Intas is hiring experienced professionals for R&D Upstream, Downstream, Analytical Development, and QA Process roles in biosimilars. Join this leading pharma company through a walk-in interview on 19th April 2026 in Bengaluru. Explore exciting pharma jobs, biotech careers, and QA jobs in India’s growing biopharmaceutical sector.
Contents
- 1 About the Company
- 2 Job Details
- 3 Job Description
- 3.1 Associate Scientist / Research Scientist – R&D Upstream Process Development (UPD)
- 3.2 Associate Scientist / Research Scientist – R&D Analytical Development Lab (ADL)
- 3.3 Associate Scientist / Research Scientist – R&D Downstream Process Development (DSP)
- 3.4 Sr. Executive / Assistant Manager – QA (Process QA)
- 4 Skills/Qualifications
- 5 Key Responsibilities
- 6 Benefits/Perks
- 7 How to Apply
- 8 Walk-in Interview Details
- 9 Why You Should Join
- 10 FAQs
About the Company
Intas Pharmaceuticals Ltd. is a leading vertically integrated global pharmaceutical company headquartered in Ahmedabad, India. With a strong focus on formulation development, manufacturing, and marketing, Intas operates in over 85 countries and generates around 70% of its revenue from international markets, including highly regulated regions like the US and EU.
The company excels in biosimilars, offering advanced EU-GMP certified biopharma capabilities. It features state-of-the-art facilities, including India’s largest single-use bioreactors, and maintains a reputation for innovation, regulatory compliance with FDA, EMA, and ROW standards, and consistent growth.
Recognized as a “Great Place to Work”, Intas fosters an open-door culture that supports professional development and long-term career stability in the pharmaceutical industry.
Job Details
- Company Name: Intas Pharmaceuticals Ltd.
- Experience: 3 to 10 Years (varies by role; 4 to 10 Years for QA)
- Qualification: M.Sc / M.Tech in Biotechnology, Bioprocess Engineering, Bio-Chemistry; B.Pharm / M.Pharm for QA roles
- Location: Bengaluru (R&D roles – Walk-in) and Ahmedabad (QA roles – Biopharma Plant)
- Work Type: On-site
Job Description
Intas is expanding its Biopharmaceutical capabilities and invites ambitious professionals with prior experience in the biotech/biosimilars industry to join its R&D and QA teams. These roles offer hands-on exposure to end-to-end single-use facilities for Upstream and Downstream Processing, advanced analytics, and global regulatory environments.
Associate Scientist / Research Scientist – R&D Upstream Process Development (UPD)
- Department: R&D – Upstream Process Development
- Experience: 3 to 10 Years in R&D Biosimilars
- Education/Qualification: M.Sc / M.Tech – Biotechnology, Bioprocess Engineering, Bio-Chemistry
Associate Scientist / Research Scientist – R&D Analytical Development Lab (ADL)
- Department: R&D – Analytical Development Lab
- Experience: 3 to 10 Years in R&D Biosimilars
- Education/Qualification: M.Sc / M.Tech – Biotechnology, Bioprocess Engineering, Bio-Chemistry
Associate Scientist / Research Scientist – R&D Downstream Process Development (DSP)
- Department: R&D – Downstream Process Development
- Experience: 3 to 10 Years in R&D Biosimilars
- Education/Qualification: M.Sc / M.Tech – Biotechnology, Bioprocess Engineering, Bio-Chemistry
Sr. Executive / Assistant Manager – QA (Process QA)
- Department: QA – Process QA
- Experience: 4 to 10 Years in Biosimilars industry
- Education/Qualification: B.Pharm / M.Pharm / M.Sc / M.Tech – Biotechnology, Bioprocess Engineering, Bio-Chemistry
- Location: Ahmedabad, Biopharma Plant
Skills/Qualifications
- Hands-on experience in cell culture handling, AMBR, bioreactors, and upstream process development
- Expertise in resin screening, optimization, viral validation, and downstream process development
- Proficiency in physicochemical characterization of recombinant proteins using HPLC, UPLC, Capillary Electrophoresis, Circular Dichroism, Fluorescence Spectrometry, and DSC
- Strong knowledge of Design of Experiments (DoE), data analysis with tools like JMP and SIMCA, process characterization, and scale-up
- Experience in reviewing and approving GMP documents, batch records, deviations, CAPA, change controls, and audit observations
- Understanding of data integrity, regulatory requirements, APQR preparation, and participation in process/cleaning validation and audits
- Prior experience in the biosimilars or biotech industry is mandatory
Key Responsibilities
- Develop and optimize upstream and downstream processes for biosimilars
- Perform resin screening, process characterization, and scale-up activities
- Conduct analytical characterization using advanced instruments
- Analyze data using statistical tools and design experiments
- Review GMP documents, batch records, deviations, and CAPA
- Ensure timely batch release and compliance with global regulatory standards
- Participate in internal/external audits and validation activities
Benefits/Perks
- Exposure to India’s largest single-use bioreactors and end-to-end single-use facilities
- Experience with global audits (EMA, FDA, ROW)
- Use of advanced data analytics tools like JMP and SIMCA
- Recognized as a “Great Place to Work” with open-door culture
- Opportunities for career growth in a fast-expanding biopharma division
- Global exposure and learning in a regulated, innovative environment
How to Apply
Interested and eligible candidates can click the link provided in the original job notification to register or scan the QR code for quick registration. For more pharma job opportunities across India, visit Pharma Recruiter.
Note: Intas Pharmaceuticals Ltd. does not charge any fee for job applications, processing, training, or testing. Candidates interviewed in the past 6 months are not eligible. This opening is strictly for those with prior biotech/biosimilars experience.
Apply now to be part of Intas’ growth story in biopharmaceuticals!
Walk-in Interview Details
- Date: 19th April 2026 (Sunday)
- Time: 09:30 AM to 05:00 PM
- Venue: Lemon Tree Hotel, 54B/55A, Hosur Main Road, Electronics City, Phase-1, Bengaluru, Karnataka – 560100, India
Why You Should Join
Intas offers a dynamic workplace certified as a “Great Place to Work” with an open-door culture that encourages innovation and collaboration. Professionals gain valuable exposure to cutting-edge biopharma technologies, global regulatory audits, and advanced analytics while contributing to affordable biosimilars for patients worldwide.
With strong emphasis on compliance, continuous learning, and career progression, joining Intas ensures long-term stability and exciting growth in India’s pharmaceutical sector.
FAQs
Who is eligible for these Intas R&D and QA jobs?
Candidates with 3–10 years of experience in the biosimilars/biotech industry and relevant qualifications (M.Sc/M.Tech Biotechnology or related fields) can apply. Prior experience is mandatory.
How can I apply for the walk-in drive on 19th April 2026?
Register via the provided link or QR code and attend the walk-in at Lemon Tree Hotel, Bengaluru, between 09:30 AM and 05:00 PM. Bring all relevant documents.
Is there any application fee for Intas pharma jobs?
No. Intas does not charge any fee for applications, processing, or training. Beware of fraudulent offers.
What career growth opportunities does Intas provide?
Intas offers global exposure, advanced facility experience, and a supportive culture recognized as a Great Place to Work, enabling rapid professional development in biopharma R&D and QA roles.
