Baxter Quality Control Job Vacancy 2021 – Apply Online
This is where you make a difference in our patients’ safety. As a member of the Baxter Quality team, you will play an essential part in our mission of saving and sustaining lives. Quality is important throughout the entire product lifecycle and works collaboratively with all areas of the organization. Because Quality touches everything Baxter does, a role in Quality provides many opportunities for growth, learning and a successful career that has a daily impact on people’s lives.
Job Title: Assoc, Quality Control – RMPM
Req Id: JR – 054393
Location Ahmedabad, Gujarat, India
Job Category: Quality Control
Eligibility Criteria:
- M Sc / M Pharm / B Pharm
- Candidate must have 3 – 6 yrs. of working experience in QC department (i.e. pharma industry)
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 [email protected] and let us know the nature of your request along with your contact information.
This is where you save and sustain lives
At
Baxter, they are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You’ll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.Baxter’s products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.
Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.
Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.
- To carry out the sampling of all the materials according to Standard Operating Procedure (SOP).
- To carry out the testing of Raw Material and Packing Material according to the approved standard test procedure.
- To support Sub-Department Manager in releasing of Raw Material and Packing Material
- To carry out the calibration of instruments as per the schedule.
- To coordinate with the stability department for the working standards as per the guidelines and various pharmacopeias.
- To ensure the status label on the material and transfer such material in the respective area.
- To prepare reagent & volumetric solution and standardize it.
- To carry out all the necessary tests as per respective specifications and procedures and record the results for all the materials.
- To check the stores and ensure the implementation of GMP norms in the stores.To inform
- to superior immediately in case of any Out of Specification result or Non-conformity or Laboratory Incident observed or any instrument breakdown.
- To review the sampling activity of all the materials performed by team members.
- To assess the results of testing of Raw Material, Packing Material products to ensure alignment with the standard operating procedure (SOP) and regulatory guidelines.
- To review results of the tests against the specification & Standard Test Procedure performed by team members.
- To ensure availability of the working & impurities standards as per various pharmacopeias.
- To ensure the status label on the material and transfer such material in the respective area.
- To support Sub-Department Manager, in the investigation of out of specification (OOS), non-conformity and Laboratory Incident Report (LIR) and take corrective and preventive actions.
- To check and verify standardization and preparation of reagents and volumetric solutions.
- To review periodic observation of retained samples done by team members
- To follow and ensure Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP) and Good Documentation Practices inside QC.
- To support & guide team members in implementing change control, Corrective and preventive actions (CAPA) and check the effectiveness of CAPA, give suggestions from Divisional Head if required.
- To train team members on current Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), and Good Documentation Practices.
- To assist the Sub-Department Manager with information of SOP and give suggestions to improve system performance.
- To check, verify, and review the calibration of all the analysis instruments whether performed as per the schedule.
- To ensure recording of all the data related to the testing online, on a day-to-day basis and ensure traceability of the same.
- To check the completion of method transfer successfully in coordination with Analytical Development Lab (ADL) Department.
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