At Bristol-Myers Squibb, our mission is to discover, develop, and deliver innovative medicines that help patients prevail over serious diseases. As a Specialist in QC, you will play a crucial role in ensuring the quality and safety of our products by conducting thorough quality control testing and analysis. We are looking for a meticulous and detail-oriented individual with a strong understanding of QC principles and experience in a pharmaceutical or biotech setting. Join our team and make a difference in the lives of patients around the world.
- Conduct quality control testing and analysis of pharmaceutical products in accordance with established protocols and procedures.
- Perform routine and non-routine testing to ensure product quality, purity, and stability.
- Maintain accurate and detailed records of all testing and analysis performed.
- Identify and troubleshoot potential issues or discrepancies in test results and communicate them to the appropriate team members.
- Adhere to all safety protocols and maintain a clean and organized work environment.
- Collaborate with cross-functional teams to investigate and resolve any quality control issues.
- Stay updated on industry regulations and guidelines related to QC testing and ensure compliance with all applicable standards.
- Participate in the development and optimization of new QC methods and procedures.
- Assist in the training of new team members and provide guidance and support to junior staff.
- Contribute to continuous improvement efforts and participate in quality improvement initiatives.
- Communicate effectively with colleagues and management to provide updates on testing progress and results.
- Represent the company in a professional and ethical manner at all times.
- Act with a sense of urgency and prioritize tasks to meet timelines and deadlines.
- Continuously strive for excellence in all aspects of QC testing and analysis.
- Embrace and embody the company's mission and values in all job duties and interactions.
Bachelor's Degree In A Scientific Field, Such As Chemistry, Biology, Or Pharmaceuticals.
Minimum Of 3-5 Years Experience In A Qc Role In The Pharmaceutical Industry.
Strong Knowledge Of Regulatory Requirements And Industry Standards, Including Fda And Ich Guidelines.
Experience With Various Analytical Techniques And Instruments, Such As Hplc, Gc, And Spectrophotometry.
Excellent Communication And Problem-Solving Skills, With The Ability To Work Independently And In A Team Environment.
Data Analysis
Communication
Time Management
Analytical skills
Attention to detail
GMP
Quality Control
Compliance
SOPs
Teamwork
Laboratory Techniques
Problem-Solving
Communication
Conflict Resolution
Emotional Intelligence
Leadership
Time management
Interpersonal Skills
creativity
Teamwork
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Specialist, QC in Devens, MA, USA is $60,000 - $80,000 per year. This may vary depending on the specific job responsibilities, experience level, and company size.
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Bristol-Myers Squibb Co. operates as a biopharmaceutical company, which engages in the discovery, development, licensing, manufacturing, marketing, distribution, and sale of biopharmaceutical products. It includes chemically-synthesized drugs or small molecules and products produced from biological processes called biologics.

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