Senior Officer - Quality Control (RM/PM)

Why This Role Matters

Raw Materials (RM) and Packing Materials (PM) form the foundation of pharmaceutical product quality. Any compromise at this stage directly impacts product safety, stability, and regulatory compliance. Strict analytical control and documentation of incoming materials are essential to ensure consistency and GMP compliance.
At APDM Pharmaceuticals, the Officer / Sr. Officer / Executive / Sr. Executive – QC (RM/PM) plays a crucial role in testing, approving, and monitoring raw and packaging materials at the Sakodara, Gujarat facility. This role ensures that only quality-approved materials are released for production use.

Job Description

APDM Pharmaceuticals is hiring qualified professionals with 2 to 5 years of pharmaceutical Quality Control experience in Raw Material and Packing Material analysis. The selected candidate will be responsible for sampling, testing, documentation, and release of RM and PM as per approved specifications and pharmacopeial standards.
The role requires strong knowledge of analytical techniques, regulatory requirements, and Good Laboratory Practices (GLP). The candidate will coordinate closely with QA, Warehouse, and Production departments to ensure timely material release.

Key Features of the Role

• Analytical testing of Raw and Packing Materials
• Exposure to pharmacopeial standards (IP, BP, USP as applicable)
• Handling of sampling and material release procedures
• Participation in OOS, OOT, and investigation processes
• Involvement in audit and inspection readiness
• Growth opportunities within QC or Analytical functions

Responsibilities

• Perform sampling of Raw Materials and Packing Materials as per SOP
• Conduct analytical testing as per approved specifications and STPs
• Operate and maintain analytical instruments such as HPLC, GC, UV, IR (as applicable)
• Review and document analytical results accurately
• Ensure compliance with Good Laboratory Practices (GLP) and GDP
• Prepare and review Certificates of Analysis (COA)
• Handle OOS, OOT, and deviation investigations related to RM/PM
• Coordinate with Warehouse for material status labeling and release
• Maintain laboratory logbooks and documentation records
• Participate in method verification and validation activities
• Support internal audits and regulatory inspections
• Ensure data integrity compliance in all testing activities

Required Qualifications

• 2 to 5 years of experience in pharmaceutical QC (RM/PM analysis)
• Strong knowledge of pharmacopeial testing requirements
• Experience in analytical instrumentation handling
• Understanding of OOS and investigation procedures
• Knowledge of GMP and GLP guidelines

Educational Requirements

• M.Sc in Chemistry / Analytical Chemistry
• M.Pharm preferred
• Strong academic background in pharmaceutical or analytical sciences

Experience and Skills

• Hands-on experience in RM and PM analysis
• Familiarity with analytical instruments and calibration practices
• Good documentation and reporting skills
• Strong analytical and problem-solving ability
• Knowledge of data integrity and compliance systems
• Ability to work within timelines and production schedules
• Good communication and coordination skills
• Basic familiarity with ERP or Laboratory Information Management Systems preferred

Salary Insights

• Performance-based growth structure
• Exposure to regulated pharmaceutical laboratory operations
• Career progression toward Assistant Manager – QC or Senior Analytical roles

Company Overview

APDM Pharmaceuticals is a growing pharmaceutical organization committed to delivering high-quality and compliant healthcare products. Operating from its manufacturing facility in Sakodara, Gujarat, the company emphasizes strict quality control systems, regulatory adherence, and continuous improvement.
The organization provides a structured environment for professionals seeking long-term careers in Quality Control and Analytical Sciences.

FAQs

Q: Is experience in RM and PM testing mandatory?
Yes, candidates must have relevant experience in Raw and/or Packing Material analysis.

Q: Are pharmacopeial standards knowledge required?
Yes, familiarity with IP, BP, USP, or other applicable standards is preferred.

Q: Will the role involve instrument handling?
Yes, analytical instrument operation is part of the responsibilities.

Q: What determines Officer vs. Executive designation?
Designation depends on experience depth, independent testing capability, and regulatory exposure.

Application Tips

• Mention specific materials tested (API, excipients, printed PM, foils, bottles, etc.)
• Highlight instruments handled (HPLC, GC, UV, IR, etc.)
• Include OOS and investigation exposure
• Quantify number of samples analyzed per month
• Showcase compliance with GLP and data integrity practices
• Clearly mention pharmacopeial standards handled