Are you an experienced pharmaceutical professional passionate about quality assurance and equipment validation? BDR Pharmaceuticals, a Great Place to Work certified company, is hiring a QA Executive – Equipment Validation (OSD) to join our dynamic team in Baska, Halol. This role offers an exciting opportunity to contribute to high-quality pharmaceutical manufacturing while advancing your career in a supportive, innovative environment. Read on to explore the responsibilities, qualifications, benefits, and how to apply for this rewarding position.
Job Responsibilities
As a QA Executive specializing in Equipment Validation for Oral Solid Dosage (OSD), you will play a critical role in ensuring compliance and quality throughout the validation lifecycle. Key responsibilities include:
- Preparing and Reviewing Validation Plans: Develop and review Validation Master Plans (VMP, PVMP, CVMP, QMP) to ensure compliance with industry standards.
- Executing Validation Protocols: Follow the validation master plan, prepare and review validation documents, and execute protocols for equipment validation.
- Document Management: Handle and store quality documents, including Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), logbooks, protocols, reports, and Standard Operating Procedures (SOPs).
- SOP Development: Create and review SOPs and procedures related to validation processes.
- Process Performance Qualification (PPQ): Prepare and review PPQ and cleaning validation protocols and summary reports.
- Monitoring and Coordination: Oversee PPQ and cleaning validation activities, collaborating with cross-functional teams to ensure smooth execution.
- Deviation Management: Address and resolve deviations identified during validation activities to maintain compliance.
Qualifications
To excel in this role, candidates should meet the following requirements:
- Education: B.Pharm or M.Pharm from a recognized institution.
- Experience: 5-7 years of experience in equipment validation, specifically in Oral Solid Dosage (OSD) within the pharmaceutical industry.
- Skills: Strong knowledge of validation protocols, SOP development, and regulatory compliance. Excellent organizational, analytical, and communication skills.
- Industry Background: Proven experience in the pharmaceutical industry, with a focus on quality assurance and equipment validation.
Benefits of Joining BDR Pharmaceuticals
At BDR Pharmaceuticals, we value our employees and offer a range of benefits to support your professional and personal growth:
- Great Place to Work Culture: Join a certified Great Place to Work, fostering collaboration and innovation.
- Career Growth Opportunities: Access training and development programs to advance your career in the pharmaceutical industry.
- Competitive Compensation: Receive a competitive salary package with additional perks.
- Work-Life Balance: Enjoy a supportive environment that prioritizes employee well-being.
How to Apply
Ready to take the next step in your pharmaceutical career? Apply now by sending your resume and cover letter to neha.thakkar@bdrpharma.com or contact 6358139082 for more details. Ensure your application highlights your experience in equipment validation and pharmaceutical quality assurance. Applications are accepted until October 02, 2025.
FAQs
Q: What is the role of a QA Executive in Equipment Validation at BDR?
A: The QA Executive ensures equipment used in OSD manufacturing meets regulatory standards by preparing validation plans, executing protocols, managing documents, and addressing deviations.
Q: What qualifications are required for this position?
A: Candidates need a B.Pharm or M.Pharm degree and 5-7 years of experience in equipment validation within the pharmaceutical industry.
