Lead the efforts of QA personnel responsible for the testing, investigations, and method transfer activities to ensure compliance with all regulatory requirements, company policies, values, and goals
Responsible for setting strategy direction for the Quality Assurance Dept. and team
Provide leadership for lot release, incoming quality, manufacturing, and labs investigations, change control and corrective and preventative action review/approval, manufacturing support, record review/approval, and ongoing projects support (if any)
Support team by guidance and coaching and provide direction/approval of activities and decisions
Cultivate and reinforce appropriate group values, ethics, norms, and behaviors
Share oversight to individuals and team on personal development, performance, and quality related issues. Write and deliver performance reviews
Ensure proper use of assets, budget, and personnel and communicate effectively with key customers and partners, both within the site and outside as appropriate
Responsible for supporting all planned and unplanned manufacturing and labs deviations, review and approval of product and equipment change controls (including SOPs and master batch records)
Conduct impact assess to design changes and participate/coordinate CAPA Review Board
Maintain the structure to ensure that all quality commitments and timelines are tracked and met. In addition, assist the senior leaders at the site in resource and budget preparations
Responsible for driving process improvements within Drug Substance, Drug Product, Site support systems
Actively with urgency when necessary to resolve issues related to production or supply as it relates to investigations or other issues
Coordinate planned and/or ad-hoc external audits and drive Internal Audit plan and share reports and outcome to the Site Management Team proposing continuous improvement action plan
Responsible for driving cross-training across Drug Substance, Drug Product, Site staff resources (as well as potentially other areas of QA)
Work directly with internal and external customers to assure Best-in-Class expectations for quality are met if not exceeded
Analyze trends, quality metrics and other data to identify quality and compliance gaps
Participates in the recruitment, selection, promotion, and performance management of QA employees
Competencies and Behaviors:
Previous experience mentoring and coaching experienced Quality professionals
Proven results using quality improvement tools and techniques to drive improvements across different functions at Multicare’s Site
Leading by example to be role model for others
Collaborative approach and ability to build strong partnerships with cross-functional teams to drive results
Demonstrate excellent communication, facilitation, and conflict resolution skills
The drive for self-development, the ability to collaborate, and an action-oriented work ethic
Excellent written and verbal skills in English
Project Management experience and/or certification is a definite plus
Experience
10 To 15 Years
Work Level
Senior Level
Employment Type
Full Time
Salary
13-18 LPA
Industry & Sub Industries
Healthcare - Clinical Research & Contract Research
Education
Pharmacy graduate preferably with related post-graduate QMS degree