HomeAhmedabad JobsAPDM Pharmaceuticals Walk-In Interview on 17th November 2026 | QA Jobs in...

APDM Pharmaceuticals Walk-In Interview on 17th November 2026 | QA Jobs in Ahmedabad

APDM Pharmaceuticals Private Limited is conducting walk-in drive for experienced pharmaceutical professionals in Quality Assurance department. The interview is conducting on Tuesday, 17th November 2026, at the company’s facility in Sakodara, Bavla, Ahmedabad, Gujarat. Candidates with 3 to 8 years of relevant pharmaceutical industry experience can attend interview at Ahmedabad.

APDM Pharmaceuticals Walk-In Interview – Recruitment Overview

 

ParameterDetails
Company NameAPDM Pharmaceuticals Private Limited
DepartmentQuality Assurance (QA)
DesignationOfficer / Executive / Sr. Executive
Areas / FunctionsValidation, Qualification, Technology Transfer, IPQA, CSV, QMS
No. of Vacancies06
QualificationM.Sc. / M.Pharm. / B.Pharm.
Experience3 to 8 Years
Mandatory RequirementUSFDA, EU, MHRA & ANVISA audits / regulatory exposure
Walk-In Date17th November 2026 (Tuesday)
Interview Time01:00 PM to 03:30 PM
Interview VenuePlot No. 775, 776 & 628, Sakodara Village, Taluka Bavla, Ahmedabad, Gujarat – 382220
CV Submission Emailcareer@apdmpharma.com

Department wise Vacancies and Job Requirements

This walk-in interview is conducting for various roles in Quality Assurance department areas like Validation, Qualification, Technology Transfer, IPQA, Computer System Validation (CSV), and Quality Management System (QMS).

Department: Quality Assurance (QA)

Positions: Officer / Executive / Sr. Executive

Qualification: M.Sc. / M.Pharm. / B.Pharm.

Experience: 3 to 8 Years

Detailed Skills and Responsibilities

1. Validation – 01 Position

  • Experience in preparation, execution and review of Process Validation, Cleaning Validation and Packaging Validation protocols and reports.

  • Knowledge of Hold Time Studies, Transport Validation.

  • Ability to handle validation documentation, deviation assessment and implementation of CAPA.

2. Qualification – 01 Position

  • Hands-on experience in qualification of manufacturing equipment, instruments and utilities.

  • Knowledge of HVAC, Purified Water System and Compressed Air System qualification and validation.

  • Experience in Temperature Mapping, preparation/review of IQ, OQ and PQ protocols and reports.

3. Technology Transfer – 01 Position

  • Handling and review of technology transfer activities, documentation and coordination with cross-functional departments.

  • Knowledge of technology transfer protocols, process evaluation, batch documentation, risk assessment and transfer reports.

  • Coordination with Production, QC, Engineering and other cross-functional departments to ensure successful technology transfer.

4. IPQA (In-Process Quality Assurance) – 01 Position

  • Hands-on experience in shop-floor QA activities, including line clearance, in-process checks and GMP compliance monitoring.

  • Experience in BMR/BPR review, dispensing and manufacturing activity verification, process monitoring and batch reconciliation.

  • Handling of deviations, incidents, change controls and CAPA related to manufacturing operations.

  • Ensuring compliance with cGMP, GDP and applicable regulatory requirements.

5. Computer System Validation (CSV) – 01 Position

  • Knowledge and experience in validation of computerized systems used in pharmaceutical manufacturing and quality operations.

  • Preparation, execution and review of CSV documentation, including validation protocols, risk assessments and validation reports.

  • Knowledge of data integrity principles, audit trails, user access controls and 21 CFR Part 11 requirements.

6. Quality Management System (QMS) – 01 Position

  • Hands-on experience in implementation, maintenance and continuous improvement of Pharmaceutical QMS as per cGMP requirements.

  • Handling of Deviations, Change Controls, CAPA, QRM, APQR and effectiveness checks.

  • Preparation, review and control of SOPs, quality documents and records.

  • Experience in internal audits, self-inspections, vendor audits and monitoring of audit CAPAs.

  • Knowledge of GDP, data integrity, document control, product complaints and product recalls.

  • Monitoring of quality metrics, trend analysis and QMS performance.

Walk-In Interview Venue details

Company: APDM Pharmaceuticals Private Limited

Address: Plot No. 775, 776 & 628, Village – Sakodara, Taluka Bavla, Ahmedabad, Gujarat – 382220.

Interview Date: Tuesday, 17th November 2026

Reporting / Interview Time: 01:00 PM to 03:30 PM

Unable to Attend the Walk-In Interview?

Candidates who cannot attend the scheduled walk-in interview share their resumes by email (mention the department and position you are applying for in the email subject line.)

HR Email: career@apdmpharma.com

Documents Required for the Interview

Candidates are who are interested join walk-in interview with us are requested to bring following documents

  • Updated resume
  • Copies of educational qualification certificates.
  • Experience letters and employment-related documents
  • A valid government-issued photo ID.
  • Relevant training or certification records, if applicable.

APDM Pharmaceuticals Walk-In Interview 2026

About APDM Pharmaceuticals Pvt Ltd

Founded in June 2022 by visionary entrepreneurs and seasoned scientists near Ahmedabad, Gujarat, APDM Pharmaceuticals Pvt Ltd is a fast-growing, research-driven Contract Development and Manufacturing Organization (CDMO) specializing in solid oral formulations. Within just 15 months of inception, the company established a state-of-the-art 15,000 sq. meter, IoT-enabled manufacturing facility and a dedicated R&D centre staffed by 50+ scientists focused on formulation development, patent landscaping, and global regulatory compliance. Committed to cutting-edge innovation, uncompromising quality, and ethical partnerships, APDM offers end-to-end pharma solutions — from R&D prototypes to high-volume commercial batches — and has strategically acquired two ANDAs to accelerate approvals from USFDA, EMEA and PIC/S markets, positioning itself as a versatile, future-ready partner advancing global access to high-quality medicines.

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