Freshers Chemistry Jobs at Zentiva | Apply Now For The Executive- Manufacturing Science and Technology (MST) Role
Zentiva is hiring an Executive – Manufacturing Science and Technology (MST) in Ankleshwar, India. This role offers an exciting opportunity for chemistry and pharmacy professionals to work on analytical method development, validation, and GMP/GLP compliance while supporting pharmaceutical and API manufacturing processes. If you’re eager to advance in the pharma industry with a focus on quality and innovation, this position is an excellent fit.
- Job Position: Executive- Manufacturing Science and Technology (MST)
- Location: Ankleshwar, Gujarat, India
- Job ID: R2468437
About the Company
Zentiva is a leading pharmaceutical company dedicated to improving healthcare accessibility across global markets. With a strong focus on high-quality, affordable medicines, Zentiva combines innovation, compliance, and operational excellence to support patients worldwide.
Job Description
The Executive – Manufacturing Science and Technology (MST) will provide analytical support for chemistry-related activities in compliance with regulatory directives, quality standards, and safety protocols. This position ensures adherence to GMP/GLP standards, supports product development, and contributes to achieving organizational objectives.
Key Responsibilities
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Analytical Method Validation & Development
- Develop, validate, and transfer analytical methods.
- Conduct sampling and testing of raw materials, intermediates, APIs, stability samples, hold time study samples, and cleaning validation samples.
- Support impurity and reference standard qualification.
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CMC Activities & Documentation
- Send samples to third parties/customers, prepare and approve CoAs.
- Generate and archive GMP documents.
- Prepare system and operational SOPs using eDMS.
- Manage inventory of reagents and chemicals.
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Quality, Compliance & Regulatory Support
- Ensure compliance with GMP, GLP, and ALCOA principles.
- Handle investigations of OOS/OOT, deviations, lab incidents, and customer complaints.
- Review pharmacopoeia and regulatory requirements regularly.
- Support change control, deviation management, and regulatory audits.
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Instrumentation Management
- Operate and calibrate HPLC, GC, HSGC, UPLC, UV, FTIR, DSC, and other laboratory instruments.
- Troubleshoot instruments and coordinate with service providers for maintenance.
- Ensure qualification and documentation of laboratory instruments.
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HSE Compliance
- Maintain safe working conditions in line with HSE guidelines.
- Identify and correct unsafe practices and report hazardous situations.
- Qualifications
-
- Postgraduate degree in Chemistry or Pharmacy.
- 0–7 years of experience as an analyst or development technologist in the Pharmaceuticals/API industry.
- Strong knowledge of GMP & GLP.
- Experience with LIMS & QMS is preferred.
- Excellent coordination, analytical, and communication skills.
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