Are you looking to excel in the field of quality assurance in the pharmaceutical industry? Join us as an Executive – Quality Assurance at our state-of-the-art manufacturing facility in Ankleshwar, India. This full-time position offers the chance to work with a team of experts in regulatory-approved oral solid dosage (OSD) manufacturing units.
About the Company
We are a reputed name in the pharmaceutical industry, dedicated to delivering high-quality products that meet global regulatory standards. Our commitment to innovation, quality, and excellence has made us a trusted partner in healthcare.
Key Responsibilities
As an Executive in Quality Assurance, your primary duties will include:
Quality Management/Continuous Improvement
- Conducting line clearance and ensuring shop floor compliance.
- Performing in-process checks and sampling activities.
- Assisting in the investigation of customer complaints at the site.
- Supporting qualification, validation systems, change control, and deviation management.
- Preparing and reviewing the Annual Product Quality Review.
- Reviewing Batch Manufacturing & Packing Records for accuracy.
- Coordinating cGMP training activities for staff.
Documentation Control
- Developing and maintaining quality system Standard Operating Procedures (SOPs).
- Managing controlled distribution, archival, and retrieval of documents and records.
- Ensuring proper control over master documents and archival rooms.
- Issuing batch records, ATRs, logbooks, and controlled formats.
Product Quality Assurance
- Overseeing in-process controls during manufacturing and packaging.
- Reviewing executed batch manufacturing and packing records.
- Implementing and ensuring the effectiveness of Corrective and Preventive Actions (CAPA) arising from deviations or complaints.
- Reviewing analytical testing records for compliance.
Required Qualifications
- Education: B. Pharm or M. Pharm from a reputed university.
- Experience: 2–4 years of experience in a similar role within regulatory-approved large OSD manufacturing units.
Desired Skills
- Strong understanding of cGMP and pharmaceutical quality standards.
- Attention to detail in documentation and process controls.
- Excellent analytical and problem-solving skills.
- Ability to coordinate effectively across departments for quality assurance tasks.
- Proficiency in using quality management systems and tools.
