Ipca Laboratories Limited is thrilled to announce a virtual recruitment drive for a Quality Assurance (QA) Validation Officer/Sr. Officer position within our esteemed Pharmaceuticals division. This exciting opportunity is based in Piparia (Silvassa) and offers a chance to join a leading player in the pharmaceutical industry. The virtual drive is scheduled for Thursday, April 24th, 2025.
About Ipca Laboratories Limited:
Ipca Laboratories Limited is a prominent pharmaceutical company with a strong reputation for quality and innovation. We are committed to developing and manufacturing high-quality medicines that improve lives globally. Our commitment to excellence extends to our employees, offering a supportive and challenging work environment for professionals to grow and thrive. Joining Ipca means becoming part of a dynamic team dedicated to advancing healthcare solutions.
Job Overview: QA Validation Officer/Sr. Officer
This crucial role within our Quality Assurance department focuses on ensuring the quality and compliance of our pharmaceutical products throughout their lifecycle. The successful candidate will play a vital role in maintaining the highest standards of quality and regulatory compliance.
Key Responsibilities:
- Validation Documentation: Prepare and compile comprehensive protocols and reports for process validation, ANDA (Abbreviated New Drug Application) submissions, and hold time studies. This includes meticulous documentation and adherence to regulatory guidelines.
- Product Quality Reviews: Develop and deliver detailed product quality review reports, analyzing data and identifying potential areas for improvement.
- Software Proficiency: Demonstrate proficiency in utilizing various software applications including Minitab (statistical analysis), EDMS (electronic document management systems), and new LIMS (Laboratory Information Management Systems). Experience with supply chain management software is also highly desirable.
- Batch Record Review: Critically review executed batch manufacturing records and batch packing records to ensure compliance with established procedures and specifications.
- Technology Transfer and Site Evaluation: Provide support and assistance in technology transfer projects and site evaluation studies, contributing to seamless transitions and consistent quality across different locations.
Qualifications and Experience:
- Education: B.Pharm or M.Pharm degree from a recognized university.
- Experience: 6 to 8 years of relevant experience in QA Validation within the pharmaceutical industry. Experience working within a regulated environment (e.g., FDA, EU GMP) is strongly preferred.
- Skills: Strong analytical skills, attention to detail, excellent documentation practices, and the ability to work effectively both independently and as part of a team are essential. Proficiency in relevant software applications is also crucial.
Why Choose Ipca Laboratories Limited?
- Industry Leader: Be part of a leading pharmaceutical company with a global presence.
- Career Growth: Enjoy opportunities for professional development and advancement within a dynamic organization.
- Collaborative Environment: Work alongside experienced professionals in a collaborative and supportive team environment.
- Competitive Compensation: Receive a competitive salary and benefits package.
- Meaningful Work: Contribute to the development and delivery of life-improving medications.
How to Apply:
Interested and qualified candidates are encouraged to apply by following these steps:
Step 1: Submit your Resume:
Send your resume to tejal.bhandari@ipca.com before April 24th, 2025. Please include the following information in your email:
- Total number of years of experience
- Current CTC (Cost To Company)
- Notice period
Step 2: Shortlisting and Virtual Interview Invitation:
Shortlisted candidates will receive a separate email containing the link and time for the virtual interview. This will be shared well in advance of the interview date.
Step 3: Virtual Interview:
The virtual interview will be conducted on April 24th, 2025, at the scheduled time.
Contact Information:
For any queries or assistance, please contact Miss Tejal Bhandari (HR) at 9687607002 or 0260 6624406.
