...situations
Plant round
Plant round in absence of QA and during IInd and IIIrd shift.
Online checking of critical process parameters during round.
ISO,cGMP,GC,HPLC
Designation: System Audit - QA / ...
...inspect accident site and identify cause of accident.
18. To conduct environment impact assessment and regulatory compliance assessment.
Safety,Environment
Designation: Head of Department - Environment & Saf...
...Validation of instruments/equipments
Appropriate training and guidance to the subordinates.
Safety in the laboratory.
Regular housekeeping and upkeep of the work area.
Maintaining adequate inventory of c...
Required Pharmaceutical Production Formulation Specialist
Location: Ankleshwar Gujarat India
Industry Pharma Formulation
Must have 35 Years of Experience (Must be from Formulation Industry)
Job Description:
As a Pharmaceutical Producti...
~ Implement quality control activities at Ankleshwar adhering to regulatory / global quality Directives and HSE guidelines with optimum utilization of resources to ensure consistent good quality of products to meet with cust...
B. Pharm / M. Pharm from reputed university
2 to 3 years in pharmaceutical manufacturing (Preferably in Granulation , compression Coating section)
Candidate should be able to discharge following roles and responsibilities
Production
...
...deploy a group level reporting mechanisms to monitor HSE programs.
Coordinate with government agencies like pollution control board, inspectorate of factories for periodical surveys and audits related to safety. ...
...time to time, new experiment for effluent disposal with the help of WWTP, EHS guidelines / local statutory compliances.
Plant Manager / Assistant Managers for Deviation / Observation / incidence pertaining to Qua...
MISSION STATEMENT
To build up Zentiva local guidelines, local procedures of packaging material management
Designs and process of packaging material changes
Direct Management of the local Artwork team
MAIN ACCOUNTABILITIES AND DUTIES
L...
Internal Job Description
~ Contribution in management and control of both site project/transfer as well as donor Documentation, such as Product transfer protocols, product transfer checklist, associated BMRs, Master Documents, etc. • Preparing & r...
