Opening For Officer-
QC @ Otsuka Pharma, Ahmedabad (Japanese MNC)
Experience: 2-6
yrs
Qualification: B.Pharm
/ M.Pharm / B.Sc / M.Sc (Chemistry, Biotech, Microbiology)
Job description:
To carry out the
sampling of all the materials according to Procedure
To carry out the
testing of Raw Material and Packing Material according to approved procedure.
To release Raw
Material and Packing Material.
To carry out the
calibration of instruments as per the schedule.
To prepare the
working standards as per the guidelines and various pharmacopoeias.
To ensure the status
tag on the released material and transfer such material in the released area.
To analyze the
artworks as per the guidelines.
To follow the Good
Laboratory practices and Good Manufacturing practices (GMP).
To prepare reagent
& volumetric solution and standardize it.
To carry out all the
necessary tests and record the results for all the material.
To record all the
data related to the testing online, on day-to-day basis and ensure easy
traceability.
To prepare
requirement list of chemical & reagent for procurement.
To perform the tests
as per the specification & method of analysis and record the necessary
results in prescribed documents.
To investigate failure
of finished product (FP) / In-process (IP) product, in case of any out of
specification (OOS) / deviation and take corrective and preventive actions.
To carry out the
calibration of all the analysis instruments as per the schedule.
We are looking for
qualified and experienced candidates for our Quality operations. Candidates
possessing good communication skill and exposure in Parental
formulations.
Opening For Officer-
QA @ Otsuka Pharmaceutical, Ahmedabad
Experience: 2-6
yrs
Qualification: B.Pharm
/ M.Pharm / B.Sc / M.Sc (Chemistry, Biotech, Microbiology)
Job description
- To verify raw material, primary packing
material at the time of material issuance and material dispensing.
- To perform routine IPQA monitoring like
volume check, critical control step verification during manufacturing of
the product, sampling and periodic verification activities.
- To verify sample / good destruction
process .
- Receipt and handling of data
loggers.
- To carry out reconciliation and physical
verification of the returned goods.
- To verify logbooks, online documents,
records, analysis report and other supporting documents related to
products manufactured in the plant.
- To execute the Corrective and Preventive
Action (CAPA) defined by Quality Management System (QMS),
- To verify secondary packing
material.
- To execute line clearance for routine
packing activity, monitor each packing line at regular time interval and
sample collection.
- To support in trend analysis of the
packing line monitoring and keep track of Out of Trend (OOT) .
- To execute the CAPA defined by QMS .
Opening For Officer/
Sr. Officer- Production@ Otsuka Pharma, Ahmedabad
Experience: 2-7
yrs
Qualification: B.Pharm
/ M.Pharm / B.Sc / M.Sc (Chemistry, Biotech, Microbiology)
Job description
- To ensure the cleanliness and
environmental norms of various area like dispensing, compounding, filling,
capping, including airlocks .
- To ensure cleaning and disinfection of
floor, ceiling, wall and equipments.
- To ensure that the maintenance of
dispensing compounding, filling, capping, including airlocks is as per
Standard Operating Procedure (SOP) norms.
- To carry out planning of material issue
and dispensing as per priority of batch manufacturing.
- To prepare documents regarding material
issue and dispensing.
- To issue the material from store as per
Batch Manufacturing Record.
- To ensure the batch manufacturing process
is done as per Batch Manufacturing record.
- To control the timing of Cleaning In
Process (CIP) / Sterile In Process (SIP) and batch manufacturing process,
to start the production timely.
- To do the Bubble Point Test (BPT) /
Forward Flow Test (FFT) of product filter before and after filtration and
Water Intrusion Test (WIT) of air filters.
We are looking for
qualified and experienced candidates for our Manufacturing operations.
Candidates possessing good communication skill and exposure in Parental
formulations
Looking For ADL
Officer _ Otsuka Pharmaceutical, Ahmedabad
Experience: 2-6
yrs
Qualification: B.Pharm
/ M.Pharm / M.Sc
Job description
- Responsible for Analytical Method
Validation and Method Development activity.
- To perform F&D sample analysis.
- Responsible for Good Lab Practices (GLP)
Activities and its complies.
- Responsible for Calibration of lab
instruments.
- Preparation and review of Validation
Protocols/Reports and Analytical Reports including data.
- Preparation/Review of SOP and its
compliance.
- Responsible for Procurement of analytical
and Lab requirements.
- To maintain the Documents of Analytical
Protocols and Reports including Validation and Development.
- Responsible for maintain the stock of
Laboratory requirements including chemicals and other analytical
requirements.
- To maintain all data and log book records
with Online as per GLP Requirement
E-Mail: hrm.opmf-amd@otsukapharma.in / sagar.somaiya@otsukapharma.in
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