Lupin Walk-In R&D, Manufacturing & QA/QC
- Company Overview
- Job Role & Responsibilities
- R&D – Biosimilar & Analytical Development
- DS Production (Upstream & Downstream)
- DP Manufacturing & Aseptic Operations
- Quality Assurance (QA)
- Quality Control (QC)
- DP Engineering (DME)
- Eligibility / Qualifications
- Required Education
- Relevant Courses
- Experience
- Skills Required
- Location & Salary
- Interview Location:
- Job Location:
- Salary:
- Application Process
- Walk-In Interview Details:
- Why You Should Apply
- FAQs
- Who can apply for these roles?
- What experience is required?
- What departments are hiring?
- Where is the interview conducted?
- Do I need prior biotech experience?
- Summary Table
Lupin Biotech Walk-In 2026 – R&D, Manufacturing & QA/QC Roles in Ahmedabad
Lupin Biotech is conducting a large-scale walk-in drive for multiple vacancies across R&D, Drug Substance (DS) Production, Drug Product (DP) Manufacturing, Quality Assurance, and Quality Control at its Ahmedabad hiring event. The company is inviting experienced professionals (2 to 10 years) for a range of roles spanning biosimilar development, upstream/downstream processing, aseptic manufacturing, and advanced analytical testing.
This is a high-impact opportunity for candidates from biopharmaceutical and life sciences backgrounds to work on cutting-edge biotech platforms, including mammalian and microbial systems, bioassays, and regulatory-compliant manufacturing operations.
Company Overview
Lupin Biotech is part of Lupin’s global pharmaceutical ecosystem, focused on advancing biologics, biosimilars, and complex injectable products. The organization is known for its strong R&D capabilities, global regulatory presence, and commitment to delivering high-quality, affordable biologic therapies.
With state-of-the-art facilities and a strong pipeline in biosimilars, Lupin Biotech operates at the intersection of science, innovation, and regulatory excellence. Teams work across process development, analytical characterization, and large-scale manufacturing aligned with international standards.
Working here offers:
- Exposure to biosimilar development and bioprocess engineering
- Hands-on work in upstream and downstream manufacturing environments
- Experience with aseptic processing and sterile manufacturing
- Opportunities to contribute to global healthcare through biologics
Job Role & Responsibilities
R&D – Biosimilar & Analytical Development
- Develop and optimize biosimilar processes and formulations
- Perform analytical characterization, bioassays, and comparability studies
- Support technology transfer from R&D to manufacturing
- Maintain detailed scientific documentation for regulatory submissions
DS Production (Upstream & Downstream)
- Execute cell culture (mammalian/microbial) and fermentation processes
- Perform downstream purification including chromatography and filtration
- Monitor critical process parameters and ensure batch compliance
DP Manufacturing & Aseptic Operations
- Handle filling, visual inspection, and packaging operations
- Ensure strict adherence to aseptic techniques and cleanroom protocols
- Maintain batch records and comply with GMP guidelines
Quality Assurance (QA)
- Manage QMS activities, deviations, CAPA, and investigations
- Work with LIMS/SAP systems for documentation and tracking
- Perform IPQA checks and support audits and inspections
Quality Control (QC)
- Conduct analytical testing using chromatography, CE, SDS-PAGE
- Perform HCP and host cell DNA analysis
- Maintain GLP-compliant documentation and stability data
DP Engineering (DME)
- Support mechanical/electrical systems for manufacturing operations
- Ensure maintenance of utilities and equipment used in sterile production
These roles are essential to ensure product quality, regulatory compliance, and successful commercialization of biologics.
Eligibility / Qualifications
Required Education
M.Pharm, B.Pharm, B.Tech, M.Tech, M.Sc (Microbiology, Biotechnology, Chemistry)
Relevant Courses
Biotechnology, Microbiology, Bioprocess Engineering, Pharmaceutical Analysis, Pharmaceutics
Experience
- 2 to 10 years in biopharmaceutical or biotech manufacturing/R&D
Skills Required
- Knowledge of bioprocessing (upstream/downstream)
- Experience with analytical techniques and bioassays
- Understanding of GMP, GLP, and regulatory compliance
- Familiarity with aseptic manufacturing and cleanroom operations
Location & Salary
Interview Location:
- Novotel Ahmedabad, Iscon Crossroads, Sarkhej–Gandhinagar Highway, Ahmedabad
Job Location:
- As per business requirement (biotech manufacturing sites)
Salary:
- Competitive and aligned with experience and role
Application Process
Walk-In Interview Details:
- Date: 12 April 2026 (Sunday)
- Time: 08:00 AM to 04:30 PM
- Venue: Novotel Ahmedabad, Iscon Crossroads
Candidates should carry updated resumes, ID proof, and relevant documents for the interview. Direct interaction with hiring managers will be part of the selection process.
Why You Should Apply
- Work on next-generation biotech and biosimilar platforms
- Exposure to global-quality manufacturing and regulatory systems
- Strong career growth in R&D, QA, QC, and production roles
- Opportunity to join a globally recognized pharmaceutical group
FAQs
Who can apply for these roles?
Candidates with relevant experience in biopharmaceutical R&D, manufacturing, QA, or QC.
What experience is required?
2 to 10 years in biotech or pharmaceutical operations.
What departments are hiring?
R&D, DS Production, DP Manufacturing, QA, QC, and Engineering.
Where is the interview conducted?
Novotel Ahmedabad.
Do I need prior biotech experience?
Yes, relevant experience in biologics or biopharma is preferred.
Summary Table
| Company | Lupin Biotech |
|---|---|
| Vacancies | R&D, DS Production, DP Manufacturing, QA, QC, Engineering |
| Required Education | M.Pharm, B.Pharm, B.Tech, M.Tech, M.Sc |
| Experience | 2–10 years |