QC Analytical Development Chemist

22h22 hours ago

Bristol Myers Squibb

Shanghai, CN · Full-time · CNY 300,000 – CNY 500,000

About this role

Working at Bristol Myers Squibb means engaging in challenging, meaningful, life-changing work. Uniquely interesting projects happen daily, from optimizing production lines to breakthroughs in cell therapy, transforming patients' lives and careers. Employees grow through opportunities uncommon in scale alongside high-achieving teams.

Test finished products, raw materials, packing materials, intermediates, stability samples, and validation samples according to testing standards, general methods, Pharmacopeia, and SOPs. Provide timely and accurate analysis results and reports. Record test procedures and lab activities following SOP requirements.

Perform product validations per protocol, prepare and test solutions and buffers, and maintain assigned instruments through calibration and upkeep. Develop new analytical methods, ensure successful method transfers to SASS, and support new product registrations. Establish and revise related SOPs while maintaining a clean, safe laboratory environment.

Bristol Myers Squibb emphasizes balance and flexibility with a wide variety of benefits, services, and programs. Resources support pursuing goals at work and in personal lives. A supportive culture empowers individual talents with shared values of passion, innovation, urgency, accountability, inclusion, and integrity.

Requirements

Knowledge of testing standards, general methods, Pharmacopeia, and SOPs
Proficiency in analytical testing of raw materials, intermediates, and finished products
Experience in product validation and stability sample analysis
Skills in solution and buffer preparation, testing, and storage
Ability to perform instrument calibration, maintenance, and troubleshooting
Expertise in developing and transferring new analytical methods
Familiarity with GMP laboratory practices and waste handling
Understanding of pharmacopeial compliance and method validation protocols

Responsibilities

Test finished product, raw material, packing material, intermediate, stability sample and validation sample according to testing standard, general method, Pharmacopeia, etc., and provide timely and accurate results
Record test procedure and lab activity, report test results following SOP
Finish the validation of product according to the protocol
Prepare, store and test solution and buffer solution following manual or SOP
Accomplish the calibration and maintenance of assigned instruments to ensure they meet analytical needs
Develop new analytical methods
Ensure successful method transfer to SASS and support registration work of new products
Establish and revise related SOPs