Axelia Laboratories

The wheel is churning as India ascends to new heights. Happy Independence Day everyone!!

Job Profile :

Responsible for the day to day manufacturing, maintenance, packing & documentation activities of the respective departments ie: Tablet/Capsule/Oral Liquid/External Dept.

Operate Manufacturing machines, equipment and instruments. Perform scheduled cleaning & preventive maintenance of all equipment.

Handling of area and equipment qualification.

Perform line clearance activities and inform QA.

Formulation development.

Preparation & timely maintenance of MFR, BMR & BPR.

Validation of processes with coordination with QA department.

Review and updation of SOP.

Calibration & Validation of instruments & equipment.

Co-ordination with Stores, QC & QA departments for smooth day to day production activity.

Issue material requisitions as per MFR and request the same as per the requirement.

Receive material indent from stores & control over raw material usage.

Taking care of test samples, test request and supervision of operators.

Provide training on manufacturing processes & GMP for internal training.

Presentation of manufacturing activities and processes to internal & external auditors.

Attend the queries related to manufacturing activities during audits.

Initiate the change control, Deviation, CAPA in coordination with QA department.

Academic credentials : B.Pharm or higher. Computer Literacy is required.

Work Experience : 1-5 years experience in pharmaceutical formulations manufacturing preferred.
Manufacturing Approval from FDA will be given weightage.
Freshers may also apply for internship.

Personal Characteristics : Knowledgeable. Team person. Good communication skills. Fast learner. Systematic & well organised.