IPQA CHEMIST

Job Description

• To perform IPQA activities at shop floor in each and every stage of sterile manufacturing and packing.

• QA overview for clean room behavior and aseptic activity.

• Review of batch processing records.

• Review of all documents relating to the manufacturing, Packaging & analysis report prior to batch release.

• Review of documents of respective areas and logbooks for adequacy and completeness.

• QA overview for receipt of material from warehouse to production.

• IPQA of Dispensing, Manufacturing, Packaging and Dispatch activities.

• Review and Control of SOP's, Specification, BPR issuance, Master Formulae and Records.

• Preparation & Review of process validation protocols and reports.

• Executing the validation/re-validation activity in the absence of authorized person.

• Any job activity assigned by HOD

• Responsible for regulatory audits.

 Execute IPQA Excellence by setting clear benchmarks.

• Smart Thinker and displays smart/ tactical moves & mental agility.

• Is open and flexible when faced with changing circumstances and finds ways and means of doing things and not get struck with the past.

• Comes up with ideas which are different and can be used commercially, profitably and growth.

• Support and guide subordinates by giving appropriate examples & feedback. Encourage team to come up with new ideas.

• Proposes solution which has elements of sustainability.