Quality Manager

Quality Systems Manager

The Quality Systems Manager is responsible for implementing, supporting, and monitoring the effectiveness of the Quality Systems and Training within the Global External Manufacturing (ExM) organization. Responsibilities include process ownership, operations support, and other ad-hoc duties.

Required Competencies:

• Works under minimum supervision and exhibits a positive work attitude and high productivity
• Detail-oriented, well organized and have excellent verbal and written communication skills as well as excellent organization and follow-up skills
• Candidate must be flexible and comfortable working in a fast-paced environment with aggressive and dynamic timelines
• Excellent interpersonal skills
• Ability to collaborate, facilitate, and support standard practices across multiple functional groups in diverse geographical locations are required; self-motivated
• Strong presentation skills; confident public speaker
• Ability to multi-task numerous projects
• Ability to achieve targets and milestones
• Can prioritize workload based on changing business needs
• Ability to recognize topics / decisions requiring escalation
• Ability to work with initiative and manage own workload
• Proficient in the use of Microsoft Office programs including One Note and SharePoint platforms
• Fluent English is required.
• Strong working knowledge of Microsoft Office

Required Qualification(s) and Desired

Experience:

• A science related degree in Chemistry, Engineering or Biotechnology or equivalent
• A minimum of four (4) years' experience in a pharmaceutical Quality related role, preferably within a Quality Systems team
• A strong working knowledge of GxP regulations in the European Union (EU), United States (US) and other relevant global markets
• Experience in leading or participation in project teams
• Experience in a GxP Manufacturing site
• Lead investigator training