The opportunity
The Quality Control Analytical Laboratory is responsible for all analytical testing to support the production of Cytotoxic injectable products. The laboratory executes a wide variety of analytical tests on active substances, excipients, packaging materials and drug products for release and stability purposes. The department is also responsible for introduction and qualification, maintenance and calibration of equipment, maintaining GMP documentation and stock keeping. In order to strengthen this responsibility, the Quality Control Analytical Laboratory is searching for a Group/Team leader Quality Control Analytical Laboratories Equipment & Support.
The group leader QC- Analytical Laboratory Equipment & Support is supported by an enthusiastic and diverse team, which closely collaborates with different stakeholders, like Procurement, E&M and Quality Systems to implement new analytical equipment and maintain existing equipment, update documentation and make sure all needed materials are available. It is your role to plan the various activities in close collaboration with stakeholders, while remaining aligned with the strategy, commitments and goals of the QC organization. You will be is a subject matter expert in equipment qualification and an expert in problem solving.
How you’ll spend your day
Manage Activities
Guide the team in equipment implementation strategies
Manage the team in establishing and maintaining quality at the lab in accordance with Site SOP’s, regulatory guidelines and cGXP compliance requirements.
Maintain a culture of enhancing quality throughout the entire Laboratory.
Performance of in-depth root cause analyses and problem solving
Act as a Subject Matter Expert during regulatory and internal audits.
Is a Subject Matter Expert with respect to equipment qualification.
Responsible for implementation of equipment which meets the business needs and current regulations.
Responsible for cross-departmental communication with stakeholders like Procurement and Quality Systems to meet project demands
Responsible for equipment maintenance and Calibration
Responsible for GMP documentation and ordering of materials
Manage Team and Resources
Manage own team through talent identification, active performance management, succession planning, employee development, mentoring and modeling behavior according to Teva values.
Run an efficient and effective QC team through managing the team budget and resources.
Manage of Culture of Safety
Maintain a culture of enhancing safety throughout the entire Laboratory.
Review and provide options to meet business needs without compromising health & safety.
