Qa Director Jobs

About The Position

Requirements

• Bachelor’s degree in Life Sciences or related field, or equivalent combination of education and experience
• minimum of 12 years experience in a Quality Operations, Quality Management or manufacturing role, in a late stage or early stage start-up Drug Substance/biologics company

Responsibilities

• Build and execute a business strategy that translates vision and corporate goals into departmental objectives
• Builds and maintains a high performing team of managers, providing effective alignment and communication with functional groups at the site and at other manufacturing sites, to successfully deliver on all commitments. Sets the course for the future- defines priorities, goals and objectives for quality team
• Provide direction, set performance standards, evaluate, develop performance and inspire direct reports
• Ensure quality floor staff are appropriately trained to support plant operations, ensuring risks are identified and resolved. Responsibilities include in-process testing oversight, line clearance checks (as necessary), batch record review, return to service requirements have been met and quality-on-the-shop-floor responsibilities of first response to product quality issues in production
• Provide career development and training advice. Provide regular feedback to direct reports on company and departmental operations
• Directs the activities of resources, both internal and outside contractors/vendors, with similar technical or functional responsibilities
• Lead cross functional teams and manages the deliverables for the assigned projects. Drives projects through completion within timeline, quality and budgetary constraints. Interfaces with senior management to report on project and program milestones and to present project needs
• Provides escalated response for Quality and Compliance issues on the manufacturing floor and assures that decisions are made at the proper level and with the appropriate insights.
• May provide review and final QA approval of deviations, and other quality events; protocols/reports; change documentation, SOPs; master batch record approval
• Ensures product, facility, and equipment holds are placed when batch, equipment or system integrity is questioned
• Responsible for representing the Company and directly interfacing with auditors during regulatory body inspections
• Ensures periodic informal audits are completed in production
• Leads teams for tracking of quality activities, metrics, CAPA tracking, etc. Reports metrics and assesses data trends to work with operating departments to facilitate process improvements
• Develops or supports procedure and process development for continual improvement of cell culture operations, centrifugation/harvest, chromatography, UFDF, viral clearance, aseptic dispensing, filling batch records, and segregation/hold process
• Provide leadership and direction to the manufacturing and support area departments to ensure a constant state of inspection readiness
• Requires the ability to influence others to achieve results and to challenge the status quo

Benefits

• annual bonuses or other incentive plans
• equity awards
• pension or retirement benefits
• 401(k) company match
• health and wellness programs
• fitness centers
• insurance benefits (e.g. medical, dental, vision, life and disability)
• paid time off
• family support benefits