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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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It 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. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer 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 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.

+ Set-up and facilitate key analytical-focused team meetings

+ Coordinate authoring, review and approval of critical analytical documents

+ Perform second-person review on analytical reports and memos

+ General operational support for analytical working groups for commercial biologic/vaccine programs

+ Collaborate across internal network, external partners, international governments and/or contract manufacturing and research organizations (CMO/CRO) in the area of large molecule analytics

+ Coordinate with analytical and process development groups to prepare for analytical troubleshooting, validation, and technology transfers

+ Support coordination of analytical activities across teams of subject matter experts to maintain or troubleshoot biochemical, immuno-chemical and chromatography-based analytical methods

+ Support coordination of analytical method transfers and/or assay method validations, including authoring and coordinating review of protocols and reports

+ Project manage change controls related to analytical method or specification change controls

Basic Minimum Qualifications:

+ Bachelor's of Science (Biology, Chemistry, Biochemistry or related sciences) AND two (2) years of working in a related role OR

+ Master's of Science preferably with experience in a related role

+ Minimum of two (2) years of large molecule (vaccine or biologics) method development, validation, or project management

+ Minimum of two (2) years of working knowledge of a GMP laboratory environment

+ Technical writing experience

+ Ability to work in a fast-paced team-oriented setting

+ Excellent communication (oral and written) and attention to detail

+ Authorization to work in the United States indefinitely without restriction or sponsorship

The Ideal Candidate would possess:

+ Proven ability to manage multiple projects/tasks simultaneously

+ Demonstrated self-starter with capability to develop innovative solutions to challenges

+ Excellent communication skills, oral and written

+ Strong organization and attention to detail

+ Ability to learn new techniques quickly, keep accurate records, follow instructions, and comply with company policies as well as regulatory/GMP requirements

+ Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude

+ GMP large molecule method development, validation, and/or project management experience

+ Understanding of regulatory filings (IND, MAA, BLA)

Change control experience

Position is full-time, Monday-Friday, generally 8 a.m. - 5 p.m. with overtime as needed. Candidates currently living within a commutable distance of West Point, PA are encouraged to apply.

+ Excellent full time benefits including comprehensive medical coverage, dental, and vision options

+ Life and disability insurance

+ 401(k) with company match

+ Paid vacation and holidays

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.