Our client Altran is a world leader in R&D and engineering consulting. They work with clients in more than 20 countries to create and develop new products and services. Innovation is our guiding principle, with which we lead in a world where change is a constant factor. In the Netherlands they also bring the most complex and innovative projects of the customers to life. More than 800 consultants use their expertise every day to improve the performance of their clients. They can proudly say that they are the partner in the field of technical innovation and process improvement.
We are looking for Lab Service Manager QC with the following Technical and job specification. A lot of Enthousiasm and flexibility.
You are responsible for a broad range of services provided by his teams such as; o Lab Automation (incl iLAB) o Equipment Life Cycle Management (ELM), o Facility, o In House Services, o Sample Management, o Compliance coordination o Environment, Health, Safety and Sustainability (EHS&S) • Ensures all forecast is in line with the timelines, resources and team-budget. • Review and authorize GMP documentation • Participate in Management meetings with internal and external stakeholders
Managerial • Mentors, coaches, trains and develops his/her team. Evaluates performance, provides opportunities for growth and develop high-performance team feeding targeted succession planning • Acts as change agent and builds and maintains team capabilities to meet current and future needs • Is responsible for setting the goals and objectives for the department and to define proper Key Performance Indicators that are indicative for excellent performance. Fosters result driven performance and holds team accountable • Manages the budget of the group and provide inputs for the OPEX and CAPEX budget, ensures an aligned planning with other team and allocations out for the costs related to her/his team • Responsibility for achieving innovation and excellence in business processes applying Faster Forward, JJOS and BEx principles and tools
Compliance Employee safety and health • Ensure that procedures and guidelines linked to safety and health are met Environmental care • Ensure that the group complies with the environmental procedures and guidelines Quality • Ensure overall compliance to regulatory cGMP requirements, global standards, procedures, etc. • Ensure that data is generated and maintained according to current regulatory requirements
Qualifications and Competences: • Bachelor/Master’s degree or equivalent in Analytical Chemistry, Biochemistry, Biotechnology, Pharmaceutical Science or equivalent • 8-10 years experienced in a Quality or related environment, of which 4 or more years were held in a leadership position
Professional experience • Experience in Quality Control • Profound knowledge of pharmaceutical regulations/cGMP principles (FDA, EU, JPN, etc.) • General knowledge of pharmaceutical development & manufacturing • Organizational planning and problem-solving experience : • Strong leadership & development qualities • Experience with principles of Process Excellence, Lean manufacturing, etc. • Good presentation skills • Excellent knowledge of English
Personal and interpersonal skills • Analytical thinking • Strong Quality Awareness • Flexible • Stress resistant • Organizational and people management skills • Dealing with intercultural differences • Work independently • Ability to empower and motivate a team that is diverse in culture, knowledge and capabilities • Capability to manage multiple priorities and unexpected changes
What do we offer: • Salary between € 3000 and € 4500 gross per month. Depending on knowledge and experience. • A variable bonus plan • A lease car or mobility budget • Flexible secondary conditions • Extensive training programs through our Academy • An annual budget for personal innovations • An InnovationLAB, fully facilitated by our client, where you can work on your own creations, alone or together with colleagues with the same interests