APDM Walk-in QA, QC, Production

BPharm MSc QA QC Production Jobs at APDM Sakodara

APDM Pharmaceuticals hiring BPharm, MPharm, MSc candidates for QA, QC, Production roles in Sakodara. Walk-in interview openings.

APDM Pharmaceuticals has announced a major walk-in interview drive for its manufacturing facility at Sakodara. The company is hiring skilled and experienced pharmaceutical professionals across Quality Control, Quality Assurance, Production, and Packaging departments. These opportunities are open to B.Pharm, M.Pharm, and M.Sc candidates who have hands-on exposure to regulated market requirements such as EU, MHRA, USFDA, and ANVISA. This hiring drive reflects APDM Pharmaceuticals’ continued expansion and commitment to building strong quality and compliance-driven teams.

Company Overview

APDM Pharmaceuticals is a rapidly growing pharmaceutical organization committed to building a healthier future through quality-driven manufacturing and regulatory excellence. The company operates with a strong focus on compliance, data integrity, and patient safety, aligning its operations with stringent international regulatory standards. With exposure to highly regulated markets including the European Union, MHRA (UK), USFDA, and ANVISA (Brazil), APDM Pharmaceuticals has established itself as a trusted name in formulation manufacturing and quality systems.

The organization emphasizes strong quality culture, cross-functional collaboration, and continuous improvement. Professionals joining APDM Pharmaceuticals gain valuable exposure to global audits, complex regulatory expectations, and advanced pharmaceutical quality systems that significantly enhance long-term career prospects in the pharma industry.

Job Role & Responsibilities

Quality Control Department

Trainee / Sr. Officer / Executive / Sr. Executive – Quality Control

Experience: 0 to 6 Years

Key Responsibilities:

• Raw material sampling and chemical analysis
• Instrumental analysis using HPLC, GC, IR, KF, UV, Polarimeter, and Dissolution
• Finished product, in-process, and stability testing as per FP, IP, and stability protocols
• Preparation and review of Methods of Analysis (MOA) and analytical protocols
• Planning and execution of AMT, AMV, and API verification activities
• Coordination for technology transfer and analytical method validation
• Maintenance of GLP compliance and laboratory documentation
• Adherence to cGMP, GLP, ALCOA++ principles, and GDP requirements
• Preparation, review, and control of analytical documents

Quality Assurance Department

Officer / Sr. Officer / Executive – Quality Assurance

Experience: 2 to 7 Years

Key Responsibilities:

• In-process quality assurance (IPQA) activities
• Vendor qualification and audit coordination
• Technology transfer and validation support
• Handling of QMS documentation, deviations, and CAPA
• Qualification of equipment and utilities
• Quality risk assessment and compliance monitoring
• Support during EU, MHRA, USFDA, and ANVISA audits

Manager / Sr. Manager – Quality Assurance

Experience: 10 to 15 Years

Key Responsibilities:

• Overall QA leadership and regulatory compliance management
• Oversight of IPQA, QMS, validation, and qualification activities
• Computer System Validation (CSV) and data integrity compliance
• Handling regulatory audits and customer inspections
• Quality risk management and compliance strategy implementation
• Cross-functional coordination and audit readiness

Production / Packaging Department

Sr. Officer / Executive – Production / Packaging

Experience: 3 to 7 Years

Key Responsibilities:

• Review and execution of BMR and BPR activities
• SOP preparation and change control management
• Deviation handling and quality risk assessment
• Line clearance, logbook maintenance, and documentation
• Coordination with QA, QC, and engineering teams
• Vendor qualification and audit readiness support

Eligibility / Qualifications

Required Education

• B.Pharm
• M.Pharm
• M.Sc

Relevant Courses Include:
B.Pharm, M.Pharm, M.Sc Chemistry, M.Sc Pharmaceutical Chemistry, M.Sc Analytical Chemistry

Experience Requirements

• Experience ranges from fresher level to 15 years depending on the role
• Mandatory exposure to EU, MHRA, USFDA, and ANVISA regulatory audits
• Strong knowledge of cGMP, GLP, ALCOA++, GDP, and data integrity principles

Location & Salary

Job Location:
APDM Pharmaceuticals Plant, Sakodara

Salary Package:
Salary will be competitive and aligned with industry standards. Final compensation will depend on qualifications, regulatory exposure, experience, and interview performance.

Walk-in Interview Details

Date: 07 February

Time: 09:30 AM to 05:00 PM

Walk-in Venue:
403, Patron,
Opp. Kensvilla Golf Academy,
Rajpath Club Road,
Bodakdev, Ahmedabad

Candidates are requested to carry their updated resume and one passport-size photograph.

Why Join APDM Pharmaceuticals

• Strong exposure to regulated markets including EU, USFDA, MHRA, and ANVISA
• Quality-driven work culture with global audit readiness
• Opportunities across QC, QA, and Production functions
• Career growth in compliance, validation, and regulatory systems
• Direct contribution to safe, effective, and compliant pharmaceutical products

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Frequently Asked Questions (FAQs)

Who can apply for APDM Pharmaceuticals walk-in interview?

Candidates with B.Pharm, M.Pharm, or M.Sc qualifications and relevant regulatory exposure can apply.

Is regulatory audit exposure mandatory?

Yes. Exposure to EU, MHRA, USFDA, or ANVISA audits is mandatory for all roles.

Are freshers eligible for these positions?

Freshers are eligible for trainee-level roles in the Quality Control department.

What documents should be carried for the interview?

Candidates should bring an updated resume and one passport-size photograph.

What is the job location?

The job location is APDM Pharmaceuticals Plant, Sakodara.

Summary Table

Company	APDM Pharmaceuticals
Vacancies	Trainee/Sr. Officer/Executive/Sr. Executive – QC, Officer/Sr. Officer/Executive – QA, Sr. Officer/Executive – Production & Packaging, Manager/Sr. Manager – QA
Required Education	B.Pharm, M.Pharm, M.Sc Chemistry, M.Sc Pharmaceutical Chemistry, M.Sc Analytical Chemistry
Experience	0 to 15 Years