Assoc, Quality Control @ Baxter
Req #: JR - 005236
Location: Ahmedabad, GJ IN
Job Category: Quality
Date Posted: 9/6/2019 7:34:51 AM
Are you looking for a career that matters?
We believe every person deserves a chance for a healthy
life, free from illness and full of possibility. We see a world full of
healing, with viable care options available to those with limited choices
today. We envision new ways of providing physicians, pharmacists and nurses
with technologies that not only treat chronic diseases, but also work to
prevent them. We’re looking for team members who are motivated to learn, grow
and innovate, while making a meaningful difference for millions of people
around the world.
To
investigate failure of finished product (FP) / In-process (IP) product, in case
of any out of specification (OOS) / Laboratory error / deviation and take
corrective and preventive actions.
To ensure
that preparation of reagents and volumetric solution and standardization
on time.
To perform
periodic observation of retained sample.
To initiate
Change control (CcM), Non conformation report (NCR), Out of Specification
(OOS), Document change record (DCR) etc.. QMS related documents.
To do the
work allocation in shift and ensure it complete within timeline.
To assess
the results of testing of In-process sample and finish products to ensure
alignment with standard operating procedure (SOP) and regulatory guidelines.
To review
results of the tests against the specification & standard test procedure
performed by team members.
To
investigate out of specification (OOS), Non-conformity and Laboratory Error
Report (LER) related to In-Process Product Testing (IPPT) & Finished
Product Testing (FP) and take corrective and preventive actions.
To follow
and ensure Good Laboratory Practices (GLP) and Good Manufacturing Practices
(GMP) inside QC.
To ensure
availability the working & impurities standards as per various
pharmacopoeias.
To support
& guide team members in implementing change control, Corrective and
preventive actions (CAPA) and check effectiveness of CAPA, give suggestions
wherever necessary.
To guide and
support team members for performing all test for in-process product &
finish product as per the specification and schedule.
To train
team members on current Good Manufacturing Practices (cGMP) and Good Laboratory
Practices (GLP) with support from Sub-Department Manager.
To prepare
SOP as and when required.
To check,
verify and review the calibration of all the analysis instruments whether
performed as per the schedule.
To check
completion of method transfer successfully in coordination with Analytical Development
Lab (ADL) Department.
Equal
Employment Opportunity
Baxter is an
equal opportunity employer. Baxter evaluates qualified applicants without
regard to race, color, religion, gender, national origin, age, sexual
orientation, gender identity or expression, protected veteran status,
disability/handicap status or any other legally protected characteristic.
EEO is the
Law
EEO is the
law - Poster Supplement
Pay
Transparency Policy
Reasonable
Accommodations
Baxter is
committed to working with and providing reasonable accommodations to
individuals with disabilities. If, because of a medical condition or
disability, you need a reasonable accommodation for any part of the application
or interview process, please send an e-mail to Americas_TTA@baxter.com and let
us know the nature of your request along with your contact information.
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