Cipla Hiring for Junior Team Member – QC/QA/Engineering /Operator – Production/Packing

Junior Operator – Production

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

Education Qualification Diploma in Pharmacy / Engineering

Relevant Work Experience 2 years of experience in packing with knowledge of handling of QMS activity, qualification and other related documents

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

Education Qualification B. Pharma/ M.Sc

Relevant Work Experience 2 years of experience in quality assurance department

Junior Team Member – QC

Job Purpose

Prepare, update and review the specifications, SOPs, policy and operating documents for analysis of materials in order to ensure alignment to predefined quality parameters and compliance to respective standards / pharmacopeia and cGMP requirements

Accountabilities

I. Prepare documents like SOPs, specifications and non-routine documentation and ensure timely availability across the site to provide support during the analysis II. Review the latest pharmacopeial updates, supplements and amendments by evaluating the updates required in the available document to ensure the compliance with the current pharmacopoeia through consent with regulatory body III. Review the assigned documents by referring the concern backup and pre-defined quality procedure to ensure its compliance against the quality requirements IV. Issue documents to applicable units, by maintaining the record of the same in the issuance record (bound book) so the current version of the common document is available at the unit V. Execute harmonization and simplification process of documents to reduce complexities in processes and ensure standardized procedures are followed

Education Qualification M.Sc. / B. Pharma Relevant Work Experience 2 years of experience in QC department of a pharmaceutical organization

Junior Officer – Engineering

Job Purpose

Execute the maintenance activities in the plant & ensure the minimum breakdown with maximum efficiency by following safety & GMP Standards

Accountabilities

I. Give inputs for preparing & adhere to unique planner for planned preventive maintenance & instrument calibrations for effective maintenance and adherence to standards. II. Handle breakdown maintenance to avoid recurrence and maintain continuous process operations III. Use new technologies initiated by Management while adhering to CAPEX and OPEX targets to improve Machine/system performance IV. Follow HSE safety standards to maintain high level of Safety during maintenance so as to avoid major breakdown and report accidents/ incidences V. Perform Material and Spare management and issue Consumables, spares , materials , log books etc. in order to avoid delays due to unavailability of materials

Education Qualification Graduate Engineer / Diploma In Engineering Relevant Work Experience 2 years of experience in Pharma / API industry (Maintenance and Projects)