Senior Analyst, QC Chemistry

BeiGene•Hopewell, NJ

7d•$90,900 - $125,900•Onsite

About The Position

Perform QC Chemistry laboratory activities to support GMP manufacturing, testing and release of materials, intermediates and finished products under FDA/EU regulations, applicable International Regulations, BeOne processes and procedures. Establishes and implements QC Chemistry procedures and supports regulatory compliance inspections. Ensures efficient and effective day-to-day operations of the Chemistry laboratory. This position reports to the QC Sr. Manager and is located full-time at the Hopewell, NJ site.

Requirements

Expertise in Quality Control (QC) within a Good Manufacturing Practice (GMP) environment, ensuring compliance with industry standards and regulations through hands-on laboratory experience.
Working knowledge and experience with analytical methods such as GC, HPLC, UPLC, IEF, TOC, UV, FTIR, etc.
Knowledgeable with USP/EP and cGMP/EU GMP regulations.
Familiar with instrument and equipment validation.
Expert knowledge of quality control principles, practices and standards for the biopharmaceutical industry.
Impressive, demonstrable track record and skills/experience gained within a similar position(s), at a similar level.
Credible and confident communicator (written and verbal) at all levels.
Strong analytical, problem-solving ability, with excellent attention to detail, with the ability to work accurately in a busy and demanding environment.
Hands-on approach, with a ‘can do’ attitude.
Ability to prioritize, demonstrating good time management skills.
Self-motivated, with the ability to work proactively using own initiative.
Committed to learning and development.
Interacts with all levels of BeOne employees
Bachelor’s or above in Chemistry, Biochemistry, or Biotechnology related scientific discipline.
Minimum of 4+ years of working experience in an FDA-regulated biotechnology, pharmaceutical company are required.
Familiar with Waters Empower Chromatography Data System.
Strong PC literacy required; MS Office skills (Outlook, Word, Excel, PowerPoint).
Ability to work on a computer for extended periods of time

Nice To Haves

Serving as subject matter expert in one or more areas of required testing.
Strong leadership/team management skills and experience.

Responsibilities

Perform routine and non-routine testing using HPLC, UPLC, UV-Vis, capillary electrophoresis, and other techniques (PS-20, HPLC-SEC, TOC, Conductivity, CZE, etc.) in the QC Chemistry and Raw Materials laboratory to ensure timely and compliant generation and reporting of in-process, release, and stability test results in support of large molecule manufacturing operations.
Review, interpret, and report analytical data in accordance with GMP regulations and internal procedures.
Ensure appropriate investigation of OOS events, discrepancies, lab errors, and equipment failures.
Implement corrective actions and preventive actions (CAPAs).
Participate in transfer and method validation activities, including protocol preparation, protocol execution and report preparation.
Support routine operations, including but not limited to instrument qualification and maintenance, SOP generation and revision, test record keeping, etc.
Maintain equipment in a qualified and calibrated state, coordinating with metrology or vendors as needed.
Manage inventory of reagents and supplies for the laboratory.
Participate in internal and external GMP audits and inspections, as needed.
Train other junior level analysts and new hires on instrumentation, GMP practices, and data analysis.
Serving as subject matter expert in one or more areas of required testing.
Undertake other duties as required.
Ensure timely completion of testing (e.g., In-process control, DS release, DP release, and stability testing) to ensure timely generation and reporting of test results in support of manufacturing operations.
Review of laboratory test results, ensuring adherence to Good Documentation Practices.