Job Description

This is where you save and sustain livesAt Baxter, we 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 ensure the analysis of the in process product or finish product sample and on time and release of it as specified under various regulatory norms and in house standards.
• To prepare the working standards as per the guidelines and pharmacopoeias.
• To record all the data related to the testing online on day-to-day basis.
• To bring to the notice the abnormalities and deviations to Manager Quality Control and Q.C. - Head.
• To be responsible for any other work this may be assigned to you by the management from time to time.
• To intimate the Executive or Manager Quality Control for any abnormality or failure of any finished product, finish product samples or in process product testing, however if he is absent then intimating the status of the same to Q.C Head.
• To perform the tests as per the specification & standard test procedure and record the necessary results in respective documents.
• To investigate failure of finished product (FP) or In-process (IP) product, in case of any out of specification (OOS) or Laboratory error or deviation and take corrective and preventive actions.
• To coordinate with stability department for the working standards as per the guidelines and various pharmacopoeias.
• To carry out the calibration of all the analysis instruments as per the schedule.
• To prepare reagents and volumetric solution and standardize it.
• To perform periodic observation of retained sample.
• To perform and implement change control, wherever necessary.
• To perform chemical analysis.

Desired Educational Qualification: M Sc. / B Sc. / B Pharm / M PharmDesired Skills & Experience: The candidate must have

• 2 - 6 years of experience in QC department in Pharmaceutical industry, preferably in injectable products

Reasonable AccommodationsBaxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the here and let us know the nature of your request along with your contact information.Recruitment Fraud NoticeBaxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our .

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