Openings for QA Sr. Executive in USP and Production, QA in Gracure pharma

Openings for QA Sr. Executive in USP and Production, QA in Gracure pharma

 About the Job

Brief Work Outline

This is a non-administrative expert position liable for supporting different Quality Confirmation exercises collaborating with the QA Office Manager to include: Working with all utilitarian groups on keeping up with the quality administration framework.

Center regions Lead lab project documentation reviews (Insightful information audits) of Reference Standard Laboratory(RSL), Biologics, Compendial Improvement lab (CDL) - Scientific Strategy Validaiton, CDL-New Use Testing, Logical Innovative work (ARD), Steadiness Delivery Review, RSL-NMR, and Check program (Synthetic and Microbial science), survey of gear intelligence level/OQ/PQ conventions reports and other need/impromptu lab project surveys.

What will YOU make mean for here at USP?

Lab Task documentation reviews:

Convenient survey and consummation of task documentation reviews (Insightful information audit).

Survey and endorsement of hardware capability/approval conventions and reports.

Keeping up with Quality administration framework:

Support boss to rehash OOS-OOT, Deviations, examinations, RCA and CAPA Adequacy checks.

Support QA/other cross useful divisions in readiness of outside ISO 9001 and 17025 reviews.

Guarantee the consistence to ISO norms and interior SOPs.

Records and information control:

Survey of SOPs, Division controlled records, structures, designs and chronicled of QA archives.

Supporting manager to rollout and execute worldwide drives.

Who USP is Searching For?

The effective up-and-comer will have a shown comprehension of our main goal, obligation to greatness through comprehensive and evenhanded ways of behaving and rehearses, capacity to rapidly fabricate validity with partners, alongside the accompanying capabilities and experience:

Graduate degree in Science with 5-8 years important involvement with a drug industry, ideally working in Programming interface or definitions industry.

Least of three (3) long stretches of active involvement with research facility, treatment of insightful hardware, capability of scientific gear, alignment, metrology and other lab exercises.

Least of two (2) years' involvement with logical survey with great specialized report composing abilities, examination of Value notices (OOS-OOT, Deviation, Occurrence, Change controls and CAPA), record control, administrative and additionally ISO reviews and other QA exercises.

Information on Scientific Strategy approvals and Biologics/Microbial science/Cell science related testing is an additional benefit.

Working information on MS Word, PowerPoint, Succeed and so forth.,

Extra Wanted Inclinations

ISO 9001 Reviewer Confirmation and information on ISO/IEC 17025

Any QA/QC course/accreditations, for example, Certificate in Drug Quality Confirmation, Far reaching Course in Quality Affirmation and Control Frameworks, Great Documentation Practices, Information respectability, Examinations (Main driver Investigation) and chance evaluation is an additional benefit.

Comprehension of GMP, GLP, and ISO guidelines and the mix of the guidelines into working frameworks in the research center.

Great composed and verbal interchanges abilities.

Results driven with showed effective results.

Administrative Obligations


Openings for Gracure - QA and Production departmenrs

Dear candidate

We have an #urgent requirement from #Gracure Pharmaceutical Ltd at Bhiwadi Location. Interview mode telephonic The Details are:

Department: Production

Designation: junior Officer

Qualification: B. Pharma/M. Pharma /

Experience: 6 month to 1 Years

Department: QA (IPQA)

Designation: junior Officer

Qualification: B. Pharma/M. Pharma /

Experience: 6 month to 1 Years

If Interested please share your resume on [email protected]

Macleods Pharmaceutical limited is hiring!

#Department : Production (OSD) & Q.C

#Experience :

Production : 2-7 years in Granulation/ Coating / Laser drilling & Imprinting / Bulk Packing / Blister .

Quality Control: 2-7 years in RM / PM / GLP / Stability / AMT& AMV.

#Education :

Production - M.Pharma/ B.Pharma / D.Pharma / Diploma / ITI

Quality Control - M.Sc / B.Pharma / M.Pharma

#Location : Pithampur , ISEZ

Interested candidates can share resume on [email protected].