Quality Manager for Sterilization Processes
1 day ago
Schott North America invites applications for a Quality Manager for Sterilization Processes to lead our efforts in ensuring compliance with ISO and cGMP regulations across our sterile products portfolio. This exciting opportunity is ideal for a seasoned professional with a strong background in chemistry, microbiology, or a related field, and a minimum of 5 years of experience in a Quality Engineer role with sterile products. Your expertise in validating and re-validating sterilization processes, managing data, and analyzing trends will be invaluable in driving continuous improvement initiatives. Additionally, your experience in product/process investigations, validations, instrument qualifications, and EM programs will serve as a solid foundation for this role. With your extensive knowledge of ISO 9001, 13485, and 15378, along with cGMP, you will play a key role in ensuring the highest level of quality and compliance across our organization.
About Our Company
At Schott North America, we pride ourselves on being a leader in the production of high-quality glass containers for the pharmaceutical industry. Our commitment to excellence and innovation drives us to continually improve our processes and products. We strive to foster a collaborative and inclusive work environment that supports the growth and development of our employees. If you share our passion for quality, innovation, and teamwork, we encourage you to apply for this exciting opportunity.
What We Offer
As a valued member of our team, you can expect a competitive salary range of $125,000 - $170,000 per year, depending on experience, excellent healthcare benefits, including medical, dental, and vision, short and long-term disability, tuition reimbursement, pet insurance, paid time off, and other supplemental benefits available upon election.
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