Commissioning & Qualification Manager IFF (all genders)
Jetzt bewerben
Commissioning & Qualification Manager IFF (all genders)

Commissioning & Qualification Manager IFF (all genders)

Frankfurt am Main Vollzeit 48000 - 84000 € / Jahr (geschätzt) Kein Home Office möglich
Jetzt bewerben
Sanofi

Auf einen Blick

  • Aufgaben: Lead and oversee commissioning, qualification, and validation activities for biopharmaceutical projects.
  • Arbeitgeber: Join Sanofi, a leader in the biopharmaceutical industry focused on global health.
  • Mitarbeitervorteile: Enjoy competitive salary, professional development, and a collaborative work environment.
  • Warum dieser Job: Make a significant impact on global health while working on cutting-edge projects.
  • Gewünschte Qualifikationen: Advanced degree in Engineering or Science; 3-5 years of relevant experience required.
  • Andere Informationen: Proficiency in English is essential; knowledge of German or French is a plus.

Das voraussichtliche Gehalt liegt zwischen 48000 - 84000 € pro Jahr.

To ensure a rapid processing of your application, please apply only via the “Apply” button. Please include a letter of motivation and a current resume with your application.

About the job

The Quality Commissioning & Qualification Manager IFF is responsible for ensuring that all aspects of Commissioning and Qualification (C&Q) activities for the project, including design, commissioning and qualification of facilities, critical utilities, equipment, and computerized systems, are executed on time and in accordance with the C&Q / Validation Master Plan, local and global requirements, and applicable regulations.

As an integral part of the project quality team, this position has overall responsibility for participating in project workstreams, ensuring proper execution of design/qualification/validation strategies as well as providing support and guidance for quality processes and procedures.

This role is expected to work independently and with a level of autonomy and authority in decision-making to ensure ongoing compliance against approved documents and current Good Manufacturing Practices across the project during conceptional, basic and detailed design, construction C&Q, PQ, Validation and future site organizations until final approval.

Main responsibilities:

  • Lead and oversee all commissioning, qualification, and validation activities for the IFF project, ensuring compliance with plans, requirements, and regulations.
  • Oversee and ensure cGMP Design and IFF Quality Concepts Development and Implementation during Design Review and Design Qualification, support Process Engineering Team.
  • Actively participate in project workstreams, providing expert guidance on quality processes and procedures.
  • Drive development and implementation of the project’s commissioning, qualification, and validation strategy, plans, and system impact assessments in collaboration with Engineering team.
  • Prepare and execute protocols, reports, and validation master plans to maintain quality standards.
  • Act as Quality oversight of Supplier Qualification Engineering activities (e.g. FAT, SAT, Vendor documentation and test execution).
  • Foster a culture of quality compliance and continuous improvement across the project and future sites.
  • Collaborate with cross-functional teams to ensure quality objectives are met throughout the project lifecycle.
  • Provide leadership and mentorship to team members, promoting best practices in quality management.

Why choose us?

  • Opportunity to work on cutting-edge projects in the biopharmaceutical industry.
  • Collaborative and innovative work environment.
  • Competitive salary and benefits package.
  • Professional development and growth opportunities.
  • Chance to make a significant impact on global health through quality management in insulin production.

About you

  • Education/Experience : Advanced degree in Engineering, Science, Pharmacy, or equivalent field. MSc or PhD preferred; 3-5 years of industry experience in biopharma or related regulated industry; Proven experience in Quality System Management, Process Validation Lifecycle, and Quality by Design principles.
  • Soft and technical skills : Strong understanding of pharmaceutical manufacturing processes and GxP regulations; Expertise in quality systems, risk management, and continuous improvement methodologies; Excellent leadership, communication, decision-making, and negotiation skills; Experience with international regulatory bodies and FDA requirements; Demonstrated ability to develop and mentor team members.
  • Languages : Proficiency in English is required; knowledge of German and French is a plus.

Pursue Progress . Discover Extraordinary .

Progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue progress. And let’s discover extraordinary together.

At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com !

