Serán is seeking a QA Associate Director,who oversees the day-to-day operations of the Quality Assurance department with oversite of clinical manufacturing and warehouse activities in addition to disposition of raw materials and drug products. Required attributes include a results-driven and broad-minded quality assurance professional with extensive experience in compliance and regulations, quality systems management, investigations, training and mentoring, client relations, performance management, and change management. Extensive experience with direct or quality oversite of manufacturing operations is required.
The successful candidate will have excellent problem-solving skills and will identify critical quality objectives, develop cross-functional, collaborative, and creative teams, and improve, adapt, and execute practical solutions in competitive and fast-paced environments.
Supervisory Responsibilities
Leads and mentors Quality Assurance personnel.
Recruits, interviews, hires and trains new staff.
Oversees daily workflow of the department.
Responsibilities
Leads and implements continuous improvement initiatives to reduce risk and improve efficiency for the company’s quality systems and department operations
Management and scheduling of department operations
Oversees and conducts review and approval of Investigations, CAPAs, Complaints, and Change Management
Review and approval of SOPs, batch records, raw material records, and certificates of conformance/compliance
Responsible for Quality oversight of activities involving raw material, drug product manufacturing, packaging, labeling, and warehouse activities
Assures cGMP compliance systems and processes are in place to support raw material and drug product review, release, storage, and shipping
Defines and maintains a strong people management, training, and engagement culture to ensure a high and constantly improving right first-time rate
Supports internal audits, client audits and regulatory inspections
Required Skills and Experience
Expert knowledge of GMP guidelines and Quality expectations for preclinical and clinical phase manufacturing operations
In-depth understanding and application of cGMP principles, concepts, practices, and standards
Experience with regulatory inspections by the FDA and EU authorities
Ability to influence diverse stakeholders and drive accountability and decision-making cross functionally
Demonstrated ability to partner with other functional groups to achieve business objectives
Experience organizing and managing group responsibilities while working independently with minimal oversight
Time and project management skills with the ability to multi-task and meet deadlines
Excellent verbal and written communication skills
Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside of the company
Excellent organizational skills and attention to detail
Strong analytical and problem-solving skills
Strong supervisory and leadership skills
Education and Experience
Minimum of a bachelor’s degree, preferably in a scientific discipline. An advanced degree is preferred
10+ years previous GMP and Quality experience in the Pharmaceutical industry with quality oversite of Oral Solid Dose manufacturing
Experience with regulatory inspections by the FDA and EU authorities
