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APDM Pharmaceuticals Walk-in Interview for QA & QC Professionals in Gujarat | Pharma Jobs on 27th June 2026

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Looking for pharma jobs in Gujarat? APDM Pharmaceuticals is conducting a walk-in interview on 27th June 2026 for experienced QA and QC professionals. Explore exciting pharmaceutical careers in India with a WHO-GMP compliant organization offering excellent growth opportunities.

About APDM Pharmaceuticals

APDM Pharmaceuticals is a rapidly growing pharmaceutical company committed to creating a healthier future through quality-driven manufacturing and regulatory excellence.

Operating in a WHO-GMP compliant environment, the company focuses on delivering high-quality pharmaceutical products while maintaining stringent quality standards and compliance requirements.

Known for its professional work culture, APDM Pharmaceuticals emphasizes innovation, continuous improvement, and employee development.

The organization offers outstanding career opportunities for pharmaceutical professionals seeking long-term growth in a regulated manufacturing environment. Candidates with experience in USFDA-regulated facilities are especially encouraged to apply.

Job Details

  • Company Name: APDM Pharmaceuticals
  • Experience: 3–15 Years (Varies by Role)
  • Qualification: M.Sc., B.Sc., M.Pharm, B.Pharm, M.Sc. Microbiology
  • Location: Bavla, Gujarat, India
  • Work Type: On-site
  • Industry: Pharmaceuticals
  • Preferred Experience: USFDA Regulatory Environment

Job Description

APDM Pharmaceuticals is hiring experienced professionals for its Quality Assurance (QA), Quality Control (QC), and QC-Microbiology departments.

The company is seeking qualified candidates who can contribute to maintaining quality systems and regulatory compliance in a WHO-GMP manufacturing facility.

Senior Officer / Executive / Senior Executive – QA

  • Department: Quality Assurance (QA)
  • Role: Quality Assurance Professional
  • Experience: 3–8 Years
  • Education/Qualification: M.Sc., M.Pharm, B.Pharm

Assistant Manager / Deputy Manager – QA

  • Department: Quality Assurance (QA)
  • Role: Quality Management & Compliance
  • Experience: 10–15 Years
  • Education/Qualification: M.Sc., M.Pharm, B.Pharm

Executive / Senior Executive – QC

  • Department: Quality Control (QC)
  • Role: Quality Control Professional
  • Experience: 3–10 Years
  • Education/Qualification: M.Sc., B.Sc., M.Pharm, B.Pharm

Executive / Senior Executive – QC Microbiology

  • Department: QC-Microbiology
  • Role: Microbiology Testing & Compliance
  • Experience: 3–10 Years
  • Education/Qualification: B.Sc. Microbiology, M.Sc. Microbiology

Skills & Qualifications

  • Strong understanding of pharmaceutical quality systems
  • Experience in WHO-GMP regulated environments
  • Knowledge of USFDA compliance requirements
  • Expertise in QA and QC operations
  • Microbiological testing knowledge for QC-Micro roles
  • Documentation and compliance management skills
  • Analytical and problem-solving abilities
  • Strong communication and teamwork skills
  • Attention to detail and accuracy
  • Regulatory inspection readiness experience

Key Responsibilities

  • Ensure compliance with GMP guidelines
  • Maintain quality management systems
  • Review and manage quality documentation
  • Support regulatory audit readiness
  • Conduct quality inspections and monitoring
  • Perform laboratory testing and analysis
  • Investigate deviations and quality issues
  • Maintain accurate records and reports
  • Implement corrective and preventive actions
  • Collaborate with cross-functional teams

Benefits & Perks

  • Excellent career growth opportunities
  • Professional and supportive work culture
  • Exposure to regulated pharmaceutical operations
  • Learning and development opportunities
  • Stable long-term career prospects
  • Industry-standard compensation package
  • Experience in a compliant manufacturing facility
  • Opportunity to work with experienced professionals

How to Apply

Interested candidates who are unable to attend the walk-in interview can send their updated CV to:

Email: career@apdmpharma.com

Applicants should mention the Position Title and Department Name in the email subject line for faster processing.

Verified Post

Verification: To confirm the legitimacy of this posting, you can view the original announcement on the APDM career page.

APDM Pharmaceuticals Walk-in Interview for QA & QC Professionals in Gujarat | Pharma Jobs on 27th June 2026

For more pharmaceutical job opportunities across India, visit Pharma Recruiter: Pharma Recruiter

Apply now and become part of APDM Pharmaceuticals’ vision of building a healthier future through quality, compliance, and innovation.

Walk-in Interview Details

  • Date: 27th June 2026 (Saturday)
  • Time: 9:00 AM to 3:30 PM
  • Venue: APDM Manufacturing Plant, Plot No. 775, 776 & 628, Bavla, Village Sakodara, Gujarat 382220
  • Email: career@apdmpharma.com

Documents Required

  • Updated CV/Resume
  • Passport Size Photograph
  • Last 3 Months Salary Slips
  • Current CTC Proof
  • Educational Certificates
  • Aadhaar Card
  • PAN Card

Why You Should Join APDM Pharmaceuticals

APDM Pharmaceuticals offers a rewarding platform for professionals seeking advancement in pharmaceutical quality functions.

The company’s commitment to WHO-GMP compliance, regulatory excellence, and employee development creates an environment where talented professionals can thrive.

FAQs

Who is eligible for the APDM Pharmaceuticals walk-in interview?

Candidates with 3–15 years of relevant experience in QA, QC, or QC-Microbiology and the required educational qualifications are eligible to apply.

Is USFDA experience mandatory?

USFDA regulatory experience is preferred and will be an added advantage during the selection process.

Can I apply if I cannot attend the walk-in interview?

Yes. Candidates who cannot attend may email their updated CV to career@apdmarma.com and mention the position and department in the subject line.

What growth opportunities are available at APDM Pharmaceuticals?

The company offers excellent career growth, professional development, regulatory exposure, and opportunities to work in a WHO-GMP compliant environment.

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