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
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• 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.

Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.