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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