QA Supervisor (Compounding)
QA Supervisor (Compounding)
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Job Description
This is where you save and sustain lives
At 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. Youll feel a sense of purpose throughout the organization as we know our work improves outcomes for millions of patients.
Baxters 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 liveswhere your purpose accelerates our mission.
Due to an internal promotion we have a great opportunity to hire a QA Supervisor. The Quality Assurance Supervisor will report to the QA Manager and be responsible to lead the overall QA Team in the continuous compliance of Compounding Unit to cGMP and Specials manufacturing requirements local procedural requirements and Baxter Corporate policies.
Baxter Compounding manufacture life saving products such as chemotherapy antibiotics and nutrition. The quality team play a vital role in ensuring these products are released safely and in a timely manner.
This role is MondayFriday with flexibility on start/finish time.
Duties and responsibilities
- Management of the QA Team including development and performance review.
- To ensure that QA procedures are written and reviewed to reflect current practice in agreed timelines.
- To ensure compliance with all QA deadlines eg: worksheet review event investigations audit actions CAPAs and change management.
- Assist in the planning and coordination of MHRA inspectors visits and selfinspection audits with regard to renewal of licence.
- To ensure all testing equipment is calibrated at agreed intervals and accompanying results are within specifications.
- To manage the recruitment of new staff to agreed staffing levels and oversee the training of new and existing staff within QA Officers team.
- To authorise written procedures and other documents including amendments.
- Ensure that all QA databases are maintained.
- Maintain all aseptic suites to the highest standards of EU GMP.
- Perform QA review/ approval of NCR Change Control and Validation documentation;
Experience required
- Graduate Qualification or BTec / equivalent in Pharmacy or a scientific subject
- Minimum three years relevant experience in a GMP Environment
- Field of Expertise Quality Assurance Production Validation Microbiology. Aseptic
- Strategic thinker
- Good interpersonal skills
- Able to manage and motivate a team
- Able to deal with pressure
- Good time management
- Good communicator both verbal and written
- Ability to work with minimal supervision
- Able to communicate effectively
- High degree of attention to detail.
- Understand the importance of accuracy and flexibility
- Ability to lead effectively and efficiently
- Ability to deal with and resolve conflict
- Able to demonstrate technical knowledge
- Foster relationships and maintain open communication with the other Compounding functions
What happens next
A member of our Talent Acquisition team will review your application and be in touch within 2 weeks. Thank you for your interest in Baxter.
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Reasonable Accommodations
Baxter 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 link here and let us know the nature of your request along with your contact information.
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Required Experience:
Manager
Employment Type
Full-Time
