Sapigen Biologix (Bharat Biotech) – Multiple Senior Roles in Production, QC & QA for Vaccines/Sterile Injectables

Vaccine Jobs – Sapigen Biologix, a Bharat Biotech subsidiary, is hiring experienced professionals for production, quality control (microbiology, virology, chemical), and quality assurance roles in vaccines and sterile injectables manufacturing.

These high-level opportunities in pharma jobs, biotech careers, and vaccine production require 8–20 years of relevant experience and are based at their facility in Bhubaneswar, Odisha. Ideal for experts in aseptic operations, cell culture, chromatography, sterility testing, virology assays, and QMS.

About the Company

Sapigen Biologix Pvt. Ltd., a wholly-owned subsidiary of Bharat Biotech International Limited, specializes in the research, development, and manufacturing of innovative vaccines and biologics. Located in Bhubaneswar, Odisha, the facility focuses on advanced vaccine production using cutting-edge technologies in viral vectors, recombinant proteins, and sterile processes.

Backed by Bharat Biotech’s legacy of developing world-class vaccines (including Covaxin®), Sapigen upholds stringent regulatory standards (WHO-GMP, USFDA-aligned), quality excellence, and innovation to deliver safe, effective biological products for global health. The company emphasizes a collaborative, science-driven culture with strong focus on aseptic manufacturing and virology expertise.

Job Details

• Company Name: Sapigen Biologix Pvt. Ltd. (Subsidiary of Bharat Biotech)
• Location: Bhubaneswar, Odisha, India
• Work Type: On-site
• Note: Candidates must have relevant experience in vaccines or sterile injectables

Job Description

Sapigen Biologix is recruiting senior talent for critical functions in vaccine and biologics production. Roles demand deep expertise in aseptic techniques, downstream processing, analytical testing, virology assays, and quality systems in a highly regulated sterile environment.

Production – Drug Substance

• Department: Production (Drug Substance – Vaccines/Biologics)
• Experience: 10–20 Years
• Qualification: M.Sc / B.Sc (Microbiology, Biotechnology, Virology, Biochemistry, Veterinary)
• Key Areas:
  • Sterile aseptic operations
  • Autoclave & DHS operation
  • Automated CIP/SIP operations
  • Cell culture aseptic operations
  • Chromatography (purification)
  • Media/buffer preparation
  • Zonal centrifuge operation
  • QMS, Change Control, CAPA, Deviation Investigation

Quality Control – Microbiology

• Department: Quality Control – Microbiology
• Experience: 15–20 Years
• Qualification: M.Sc / B.Sc (Microbiology / Biotechnology preferred)
• Key Areas:
  • Sterility testing
  • Bioburden & microbial enumeration
  • Endotoxin testing (BET)
  • Media preparation, qualification & growth promotion testing
  • Sterility/BET testing of RM, PM, bulk & finished product

Quality Control – Virology

• Department: Quality Control – Virology
• Experience: 0–15 Years
• Qualification: M.Sc / B.Sc (Virology, Microbiology, Biotechnology)
• Key Areas:
  • PCR / qPCR / RT-PCR
  • Cell culture-based virology assays
  • Cell culture techniques
  • ELISA & immunoassays
  • Viral infectivity assays
  • Method validation protocols & reports
  • OOS / OOT / deviation investigations
  • Batch release for finished product

Quality Control – Chemical

• Department: Quality Control – Chemical
• Experience: 8–12 Years
• Qualification: M.Sc / B.Sc (Chemistry / Analytical Chemistry)
• Key Areas:
  • Raw material & finished product testing
  • HPLC / GC / UV / IR analysis
  • Stability & validation sample analysis
  • OOS / OOT handling & documentation
  • Preparation of SOPs, STPs, specifications
  • Deviation / change control / CAPA

Quality Assurance – IPQA

• Department: Quality Assurance – In-Process QA
• Experience: 10–15 Years
• Qualification: M.Sc / B.Pharm / M.Pharm
• Key Areas:
  • Line clearance & in-process compliance
  • Batch manufacturing & packing record review (BPR)
  • Deviations, OOS investigations & trend analysis

Skills/Qualifications

• Proven experience in vaccines, biologics, or sterile injectables manufacturing/testing
• Strong knowledge of GMP, GLP, WHO-GMP, and regulatory guidelines
• Expertise in aseptic processing, cell culture, chromatography, sterility/virology testing
• Proficiency in QMS tools (CAPA, deviation, change control, investigation)
• Analytical instrument handling (HPLC, GC, PCR, ELISA, etc.)
• Documentation excellence and audit readiness

Key Responsibilities

• Execute sterile production processes and downstream purification
• Perform microbiological, virological, and chemical quality testing
• Ensure compliance during in-process checks and batch release
• Investigate deviations, OOS/OOT, and implement corrective actions
• Prepare/review SOPs, protocols, reports, and validation documents
• Maintain aseptic integrity, equipment qualification, and media management

Benefits/Perks

• Opportunity to work on cutting-edge vaccine and biologics projects
• Career growth in a reputed Bharat Biotech subsidiary
• Exposure to advanced sterile and virology technologies
• Supportive, innovation-focused culture
• Competitive compensation aligned with experience

How to Apply

Send your updated CV and portfolio (highlighting relevant vaccine/sterile injectable experience) to hrd@sapigen.com. For more vaccine jobs, biologics opportunities, and pharma roles in Odisha, visit Pharma Recruiter.

Apply now—join Sapigen Biologix and contribute to life-saving vaccine innovation!

Why You Should Join

Sapigen Biologix, backed by Bharat Biotech’s proven success in vaccine development, offers a rare chance to work on high-impact biologics in a state-of-the-art facility.

With a strong emphasis on quality, compliance, and scientific advancement, the company provides professional fulfillment, exposure to global standards, and long-term stability in India’s growing vaccine ecosystem—ideal for seasoned experts passionate about public health and sterile manufacturing.

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