REQUIREMENTS
Education / Experience
Education:
Graduate / Post Graduate in Pharmacy or Chemistry
Experience:
2-3 years in Pharma industry with awareness of Quality management systems, manufacturing activities, process validation, Quali...
QMS: Maintain detailed documentation of QMS(change control, deviation, incident, market complaints, product recall)
VMP: maintain and execution of Validation plan as per schedule
Master index: Prepare and maintain of Master index for SOP, STP, ...
...Maintenance program for the site to ensure all Equipment/Structure/Buildings/Facilities related Preventive Maintenance carried out.... ...Local Boiler Authority, GIDC Department, DGVCL, Elect...
Fibre analysis
Should able to handle all the activities of quality control, should be familier with fibre testing such as Tensile testing, Fibre Finish, Fibre Crimp, Fibre colour, fibre shrinkage, lab grade carding machine, fibre moisture, ...
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...
ACTIVITIES
RESPONSIBILITIES
1
TESTING
Maintain each Lab Instrument operations as per SOP.
Ø
Arrange & check raw materials testing as per received supplier. Check the RM description on bags/ drums, in case of any ...
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...
Master data creation of existing and future requirements.
Co-ordinating with PM new product routing developments.
CO-ordination with Business controller for Pk calculations.
Co-ordination with production for implementation of processes me...
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...
