About :- Shilpa
Medicare Limited (SML) started its operations as API manufacturer way back in
1987 at Raichur, Karnataka- India. The commercial production in the SML was
started in November 1989. We initially started producing Trimethoprim IP/BP
with in-house developed technology. During the first year of its operation, the
Company had expanded the production facilities to manufacture Trimethoprim
apart from selling on its own, for other reputed Companies like Eskayef
Limited, Bombay Drugs and Pharmas Limited, Bombay Drug House Ltd., US Vitamins
Ltd, Sandoz India Ltd etc. for their export commitments.
Production
Dept Openings
Link
to apply :- http://www.vbshilpa.com/currentopenings.php
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Post :- Executive / Sr. Executive
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Post:- Chemist / Sr.Chemist
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Education:- B.Sc/M.Sc MSc (Org. Chemistry)
Experience:- 8 - 12 Years
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Education:- B.Sc/M.Sc
Experience:- 2-8 Years
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Job Description :
Execute
the production plant as per shift operations to achieve consistent product
quality, quantity and yield.
Trouble
shooting of process and operational issues on shop floor.
Supervise
batch charging and verification of RM Quantities and responsible for
maintaining Batch Production records.
Check
equipments and connected accessories and operate them as per the process
norms.
Monitor
and maintain all parameters as per SOPs and ensure strict compliance with GMP
and safety norms
Experienced
candidates from Pharmaceutical / Chemical Industry only may apply.
Knowledge
of SOP's and manufacturing processes will be an added advantage.
Exposure
to regulatory audits and eagerness to work on the shop floor is desired
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Job Description :
Supervise
batch charging and verification of RM Quantities and maintain Batch
Production records.
Check
equipments and connected accessories for cleanliness and operate them as per
the process norms.
Monitor
and maintain all parameters as per SOPs and ensure strict compliance with GMP
and safety norms.
Seek
assistance for or escalate all process deviations/maintenance
jobs. Experienced candidates from Pharmaceutical / Chemical Industry
only may apply.
Knowledge
of SOP's and manufacturing processes will be an added advantage.
Experience
in manufacturing processes such as compression, granulation, coating, capsule
filling will be an added advantage.
Exposure
to regulatory audits and eagerness to work on the shop floor is desired.
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Post:- Shift In-charge
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Post:- Chemist:
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M.Sc./B.Sc./B.Pharma
8-10 Years experience in API bulk drug
production activities as per cGMP guidelines.
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M.Sc./B.Sc./B.Pharma
1-4 Years experience in API bulk drug
production activities as per cGMP guidelines.
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Apply :- Production Dept Openings
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Quality Control Dept
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Microbiology Dept
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Post -
Chemist
/ Executive / Sr. Executive
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Post :- Manager / Executive
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Education
:- B.Sc/M.Sc (Chemistry)
experience.
Years 5- 8 years |
Education :- B.Sc/M.Sc
experience
2 - 8 Years
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Job
Description :
Responsible for allocation and
review of analysts work against standards.
Maintaining RM control samples,
performing routine analysis and reporting test results, conducting internal
audits and preparing trend reports.
Taking necessary investigative
measures for out-of-specification laboratory results and facilitating
achievement of production schedules.
Responsible for staff
development through proper induction and training.
Analytical experience in the
pharma industry will be preferred.
Should be well versed with QC
activities of API in process labs.
Exposure to regulatory audits
and eagerness to work on the shop floor is desired
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Job
Description :
Responsible for maintaining of
SOP’S,STP’S,Validation Protocols and reports.
Implementation and ensuring the
Quality Management system in Microbiology department.
Maintaining of inspection &
Test Methods.
Responsible for overall
Microbiology Department functions.
Exposure to regulatory audits
and eagerness to work on the shop floor is desired
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Apply for Quality Control Dept & Microbiology Dept
Click here
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Quality Assurance Dept
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Post:- Manager QA
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Post :- Executive / Sr. Executive :
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B.Sc/M.Sc
(Chemistry) : 10 - 15 Years experience.
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B.Sc/M.Sc
(Chemistry) : 5 - 8 Years experience.
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Job
Description :
Follow up with Regulatory
Audits and Customer Audits.
Reviewing all Regulatory
documents prior to submission to Regulatory Affairs Department.
Implementation of Quality
Management System across the site.
Data review and submission to
RA for DMF deficiencies.
Investigations are carried out
during Batch deviations, OOS results and customer complaints.
Validation Master Plan,
Validation Protocols Validation Reports and qualification documents
Approving changes to the
existing systems, documents, processes, specifications and test methods of
Raw materials, Intermediates and Finished Products.
Exposure to regulatory audits
and eagerness to work on the shop floor is desired
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Job
Description :
Review process documents
stage-wise and facilitate timely release of batches.
Perform IPQA checks during
production.
Review and compile deviations
and change controls. Ensure quality compliance of the product through
internal audits.
Knowledge of SOP's and IPQA
processes and exposure to external audits.
Experienced candidates from
Pharmaceutical / Chemical Industry preferred.
Exposure to regulatory audits
and eagerness to work on the shop floor is desired
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Apply for Quality Assurance Dept
Click here
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Analytical Research & Development
Dept
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Engineering Dept
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Asst.
Manager/Sr. Executive
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Sr.Manager:
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M.Sc. Chemistry, 5-7 Years hands on experience of XRPD, DSC, TGA, SEM and Particle size analysis
etc.
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BE/B.Tech/ M.Tech [Mech]: 10-12 years
experience in Engineering Maintenance of cGMP Compliant API /
Chemical Plant. Independently responsible for all maintenance activities,
documentation as per cGMP, OSHA, ISO in the respective areas.
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Apply for Analytical Research & Development Dept
& Engineering Dept
Click here
http://www.vbshilpa.com/currentopenings.php
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2 comments:
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Share&Stock
FMCG
sectoral investment caps
National Stock Exchange Nifty
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