BDR Pharma Hiring Executive QA – OSD

BDR Pharmaceutical International Pvt Ltd; Panchmahal District; On-site; INR 900,000 - 1,300,000; Full time

Benefits offered by this job

Great Place to Work certified

Halol facility

Job summary

BDR Pharmaceuticals International Pvt. Ltd. at Halol in Gujarat seeks an experienced Executive – QA (Process Validation – OSD) to lead and execute validation activities, ensuring compliance with global regulatory requirements.

The role covers VMP/PVMP/CVMP/QMP preparation and review, PPQ, qualification protocols, and maintenance of quality documentation, with collaboration across cross-functional teams and CAPA investigations. 5–7 years' QA/Validation experience is desirable.

Qualifications

• B Pharm or M.Pharm degree required.
• 5–7 years of QA/Validation experience in OSD.
• Strong knowledge of validation protocols and regulatory compliance.

Responsibilities

• Prepare and review Validation Master Plan (VMP, PVMP, CVMP, QMP).
• Execute qualification and validation documents as per protocol.
• Prepare and review URS, FS, DS, DQ, IQ, OQ, PQ documentation.
• Conduct PPQ and cleaning validation protocols and summary reports.
• Monitor PPQ and cleaning validation activities.
• Collaborate with cross-functional teams for qualification and validation activities.
• Address deviations and participate in investigations.
• Support change management, deviations, CAPA, and other QMS activities.

Skills

Validation knowledge

QMS

CAPA

Regulatory compliance

Education

B Pharm / M.Pharm

Job description

BDR Pharma Hiring Executive QA – OSD Validation

BDR Pharmaceuticals, a Great Place to Work certified company, is inviting applications for the role of Executive – QA (Process Validation – OSD) at its Halol facility. This is an excellent opportunity for experienced professionals to advance their careers in one of India’s fastest-growing pharmaceutical companies.

Company Overview

BDR Pharmaceuticals International Pvt. Ltd. is a recognized player in the global pharmaceutical industry with a strong focus on oncology, critical care, and specialty medicines. Known for its innovation-driven approach, BDR Pharma emphasizes compliance, research excellence, and patient-focused healthcare. The company’s continuous growth offers professionals a platform to enhance their skills in a dynamic and supportive work environment.

Job Role & Responsibilities

As Executive – QA (Process Validation – OSD), you will be responsible for managing and executing process validation activities while ensuring compliance with global regulatory requirements.

Key Responsibilities:

• Prepare and review Validation Master Plan (VMP, PVMP, CVMP, QMP)
• Execute qualification and validation documents as per protocol
• Prepare and review Continued Process Verification protocols and summary reports
• Manage equipment and utility periodic requalification/re-verification schedules
• Handle quality documentation: BMR, BPR, log books, SOPs, protocols, reports
• Prepare and review URS, FS, DS, DQ, RA, IQ, OQ, PQ documentation
• Conduct PPQ and cleaning validation protocols and summary reports
• Monitor PPQ and cleaning validation activities
• Collaborate with cross-functional teams for qualification and validation activities
• Address deviations and participate in investigations
• Support change management, deviations, CAPA, and other Quality Management Systems (QMS)

Eligibility / Qualifications

• Education: B Pharm / M.Pharm
• Experience: 5–7 years in pharmaceutical quality assurance and process validation (OSD)
• Preferred Skills: Strong knowledge of validation, qualification protocols, QMS, CAPA, and regulatory compliance

Relevant courses: Pharmaceutical Quality Assurance, Industrial Pharmacy, Pharmaceutical Analysis, Pharmaceutical Technology, GMP & Regulatory Compliance.

Location & Salary

• Work Location: Baska, Halol (Gujarat)
• Salary: Competitive salary package based on experience and company standards

Why Join BDR Pharma?

• Certified as a Great Place to Work
• Opportunity to work in a leading Indian pharmaceutical company with global reach
• Exposure to cutting-edge validation and QA practices
• Professional growth in a compliance-driven environment

FAQs

1. Who can apply for this position? Candidates with B Pharm or M.Pharm degrees and 5–7 years of QA/Validation experience in OSD can apply.

2. What is the work location? The position is based at Baska, Halol (Gujarat).

3. What are the key responsibilities? Process validation, qualification, QMS support, handling quality documents, and regulatory compliance.

4. What is the application deadline? 23rd August 2025.

5. How can I apply? Send your CV to [e-mail] or call 6358139082.