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Senior Executive Quality Control

3-6 years
Not Disclosed
10 June 20, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Job Summary

We are hiring a Senior Executive – Quality Control for our pharmaceutical manufacturing unit in Ahmedabad, India. The role demands expertise in analytical method validation, instrument calibration, and ensuring GLP/GMP compliance. This is an excellent opportunity for quality professionals with a background in chemical and instrumental analysis to contribute to maintaining high-quality pharmaceutical standards.


Key Responsibilities

  • Perform analytical activities as per the Analytical Competency Matrix.

  • Conduct on-job training and practical demonstrations for chemical and instrumentation processes.

  • Analyze in-process, semi-finished, finished goods, raw materials, and stability samples for OSD and LVP products.

  • Handle analytical method validation and verification according to defined protocols.

  • Manage sample receiving, documentation, and SAP data entry.

  • Coordinate with external commercial labs for sample analysis when required.

  • Prepare volumetric solutions, reagents, and test solutions as necessary.

  • Calibrate laboratory instruments and ensure documentation as per pharmacopeial updates.

  • Maintain quality control resources and ensure compliance with cGDP, cGMP, and data integrity.

  • Implement EPD Global Guidelines and COBC requirements.

  • Support and face internal and external audits to ensure regulatory compliance.

  • Complete SOP training in Isotrain within stipulated timelines.

  • Execute additional tasks as assigned by the reporting manager.


Required Skills & Qualifications

  • Bachelor’s or Master’s degree in Pharmaceutical Sciences, Chemistry, or related field.

  • 3–6 years of experience in Quality Control within the pharmaceutical industry.

  • Strong knowledge of GLP, GMP, cGDP, cGMP, and data integrity requirements.

  • Proficient in analytical method validation and verification.

  • Experience with SAP and laboratory documentation.

  • Familiarity with EPD Global Guidelines and COBC compliance.

  • Excellent understanding of laboratory instrument calibration.

  • Strong attention to detail and problem-solving skills.


Perks & Benefits

  • Competitive salary as per industry standards (Not specified in JD).

  • Opportunity to work in a globally compliant pharmaceutical environment.

  • Exposure to audits and global regulatory guidelines.

  • Training and skill development programs.

  • Supportive and collaborative team culture.


Company Description

A leading pharmaceutical company in Ahmedabad, India, committed to excellence in manufacturing and quality assurance. The organization upholds global regulatory standards and fosters a culture of continuous improvement and integrity across all operations.


Work Mode

On-site – Ahmedabad, India


Call-to-Action

If you are passionate about quality control in pharmaceuticals and meet the above qualifications, apply now to join our dynamic team and contribute to global healthcare excellence!