Company Description
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.
Job Description
We are seeking a solid oral dosage form pharmaceutical formulation expert to:
- Support the design, execution, and analysis of drug product experimentation for establishing the pathway from early to late-stage development of commercial drug product manufacturing processes and regulatory control strategies.
- Contribute to the authorship of development and regulatory documentation, including technical contributions to new drug product submissions.
- Assist in the build and review of formulation recipes and manufacturing batch records.
- Participate regularly in team meetings to contribute their technical knowledge for analysis of development data and provide recommendations for troubleshooting remediation.
Qualifications
The individual should have a BS or MS in chemistry or related science, extensive experience (15+ years) in solid oral dosage form (tablets and capsules) development, regulatory interactions, and manufacturing processes.
Additional Information
Position is Monday- Friday 8:00 am-5:00 pm. Overtime as needed. Candidates currently living within a commutable distance of Groton, CT 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.
- Authorization to work in the United States indefinitely without restriction or sponsorship.
Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
