Job Description

• Perform chemical testing of raw materials, intermediates, and Active Pharmaceutical Ingredients (APIs) in support of process research, discovery research, GMP production, and stability testing.
• Responsible for utilizing common analytical techniques such as: HPLC, GC, UV-Vis, LC-MS, KF, FTIR, NMR, Refractive index, and wet chemical methods such as titrations.
• Execute routine analysis with direction on more complicated analysis, method development, and project management.
• Apply basic scientific knowledge to perform analysis and to solve simple analytical problems.
• Learn and follow all Standard Operating Procedure (SOPs) and Good Manufacturing Practices. (GMPs)
• Revise SOPs, test methods, and GMP documents with guidance
• Conduct analysis and interpret results
• Transfer, modify, and improve analytical methods with guidance from experienced team members 
• Prepare scientific reports with guidance from experienced team members
• Review all data regarding raw materials, intermediates, and APIs
• Performs testing for the qualification of reference standards
• Perform cleaning validations and verifications
• Calibrate instruments and contribute to laboratory organization and compliance

Qualifications

• BS in Analytical Chemistry or equivalent with 1-2 years related experience in a pharmaceutical Quality Control environment
• Experience with common analytical techniques such as: NMR, UV, pH meter, KF, FTIR, Refractive index is required
• Experience with common analytical techniques such as: HPLC, GC, LC-MS is preferred
• Ability to read, analyze, and interpret English-language chemical periodicals, scientific journals, and regulatory documents
• Good written and verbal communication skills
• Good understanding of Microsoft Office and statistical software
• Ability to write clear and concise technical reports
• Ability to work independently with minimal supervision and in a team environment
• Demonstrate ability to exercise good judgment and make decisions quickly  
• Experience communicating effectively to management
• Experience in establishing integrated plans with resource and task constraints

Additional Information

Position is full-time, working four 10 hour days. Shifts will be either Monday - Thursday or Thursday - Sunday.  Candidates currently living within a commutable distance of Devens, MA 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 IS A M/F, DISABLED, AND VETERAN EQUAL EMPLOYMENT OPPORTUNITY AND AFFIRMATIVE ACTION EMPLOYER.