Assistant Manager : Manufacturing Science and Technology (MST)
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Before you apply
Work modeon-site
Typefull-time
SeniorityMid
Experience3–12 yrs
DepartmentManufacturing Science and Technology (MST)
Company size1,001–5,000 people
PostedSep 16, 2026 · 1mo ago
Verified live14h ago
At a glanceSummarised by Seekless from the posting.
M.Sc. or Ph.D. in Organic Chemistry
Experience: 3-12 years
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)
Accountability
Authenticity
Collaboration
Courage
Trust
Knowledge of NMR, Mass, HPLC, GC, UV, FITR, DSC for interpretation of results
Must follow the data integrity principles
Identifying and correcting unsafe conditions or behaviours
Lab maintenance and asset preventative maintenance activities
Carrying out any other assignments or projects as per the instruction of the Dept. Head
Complying to HSE Requirements
Skills
design of experiments (DOEs)
Quality by Design (QbD)
ELN
NMR
Mass
HPLC
GC
UV
FITR
DSC
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.