Sanofi Hiring Production Specialist, Officer- VI & P Bachelor Degree in Science / Pharmacy Apply Now
Visual
inspection and packing
Will be
responsible for troubleshooting in visual inspection and packing related
machines.
Will be
responsible for effective installation, commissioning and qualification of
equipment’s in Inspection and Packing area.
Will be
responsible for operation of machines in visual inspection and packing area.
Perform
manual inspection of cartridges and loading / unloading of cartridges.
Perform
execution of in-process checks as per current SOP's and BMR's.
Accountable
for handling and transfer of secondary packaging materials.
Ensure
maintenance and validation activities for visual inspection and packaging
equipment’s in compliance with the current GMP practices and support in failure
investigations.
Execute the
actions described in the SOP's and BMR's includes cleaning and line clearance
of visual control and packing machines.
Support in
continuous improvement of industrial performance in visual inspection and
packaging area.
It is
required to operate and troubleshoot the visual inspection and packing related
equipment (automatic inspection machine, labelling machine, blister packing
machine, cartonator machine etc)- hence maintenance and troubleshooting
experience of automatic VI & P machines is required
Excellent
verbal and written communication skills in English are required.
Knowledge on soft skills like MS office is
required.
Knowledge on
GXP and technical skills involved in relevant manufacturing activities
Medical
device packing
To ensure GMP
and GDP is followed at all levels of medical device packing activities and
relevant activities.
To ensure
adherence to ISO 13485 and laid down standards, Laws & Acts.
Will be
responsible for troubleshooting in medical device packing related machines.
Will be
responsible for operation of machines in medical device packing.
Supervise manual
packing of medical device and document the activities performed.
Perform
execution of in-process checks as per current SOP's and BR's.
Accountable
for handling and transfer of secondary packaging materials.
Ensure
maintenance and validation activities for medical device packing in compliance
with the current GMP practices and escalate the Non-compliance and
non-conformance.
Ensure the
actions described in the SOP's and BR's includes cleaning and line clearance of
medical device packing area.
Training and
Documentation
Responsible
to training and qualification of the people in the team.
Complete the
assigned training and maintain the training file updated.
Accountable
for online entries of batch records, record sheet template, log books etc. for
the operation of visual inspection and packing area and medical device packing.
Support for
preparation of production operations and SOPs, batch production records, record
sheet template, log books, etc.
Working in
teams and Inspection readiness
Ensure the
compliance of area/activity for various regulatory inspections/ audits and GMP
compliance.
Create good
working relation within the team and cross functional teams.
Health,
safety and environment
To identify,
correct and promptly report unsafe conditions, behaviours, or potentially
hazardous situations.
To animate a
strong, proactive culture oriented towards promoting positive behaviours at all
levels of the organization.
Knowledge,
Skills & Competencies / Language
Demonstrated
capacity to efficiently prioritize work and timely inform supervisor on the
progress
Excellent
verbal and written communication skills in English are required.
Knowledge on
soft skills like MS office is required.
Qualifications
A minimum of
Bachelor Degree in Science / Pharmacy.
2 -3 years of
relevant experience in visual inspection and packing.
Relevant
working experience in a Pharmaceutical industry.
Requirements
of the job
This position
requires the incumbent to work in shifts.
This position
requires to maintain the positive working relation with all the stakeholders to
meet the supply
TO APPLY CLICK HERE
Join for Regular Job Updates in What's App & Telegram
No comments:
Post a Comment