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Salary
$26k – $64k per year (Estimated)
Location
In office (India)
Seniority
Middle · 3+ years exp
Employment
Full-Time
Overview
Company
Impact
Profile match
Zentiva is a prominent European pharmaceutical enterprise specializing in the production and supply of high-quality generic medicines and consumer healthcare products. Headquartered in Prague, Czech Republic, the company operates across dozens of international markets, delivering accessible treatments to millions of patients. Managing the complete lifecycle from laboratory research and manufacturing to global distribution, it focuses on expanding access to affordable, essential medications.

JOB TITLE

Assistant Manager : Manufacturing Science and Technology (MST)

REQUIREMENTS

Education / Experience

M.SC OR PH.D. IN ORGANIC CHEMISTRY

Experience: 3-12 years

Technical skills &

Competencies / Language

  • Knowledge of modern organic Chemistry
  • Knowledge of performing synthetic experiments.
  • Application of varied analytical methods.
  • Troubleshooting
  • Knowledge of design of experiments (DOEs).
  • Knowledge of Quality by Design (QbD).

Zentiva values

  • Accountability, Authenticity, Collaboration, Courage and Trust

JOB PURPOSE

Generic

Providing synthetic organic chemistry expertize for the development of processes for APIs/intermediates and DMF compilation support to the customer, ensuring compliance to regulatory, group directives, quality requirements, safety standards and effective utilization of resources, transversal cooperation with cross functional teams to fulfill the organization’s objective, living Group’s Values and Code of Ethics

KEY ACCOUNTABILITIES

Process development:

Execute experiments with analysis on own in laboratories for developing cost-effective processes of APIs/intermediates

Isolation, Purification and characterisation of APIs/intermediates/impurities

Facilitate Technology transfers/ shift in charge in case of Pilot plant technology transfer/production

Support the production team for investigation of deviations. Identify the root cause, perform the experiments and provide a concise report to QA.

Providing required data for the DMF compilation.

New ideas generation for new APIs/Intermediates/COGs estimation

Timely closure of experiments and data compilation in report format.

cGMP:

Compliance to current GMP/Regulatory guidelines.

Compliance to local and global norms of Quality/Regulatory and HSE.

Regulatory compliance (Global/Local)

Regular Pharmacopoeia and regulatory requirement review

Training of self and subordinates on quality and HSE systems.

Instrumentation:

Effective use of Electronic Lab Notebook (ELN) for recording lab experiments making sure each experiment is signed and closed electronically within stipulated time.

Knowledge of NMR, Mass, HPLC, GC, UV, FITR, DSC, etc for interpretation of results

Must follow the data integrity principles

Other

Complying to HSE Requirements

Identifying and correcting unsafe conditions or behaviours and promptly reporting others potentially hazardous situations.

Lab maintenance and asset preventative maintenance activities.

Carrying out any other assignments or projects as per the instruction of the Dept. Head to meet with the organizational objectives and priorities.

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