Opportunity for B. Pharma/ M. Pharma as a Quality Specialist III (Hybrid Mode) – Apply Now

Looking to advance your career in pharmaceutical quality assurance? Teva Pharmaceuticals invites skilled B. Pharma/ M. Pharma professionals to join our team as Quality Specialist III. Embrace a dynamic role where you’ll ensure top-notch quality standards in a hybrid work environment. Explore this opportunity to make a meaningful impact in the pharmaceutical industry while enjoying flexibility in your work-life balance. Join Teva Pharmaceuticals today and embark on a rewarding journey towards excellence.

Job Description

This section is where we attract the attention of potential candidates and sell the role. How has the role come about? What makes it appealing? What are the key responsibilities? How is the role better with Teva than with another company? Wherever possible, we should bring through the essence of our EVP pillars, i.e., we care, we’re in it together, and we make work fulfilling.

Responsibility

1. Complaint Processing:

Performs the functions associated with receiving, trending, logging and coordinating the return of the Samples for product quality related Complaints. This includes complaints received via phone, email, and internet. Utilize knowledge and experience from processing of live complaint calls to lead by example.

2. Assists QAS Intake team management in handling of QAS Intake team activities :

Serves as a Subject Matter Expert on all In-Take Team complaint processes and scenarios and assists QAS employees to ensure compliance with Quality Assurance Services Standard Operating Procedures and Work Instructions. Collaborate with QAS Daily review team and/or closing team to discuss and calibrate on varying views on how records should be handled. Responsible for handling High Profile complaints. Conduct a day end review to ensure that proper justification is provided for and documented in all High Profile complaints.

3. Participate and contribute to the continuous improvement activities of the QAS group:

Participate in the continuous improvement of the QAS Group to drive operational excellence by performing a variety of tasks and projects to increase compliance, efficiencies and effectiveness of actions within the Group. Tasks and Projects may include but are not limited to:
a. Support audits and inspections of QAS group
b. Provide data related to product complaints, volumes, Deviation reports as required
c. Identify automation and defect proofing opportunities and highlight the same to QAS management via business cases, quantifiable data.

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