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Commissioning & Qualification Manager IFF (all genders) Arbeitgeber: Sanofi

At Sanofi, we pride ourselves on being an exceptional employer, offering a collaborative and innovative work environment that empowers our employees to thrive. As a Commissioning & Qualification Manager, you will have the opportunity to work on cutting-edge biopharmaceutical projects, with competitive salaries and comprehensive benefits that support your professional growth. Join us in making a significant impact on global health while fostering a culture of quality compliance and continuous improvement.
Sanofi

Kontaktperson:

Sanofi HR Team

StudySmarter Bewerbungstipps 🤫

So bekommst du den Job: Commissioning & Qualification Manager IFF (all genders)

Tip Number 1

Familiarize yourself with the latest trends and regulations in the biopharmaceutical industry, especially around Commissioning and Qualification (C&Q) processes. This knowledge will not only help you during interviews but also demonstrate your commitment to staying updated in a rapidly evolving field.

Tip Number 2

Network with professionals in the biopharma sector, particularly those who have experience in quality management and C&Q activities. Engaging with industry experts can provide valuable insights and potentially lead to referrals that could enhance your application.

Tip Number 3

Prepare to discuss specific examples from your past experiences where you successfully led quality initiatives or overcame challenges in compliance. Highlighting these instances will showcase your leadership skills and ability to drive quality standards.

Tip Number 4

Demonstrate your understanding of Good Manufacturing Practices (GMP) and how they apply to the role. Being able to articulate how you would ensure compliance throughout the project lifecycle will set you apart as a candidate who is ready to take on the responsibilities of this position.

Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Commissioning & Qualification Manager IFF (all genders)

Commissioning and Qualification Expertise
Quality System Management
Process Validation Lifecycle
Quality by Design Principles
Pharmaceutical Manufacturing Processes
GxP Regulations Knowledge
Risk Management
Continuous Improvement Methodologies
Leadership Skills
Communication Skills
Decision-Making Skills
Negotiation Skills
Experience with Regulatory Bodies
FDA Requirements Knowledge
Team Development and Mentorship

Tipps für deine Bewerbung 🫡

Craft a Compelling Motivation Letter: Your motivation letter should clearly express your interest in the Commissioning & Qualification Manager position. Highlight your relevant experience in biopharma, your understanding of quality systems, and how you can contribute to the project’s success.

Update Your Resume: Make sure your resume is current and tailored to the job description. Emphasize your educational background, industry experience, and specific skills related to quality management and compliance in pharmaceutical manufacturing.

Highlight Relevant Experience: In both your motivation letter and resume, focus on your previous roles that involved commissioning, qualification, and validation activities. Provide examples of how you have successfully led projects or teams in similar environments.

Follow Application Instructions: Ensure you apply only via the 'Apply' button as specified in the job description. Double-check that all required documents, including your motivation letter and resume, are included before submitting your application.

Wie du dich auf ein Vorstellungsgespräch bei Sanofi vorbereitest

Prepare Your Motivation Letter

Make sure your motivation letter clearly outlines why you are interested in the Commissioning & Qualification Manager position. Highlight your relevant experience in biopharma and how it aligns with the responsibilities of the role.

Showcase Your Technical Expertise

Be ready to discuss your understanding of pharmaceutical manufacturing processes, GxP regulations, and quality systems. Prepare examples from your past experiences that demonstrate your expertise in these areas.

Demonstrate Leadership Skills

Since this role involves providing leadership and mentorship, think of specific instances where you successfully led a team or project. Be prepared to discuss your approach to fostering a culture of quality compliance and continuous improvement.

Engage with Cross-Functional Teams

Highlight your experience working with cross-functional teams. Discuss how you have collaborated with different departments to achieve quality objectives and ensure compliance throughout the project lifecycle.

Commissioning & Qualification Manager IFF (all genders)
Sanofi
Jetzt bewerben
Sanofi
  • Commissioning & Qualification Manager IFF (all genders)

    Frankfurt am Main
    Vollzeit
    48000 - 84000 € / Jahr (geschätzt)
    Jetzt bewerben

    Bewerbungsfrist: 2027-02-04

  • Sanofi

    Sanofi

    10,001 - 50,000
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