Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers’ therapies from curiosity to cure and ultimately to improve patients’ lives.
Director, Quality Operations Support
Location
United States
Posted
6 days ago
Salary
$148K - $184.7K / year
Seniority
Lead
No structured requirement data.
Job Description
Director, Quality Operations Support
Curia
Role Description The Director of Quality Operations Support is responsible to enable the Business Unit (BU) Quality Head for API (Small Molecule and Generic APIs) and Biologics, in delivering Curia’s strategic objectives. This position also enables the site Quality Heads in the effective implementation of global quality standards, global procedures, and other strategic initiatives. - Providing onsite support to the sites for inspection readiness, during regulatory agency inspections or customer audits. - Managing day to day quality operations. - Serving as a subject matter expert for complex investigations. - Acting as a delegate for BU Quality Head in customer and internal meetings. Responsibilities - Key enabler for BU Quality Head – Support the sites in quality operational activities including regulatory inspections and customer audits, investigation reviews, and batch record reviews related oversight activities. - Role requires significant travel to the sites as needed. - Participates in the BU and site’s Quality Management Review meetings and Inspection Readiness meetings; verifies effectiveness of the Quality Systems through site visits and deviation/CAPA reviews. - Collaborates between sites and customers for finalizing quality agreements to standardize the requirements across all sites. - Provides technical and quality support for the implementation of global standards and procedures at the sites. - Acts as an extension of the BU Quality Head when attending site leadership team meetings as well as quality team meetings. - Develops and delivers various training to the sites to emphasize compliance to site and global procedures, including leading qualification programs (e.g., Investigations) at the sites. - Provides technical support as required for the implementation of electronic systems such as DMS and LIMS at the sites. - Participates in the development of responses at the sites to address regulatory inspection findings. - Facilitates and reviews gap assessments performed by the sites for inspectional findings across the network; supports the sites in meeting requirements, as needed. - Plays a key role as above site Quality representative in customer business reviews, escalations and other meetings to drive Quality decisions. - Readily available to travel to the sites, to assess the Quality Systems, provide trainings and during inspection readiness preparation activities (facility walkthroughs) and during regulatory inspections. - May serve as staff augmentation on an interim basis, in Quality Leadership; including staff reviews/goal setting, as needed. Qualifications - B.S./B.A. or M.S. degree in Chemistry, Microbiology, Chemical Engineering or related field. - 15+ years of experience in the pharmaceutical industry, with at least 8 of those years of experience being in Quality, Quality Assurance, and/or Quality Systems/Compliance, and at least 5 of supervisory experience. - Strong knowledge of the pharmaceutical industry regulations applicable to API and Biologic manufacturers. - Demonstrated experience in mentoring and coaching, with ability to motivate teams to reach a common goal. - Strategic thinking—problem solver. Requirements - Must pass a background check. - Must pass a drug screen. - May be required to pass Occupational Health Screening. - May be required to obtain and maintain gowning certification. - May be required to obtain and maintain media qualification. Benefits - Generous benefit options (eligible first day of employment). - Paid training, vacation and holidays (vacation accrual begins on first day of employment). - Career advancement opportunities. - Education reimbursement. - 401K program with matching contributions. - Learning platform. - And more! Company Description Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers’ therapies from curiosity to cure and ultimately to improve patients’ lives.
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