QC Executive - Pharmaceutical

Umendra Life Sciences Pvt. Ltd.; Ahmedabad District; On-site; INR 400,000 - 650,000; Full time

Job summary

Umendra Life Sciences Pvt. Ltd. is expanding its Quality Control team at the Bavla plant, 35–40 km from central Ahmedabad.

This on-site role involves testing across raw materials, packing materials, bulk and finished goods against approved specifications, with COA preparation and review. Candidates should have 1–9 years of hands-on QC experience in pharma or personal-care manufacturing, and hold a B.Sc./M.Sc. (Chemistry) or B.Pharm/M.Pharm.

Qualifications

• B.Sc./M.Sc. in Chemistry or B.Pharm/M.Pharm; bench experience with instruments.
• Strong GMP and data integrity adherence; SOP-driven work.
• 1–9 years hands-on QC in pharma/personal-care manufacturing.
• Able to work on-site at Bavla plant; non-negotiable.

Responsibilities

• Test across RM/PM, bulk and finished goods vs specs; prepare COA.
• Sampling and testing of RM/PM; TOC/water testing; instrument calibration.
• Stability testing and documentation kept audit-ready.
• OOS/OOT investigations and closure; data traceability (ALCOA+).
• Mentor officers/chemists; own RM review and stability documentation for seniors.

Skills

Laboratory testing

Analytical thinking

Data integrity

Documentation

ALCOA+

Education

B.Sc./M.Sc. (Chemistry)

B.Pharm/M.Pharm

Tools

HPLC

GC

UV-Vis Spectrophotometer

Instrument calibration

Stability testing

COA preparation

STPs/STSs

SOP upkeep

Job description

Umendra Life Sciences manufactures OTC topical products — creams, gels, lotions, ointments — for regulated export markets, primarily the US. We are looking to expand our Quality Control team, and individuals with varying degrees of experience are encouraged to apply

What you'll own

• Testing across raw materials, packing materials, bulk and finished goods against approved specifications, with COA preparation and review.
• Sampling and testing of RM/PM, TOC/water testing, and instrument calibration.
• Stability testing and stability documentation kept audit-ready.
• Working standards management, STPs, STS and SOP upkeep.
• OOS/OOT and incident handling — documentation, investigation, closure.
• AMV & CV (analytical method and cleaning validation) support.
• Contemporaneous, data-integrity-compliant (ALCOA+) recording — no back-filling, no shortcuts — keeping the lab inspection-ready at all times.
• Officer: sampling and routine RM/PM/FG testing, COA preparation, documentation.
• Executive: independent testing across streams, stability and validation execution, STP/STS ownership.
• Senior Executive: owns RM review, stability documentation, OOS/OOT investigations, calibration and training; mentors officers and chemists.

Who fits

• Able to work on-site at our Bavla plant (35–40 km from central Ahmedabad). This is a plant role — non-negotiable.
• 1–9 years of hands-on QC experience in pharma or personal-care manufacturing — the offer level matches your depth.
• B.Sc./M.Sc. (Chemistry) or B.Pharm/M.Pharm; genuinely comfortable on the bench and on the instruments.
• Strong grip on GMP, data integrity and SOP-driven working. Compliance is the job, not overhead.
• Senior candidates: demonstrable ownership of stability, method/cleaning validation and investigations — not just routine analysis.

What this role is not

• Not remote, not a corporate or head-office QA desk.
• Not a paperwork-only position — you'll be on instruments and in the lab daily.