect.- Document results accurately and in a timely manner using e:notebook, technical reports, and invention reports, as required- Network with a cross functional team across R and D, marketing, sales and manufacturing to develop products and understand the application of these products so that they can be translated quickly from the lab to commercial scaleQualifications: Master/PhD in coatings, polymer science, physics, chemical engineering, chemistry, materials science, or a related field: At least 5 years of research experience working with coatings design, formulation and testing. Experience with coil, wood or protective coatings is highly desired: Excellent written and oral communication skills in English. Knowledge of other European languages is a plus.: Ability to work in Ghent, Belgium: The candidate is required to travel up to 25 of their time.