Instagram
youtube
Facebook

Senior Executive - Manufacturing Qms

0-2 years
Not Disclosed
10 Oct. 31, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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

Senior Executive – Manufacturing QMS

📍 Location: Ahmedabad City, Gujarat, India
🕓 Job Type: Full-time
📅 Posting Date: 29 September 2025, 04:13 PM
Apply Before: 31 December 2025, 04:13 PM
🆔 Job ID: 6578
🏭 Department: Manufacturing Process Operations
🎓 Qualification: Bachelor of Pharmacy (B. Pharm)
📍 Work Location: Survey No. 506, At-Palli, Mehsana, Gujarat, 382165


Job Summary

The Senior Executive – Manufacturing QMS is responsible for managing and ensuring the quality and compliance of manufacturing documentation and processes. The role involves preparation, review, and control of key quality documents, execution of CAPA and deviation management, and supporting process improvements as per cGMP and QMS requirements.


Key Responsibilities

  • Maintain personal hygiene and ensure strict compliance with cGMP, GDP, and departmental discipline.

  • Prepare and review master documents, protocols, and production reports as per regulatory and internal requirements.

  • Manage and control Exhibit batch documentation such as Batch Manufacturing Records (BMRs) and Batch Packaging Records (BPRs).

  • Handle Change Control, Deviations, CAPA, and Investigations in coordination with Quality Assurance and Production teams.

  • Conduct training sessions for subordinates, technicians, and operators in accordance with department needs.

  • Participate in and ensure compliance with the Training Schedule and TNI (Training Need Identification) plan.

  • Perform additional activities as assigned by the Head of Department (HOD).

  • Review all Exhibit batch–related documents to ensure accuracy and regulatory compliance.


Required Skills

  • Strong knowledge of Change Control, Deviations, CAPA, and Investigations

  • Proficiency in managing BMR, BPR, and SOP documentation

  • Excellent understanding of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP)

  • Effective training and leadership abilities

  • Strong attention to detail and documentation accuracy


Education & Experience

  • Qualification: Bachelor of Pharmacy (B. Pharm)

  • Experience: Relevant experience in manufacturing QMS or production documentation preferred


Job Schedule

  • Type: Full-time

  • Shift: As per company requirements