Sr.Executive QC

About this role

Not quite right? These jobs in Bharuch match the same skills — apply to a few to improve your chances.

Mega Walkin - 12th Sept , Saturday @ Unit 1 Ankleshwar

Zydus

In OfficeBharuch

Apply

SENIOR EXECUTIVE - PLANT ENGINEERING (Instrumentation)

Asian Paints

In OfficeBharuch

Apply

Executive & Technical Assistant-EHS

Piramal Pharma

In OfficeBharuch

Apply

Executive - Portfolio Program

Zentiva

In OfficeBharuch

Apply

Skills you'll use

What you'll do

• BSC / MSC Chemistry with 4 to 6 Yrs Experience
• · Analysis of in process, intermediate, raw material, packaging material, ETP and utility samples, stability samples, R&D samples and other samples as per plant requirement as per defined STP’s.
• · Well versed with advance analytical instrument like HPLC, GC, UV, IR, particle sizer, KF titrator.
• · Calibration of all equipment in QC department as per SOP’s.
• · To maintain the records of calibration, working standards, stability data, AMC, outside calibration records, instrument log book, validation report, in process and intermediates test reports as per GLP.
• · To perform analytical method validation as and when required.
• · To perform analytical method development project as and when required.
• · To prepare and update the SOP’s and STP’s of QC department.
• · To maintain 21 CFR part 11 compliance in the laboratory.
• · To release the in process, intermediates samples within defined time line.

Who can apply

• · Analysis of in process, intermediate, raw material, packaging material, ETP and utility samples, stability samples, R&D samples and other samples as per plant requirement as per defined STP’s.
• · Well versed with advance analytical instrument like HPLC, GC, UV, IR, particle sizer, KF titrator.
• · Calibration of all equipment in QC department as per SOP’s.
• · To maintain the records of calibration, working standards, stability data, AMC, outside calibration records, instrument log book, validation report, in process and intermediates test reports as per GLP.
• · To perform analytical method validation as and when required.
• · To perform analytical method development project as and when required.
• · To prepare and update the SOP’s and STP’s of QC department.
• · To maintain 21 CFR part 11 compliance in the laboratory.
• · To release the in process, intermediates samples within defined time line.
• · To perform the sampling of raw materials, packaging materials as per sampling plan.

About Piramal Pharma

Searching for “Piramal Pharma jobs” or “jobs at Piramal Pharma”? You’re in the right place.