Cipla Released Job Openings On 22/09/2022.Cipla Limited is an Indian multinational pharmaceutical company, headquartered in Mumbai, India.Interested and eligible candidates required to fill application form in online with Education and personal details and submit application along with resume .Job application form link provided at the end of post. Eligibility for the Therapy Manager / Medical Represetative as follows.
Vacancy Details:
Cipla Recruiting Bachelor in Pharmacy,Diploma in Pharmacy / Engineering,B. Pharm/B.Sc. for BABE and For clinical B. Pharma or M.Sc. Or M.B.B.S.B. V. Sc. & A.H is compulsory. M. V. Sc. (Pharmacology and Toxicology) Graduates with 01+ yrs of relevant experience for Junior Officer-Production,Junior Operator-Packing,Team Member – Clinical/Pre-Clinical/BABE Position.
Important Details :
- Location:Mumbai ,Goa
- No of Vacancies:NA
- Details of Salary:NA
- Opening date for online Application:22/09/2022
- Mode of application :Online
- How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps
Related Job : Lupin Hiring B.sc,B.pharm,D.pharm,Diploma Freshers-Send Your Resume To HR
Job Description/Skills Required
Junior Operator – Packing
Operate & maintain packing machines to achieve quality product & shift wise targeted output with maximum utilisation
AccountabilitiesI. Prepare the machine for packing operation as per production plan by using proper resources to ensure smooth operationsII. Operate the packing machines by using minimum resources to get quality productIII. Execute and update online documentation to meet cGMP requirements and maintain data integrity Fill Machine logs. Document entries/SOP and process simplification to meet cGMP.IV. Perform packing machine operations safely to avoid safety incidences by appropriately handling the machines and thereby maintaining high standard of safetyV. Deliver training to workmen and adhere cGMP and safety guidelines in production process to ensure smooth operations
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Junior Officer – Production
Job Purpose
Monitor and execute the production activities in an area during the shift by maintaining cGMP and safety norms to achieve production targets
Accountabilities
I. Execute production activities in a shift by managing available resources to achieve production target
II. Maintain standard process parameters as per BMRs and other supporting documents for achieving production target and maintaining quality
III. Prepare manufacturing records and update online documentation to meet production and cGMP requirements
IV. Follow safe work processes and ensure safety appliances are utilised during production activities in shifts to create a safe working environment
V. Execute production activities in a shift by managing available resources to achieve production target
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Team Member – Clinical/Pre-Clinical/BABE
Execute, monitor, report and interpret preclinical, clinical and BABE studies at CROs to support various regulatory submissions within targeted timelines, budgets, quality and regulatory guidelines; identify health hazard and assess risks associated with pharmaceuticals/ chemicals/ intermediates/ impurities, etc. by toxicological review and derivation (Only for preclinical)
Accountabilities
I. Gather preclinical/ clinical/ BABE study outline data by understanding the specific regulatory requirements and project constraints to ensure successful conduct of studies/trials cost effectively and within timelines
II. Check CROs for conducting preclinical/ clinical/ bio equivalence studies by site feasibility/ selection visits or evaluation for ensuring adequate facility, skill and experience for conducting the studies as per requirements
III. Liaise with CROs and internal team to enable preparation, review, and finalization of study protocol as per the defined strategy to ensure that protocol is approved by all relevant stakeholders, Ethics Committee, and/or Regulatory authorities within targeted timelines
IV. Ensure procurement and dispatch of Innovator samples/ RLD and availability of test formulation along with relevant documents (like COA, GMP statements, batch size information etc.) before study initiation
V. Monitor and/or audit ongoing studies at CROs to ensure satisfactory conduct as per requirements (guidelines, regulatory, study specific, etc.) and project timelines
VI. Act as the project coordinator for the entire study by liaising with internal team members, cross-functional teams, CROs and Project Managers to align all stakeholders and successfully conduct the BE study
VII. Identify health hazard and assess risk of pharmaceuticals/ chemicals/ intermediates/ impurities, etc. by toxicological review and derivation of PDE (permitted daily exposure)/ OEL (occupational exposure limit)/ TTC (Threshold of toxicological concern) for pharmaceuticals/ chemicals – (only for preclinical team)
