Quality Control Analyst II at BioPharma Consulting JAD Group

Norton, Massachusetts, United States -

Full Time

Start Date

Immediate

Expiry Date

06 Jun, 26

Salary

0.0

Posted On

08 Mar, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Hplc/Uplc, Microbiological Assays, Method Transfers, Validation, Data Review, Sop Creation, Gmp, Glp, Ich Guidelines, Continuous Improvement, Audit Support, Technical Writing, Data Analysis, Problem-Solving, Organizational Skills, Communication

Industry

Biotechnology Research

Description

The Quality Control Operations (QCO) Analyst II Contractor plays a key role in ensuring the highest standards of quality and compliance across development, manufacturing, and commercialization activities. This position performs routine and non‑routine testing, supports method transfers and validation activities, contributes to investigations and data trending, and assists with daily laboratory operations. The role is essential in driving QC efficiency, accuracy, and continuous improvement. Key Responsibilities Perform routine and non‑routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in‑process samples, product release, and stability studies in accordance with SOPs. Support weekend laboratory operations and maintain up‑to‑date training records. Assist with laboratory equipment maintenance, inventory management, reagent preparation, and sample handling. Review analytical data in a timely manner and serve as a qualified data reviewer. Execute operational assignments including raw material processes, environmental monitoring, and in‑process testing. Contribute to the revision and creation of controlled documents such as SOPs, work instructions, and test methods. Adhere to internal policies, SOPs, and regulatory requirements including GMP, GLP, and ICH guidelines. Participate in continuous improvement initiatives and collaborate cross‑functionally to enhance QC operations. Support regulatory submissions, inspection readiness activities, and internal/external audits. Qualifications: B.S. in Chemistry, Biology, Biochemistry, or a related scientific discipline. 4–8 years of pharmaceutical or biotech experience in a GMP QC environment or equivalent. Experience with method transfer and implementation; familiarity with method lifecycle management is preferred. Strong technical writing, data analysis, problem‑solving, and organizational skills. Excellent communication skills and ability to work effectively in a team‑oriented environment. Proficiency with LabWare LIMS, Microsoft Excel, Word, and PowerPoint preferred. Weekend Shift Role 10-month contract with possible extension

Responsibilities

This role involves performing routine and non-routine analytical and microbiological testing for various samples in compliance with standard operating procedures. The analyst will also assist with laboratory operations, including equipment maintenance, inventory management, and contributing to controlled document revisions.