Quality Control Jobs at GSK
A rare chance has emerged for qualified professionals to join GSK as a QC Analyst in Nashik, Maharashtra. The Quality Control Jobs at GSK Careers in Nashik require 3–4 years of experience in a QC laboratory, focusing on HPLC, stability, and formulations. Interested candidates are encouraged to apply before the deadline for the HPLC stability analyst Role.
About GSK
GlaxoSmithKline (GSK) is a global biopharma company dedicated to uniting science, technology, and talent to combat diseases. With a commitment to delivering high-quality medicines and vaccines, GSK operates a network of manufacturing sites that produced 1.7 billion packs of medicines and 409 million vaccine doses in 2024. The organization is focused on innovation in specialty medicines and vaccines, aiming to positively impact the health of 2.5 billion people by the end of the decade.
- Company: GlaxoSmithKline
- Location: Nashik, Maharashtra, India
Job Description
The QC Analyst will join the Quality Control team and will be responsible for performing laboratory testing, managing samples, and recording clear, accurate data. The role involves collaboration with colleagues across QC, production, and quality systems to ensure tests meet regulatory and company standards.
Key Responsibilities
- Perform routine and non-routine analytical tests following approved methods and good documentation practices in the Quality Control Jobs in Nashik.
- Receive, register, prepare, and store samples according to laboratory procedures and safety rules as an HPLC stability analyst.
- Record and review test results against specifications and report deviations or unexpected trends promptly in the Quality Control Jobs.
- Carry out basic equipment checks, clean work areas, and support calibration and maintenance activities at GSK Careers.
- Support method transfers, validations, and investigations into unexpected results or out-of-specifications.
- Maintain clear laboratory records and contribute to continuous improvement and efficiency projects.
Eligibility Criteria for the Quality Control Jobs
- Experience Required: 3–4 years in a QC laboratory (stability, creams/ointments/tablets)
- Educational Qualifications: M.Pharm / M.Sc / B.Pharm
- Diploma or degree in Chemistry, Microbiology, Biotechnology, Life Sciences, or a related field.
- Hands-on experience or coursework in laboratory techniques and safe sample handling.
- Strong attention to detail and accurate record keeping.
- Ability to follow written procedures and laboratory protocols.
- Effective verbal and written communication skills in English.
- Willingness to work on-site in a laboratory environment and follow site safety requirements.
Required Skills
- Hands-on experience in operation, analysis, troubleshooting, and maintenance of HPLC / UPLC, UV, FTIR, and other analytical instruments.
- Knowledge of analytical testing and method execution as per pharmacopoeial requirements is required for the Quality Control Jobs.
- Experience in stability testing and routine QC laboratory operations.
- Strong analytical, documentation, and problem-solving skills.
