Shilpa Medicare Ltd Openings for Prodcution,QC,QA,Engi,Research dept , Position:- Chemist to Manager for all Post 2 to 15 years as per position in industry - My Hope Portal

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Saturday 16 September 2017

Shilpa Medicare Ltd Openings for Prodcution,QC,QA,Engi,Research dept , Position:- Chemist to Manager for all Post 2 to 15 years as per position in industry


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

 

Post :- Executive / Sr. Executive
Post:- Chemist / Sr.Chemist 
Education:- B.Sc/M.Sc MSc (Org. Chemistry)

Experience:- 8 - 12 Years
Education:- B.Sc/M.Sc


Experience:- 2-8 Years
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

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.

Post:- Shift In-charge
Post:- Chemist:
M.Sc./B.Sc./B.Pharma

8-10 Years experience in API bulk drug production activities as per cGMP guidelines.
M.Sc./B.Sc./B.Pharma

1-4 Years experience in API bulk drug production activities as per cGMP guidelines.
Apply :- Production Dept Openings

Quality Control Dept


Microbiology Dept


Post - Chemist / Executive / Sr. Executive

Post :- Manager / Executive

Education :- B.Sc/M.Sc (Chemistry)

 

experience.

Years 5- 8 years 

 Education :- B.Sc/M.Sc

experience
2 - 8 Years
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

 

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

Apply for Quality Control Dept & Microbiology Dept

Click here


Quality Assurance Dept

Post:- Manager QA

Post :- Executive / Sr. Executive : 

B.Sc/M.Sc (Chemistry) : 10 - 15 Years experience.

B.Sc/M.Sc (Chemistry) : 5 - 8 Years experience.
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

 

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

Apply for Quality Assurance Dept

Click here


Analytical Research & Development Dept


Engineering Dept

Asst. Manager/Sr. Executive

Sr.Manager:

M.Sc. Chemistry, 5-7 Years hands on experience of XRPD, DSC, TGA, SEM and Particle size analysis etc.

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.  

Apply for Analytical Research & Development Dept

& Engineering Dept

 

Click here

http://www.vbshilpa.com/currentopenings.php