EA

Lupin; Panaji; On-site; INR 240,000 - 360,000; Full time

Job summary

Lupin in Panaji, Goa invites an Associate- Production to work in Granulation, Compression, Coating and Encapsulation sections. The role requires adherence to cGMP, SOPs and BMR documentation, with focus on quality and traceability in a highly regulated pharmaceutical manufacturing environment.

The candidate should have a Diploma in Pharmacy or a Graduation in Science, with 2-5 years of relevant production experience, and willingness to uphold EH&S standards while supporting continuous

Qualifications

• Diploma in Pharmacy
• Graduation in Science
• 2-5 years of work experience in production/manufacturing

Responsibilities

• Comply with cGMP, GxP and EH&S requirements.
• Operate and document production steps per SOPs and BMR.
• Handle raw materials, bulk, semi-finished and finished goods.
• Maintain hygiene and cleanliness of production areas and equipment.
• Report quality concerns and participate in cGMP training.

Skills

Innovation

Creativity

Education

Diploma in Pharmacy

Graduation in Science

Job description

Job Description:

Job Description

Department: Production
Designation: Associate- Production
Working Section: Granulation, Compression, Coating and Encapsulation

• Comply with all cGMP, GxP and any other applicable regulatory requirement, including EH&S requirements.
• Complete training on relevant SOPs and develop an understanding of the activities to be conducted prior to undertaking any task.
• Conduct all tasks/activities as per the applicable SOPs. Report any difficulty or deviation in following the procedure/instruction to immediate supervisor/managers.
• Report any quality concern or suggestion for improvement to supervisors/ managers.
• Manufacturing / processing of batches of assigned products under supervision as per instructions given in the BMR.
• Handling and movement of raw material, bulk, semi-finished and finished goods.
• Operation, washing and cleaning of equipment’s and accessories used in related production activities as per respective SOP.
• Up-keeping area and machines as per GMP requirements.
• To Support Quality Management Systems and to report any discrepancy, abnormity, non-conformance or any incidence observed to the Department Head and QA Head.
• Receipt of RM and PM from Warehouse and ensuring overall cleanliness of areas.
• Doing operations as per the SOPs and BMR with online recording in respective documents as applicable.
• To ensure self-hygiene before entering in the production area and follow all the other rules & regulation set by HR department.
• Performing in-process checks as per respective BMR and recording of results of in respective documents as applicable.
• To fulfil the training need as per current needs with respect to cGMP, Job, safety, health & Hygiene by attending the training programmes.
• Cost effectiveness in production operation by controlling overtime, revenue expenses and achieving standard yield.
• Critically monitoring of the environmental conditions with a view to meet the standards mentioned in BMR and SOP.
• Ensure calibration and preventive maintenance of manufacturing equipment and instruments as per approved schedule and the results of same meeting the standards.
• To perform line clearance activity during batch to batch and product to product change over and ensure the compliance as per SOP.
• Issuance, retrieval and destruction of dies and punches, product dedicated bags and sieves, silicon sleeves, pipes, hose pipes and screens.
• To ensure the audit compliance.
• Trouble-shooting: To attend the problems of machine and process as and when necessary.
• Any other assignment allocated by production Head.
• To attend required cGMP/ On Job /Functional training activities as per planner.

Work Experience

2-5 years

Education

• Diploma in Pharmacy
• Graduation in Science

Competencies

• Innovation & Creativity
• Result Orientation
• Collaboration
• Customer Centricity
• Developing Talent
• Stakeholder Management
• Strategic Agility
• Process Excellence