Cipla is Hiring for Junior Operator – Production,Junior Team Member – QA,RA Compliance Officer,Senior Operator – Production,Junior Operator – Packing and has issued notification to accept Applications. 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 Junior Operator – Production,Junior Team Member – QA,RA Compliance Officer,Senior Operator – Production,Junior Operator – Packing as follows.
Vacancy summary details :
- Company Name: Cipla
- Location : Goa
- Post Name: Junior Operator – Production,Junior Team Member – QA,RA Compliance Officer,Senior Operator – Production,Junior Operator – Packing
- Qualification: B.sc, M.sc, B.pharm, M.pharm, diploma
- Experience: 02-05 years of experience
- No of Vacancies: NA
- Details of Salary: NA
- Closing date for online Application : Apply as soon as possible
- Date of examination: NA
- Time and Venue :NA
- Mode of application : online
- Selection Process: Shortlisted candidates may called for selection process ( Personal interview , Group discussion , etc…,)
Job Description/Skills Required:
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
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