APDM Pharmaceuticals Walk-In Interview for Quality Assurance Jobs in Ahmedabad
APDM Pharmaceuticals Private Limited is conducting a walk-in interview for experienced professionals in its Quality Assurance (QA) department at Ahmedabad, Gujarat. The company has announced six openings across Validation, Qualification, Technology Transfer, IPQA, Computer System Validation (CSV) and Quality Management System (QMS).
Candidates holding M.Sc., M.Pharm. or B.Pharm. qualifications with 3–8 years of experience can attend the recruitment drive. The company has specified that exposure to USFDA, EU, MHRA and ANVISA audits or regulatory requirements is mandatory.
APDM Pharmaceuticals Recruitment 2026 – Overview
| Particulars | Details |
|---|---|
| Company Name | APDM Pharmaceuticals Private Limited |
| Department | Quality Assurance |
| Positions | Officer / Executive / Senior Executive |
| Total Vacancies | 6 |
| Qualification | M.Sc. / M.Pharm. / B.Pharm. |
| Experience | 3–8 Years |
| Job Location | Ahmedabad, Gujarat |
| Interview Date | 17 November 2026 |
| Interview Day | Tuesday |
| Interview Time | 1:00 PM to 3:30 PM |
| Interview Type | Walk-In |
| career@apdmpharma.com |
Department-Wise Vacancies at APDM Pharmaceuticals
APDM Pharmaceuticals has announced six Quality Assurance vacancies across the following functions:
| QA Department | Vacancies |
|---|---|
| Validation | 1 |
| Qualification | 1 |
| Technology Transfer | 1 |
| IPQA | 1 |
| Computer System Validation (CSV) | 1 |
| Quality Management System (QMS) | 1 |
| Total | 6 |
1. Validation – 1 Vacancy
Candidates applying for the Validation function should have experience in:
- Preparation, execution and review of Process Validation protocols and reports.
- Cleaning Validation and Packaging Validation.
- Hold Time Studies and Transport Validation.
- Validation documentation and deviation assessment.
- Implementation of Corrective and Preventive Actions (CAPA).
2. Qualification – 1 Vacancy
Relevant experience and knowledge include:
- Qualification of manufacturing equipment, instruments and utilities.
- HVAC system qualification and validation.
- Purified Water System qualification.
- Compressed Air System qualification.
- Temperature Mapping.
- Preparation and review of IQ, OQ and PQ protocols and reports.
3. Technology Transfer – 1 Vacancy
Candidates should have knowledge and experience in:
- Handling and reviewing technology transfer activities.
- Technology transfer documentation and cross-functional coordination.
- Technology transfer protocols and process evaluation.
- Batch documentation and risk assessment.
- Preparation of technology transfer reports.
- Coordination with Production, QC, Engineering and other departments to support successful technology transfer.
4. IPQA (In-Process Quality Assurance) – 1 Vacancy
The IPQA function requires hands-on experience in:
- Shop-floor Quality Assurance activities.
- Line clearance and in-process checks.
- GMP compliance monitoring.
- BMR/BPR review.
- Dispensing and manufacturing activity verification.
- Process monitoring and batch reconciliation.
- Handling deviations, incidents, change controls and CAPA related to manufacturing operations.
- Compliance with cGMP, GDP and applicable regulatory requirements.
5. Computer System Validation (CSV) – 1 Vacancy
Candidates interested in CSV should have knowledge of:
- Validation of computerized systems used in pharmaceutical manufacturing and quality operations.
- Preparation, execution and review of CSV documentation.
- Validation protocols and risk assessments.
- Preparation and review of validation reports.
- Data integrity principles.
- Audit trails and user access controls.
- 21 CFR Part 11 requirements.
6. Quality Management System (QMS) – 1 Vacancy
The QMS function requires experience in:
- Implementation, maintenance and continuous improvement of pharmaceutical QMS as per cGMP requirements.
- Handling Deviations, Change Controls, CAPA, QRM and APQR.
- Effectiveness checks.
- Preparation, review and control of SOPs, quality documents and records.
- Internal audits and self-inspections.
- Vendor audits and monitoring of audit CAPAs.
- GDP, data integrity and document control.
- Product complaints and product recalls.
- Quality metrics, trend analysis and QMS performance monitoring.
Mandatory Regulatory Audit Requirement
Exposure to the following regulatory audits and requirements is mandatory:
- USFDA
- EU
- MHRA
- ANVISA
Candidates should review this requirement carefully before attending the interview.
Qualification and Experience
Educational Qualification:
- M.Sc.
- M.Pharm.
- B.Pharm.
Experience: 3–8 years.
Designation: Officer / Executive / Senior Executive.
The recruitment details specify the overall experience range but do not provide separate experience requirements for each QA function.
APDM Pharmaceuticals Walk-In Interview Details
Interview Date: 17 November 2026 (Tuesday)
Interview Time: 1:00 PM to 3:30 PM
Interview Venue:
APDM Pharmaceuticals Private Limited
Plot No. 775, 776 & 628,
Village Sakodara, Taluka Bavla,
Ahmedabad, Gujarat – 382220.
Candidates should plan their travel to reach the venue within the announced interview time.
How to Apply for APDM Pharmaceuticals Jobs?
Interested and eligible candidates can attend the walk-in interview directly with their updated resume.
Candidates who are unable to attend the interview can share their CV through email.
Email: career@apdmpharma.com
Walk-In Date: 17 November 2026
Interview Timing: 1:00 PM to 3:30 PM
Applicants should ensure that their experience matches the relevant QA function and that they meet the mandatory regulatory audit exposure requirement.
Important Points for Candidates
- Total vacancies: 6.
- All openings are in the Quality Assurance department.
- Experience required: 3–8 years.
- Qualification: M.Sc., M.Pharm. or B.Pharm.
- Regulatory audit exposure to USFDA, EU, MHRA and ANVISA is mandatory.
- Candidates unable to attend can email their CV to the company.
- Salary details have not been provided in the recruitment information.
Frequently Asked Questions (FAQs)
Q1. Which company is conducting the walk-in interview?
APDM Pharmaceuticals Private Limited is conducting the walk-in interview.
Q2. Which department has vacancies?
The vacancies are in the Quality Assurance department.
Q3. How many vacancies are available?
There are six vacancies across six QA functions.
Q4. Which positions are available?
Officer, Executive and Senior Executive positions are available across Validation, Qualification, Technology Transfer, IPQA, Computer System Validation and QMS.
Q5. What qualifications are required?
Candidates should have M.Sc., M.Pharm. or B.Pharm. qualifications.
Q6. What is the required experience?
Candidates should have 3–8 years of experience.
Q7. Is regulatory audit experience mandatory?
Yes. Exposure to USFDA, EU, MHRA and ANVISA audits or regulatory requirements is mandatory.
Q8. When is the APDM Pharmaceuticals walk-in interview?
The interview is scheduled for 17 November 2026, Tuesday, from 1:00 PM to 3:30 PM.
Q9. Where is the interview venue?
APDM Pharmaceuticals Private Limited, Plot No. 775, 776 & 628, Village Sakodara, Taluka Bavla, Ahmedabad, Gujarat – 382220.
Q10. Can candidates apply by email?
Yes. Candidates who cannot attend the walk-in interview can send their CV to career@apdmpharma.com.
Q11. What is the salary offered by APDM Pharmaceuticals?
Salary details have not been specified in the available recruitment information.

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