Analytical Chemist – Product Development

Job Description

• Ability to work in a GLP or GMP environment with appropriate documentation and safety practices
• Support formulation development through hands-on generation of accurate and precise analytical chemistry data using routine laboratory techniques such as liquid chromatography (HPLC, UPLC), NMR (liquid), mass spectrometry, vibrational spectroscopy, USP/EP dissolution testing, Karl Fischer titration
• Development of dissolution methodology that will provide some measure of an in vivo / in vitro relationship and serve as a quality control procedure
• Development and execution of studies to ascertain degradation mechanisms in the solution and solid state
• Assessment of stability risks by evaluating process changes and impact on degradation chemistry or dissolution profile. This would involve DoEs and accelerated stability studies
• Development of assay/purity methods and assessment of method robustness/ruggedness
• Development and execution of method validation protocols
• Transfer of analytical methods to other laboratories and remote sites
• Hands-on generation of data in support of accelerated and registration stability studies
• Leadership responsibilities are in addition to technical roles both in and outside of the lab
• Provide managerial oversight of on-site team personnel
• Serve as liaison between the client and the team
• Lead team, schedule, and train employees in client environment
• Ensure adherence to highest quality and efficiency standards in laboratory operations
• Ensure coverage and performance
• Foster morale and teamwork
• Provide process improvements and best practices to support productivity initiatives

Qualifications

• Bachelor’s degree in chemistry or other related degree concentration and 5+ years of experience in product development analytical chemistry, or a Master’s degree in chemistry and 2+ years of experience in product development analytical chemistry
• Master’s degree in analytical chemistry is preferred
• Minimum 5 years of experience in the pharmaceutical industry
• Experience supervising a team
• Strong computer, scientific, and organizational skills
• Excellent communication (oral and written) and attention to detail
• Ability to work independently and as part of a team, self-motivated, adaptable, andapositive attitude
• Proficient in analytical chemistry techniques, able to perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
• Strong leadership, initiative, and team building skills
• Authorization to work in the United States indefinitely without restriction or sponsorship

Additional Information

Position is full-time Monday-Friday, 8a.m.-5p.m. Candidates currently living within a commutable distance of Groton, CTare 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