Quick Summary
1. Implementation of quality assurance standards, processes, controls and cGMP in warehouse. 2. Preparation of SOPs and ensure effective implementation. 3.
Qualification : BE Mechanical/Electrical/Instrumentation or B pharma …preferably BE
Experience : 6-7 years experience in handling engineering department GMP documentation activities and supporting engineering function as SME in QMS documentation
Responsibilities :
1. Implementation of quality assurance standards, processes, controls and cGMP in warehouse.
2. Preparation of SOPs and ensure effective implementation.
3. should be well versed with deviation management SOP
4. Should be well versed with change control and CAPA management related to engineering department
5. Should be familiar with documentation like DQ, IQ, OQ and PQ.
6. To ensure that training for SOP’s, GDP, cGMP and On the Job training are imparted to staff as per
Schedule
7. Routine Requalification & Validation of HVAC systems, compressed gases and equipment.
8. Preparation of all planners like Preventive maintenance, calibration, requalification etc in engineering function
9. To ensure compliance to Regulatory, ISO and WHO GSDP requirements.
10. should coordinate for the drawing preparation and approvals.
11. should have experience on working with QMS software like trackwise
If this job description resonates with you, we encourage you to apply even if you don’t meet all of the requirements. We’re interested in getting to know you and what you bring to the table!
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Location & Eligibility
About this job
- Who can apply
- Marshall Islands
- Posted
- 10 days ago
Listing Details
- Posted
- October 5, 2026
- First seen
- October 5, 2026
- Last seen
- October 9, 2026
Posting Health
- Days active
- 9
- Repost count
- 0
- Trust Level
- 28%
- Scored at
- October 15, 2026
Signal breakdown
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