APDM walk-in QA, TT, ADL & FD
- Company Overview
- Job Role & Responsibilities
- Quality Assurance – Officer / Senior Officer
- Technology Transfer – Officer / Senior Officer
- Analytical Development Laboratory (ADL)
- Formulation Development (FD)
- Eligibility / Qualifications
- Educational Qualifications
- Experience Requirements
- Location & Salary
- Walk-In Interview Details
- Application Process
- Why Join APDM Pharmaceuticals?
- Frequently Asked Questions (FAQs)
- APDM Pharmaceuticals Walk-In Interview – Vacancy Summary
APDM Pharma Walk In 2026 – M.Pharm, M.Sc Jobs Changodar
APDM Pharmaceuticals walk-in interview at Changodar for QA, TT, ADL & FD roles. M.Pharm, M.Sc vacancies with 0–6 years experience.
URL Slug: apdm-pharmaceuticals-rd-qa-tt-adl-fd
APDM Pharmaceuticals is conducting a walk-in interview drive at its R&D facility in Changodar, Ahmedabad, inviting skilled and motivated pharmaceutical professionals to join its growing research and development teams. This hiring initiative covers Quality Assurance, Technology Transfer, Analytical Development Laboratory, and Formulation Development functions, offering strong career opportunities in regulated pharmaceutical R&D environments.
These openings are ideal for candidates seeking hands-on exposure to regulatory filings, analytical method development, and formulation research aligned with global regulatory expectations. APDM Pharmaceuticals offers a collaborative work culture focused on innovation, compliance, and long-term professional growth.
Company Overview
APDM Pharmaceuticals is a research-driven pharmaceutical organization committed to building a healthier future through high-quality, compliant, and innovative medicines. With a strong focus on R&D excellence, APDM supports development programs aligned with Indian and global regulatory standards including CDSCO, State FDA, and WHO-GMP requirements.
The company operates dedicated R&D facilities designed to support analytical development, formulation innovation, and technology transfer activities. APDM’s emphasis on regulatory compliance, scientific documentation, and cross-functional collaboration makes it a credible employer for professionals looking to build careers in regulated pharma research and development.
Job Role & Responsibilities
Quality Assurance – Officer / Senior Officer
This role supports regulatory and licensing activities for R&D and manufacturing operations.
Key responsibilities:
- Preparation and submission of regulatory documents to CDSCO, State FDA, DSIR, and WHO-GMP
- Support for manufacturing, import, and test licence applications
- Tracking regulatory approvals, renewals, and validity timelines
- Maintenance of regulatory licence records and compliance trackers
- Ensuring compliance with Drugs & Cosmetics Act and applicable rules
Technology Transfer – Officer / Senior Officer
This role focuses on pharmaceutical documentation and product lifecycle support.
Key responsibilities:
- Preparation of product specifications, STPs, and test data sheets
- Creation and maintenance of comprehensive product documentation
- Support for smooth technology transfer between R&D and manufacturing
- Documentation compliance as per GDP and regulatory guidelines
Analytical Development Laboratory (ADL)
Officer / Senior Officer / Executive / Senior Executive
This role supports analytical method development and validation activities.
Key responsibilities:
- Analytical method development for assay, dissolution, and related substances
- Method validation, verification, and transfer activities
- Multimedia dissolution profiling and R&D stability studies
- Plant support during investigations and troubleshooting
- Preparation of STPs, specifications, validation protocols, and reports
- Maintenance of raw data in compliance with GLP and GDP requirements
Formulation Development (FD)
Officer / Senior Officer / Executive / Senior Executive
This role supports development of injectable and ophthalmic dosage forms.
Key responsibilities:
- Development of simple and complex parenteral and ophthalmic formulations
- Work on Generic and 505(b)(2) development programs
- Literature review and evaluation of new excipients and technologies
- Preparation of MFRs, PDRs, protocols, SOPs, and tech transfer documents
- Support scale-up, exhibit batches, and technology transfer
- Cross-functional collaboration with Analytical, QA, RA, and Production teams
Eligibility / Qualifications
Educational Qualifications
Role-specific qualifications include:
M.Pharm, B.Pharm, M.Sc, B.Sc
Relevant courses include:
Pharmaceutical Sciences, Pharmaceutics, Pharmaceutical Analysis, Analytical Chemistry, Organic Chemistry, Life Sciences, Biotechnology
Experience Requirements
- QA – Officer / Senior Officer: 2 to 4 years
- TT – Officer / Senior Officer: 0 to 2 years
- ADL – Officer to Senior Executive: 2 to 6 years
- FD – Officer to Senior Executive: 2 to 6 years
Candidates with prior exposure to R&D environments and regulated pharma documentation will be preferred.
Location & Salary
Job Location:
R&D Unit, Changodar, Ahmedabad, Gujarat
Walk-In Venue:
Unit No. 90 & 91, Parishram Industrial Hub,
Chacharwadi–Vasna, Changodar,
Ahmedabad, Gujarat – 382213
Salary & Benefits:
Salary packages will be competitive and aligned with pharmaceutical R&D industry standards, based on experience and role level. APDM Pharmaceuticals offers structured growth, regulatory exposure, and long-term stability, making these roles attractive high-CPC pharma R&D jobs.
Walk-In Interview Details
Dates:
30th & 31st January 2026
Time:
08:30 AM to 04:30 PM
Candidates are advised to report early with complete documents for smooth interview processing.
Application Process
This recruitment will be conducted through a direct walk-in interview.
Documents to carry:
- Updated resume
- One passport-size photograph
Candidates must attend the interview at the mentioned venue on the scheduled dates.
Why Join APDM Pharmaceuticals?
- Strong focus on regulated pharmaceutical R&D
- Exposure to CDSCO, WHO-GMP, and licensing activities
- Opportunities in analytical, formulation, QA, and tech transfer domains
- Collaborative and growth-oriented work culture
- Direct contribution to development of quality medicines
Frequently Asked Questions (FAQs)
Q1. Is this walk-in open for freshers?
Yes. TT roles are open for candidates with 0–2 years of experience.
Q2. What regulatory exposure is required for QA roles?
Experience with CDSCO, State FDA, DSIR, or WHO-GMP documentation is preferred.
Q3. Where will the selected candidates be posted?
All positions are based at the R&D Unit in Changodar, Ahmedabad.
Q4. Is there any application fee?
No. APDM Pharmaceuticals does not charge any recruitment fees.
APDM Pharmaceuticals Walk-In Interview – Vacancy Summary
| Company | APDM Pharmaceuticals |
|---|---|
| Vacancies | Officer / Sr. Officer – QA, Officer / Sr. Officer – Technology Transfer, Officer / Sr. Officer / Executive / Sr. Executive – ADL, Officer / Sr. Officer / Executive / Sr. Executive – Formulation Development |
| Required Education | B.Pharm, M.Pharm, B.Sc, M.Sc |
| Experience | 0 to 6 Years |

