QE Head (Greenfield Project)

QE Head (Greenfield Project)

Location : Central or South India

Job Summary

QE (Quality Engineer) Lead's responsibilities encompass leading a QE team, defining quality standards, developing testing strategies, and ensuring software quality throughout the development lifecycle.

Responsibilities :

1) To aware about the process like vial washing, depyrogenation, filtration, filling, manufacturing, lyophilizer, component washing and sterilization, terminal sterilization, isolators, CIP SIP skid, leak test, X ray inspection, VHP, clean utility like Clean steam, compressed air, PW and WFI generation system, AHU, FFM.

2) To handle the designing and qualification activity of Utility like Pure steam generation and distribution system, Purified water and WFI generation and distribution system, Nitrogen and compressed air generation and distribution system, AHU, FFM, LAF, area, cold storage etc

3) To handle preparation, review and execution of qualification protocol of new equipment like, User requirement specification, Design qualification, Installation qualification, operational qualification, performance qualification and Computer system validation and qualification

4) To prepare and execution of schedule requalification protocol of equipments and utility.

5) To prepare new standard operating procedure for qualification activity and also review SOP of process equipments.

6) To handle communication with vendor and procurement team on design parts of new equipments.

7) Issuance, retrieval and storage of qualification documents.

8) Exposure of regulatory auditors like USFDA, EU, ANVISA, CANADA etc.

9) To handle the designing and qualification activity of process equipments like vial washing, tunnel sterilizer, filling machine, capping machine, Lyophilizer loading and unloading system, Lyophilizer, filtration skid, and isolators, VHP passbox, manufacturing skid, suspension manufacturing skid, CIP SIP skid for manufacturing and filtration equipments, dispensing isolators, manufacturing isolators, pH meter, DO meter, integrity tester, Autoclave, Terminal sterilizer, ultrasonication machine, GMP washer, external washing machine, leak test and X ray inspection machine, packing equipment’s etc.

10) To handle indenting to procurement of accessories and equipment’s required for qualification activity of above equipment’s and area.

11) To prepare schedule for qualification activity, calibration activity, updation of status label of qualification activity etc.

12) To handle the QMS documents like change control, CAPA, risk assessment, deviation etc.

13) To handle the QMS documents like change control, CAPA, risk assessment, deviation etc.

14) To ensure compliance to cGMP and documentation for various qualification activities.

15) Ensure proper planning and execution of the qualification activity in accordance with the plan and allocation of man power.

B. Pharmacy, M. Pharmacy

Experience : 12 to 15 Years of experience in relevant field in Pharmaceutical Industry