We are looking for a Analytical Chemist, working in the Pharmaceuticals & Medical Products industry in Andover, Massachusetts, United States.
Facilitates, proposes and/or performs analytical method validation gap assessments through collaboration with SMEs
Authors and reviews findings from the assessments into reports utilizing a supplied format
Supports gap remediation work in the form of executing laboratory validation test plans/protocols when required per remediation plans
Provides input to SOPs, validation protocols and reports
The pay we are offering is 33 per hour. This position may present an opportunity to go permanent.
Our client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
BS/MS degree in chemistry, biochemistry, biology or related discipline
Proficiency in standard bioanalytical techniques such as HPLC and UV-Vis spectroscopy is highly preferred
Experienced in authoring technical reports, documents and/or professional journal articles
Prior biopharmaceutical experience in a relevant GMP role (validation, quality control, quality assurance etc.), as well as familiarity of cGMPs, FDA and other regulatory guidelines (ICH, USP, EP) as it pertains to analytical method validation, is preferred but not required
Proficiency in Microsoft Office (Excel functions, Word and PowerPoint)
What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.