Company Description The company is renowned FMCG Company
CTC :- Upto 30L
Role Description
The Process Excellence Manager - Six Sigma Black Belt will be responsible for leading continuous improvement initiatives across our Baddi location....
...Experience
1. Knowledge of Contract Manufacturing Operations (CMO) process for the Pharmaceuticals.
2. Knowledge of current regulatory requirements such as Schedule M, Eu GMP, USFDA, ICH etc.
3. Rich experienc...
...efficiency in combustion and value for money.
Role Description
This is a contract role for an Electrical cum Instrumentation Technician for Boiler at Universal Fuel Industries located in Baddi. The Technicia...
...Job Description
Title : Utility Engineer
Location : Baddi, Himachal Pradesh
Utilities Engineer will take the ownership of operational... ...holders concerns.
The Utilities Engin...
...Job Description:
Title : Project Manager - Process and Packaging technology
Location... ...Standardisation and the Best Practice communities (upon appointment).
...
...provide maximum availability and running at optimum efficiency within Utility system.
Ensure team is strictly following all Safety, Q&FS, Sustainability, HACCP, Local regulations and ISO requirements.
SPOC for...
...Responsibilities
An ointment manufacturing chemist is responsible for overseeing the formulation, development, and production of ointments and related pharmaceutical products. Their job responsibilities may inclu...
...Job Responsibilities
Job Location in Himachal Pradesh
#- Good Knowledge of machine maintenance.
#- Good Knowledge of complete production process (Plastic Injection Moulding).
#- existing processes designed ...
A Product Engineer is a professional who is responsible for designing commercial products and their production processes. This position works closely with product development teams to turn ideas into marketable items based on industry research.
s...
Experience Required: B.Pharm / M. Sc. with 6-10 years of experience in Micro QC. Approved chemist licensed candidate shall be preferred. Well versed with CAPA, GMP Documentation, should have exposure to regulatory audits such as MHRA, USFDA etc...
