Thursday, May 6, 2021

Cipla Hiring B.Sc, M.Sc, B.Pharm, M.Pharm, Diploma for Multiple Openings

Cipla Hiring B.Sc, M.Sc, B.Pharm, M.Pharm, Diploma for Multiple Openings



Cipla Recruitment 2021.Cipla Notification full detailes below.Cipla is one of the most respected pharmaceutical companies not just in India but across more than 170 countries. Our portfolio includes 2000 products in 65 therapeutic categories with one quality standard globally. Cipla€™s turnover in FY13 was 1.5 billion USD.

Important Vacancy details:

Post Name: Junior Operator – Production,Junior Team Member – QA,RA Compliance Officer,Senior Operator – Production,Junior Operator – Packing

Education:Diploma in Pharmacy / Mechanical Engineering,B. Pharma,B.Sc (Microbiology),M.sc,M.pharm

Experience:02-5 years of experience

Location:Goa,Sikkim

Job Description: Junior Operator – Production

Job Purpose

Execute the production operations in line with safety and GMP requirements to meet the manufacturing targets in shift

Accountabilities

I. Operate the equipment efficiently without error and deviation as per SOP to meet shift targets

II. Provide suggestions for optimization of processes to manufacture quality product

III. Execute and update online documentation to meet cGMP requirements IV. Deliver training to workmen and adhere cGMP and safety guidelines in production process to ensure smooth operations

Junior Team Member – QA

Job Purpose

Review the compliance level of site for deficiency response, prepare master validation protocol and report as per company quality policy and applicable regulatory guidelines

Accountabilities

I. Collate, review and provide required work plans on received deficiencies to HO in order to respond to regulatory authorities in a timely manner

II. Review Master Validation protocol and report for timely execution of validation batches and timely submission of documents in order to response for deficiencies

III. Review annual product quality review report at units for completeness and data correctness to ensure compliance to cGMP requirements and audit readiness

IV. Review, upkeep and issue regulated market technical agreements at site for execution of batches as per customer requirement

V. Receive and distribute approval certificate, dossiers (TDP & RAP) and development report at unit for execution of new products smoothly VI. Coordinate with auditors and site teams for regulatory and customer inspection/ audit at site to meet regulatory expectation and acquire GMP approvals

VII. Prepare final draft of compliance to audit observation and check whether it is in line with cGMP requirement to avoid regulatory action and continual improvements

VIII. Collect, compile and review raw data and finalise the same for timely submission of MHRA, UK interim update document to corporate as per agency requirement by tracking interim updates at a site level, for risk based inspection planning

IX. Drive continuous improvement initiatives in CQA to facilitate adherence to cGMP

X. Execute on time and errorless submissions by reviewing product license, all certificates for product registration and tender , staff approvals and other applications to adhere to legal requirements

XI. Support in CDSCO and state FDA inspection to be GMP compliant and getting product licence, FDA stall approvals by ensuring cross functional interaction

: RA Compliance Officer

Job Purpose

The Regulatory Affairs Compliance Officer is responsible for the review and approval for all artwork components to ensure compliance to the relevant Acts, regulations and guidelines,and the maintenance of electronic artwork on designated server. This individual will be the designated responsible individuals within the department that maintains the standards when it comes to Artwork and whom will also be the point of contact in terms of Artwork status. This individual will also be responsible for reviewing and approving the signing off Promotional material (SEP and OTC) to ensure compliance to the relevant Acts, regulations and guidelines.

Junior Operator – Production

Job Purpose

Execute the production operations in line with safety and GMP requirements to meet the manufacturing targets in shift Accountabilities

I. Operate the equipment efficiently without error and deviation as per SOP to meet shift targets II. Provide suggestions for optimization of processes to manufacture quality product

III. Execute and update online documentation to meet cGMP requirements IV. Deliver training to workmen and adhere cGMP and safety guidelines in production process to ensure smooth operations

Junior Operator – Packing

Job Purpose

Operate & maintain packing machines to achieve quality product & shift wise targeted output with maximum utilisation Accountabilities

I. Prepare the machine for packing operation as per production plan by using proper resources to ensure smooth operations

II. Operate the packing machines by using minimum resources to get quality product

III. 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 safety

V. Deliver training to workmen and adhere cGMP and safety guidelines in production process to ensure smooth operations

For More Detailes

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