Senior Manager Quality Control [Germany]

 

The Quality Difference at Thermo Fisher Scientific: What makes our quality teams unique is a shared passion for getting it done right the first time and working for the right reasons with our customers always in mind. Our team of Quality professionals understand our customers rely on the accuracy, safety, and effectiveness of our products and services that are improving lives around the world. When you join our team of quality professionals, you’ll collaborate on projects on a global scale while being encouraged to grow your skills and discover new career paths with us.

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team of more than 100,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD.

Location/Division Specific Information

Fisher Clinical Services GmbH is a subsidiary of Thermo Fisher Scientific with almost 200 employees in Germany and is the market leader in clinical supply chain management services and clinical trial sample manufacturing and logistics for patients worldwide. Further information on the locations in Weil am Rhein and Rheinfelden can be found on our website: www.fisherclinicalservices.com

Discover Impactful Work:

The Senior Manager (m/f/d) Quality Control is responsible for management of the Quality Control team at the Weil am Rhein and Rheinfelden sites. The position holder will lead of QC Supervisors and drive process and quality improvement initiatives. Additional responsibilities include development of training plans, performance of Quality investigations and trending of effectiveness of proposed corrective and preventive actions. Interaction with customers is also required.

A Day in the Life:

• Applies Good Manufacturing Principles in all areas of responsibility.
• Demonstrates and promotes the company vision.
• Maintains and analyzes Key Performance Indicators and develops action plans to ensure in response to trends
• Manage all activities and all projects in conjunction with local change control procedures.
• Apply company HR policies consistently throughout the area of managerial responsibility
• Lead, participate, and contribute to practical process Improvement (PPI) projects that deliver business objectives in a cost-effective manner.
• Demonstrates and promotes the company vision of the 4 I’s: Integrity, Intensity, Innovation and involvement; conducts all activities in a safe and efficient manner.
• Ensures appropriate scheduling of QC team to ensure business needs are met
• Oversees training programs designed to improve and maintain awareness of
• SOP’s, cGMP’s and clinical packaging requirements within Quality Assurance and all functional areas of the site.
• Ensures that QC personnel receive the training required to perform their jobs effectively, including company policies and procedures, cGMP training and processes.
• Ensures the continuing review of the Quality System and the creation of new or revised procedures to effect quality improvements, reduce costs, and enhance efficiency.
• Plans, organizes and directs QC functions that assure meeting or exceeding customer requirements. Develops goals and objectives for team members.
• Maintains excellent client relationships by providing a technically competent QC Dept.

Keys to Success:
Education

• A Bachelor Degree in a technical field such as Pharmacy, Science, or Engineering from an accredited college or university is preferred.

Experience

• Prior leadership skills required
• Prior Quality System experience in the pharmaceutical, food, or regulated industry.
• Experience managing regulatory and client audits.
• Able to manage personnel in a dynamic cGMP environment

Knowledge, Skills, Abilities

• Excellent verbal and written communication skills.
• Excellent interpersonal skills.
• Excellent organizational and planning skills.
• Excellent influencing skills.
• Excellent problem solving and root cause analysis skills
• Strong knowledge of cGMP’s
• Knowledge and experience with EU regulations and audits.

What we offer:

• Employment with an innovative, future-oriented organisation
• Outstanding career and development prospects
• Company pension scheme and other fringe benefits
• Exciting company culture which stands for integrity, intensity, involvement and innovation

If you are interested, please apply online with your CV and Motivation Letter including possible start date and salary expectations.

At Thermo Fisher Scientific, each one of our 100,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission—enabling our customers to make the world healthier, cleaner and safer.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability or any other legally protected status.

Apply today!

Agency notice!
Please note we are not interested in receiving unsolicited CVs from any personnel service providers. Should you choose to send us or upload any such candidate document they will not be acknowledged and will be deleted in line with our privacy policy.

 

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