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Ds Manufacturing Executive – Drug Substance Production (Usp / Dsp / Bioprocessing)

IPCA Laboratories Limited
0-3 years
Not Disclosed
Dhar, India
1 June 4, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Clinical Trials, Functional Teams, Literature Review, Management Skills, Medical Information, Medical Records, Medical Strategy, Pharmacovigilance, Regulatory Compliance, Risk Management, Safety Scien, Coaching Skills, Data Science, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Pro, Collaboration, Communication Skills, gmp, GMP Guidelines, Operational Excellence, Problem Solving Skills, Quality Agreements, Quality Compliance, Quality Management, Quality Standards, Regulatory Requ, Communication Skills, Continual Improvement Process, Master Data, Material Requirements Planning (Mrp), Materials Management, People Management, Production Planning, Supplier Relationship Management (Srm), Supply-Chain Man, CPC Certified

DS MANUFACTURING EXECUTIVE – DRUG SUBSTANCE PRODUCTION (USP / DSP / BIOPROCESSING)

JOB SUMMARY
A Drug Substance (DS) Manufacturing role responsible for execution of upstream and downstream bioprocessing operations in a GMP-regulated biopharmaceutical manufacturing environment. The role involves fermentation, purification, batch processing, and compliance-driven manufacturing activities to ensure consistent production of high-quality biologics and drug substances.

EXPERIENCE REQUIRED
Fresher to 3 years of experience in biopharmaceutical manufacturing, biotechnology production, or upstream/downstream processing. Freshers with strong industrial training or bioprocess exposure are eligible.

EDUCATION QUALIFICATION
M.Sc / M.Tech in Biotechnology or related life science discipline.

KEY RESPONSIBILITIES

  • Execute drug substance manufacturing operations as per GMP guidelines and production schedules

  • Perform upstream processing (USP) activities including fermentation, cell culture, and bioreactor operations

  • Carry out downstream processing (DSP) including purification, filtration, and separation techniques

  • Monitor and control bioprocess parameters to ensure product quality and yield

  • Operate and maintain manufacturing equipment as per SOPs and validated procedures

  • Ensure proper cleaning validation and equipment preparation for production cycles

  • Maintain accurate batch manufacturing records (BMR) and process documentation

  • Follow GMP, safety, and environmental health standards during all manufacturing activities

  • Support process optimization and continuous improvement initiatives in production workflows

KEY SKILLS REQUIRED

  • Strong understanding of bioprocessing principles (USP and DSP)

  • Knowledge of fermentation, purification, and bioreactor operations

  • Familiarity with GMP manufacturing systems and pharmaceutical SOPs

  • Strong documentation and batch record handling skills

  • Awareness of cleaning validation and equipment operation procedures

  • Ability to work in a regulated, production-driven environment