Cipla Ltd – Openings for QC / Production / Microbiology / SCM / Engineering / Warehouse
At Cipla Ltd, we constantly work towards ensuring access to
high quality and affordable medicines to support patients in need. Which is
why, we have been trusted by health care professionals and patients across
geographies for the last 8 decades. We are hiring for following departments
Job Location: Goa, Bangalore, Indore
Departments: QC / Production / Microbiology / SCM /
Engineering / Warehouse
Job Description:
Junior Team Member – QC Accountabilities
1. Prepare
documents like SOPs, specifications and non-routine documentation and ensure
timely availability across the site to provide support during the analysis
II. Review the latest pharmacopeial updates, supplements and
amendments by evaluating the updates required in the available document to
ensure the compliance with the current pharmacopoeia through consent with
regulatory body
III. Review the assigned documents by referring the concern
backup and pre-defined quality procedure to ensure its compliance against the
quality requirements
IV. Issue documents to applicable units, by maintaining the
record of the same in the issuance record (bound book) so the current version
of the common document is available at the unit
V. Execute harmonization and simplification process of
documents to reduce complexities in processes and ensure standardized
procedures are followed.
Manager – Microbiology (EM & QMS)
Accountabilities:
1. Ensure
proper organisation of the activities in the individual team of Enviornment
Monitoring by routine monitoring of each team member in order to ensure that is
performing to the best and in compliance to the cGMP requirements
2. Handling
QMS activities for Microbilogy department, participate in investigations of non
compliance
II. Ensure the smooth functioning of the activities relevant
to the cross functional departments and teams by conducting periodic
interactions/ meetings in order to ensure smooth functioning of each team and
to provide necessary support to the manufacturing task and schedules.
III. Ensure the availability and effective implementation of
different quality systems and controls across the different teams in the non
-routine section by confirming availability of required standard procedures and
its trainings in order to ensure that all the operations in section are performed
referring the valid standard approved
1. procedures
and in compliance to the cGMP requirements to finally support the quality
agenda of the organisation.
IV. Ensure the continuous improvements at all the teams of
non-routine section by implementing different good practices in the section in
order to achieve good output and cost savings.
Junior Officer – Production
Job Purpose:
Monitor and execute the production activities in an area
during the shift by maintaining cGMP and safety norms to achieve production
targets
Accountabilities:
1. Execute
production activities in a shift by managing available resources to achieve
production target
2. II.
Maintain standard process parameters as per BMRs and other supporting documents
for achieving production target and maintaining quality
III. Prepare manufacturing records and update online
documentation to meet production and cGMP requirements
IV. Follow safe work processes and ensure safety appliances
are utilised during production activities in shifts to create a safe working
environment
V. Execute production activities in a shift by managing
available resources to achieve production target
Apply Online – Click Here
No comments:
Post a Comment