Quality Control (QC), Quality Assurance (QA)

Morepen Laboratories Ltd., one of India's leading pharmaceutical and API manufacturing companies, has announced a Walk-In Recruitment Drive for experienced professionals in the Quality Control (QC) and Quality Assurance (QA) departments at its Baddi API Division. This recruitment offers an excellent opportunity for candidates with experience in API manufacturing, analytical instrumentation, and quality systems to become part of a reputed organization known for its commitment to quality and innovation.

The walk-in interview is scheduled for Sunday, 09 August 2026, at the company's Baddi API manufacturing facility in Himachal Pradesh.

Company Name

Morepen Laboratories Ltd.

Division

Baddi API Division

Departments Hiring

• Quality Control (QC)

• Quality Assurance (QA)

Open Positions

Chemist / Senior Chemist – Quality Control (Instrumentation)

The company is looking for experienced Quality Control professionals with strong expertise in analytical instrumentation used in pharmaceutical laboratories.

Key Responsibilities

• Perform analytical testing using sophisticated laboratory instruments.

• Maintain high standards of quality and laboratory compliance.

• Operate and troubleshoot analytical instruments.

• Ensure accurate documentation and adherence to GMP and laboratory procedures.

• Follow SOPs and regulatory guidelines during analysis.

Preferred Instrument Experience

Candidates should have hands-on experience with:

• High Performance Liquid Chromatography (HPLC)

• Gas Chromatography (GC)

• Mass Spectrometry (MS)

• Dissolution Testing

• HPLC Systems

• UV/Visible Spectrophotometer (PC-Vis)

• Instrument Control Software

• Laboratory Instrumentation and Power Systems

Chemist / Senior Chemist – Quality Assurance

Morepen Laboratories is also hiring experienced professionals for the Quality Assurance department.

Key Responsibilities

• Perform in-process quality assurance activities.

• Monitor shop-floor GMP compliance.

• Handle investigations related to Out of Specification (OOS) results.

• Manage Deviations and CAPA (Corrective and Preventive Actions).

• Prepare and review QMS documentation.

• Ensure compliance with cGMP, regulatory requirements, and internal quality systems.

Experience Required

1 to 4 Years

Eligibility Criteria

Candidates should have:

• Experience in pharmaceutical API manufacturing.

• Knowledge of analytical instruments and laboratory operations (for QC roles).

• Understanding of GMP, QMS documentation, regulatory compliance, and quality systems.

• Experience in OOS investigations, Deviations, CAPA, and in-process quality assurance for QA positions.

Walk-In Interview Details

Interview Date: Sunday, 09 August 2026

Interview Venue

Morepen Laboratories Ltd.
Village Morepen,
Tehsil Nalagarh,
District Solan – 173205,
Himachal Pradesh

Application Process

Candidates who are unable to attend the walk-in interview may share their updated resume with the HR team.

Email: baddi@morepen.com

Candidates may also contact the Baddi Office for further information regarding the recruitment process.

Why Join Morepen Laboratories?

• Opportunity to work with one of India's well-established API manufacturers.

• Exposure to advanced analytical instruments and modern quality systems.

• Career growth in Quality Control and Quality Assurance functions.

• Professional work environment with continuous learning opportunities.

• Strong focus on innovation, regulatory compliance, and employee development.