Biocon - Walk-In Interviews for Q.A & Production Departments on 10/11/2016 @ Hyderabad - PHARMA WISDOM

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Friday, 4 November 2016

Biocon - Walk-In Interviews for Q.A & Production Departments on 10/11/2016 @ Hyderabad

Walk-In for Quality Assurance (QA) & Production @ Biocon
Location: Hyderabad / Secunderabad
We are hiring experienced candidates for our API Plant-Hyderabad.
Departments: Quality Assurance & Production
Quality Assurance:
Job Title: Assistant Manager
Job Description:
-To handle Quality Assurance analysis/documentation
-Planning and scheduling the department activities.
-Review and approval of qualification / Validation and Protocols and Procedures such as a SOP's, EOP's, IOP's, etc.
-Handling of change controlling and deviations arising from all the department.
-Handling of process validations and cleaning validations and verification for API's and intermediates at SMV.
-Handling of CAPAs.
-Provide training on QA SOP's, cGMP and Induction training.
-Preparation/Review of annual product quality reports for every financial year.
-Review / Approval of New/Revised BMRs, PDRs, and ECCs.
-Responding and complying with internal and external audit observations.
-Document and DATA control.
-Handling of returned goods / reprocess.
-Preparation and review of trend analysis.
-Internal Audit coordinator.
-Review of quality system documents as and when applicable.
-Continuous monitoring of records, labelling and archival.
-Review of technology transfer documents .
-CGMP regulations, GLP and Quality system.
-Retrieval / Review / Approvals of executed BMRs, PDRs, and Dispatch inspection as per the PDR.
-Coordinating for investigations of deviations, batch failures, OOTs and if any incident arises.
-GAP analysis participation in the procedures vs practice and risk assessment.
Qualification: M.Sc/M.Pharm with good percentage.
Experience: 8'Year - 12'Years in Quality Assurance - API /Bulk Drugs.
Production - API Manufacturing:
Job Description:
-Monitoring and control of production operations
-Following SOP's, EOP's, SCP's and OCP's
-Should be responsible for compliance wrt cGMP & EHS
-Should be responsible for Shift Activities
-Maintain & control process parameter as per BPR & perform activity safely.
-Allocation of work to workmen as per days plan
-Looking after daily Production activities and shift work execution in Effective Manner
-To enhancement in production by studying time cycle of the batch.
-Maintaining and updating the batch production records.
-To implement and maintain cGMP guidelines during production activity.
-Trouble shooting process and quality issues.
-Production planning and optimization in the production.
-Continuous improvement so as to reduce production cost, get better yield and Quality Product.
-Handling manpower effectively and efficiently.
-Reporting production and plant details to the Manager.
-To take care of inter departmental Co-ordination to get done work in plant.
-To provide on the job training and guidance to the operators if required.
-Must have API Pharma Production Experience.
Qualification: B.Sc/M.Sc (Chemistry /Biochem) / Diploma in Chemical / Petrochemical Eng.
Experience: 1-10 Years in API Production/Bulk Drugs.
Date of Walk-In: 10th November 2016,
Timings: 9:00AM to 12:30PM & 2.00PM to 5:00PM
Registration: Will be closed at sharp 10:00 AM.
Biocon Limited
Plot Number 213-215,Phase II
Near Patancheru, Via Insapur,
Sanga Reddy Dist-502307
Visit our website:
You must carry a copy of updated Resume, all educational documents, recent salary slips, and experience letters.
Note: Only Male Candidates are preferred due to shifts, Candidates unable to attend the walk-in may mail their resumes.

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