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Associate - Manufacturing

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

Associate – Manufacturing

📍 Location: Ahmedabad City, Gujarat, India
🕓 Job Type: Full-time
📅 Posting Date: 29 September 2025
Apply Before: 31 December 2025, 04:12 PM
🆔 Job ID: 6580
🏭 Department: Manufacturing Process Operations
🎓 Qualification: ITI / Diploma / B.Sc
📍 Work Location: Survey No. 506, At-Palli, Mehsana, Gujarat, 382165


Job Summary

The Associate – Manufacturing is responsible for executing and monitoring manufacturing operations in aseptic and controlled areas in compliance with cGMP standards. The role involves operation, cleaning, maintenance, and documentation of all equipment and processes to ensure product quality, safety, and regulatory compliance.


Key Responsibilities

  • Follow the preventive maintenance schedule for machines, instruments, and equipment in the area.

  • Ensure cleaning and sanitization of machines, instruments, equipment, and area as per SOP.

  • Perform line clearance activities before operations in accordance with SOP.

  • Operate all machines and instruments within the assigned area effectively and safely.

  • Immediately inform the supervisor of any abnormalities, disturbances, or observations in the aseptic area.

  • Maintain self-hygiene and adhere strictly to cleaning, sanitization, and documentation procedures.

  • Complete and verify logbooks and area records accurately as per SOP.

  • Ensure UAF (User Authorization Form) compliance and proper functioning in the area.

  • Follow cGMP, GDP (Good Documentation Practices), and department discipline at all times.

  • Execute all activities related to general, controlled, and aseptic areas.

  • Participate in training programs as per the Training Need Identification (TNI) and apply learned skills effectively.


Required Skills

  • Knowledge of aseptic and terminally sterilized processes

  • Expertise in filling, stoppering, and sealing of sterile drug products

  • Strong understanding of Good Manufacturing Practices (GMP)

  • Familiarity with regulatory and compliance requirements

  • Attention to detail and adherence to quality standards


Education & Experience

  • Qualification: ITI / Diploma / B.Sc (Science or related field)

  • Experience: Freshers or candidates with relevant manufacturing experience preferred


Job Schedule

  • Type: Full-time

  • Shift: As per company requirements