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Head of Quality Neuchatel - QMR

Neuchâtel, Switzerland

Overview

Every day, employees working in Takeda’s Global Manufacturing and Supply Chain, and Global Quality business unit are shaping the future of healthcare. They are breaking down barriers and ensuring our life-changing medicines are available, accessible, and affordable to patients. Life-changing for you. Life-changing for patients.

Global Manufacturing and Supply Chain, and Global Quality is the backbone of Takeda, and our employees are the guardians for our patients, our products, and our reputation. As a member of our team, we can offer you the opportunity to grow in a meaningful career, develop your skills, and come to work every day knowing that what you do makes a genuine difference.

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Success

What makes a successful member of our team? Check out the traits we’re looking for and see if you have the right mix.

  • Agile
  • Ambitious
  • Analytical
  • Collaborative
  • Enthusiastic
  • Entrepreneurial

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Opportunity

  • Innovation

    Bold initiatives, continuous improvement, and creativity are at the heart of how we bring scientific breakthroughs from the lab to patients.

  • Inclusive

    Here, you will feel welcomed, respected, and valued as a vital contributor our global team.

  • Empowerment

    Through trust and respect, you will have genuine support from leaders, managers, and colleagues to do your best work.

  • Collaboration

    A strong, borderless team, we strive together towards our priorities and inspiring mission.

  • Top Workplace

    Recognized for our culture and way of working, we’re one of only 13 companies to receive Top Global Employer® status for 2018.

  • Work-Life

    Our people-first mission extends beyond patients to include their families, communities, and our own Takeda family.

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Head of Quality Neuchatel - QMR

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Job ID SR0011818 Date posted 01/17/2019 Location Neuchâtel, Canton of Neuchâtel

Takeda is the leading global biotechnology company focused on serving people with rare diseases and other highly specialized conditions. We have best-in-class novel products available in more than 100 countries across core therapeutic areas including Hematology, Immunology, Neuroscience, Lysosomal Storage Disorders, Gastrointestinal / Internal Medicine / Endocrine and Hereditary Angioedema; a growing franchise in Oncology; and an emerging, innovative pipeline in Ophthalmic and Gene Therapy. Our employees come to work every day with a shared mission: to develop and deliver breakthrough therapies for the hundreds of millions of people globally affected by rare diseases and other high-need conditions, and who lack effective therapies to live their lives to the fullest. About the Role: This is an exciting and challenging role where you will be responsible for leading all aspects of the Quality Operations at the Neuchâtel facility. Job Summary: The scope of the role is to ensure that quality systems and all quality related functions are in place and compliant with current Good Manufacturing Practices (cGMP), Takeda and other global regulatory standards and requirements. This person will also manage application of Takeda strategic goals and develop Neuchâtel Strategic plan; staffing, organization and development of personnel organization and achievement of defined goals and targets in order to drive the Neuchâtel plant to reach operational excellence. Member of the Core and Local Leadership Team. Pharmaceutical responsibilities as Qualified Person (delegation). Signature delegation of the Qualified Person for the Pharmaceutical responsibility related to Release activities. Number and position of functional assigned employees: Approx. 140 Core Business: Manage all aspects of the Quality Operations at the Neuchâtel facility Implement Takeda strategy within the area of responsibility (Quality Control & Quality Assurance). Maintain and continuously improve quality systems to support national, international and division requirements Ensure the Neuchatel site is inspection ready at all time. Manage quality process assuring product compliance to applicable regulations and standards Supervise and coach managers Manage budget including financial improvement (VIPs) Regular reporting of key numbers Cooperation with other Takeda facilities, especially process related facilities (TO, Lessines, Vienna, Singapore) Function/Specific competencies Lead and direct the Quality Operations functions. Ensure safety, EHS, GMP rules are followed as well as related national and international rules within department. Setup PMO´s and projects for team members to achieve daily operations goals as well as strategic quality goals. Identify high potential individuals and set appropriate development plans. Support the development and training of team members. Motivate and encourage team members. Report to VP Quality- Biologics on a routine basis the goals, the achievements, the gaps and the opportunities for improvement. Implement and review of the effectiveness of quality systems. Build-up and maintain good relationship with operations and other functions (e.g. R&D, RA, Marketing). Manage inspections by third parties (e.g. inspections by notified bodies and by regulatory agencies) incl. internal assessments. Drive continuous improvement and QLP activity within the area of responsibility. Drive and/or support continuous improvement outside the area of responsibility as defined in the relevant project. Regularly review quality and business activities during e.g. Quality Management Review, Business Review, Project Review, CAPA Review and set corrective and preventive measures Agrees with acting respectfully and fair towards other people according to Business Ethics Takeda Corporation. Education & Experience: Degree in technical/ scientific discipline such as biochemistry, chemistry, engineering or equivalent Advanced degree in complimentary field of study At least 15 years of experience in the biotechnology and/or pharmaceutical industry, preferably both Experience leading large teams in a manufacturing environment. Experience with large molecule production processes, and aseptic processing, Leading a QC laboratory Proven people manager and effective leader capable of developing people and teams with at least 10 years of management experience. Track record of effective QA leadership for internal production facilities and product disposition. Experience leading, training and/or implementing root cause analysis and effective investigation practices Strong operations background to ensure value added and effective quality operations. Experience driving out inefficiencies and improving turnaround times Understands regulations pertaining to licensing, import/export and transportation requirements. Fluent in English and French, other European language is an asset? Knowledge Skills & Abilities: Professional Experience of Releasing pharmaceutical Products (aseptic products, investigational products) Excellent knowledge of all global cGxP Regulations Understands current pharmacopeia requirements including technical methods (USP, NF, Ph.Eur) Sets clear Priorities, manages through KPIs as well as direct supervision, Excellent communication Skills with teams, peers, global partners Understands the Risk Profile of the Neuchatel Site (with respect to processes, facilities, products, utilities) and is able to provide technical instructions / guidance. Living our leadership behaviors is a basic expectation for all Takeda employees. Takeda expects all employees to embody the following: Leadership Behaviors Be Positive Be Accountable Be Results Oriented Be An Excellent Manager of Self and Others

Notice to Employment / Recruitment Agents:

Employment / Recruitment agents may only submit candidates for vacancies only if they have written authorization to do so from Shire, a wholly-owned subsidiary of Takeda’s Talent Acquisition department. Any agency candidate submission may only be submitted to positions opened to the agency through the specific Agency Portal. Shire, a wholly-owned subsidiary of Takeda will only pay a fee for candidates submitted or presented where there is a fully executed contract in place between the Employment / Recruitment agents and Shire, a wholly-owned subsidiary of Takeda and only if the candidate is submitted via the Agency Portal. Candidates submitted or presented by Employment / Recruitment Agents without a fully executed contract or submitted through this site shall not be deemed to form part of any Engagement for which the Agency may claim remuneration.



Job ID SR0011818

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