Director Quality Control

We Are Teva We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

Our Team, Your Impact This Director of Quality Control is responsible for overseeing QC testing for Chemistry and Microbiology functions for raw materials, in process, and finished product at the Davie and Sunrise sites. It includes release testing, stability testing or analytical support testing to R&D site and/or contract partners to support new product introductions and quality improvement initiatives. Review and approve analytical documents for experimental and submission batches.  

Interpret and assure that all cGMP and applicable regulations are followed while anticipate and satisfy internal and external customer requirements to robust laboratory procedures and technologies.

The position provides strategic leadership for laboratory operations, compliance, modernization, and continuous improvement initiatives. This role is responsible for driving digital transformation, automation, and innovative quality solutions that enhance regulatory compliance, operational performance, data integrity, and organizational effectiveness while supporting the site's long-term business objectives.

How You’ll Spend Your Day All areas of responsibility listed below are essential to the satisfactory performance of this position by any incumbents with reasonable accommodation, if necessary. Any non-essential functions are assumed to be included in other related duties or assignments. Support the implementation and maintenance of sample management, stability testing program, and general laboratory operational systems in accordance to cGMP requirements.

Manage a team of QC laboratory professionals and oversee performance management, mentoring, and career development.

Collaborate closely with our network of QC laboratories, internally and externally, around the globe and partner with onsite Supply Chain, Project Management, R&D, and Commercial to ensure project deadlines and objectives are met Provide knowledge to the development, implementation, and maintenance of QC Analytical Chemistry and Microbiology.

Support sites in regulatory and third party inspections, and provide technical support for specification and method development, laboratory equipment troubleshooting, and laboratory OOT and OOS investigations.

Advise management on U.S. and foreign regulatory requirements and serve as liaison with FDA and other regulatory agencies. Conduct all activities toward qualification and maintenance of QC activities and ISO registration.

Assist in the development of a company-wide LIMS system. Optimize workflow by eliminating manually written QC records, maximize the use of the LIMS system, and support reduce testing initiatives.

Connect to Analytical Research teams (e.g. Weston Florida) for the early transfer and/or validation of analytical methods of the new products assuring the process for the knowledge transfer to Florida commercial laboratories team to properly implement the new methodology for the validation campaigns.

Support Florida sites in regulatory and third party inspections, and provide technical support for specification and method development.

Provide technical expertise during the troubleshooting related to laboratory OOT and OOS investigations. Review and approve…