We're looking for a Quality Control Scientist I, working in the Pharmaceuticals & Medical Products industry in Framingham, Massachusetts, United States.
Performs qualification in a cGMP biotech manufacturing facility.
Manages multiple complex qualification projects and provides technical assistance to less experienced team members.
Writes and reviews qualification protocols and reports as well as execute protocol.
Resolves protocol discrepancies and deviations.
Evaluates new technologies platforms for implementation in the quality control laboratories.
We are offering Competitive Compensation and Benefits. 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
Bachelors degree in Life Sciences discipline and 5 years of experience in cGMP lab environment; Masters degree in Life Sciences discipline and 3 years experience in cGMP lab environment; PhD in Life Sciences discipline and 0-3 years experience in cGMP lab environment.
Ability to present technical data.
Ability to work independently on scientific projects.
Scientific technical writing ability authoring and reviewing SOPs, qualification protocols and technical reports.
Experience troubleshooting of assay and equipment issues Knowledge of Validation Lifecycle Approach.
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.