Explore rewarding pharma jobs at Intas Pharmaceuticals. Apply for Sr. Executive and Executive roles in Upstream Manufacturing, Artwork QA, Development QA, and Biochemical QC. Build your pharmaceutical career with a global leader.
About the Company
Intas Pharmaceuticals (Accord Healthcare) is a leading multinational pharmaceutical organization driven by innovation, regulatory excellence, and patient-centric healthcare solutions. With a robust global presence across more than 85 countries, Intas fosters continuous professional growth and dynamic career development.
Job Details
- Company Name: Intas Pharmaceuticals (Accord)
- Experience: 3 to 9 Years (varies by role)
- Qualification: B. Tech, M. Sc (Biotechnology, Biochemistry, Microbiology, MLT, Chemistry), M. Pharm in QA
- Work Type: On-site
Job Description
Intas Pharmaceuticals is currently inviting application profiles for multiple critical positions across core technical departments. These roles support cutting-edge manufacturing operations, strict quality assurance frameworks, and advanced laboratory testing protocols.
Sr. Executive – Upstream Manufacturing / Fractionation
- Department: Manufacturing (Upstream/Fractionation)
- Role: Operations & Equipment Handling
- Experience: 5 to 8 Years
- Education/Qualification: B. Tech / M. Sc (Biotechnology / Biochemistry / Microbiology)
Sr. Executive – Artwork Quality Assurance
- Department: Quality Assurance (Art Work QA)
- Role: Artwork Document Control & Vendor Audits
- Experience: 5 to 8 Years
- Education/Qualification: M. Sc (MLT / Chemistry)
Sr. Executive – Development Quality Assurance
- Department: Development QA
- Role: R&D Quality Documentation & Tech Transfer
- Experience: 5 to 8 Years
- Education/Qualification: M. Pharm in Quality Assurance
Executive / Sr. Executive – Quality Control (Biochemical)
- Department: Quality Control (QC-Biochemical)
- Role: Analytical Data Review & Sample Testing
- Experience: 3 to 9 Years
- Education/Qualification: B. Tech / M. Sc (Biotechnology)
Skills & Qualifications
- Expertise in operating centrifuges, filtration systems, TFF, and AKTA chromatography.
- Hands-on experience with CIP, SIP, autoclaves, and filter integrity testing.
- Proficiency in handling ELISA and PCR testing instruments.
- Strong command of document control, SOP management, CAPA, and deviations.
- Working knowledge of SAP transactions, purchase requisitions, and vendor qualification.
- Solid understanding of R&D documentation, tech transfer, and method reviews.
Key Responsibilities
- Operate upstream manufacturing equipment, including AKTA systems, centrifuges, and filtration setups.
- Perform CIP, SIP, autoclave operations, and execute EBMR documentation.
- Manage artwork reviews, vendor audits, SOP revisions, and archival records.
- Support QMS activities, including change controls, CAPA, deviations, and complaints.
- Oversee analytical method reviews, tech transfer protocols, and regulatory compliance.
- Coordinate equipment calibration, annual maintenance contracts, and SAP requisitions.
- Execute ELISA and PCR assays, sample handling, and analytical data releases.
Benefits & Perks
- Accelerate career advancement within a rapidly expanding global pharmaceutical firm.
- Gain exposure to advanced technologies and state-of-the-art biopharmaceutical equipment.
- Benefit from competitive industry compensation packages and merit-based incentives.
- Thrives in a supportive, compliant, and collaborative work environment.
- Expand professional skill sets through comprehensive Quality Management System processes.
How to Apply
Eligible candidates interested in these high-growth pharmaceutical careers are encouraged to apply directly through official corporate channels.
Check open positions and application instructions on Pharma Recruiter to submit your updated resume today.
Why You Should Join
Joining Intas Pharmaceuticals means becoming part of a highly respected global healthcare brand dedicated to quality and innovation. Employees enjoy long-term career stability, continuous learning opportunities, and a progressive work environment focused on excellence.
FAQs
What experience is required for QC BWhat qualifications are required for these roles?
Candidates need a B. Tech, M. Sc, or M. Pharm degree in relevant fields like Biotechnology, Biochemistry, Microbiology, Chemistry, or QA.
How can candidates submit their applications?
Interested applicants can review detailed requirements and submit their CVs through the application portal on Pharma Recruiter.
What experience is required for QC Biochemical roles?
QC Biochemical roles require 3 to 9 years of hands-on experience handling ELISA and PCR instruments in laboratory environments.
