Executive, Officer - Quality Assurance

Role & responsibilities

1) To be prepared document related to audit as per audit agenda.

2) Filled vendor questionnaires & prepared related documents.

3) Keeping record of key Customer.

4) To be prepared process validation protocol and report as per seniors guidance.

5) To be prepare cleaning validation protocol and report as per seniors guidance.

7) To be prepared master, controlled, uncontrolled, reference, obsolete & distribute documents as per SOPs and formats requirement.

8) To help the senior for preparation of CAPA according to audit report.

9) Issuance of Change control, OOS, deviation & other QMS formats whenever required from respective department and retained record in logbook.

10) To be prepared BPCR as per procedure.

11) To be issue BPCR to all blocks as per prerequisite.

14) To be handle change control, market complaint, deviations, CAPA.

15) To be issue documents, protocols, log book and format to all department as per prerequisite.

16) Retrieval of documents.

17) To be controlled all master documents.

18) To be prepared schedule & conduct Internal audit.

19) To be prepared APQR of all products.

20) Preparation of documents for Certification & product registrations work i.e. FDA, Halal, Kosher, Reach. etc.

Review specification, test procedure and SOP's for their deficiencies according to audit points

1) To be prepared document related to audit as per audit agenda.

2) Filled vendor questionnaires & prepared related documents.

3) Keeping record of key Customer.

4) To be prepared process validation protocol and report as per seniors guidance.

5) To be prepare cleaning validation protocol and report as per seniors guidance.

6) To be conduct training and evaluation done as per Schedule.

7) To be prepared master, controlled, uncontrolled, reference, obsolete & distribute documents as per SOPs and formats requirement.

8) To help the senior for preparation of CAPA according to audit report.

9) Issuance of Change control, OOS, deviation & other QMS formats whenever required from respective department and retained record in logbook.

10) To be prepared BPCR as per procedure.

11) To be issue BPCR to all blocks as per prerequisite.

13) To be prepared data for monthly report as per QMS and submit to senior.

14) To be handle change control, market complaint, deviations, CAPA.

15) To be issue documents, protocols, log book and format to all department as per prerequisite.

16) Retrieval of documents.

18) To be prepared schedule & conduct Internal audit.

19) To be prepared APQR of all products.

Preferred candidate profile

Role: Quality Assurance - Other
Industry Type: Pharmaceutical & Life Sciences
Department: Quality Assurance
Employment Type: Full Time, Permanent
Role Category: Quality Assurance - Other

Education
UG: B.Sc in Chemistry
PG: MS/M.Sc(Science) in Chemistry