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 is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. 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.
In 2020, Eurofins generated total revenues of EUR € 5.4 billion, and has been among the best performing stocks in Europe over the past 20 years.
Summary: Supports lifecycle management within the QC Technical Resources groups. Utilizes and applies scientific knowledge and techniques to complete change controls, corrective actions, protocols and reports for transfers, validations and method performance
Analyzes and Monitors day-to-day method performance in QC lab, including determining if problem resolution requires appropriate subject matter expert to help with any method-related issues.
Works directly with Regulatory Sciences and External Manufacturing and partners and communicates timelines for method validation/transfers to managers in QC Tech Resources.
Communicates method updates to partners and tracks progress of updates.
Analyzes, assembles and/or coordinates method performance reports and quality metrics.
Implements multi-site method harmonization and reviews of method performance.
Participates in and coordinates post-transfer investigations between contract sites and collaborative partners.
Tracks team activities and timelines to ensure that the deliverables within the project plans are met and on time.
Escalates issues to management, as needed.
Coordinates multi-site trending and reviews and communicates information to SMEs, as needed.
Continuously drives to improve processes for improved performance.
Performs and/or coordinates assay qualification for the QC Group.
Drafts new or updated test procedures and assays for QC Group.
Performs and/or coordinates assay transfers from R&D, internally within QC or to business partners.
Authors and/or coordinates technical document preparation.
Owns and coordinates change controls and corrective/preventative actions
Participates in training programs for QC personnel.
Education and Experience:
Requires BS/BA in a Life Sciences field or equivalent combination of education and experience.
Knowledge, Skills and Abilities:
Additional Information
Position is full-time, 1st shift, Monday – Friday, 8:00am-4:30pm. Candidates currently living within a commutable distance of Rensselaer, NY and the surrounding areas are encouraged to apply.
Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
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