Role & responsibilities

QC Incharge and Micro Incharge.

- Lead and manage Quality Control (QC) operations for Chemical, Instrumental and Microbiology laboratories.
- Ensure testing of Raw Materials, Packaging Materials, In-process Samples, Finished Products, Stability Samples and Water Samples as per approved specifications.
- Review and approve analytical reports, laboratory records, SOPs, STPs and specifications.
- Handle and troubleshoot analytical instruments such as HPLC, GC, UV-Visible Spectrophotometer, FTIR, Dissolution Apparatus and other QC instruments.
- Supervise microbiological activities including environmental monitoring, water testing and microbial limit testing.
- Investigate OOS, OOT, deviations and implement CAPA.
- Ensure compliance with cGMP, GLP, Data Integrity (ALCOA+) and regulatory requirements.
- Coordinate method validation, method transfer and stability studies.
- Lead and mentor the QC team and ensure timely completion of testing and documentation.




- Support internal, customer and regulatory audits.

Preferred candidate profile

- Bachelor's or Master's degree in B.Pharm, M.Pharm, M.Sc. (Chemistry) or M.Sc. (Microbiology).
- 813 years of experience in Pharmaceutical Quality Control (Formulation).
- Strong hands-on experience in Chemical QC, Instrumental Analysis and Microbiology.
- Hands-on experience with HPLC, GC, UV-Visible Spectrophotometer, FTIR, Dissolution and other analytical instruments.
- Good knowledge of cGMP, GLP, Data Integrity (ALCOA+), OOS/OOT, CAPA and Regulatory Compliance.
- Experience in handling laboratory documentation, stability studies and audit readiness.
- Robust leadership, communication and team handling skills.
- Experience in OSD and/or Ointment/Cosmetic Formulation will be preferred.

📌 Manager/ Assistant Manager- QC/ Micro (Baddi)
🏢 Allrite Pharmaceuticals
📍 Baddi