Role & responsibilities

- Analyse raw materials, intermediates, in-process samples, finished APIs, and stability samples as per approved specifications and analytical methods.
- Operate and maintain HPLC, GC, UV-Visible spectrophotometer, FTIR, Karl Fischer apparatus, and other QC instruments, as applicable.
- Perform wet chemical analysis, titrations, assay, impurity profiling, and other routine laboratory tests.
- Prepare reagents, mobile phases, volumetric solutions, and reference standards.
- Maintain accurate analytical records, test reports, Certificates of Analysis (CoAs), and instrument logbooks.
- Ensure compliance with cGMP, GLP, GDP, SOPs, and ALCOA+ data integrity principles.
- Report and support investigations of OOS/OOT results, deviations, and laboratory incidents.
- Support method validation, verification, transfer, CAPA, audits, and regulatory inspections, as assigned.




- Ensure laboratory safety, proper chemical handling, sample traceability, and timely completion of testing.

Preferred candidate profile

- Qualification: M.Sc. Chemistry (Analytical/Organic),
- Experience: 3-5 years Quality Control in an API/pharmaceutical
- Technical Skills: Hands-on experience in HPLC, GC, wet chemical analysis, and other relevant analytical instruments.
- Quality Compliance: Working knowledge of cGMP, GLP, GDP, SOPs, , and data integrity practices.
- Key Competencies: Robust analytical ability, attention to detail, troubleshooting skills, documentation accuracy, integrity, and commitment to quality and safety.

Freshers M.Sc. Chemistry may be considered for trainee positions.

📌 Quality Control Analyst / Chemist (Rajpura)
🏢 Valence Labs
📍 Rajpura