Quality Control Documents in Pharmaceutical

ABP EMPOWER

Urgent opening for Quality Control Documentation in Pharma Company @ Solan Himachal Pradesh.

Experience - 6 Yrs in Pharmaceutical Quality Documentation

Salary - 30,000 to 35,000 Per Month

Monitor the testing and Release of Raw materials, In process and finish products in stipulated time.

Manage all quality documentation.

Sample management of RM/PM/in process/FP.

Monitor stability sample testing and preparation of stability report.

Preparation of AMV protocol and report

Responsible for routine release of swab and rinse water analysis

Responsible for HPLC operations

Responsible for preparation and implementation of qualification/calibration schedule.

Responsible to prepare/update STS/STP/worksheet/COA of RM, PM, In process, FP..

Preparation and maintain preventative maintenance (AMC) and calibration calendar.

Maintain laboratory in good condition to face the regulatory audits.

Responsible for Calibrations of all QC instruments.

Responsible to follow related SOPs

Job Allocation of QC persons.

Initiation and closing of QMS documents like Out Of Specification, Change Control, Deviations, CAPA, Incidence report, etc.

Facing the Internal/External audits.

Responsible for Analyst qualification and training.

Responsible for completion of log books.

Procurement of Chemicals/Reagents/Reference standard/impurity and maintain the inventory.

Responsible for timely review the raw data generated in Quality Control Laboratory.

Experience : 5 - 7 Years

No. of Openings : 5

Education : Professional Degree

Role : Pharmaceutical Quality Control Engineer

Industry Type : Pharma / BioTech / Clinical Research

Gender : Male

Job Country : India