Quality Control (QC) Officer / Executive – Pharmaceutical Manufacturing

Umendra Life Sciences Pvt. Ltd.; Ahmedabad District; On-site; INR 300,000 - 400,000; Full time

Job summary

A pharmaceutical manufacturing facility in Gujarat seeks motivated individuals for a QC role. Responsibilities include HPLC testing, raw material sampling, and maintaining GLP-compliant records. Candidates should possess a B.Pharm or similar degree; freshers and those with 1-3 years of relevant experience are encouraged to apply. A strong understanding of QC instruments and documentation practices is essential. If you're detail-oriented and ready for a structured lab environment, consider joining the team.

Qualifications

• Freshers welcome; 1–3 years hands-on experience preferred.
• Strong academic lab fundamentals are essential.

Responsibilities

• Perform HPLC, IR, pH, and testing of bulk and finished products.
• Conduct chemical and physical tests on raw materials and packaging.
• Collect and test water samples for quality monitoring.
• Maintain GLP-compliant records and documentation.
• Assist in COA preparation and product release documentation

Skills

HPLC experience

IR spectroscopy knowledge

Understanding of GLP principles

Knowledge of GMP documentation standards

Familiarity with COA preparation

TOC analysis experience

OOS/OOT handling

Water QC testing

Education

B.Pharm / M.Sc Chemistry / B.Sc Chemistry

Tools

pH meters

Viscometers

Job description

Umendra Life Sciences Pvt Ltd is an export-oriented pharmaceutical manufacturing facility based in Bavla, Gujarat, specializing in topical OTC products including creams, ointments, gels, and lotions. Our QC laboratory operates to international GMP/GLP standards and supports end-to-end quality assurance — from raw material intake to finished product release. We are expanding our QC team and are looking for motivated individuals who are ready to work in an active manufacturing lab environment.

About the Role

Depending on your specialization, you will be assigned to one or more of the following QC functions:

Responsibilities

Analytical Testing

• Perform HPLC, IR, pH, and other instrument-based testing of bulk and finished products
• Interpret results, identify deviations, and elevate OOS findings per SOP
• Prepare and review Certificates of Analysis (COA)
• Perform routine calibration checks, system suitability tests, and basic instrument troubleshooting as per SOP

Raw Material & Packing Material QC

• Perform sampling of incoming raw materials and packaging components per approved sampling plans
• Conduct chemical and physical tests; record and review results against specifications
• Maintain traceability and disposition records

Water System Monitoring

• Collect and test water samples from designated sampling points (purified water, WFI where applicable)
• Operate and maintain TOC analyzer; record and trend water quality data
• Flag exceedances and elevate as per water monitoring SOP

GMP/GLP Documentation & QC Records

• Maintain raw data sheets, logbooks, and analytical records in GLP-compliant format
• Support QC document review, batch record checks, and data integrity verification
• Assist in preparation of COAs and product release documentation
• Follow GMP and GLP guidelines during all sampling, testing, documentation, and data recording activities.
• Support internal, regulatory, and customer audits by maintaining accurate and retrievable QC records.

Qualifications

• Education: B.Pharm / M.Sc Chemistry / B.Sc Chemistry or a closely related science discipline
• Experience: Freshers with strong academic lab fundamentals are welcome; candidates with 1–3 years of hands‑on experience in a pharmaceutical manufacturing QC lab are preferred

Please note: This is a manufacturing QC role. Candidates with experience limited to academic research labs, college labs, or R&D/analytical research settings should assess carefully before applying — the day‑to‑day work is production‑support focused, documentation‑heavy, and operates under strict GMP/GLP compliance requirements.

Required Skills

• Hands‑on experience or strong working knowledge of HPLC, IR spectroscopy, pH meters, viscometers, and other QC instruments
• Understanding of pharmacopoeial methods (IP/BP/USP) for raw materials and finished products
• Knowledge of GLP principles and GMP documentation standards
• Familiarity with COA preparation and OOS/OOT handling procedures
• TOC analysis experience is a plus
• Facility type: Active pharmaceutical manufacturing site — this is not an office or R&D environment
• Lab setting: Regulated QC laboratory operating under GMP/GLP; all activities are documented and subject to audit
• Pace: Production‑linked; test turnaround times are tied to manufacturing schedules
• Shift: General shift with potential for schedule adjustments based on production demand
• Physical requirements: Standing for extended periods, handling chemical reagents and solvents, routine instrument operation and maintenance

If you thrive in structured environments, care about precision, and want to build a career in pharmaceutical quality — this is a good fit.

Application Instructions

To apply, please:

• Click Apply and answer all screening questions completely — incomplete responses will not be reviewed
• Attach your updated resume (PDF or Word format)
• In your application, mention your area of QC experience (Analytical / RM‑PM / Water / Documentation) so we can route your profile to the right team lead

Shortlisted candidates will be contacted for an initial telephonic/video discussion followed by a practical and technical interview at our Bavla facility.

Equal Opportunity Statement

We are committed to diversity and inclusivity in our hiring practices.