Auf einen Blick
- Aufgaben: Lead lab support and compliance for innovative drug development.
- Arbeitgeber: Join Roche, a global leader in healthcare innovation and diversity.
- Mitarbeitervorteile: Enjoy flexible work options, extensive training, and generous parental leave.
- Warum dieser Job: Make a real impact in healthcare while fostering a culture of growth and collaboration.
- GewĂĽnschte Qualifikationen: PhD or Master's in a technical field with 10+ years in pharma/biopharma.
- Andere Informationen: Application deadline is January 5, 2025.
Das voraussichtliche Gehalt liegt zwischen 72000 - 100000 € pro Jahr.
Roche fosters diversity, equity and inclusion, representing the communities we serve. When dealing with healthcare on a global scale, diversity is an essential ingredient to success. We believe that inclusion is key to understanding people’s varied healthcare needs. Together, we embrace individuality and share a passion for exceptional care. Join Roche, where every voice matters.The PositionAs part of our Pharma Technical Development (PTD) organization, we are committed to delivering the Pharma ambitions by bringing game-changing therapies from clinical phase I into the market to serve every patient, every day. Our core business is to develop safe, innovative, and effective drugs using cutting-edge technologies for manufacturing processes (Drug Substance and Drug Product), clinical supply, formulation, device, packaging, and analytical development.The opportunityAs the Head of Lab Support & Compliance, you will lead a section within the department Operations Support & Compliance (PTDC-T) to provide specific services and support in the area of analytical equipment qualification, calibration and life cycle, stability/reference sample management, GMP compliance in these areas, and preparation of respective SOPs. This role is key to enabling smooth operations for colleagues in Technical Development and aligns with business requirements with several partners and stakeholders. The role covers and serves regional needs for PTD Basel, for Drug Substance/Drug Product manufacturing as well as Analytics & QC for Synthetic Molecules and Biologics and Devices. The role is anchored in PTDC “Synthetic Molecules Technical Development.”Leading the Lab Support & Compliance section, your key contributions will include:Engaging employees in the department, enabling their performance, and providing opportunities for personal and professional growth.Managing a portfolio of activities in lab support and compliance, including resource allocation, priority setting, decision-making, and ensuring a GMP-compliant testing environment for Drug Substance, Drug Product, and Device testing in PTD Basel.Maintaining analytical equipment and infrastructure at state-of-the-art standards, overseeing qualification, calibration, change control, and maintenance.Overseeing sample and stability management for synthetic and large molecules, as well as devices.Providing leadership within the organization, participating in extended and functional leadership teams, contributing to long-term strategy, fostering a culture of continuous improvement, and collaborating with leaders and employees to build strong relationships across functional boundaries.Who you areYou have a PhD, an engineering degree, or a Master’s Degree in a technical or scientific discipline and at least 10 years of industry experience in the pharma/biopharma business with a minimum of 5 years of experience in technical and/or GMP-related disciplines. Experience within Small or Large Molecules GMP analytics or analytical development in Pharma is a plus.For this position, you bring the following qualifications:Excellent leadership and coaching skills with experience.Sound knowledge of GMP regulations and a deep understanding of health authority expectations.Strong ability to make decisions, inspire and lead changes, and assess risks.Excellent collaboration, interpersonal, influencing, and negotiation skills. Proven ability to build and maintain effective relationships with team members, internal and external partners, and stakeholders.Excellent verbal and written communication skills in English and German.Application deadline: 5 January 2025Who we areAt Roche, more than 100,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity, and diversity.Basel is the headquarters of the Roche Group and one of its most important centers of pharmaceutical research. Over 10,700 employees from over 100 countries come together at our Basel/Kaiseraugst site, which is one of Roche’s largest sites. Read more.Besides extensive development and training opportunities, we offer flexible working options, 18 weeks of maternity leave, and 10 weeks of gender-independent partnership leave. Our employees also benefit from multiple services on-site such as child-care facilities, medical services, restaurants and cafeterias, as well as various employee events.We believe in the power of diversity and inclusion and strive to identify and create opportunities that enable all people to bring their unique selves to Roche.Roche is an Equal Opportunity Employer. #J-18808-Ljbffr
Head of Lab Support & Compliance Arbeitgeber: F. Hoffmann-La Roche Gruppe
Kontaktperson:
F. Hoffmann-La Roche Gruppe HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Head of Lab Support & Compliance
✨Tip Number 1
Familiarize yourself with GMP regulations and health authority expectations. Understanding these guidelines will not only help you in the interview but also demonstrate your commitment to compliance and quality in the pharmaceutical industry.
✨Tip Number 2
Highlight your leadership and coaching experience during networking opportunities. Engage with professionals in the pharma/biopharma sector to build relationships and showcase your ability to inspire and lead teams effectively.
✨Tip Number 3
Prepare to discuss specific examples of how you've managed lab support and compliance activities in previous roles. This will illustrate your hands-on experience and decision-making skills, which are crucial for this position.
✨Tip Number 4
Stay updated on the latest trends and technologies in analytical development and drug manufacturing. Being knowledgeable about cutting-edge practices will set you apart as a candidate who is ready to contribute to Roche's innovative environment.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Head of Lab Support & Compliance
Tipps für deine Bewerbung 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of the Head of Lab Support & Compliance position. Tailor your application to highlight your relevant experience in GMP compliance, analytical equipment management, and leadership.
Highlight Relevant Experience: In your CV and cover letter, emphasize your 10+ years of industry experience, particularly in pharma/biopharma. Showcase specific examples of your leadership skills, decision-making abilities, and any experience with small or large molecules GMP analytics.
Showcase Communication Skills: Since excellent verbal and written communication skills in English and German are required, ensure that your application is well-written and free of errors. Consider including examples of how you've effectively communicated with stakeholders in previous roles.
Express Your Passion for Diversity and Inclusion: Roche values diversity and inclusion, so make sure to express your commitment to these principles in your application. Share any experiences or initiatives you've been involved in that promote a diverse and inclusive workplace.
Wie du dich auf ein Vorstellungsgespräch bei F. Hoffmann-La Roche Gruppe vorbereitest
✨Showcase Your Leadership Skills
As a candidate for the Head of Lab Support & Compliance, it's crucial to demonstrate your leadership and coaching abilities. Prepare examples from your past experiences where you successfully led teams, inspired change, or improved processes.
✨Understand GMP Regulations Thoroughly
Since this role involves ensuring a GMP-compliant testing environment, make sure you are well-versed in GMP regulations and health authority expectations. Be ready to discuss how you've applied these regulations in your previous roles.
✨Highlight Collaboration and Relationship-Building
Roche values strong relationships across functional boundaries. Prepare to share specific instances where you effectively collaborated with internal and external partners, showcasing your interpersonal and negotiation skills.
✨Communicate Clearly in Both Languages
Given the requirement for excellent verbal and written communication skills in both English and German, practice articulating your thoughts clearly in both languages. This will demonstrate your ability to communicate effectively in a diverse workplace.