Method Validation and Method Transfer Specialist
* Full-time
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.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 62,000 staff across a network of more than 1000 independent companies in over 62 countries and operating more than 900 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.
The Method Validation and Method Transfer Specialist will play a crucial role in the validation, verification, and transfer of analytical methods within the company. The ideal candidate will have substantial experience in analytical method validation/verification in the pharmaceutical industry and a strong understanding of Compendial and ICH requirements. This position requires basic knowledge of statistics and the ability to manage a diverse portfolio of activities including planning, resource estimation, risk identification, decision making, communication, and team leadership.
Key Responsibilities:
* Conduct and oversee analytical method validation, verification, and transfer activities in accordance with regulatory guidelines and company standards.
* Ensure compliance with Compendial (USP, EP, JP) and ICH requirements for analytical methods.
* Develop and execute method validation protocols and reports.
* Perform statistical analysis and interpretation of validation data.
* Coordinate cross-functional teams to ensure timely and successful method transfers.
* Identify and mitigate risks associated with method validation and transfer activities.
* Plan, organize, and manage resources effectively to meet project timelines.
* Communicate project status, issues, and risks to stakeholders and senior management.
* Participate in internal and external audits and regulatory inspections.
Minimum Requirements:
* Bachelor's or Master's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field.
* Minimum of 1 year of experience in analytical method validation/verification within the pharmaceutical industry.
* Experience with chromatographic techniques (HPLC, GC) and spectroscopic methods (UV, IR).
* Good knowledge of Compendial and ICH requirements.
* Familiarity with regulatory submission processes.
* Experience with Laboratory Information Management Systems (LIMS).
* Strong project management skills, including planning, resource estimation, and risk management.
* Excellent communication and interpersonal skills.
* Detail-oriented with strong problem-solving skills.
* Proficiency in Microsoft Office Suite and relevant analytical software.
* Ability to communicate in both English and French.
Benefits:
* A full-time (40 hours/week) Monday – Friday job.
* A Permanent contract with flexible working hours.
* Work in a fast-growing international organization.
* Eco-Cheques +/- 250 Euro/Year.
* Additional 12 ADV days.
* A company well-being program targeting both mental and physical well-being.
* A fantastic team with monthly team lunches, fun teambuilding activities (laser tag, escape rooms, sports, etc.) and above all; a great collaborative international work environment.
* Personal development through learning on the job and additional trainings.
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