Auf einen Blick
- Aufgaben: Ensure product labels meet global regulatory standards and collaborate with diverse teams.
- Arbeitgeber: Lonza is a leading life sciences company making a positive impact worldwide.
- Mitarbeitervorteile: Enjoy relocation assistance, career ownership, and the chance to improve lives globally.
- Warum dieser Job: Join a creative team solving complex problems in a responsible and ethical environment.
- GewĂĽnschte Qualifikationen: University degree in Chemistry/Biology or Life Sciences, plus relevant experience required.
- Andere Informationen: Mentorship opportunities available; work with international standards and regulations.
Das voraussichtliche Gehalt liegt zwischen 48000 - 84000 € pro Jahr.
Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of. Responsible for labeling compliance at Lonza Visp. Accountable for combining scientific, regulatory and business requirements to ensure compliance with safety and regulatory in line with global Lonza standards. Process owner and responsible for monitoring and interpreting changes in global regulations. Demonstrates high understanding of applicable international standards and global regulations in collaboration with the “Operational Labeling expert, Visp” guide and communicates across multiple collaborators within Lonza. Role / Main Responsibilities: Ensures that all product labels at the Visp site align with relevant regulatory requirements, including FDA regulations, EU directives, and other applicable standards in different regions. Work in close collaboration with Product Safety and EHS teams. Accountable for adhering to ADR, ICH, GHS, and CLP standards for chemicals and pharmaceutical labeling. Identify potential risks related to regulatory changes and implement strong strategies to minimize risks of customer & legal complaints as well as financial impacts on our business. Provide mentorship and training to staff and collaborators on labeling regulations, processes, and standard methodologies. Monitor and anticipate evolving regulatory requirements. Identify and ensure appropriate responses or adaptations. Accountable for the timely availability of all product labels in Visp to ensure business continuity of small molecules and biologics operations. Minimum Required Qualifications / Skills: Candidates should have a University degree in Chemistry/Biology or Life Sciences, or possess equivalent experience of at least several years. Advanced work experience in Manufacturing, Product Safety, Chemistry, GMP, and Classification. Assertiveness in interacting with different functions and the ability to work with diverse teams. Relocation assistance available for candidates applying inside of the EU Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Pharma Labelling Compliance Expert - Logistics (F/D/M) Arbeitgeber: public.client.lonza.display.name
Kontaktperson:
public.client.lonza.display.name HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Pharma Labelling Compliance Expert - Logistics (F/D/M)
✨Tip Number 1
Familiarize yourself with the specific regulatory requirements relevant to labeling in the pharmaceutical industry, such as FDA regulations and EU directives. This knowledge will not only help you understand the role better but also demonstrate your commitment to compliance during discussions.
✨Tip Number 2
Network with professionals in the life sciences and pharmaceutical sectors, especially those who have experience in labeling compliance. Engaging with these individuals can provide valuable insights and potentially lead to referrals or recommendations for the position.
✨Tip Number 3
Stay updated on the latest changes in global regulations related to pharmaceutical labeling. Being proactive about regulatory trends will showcase your initiative and readiness to adapt to evolving requirements, which is crucial for this role.
✨Tip Number 4
Prepare to discuss your experience with cross-functional collaboration, particularly in relation to Product Safety and EHS teams. Highlighting your ability to work effectively with diverse teams will be key in demonstrating your fit for the collaborative nature of this position.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Pharma Labelling Compliance Expert - Logistics (F/D/M)
Tipps für deine Bewerbung 🫡
Understand the Role: Make sure to thoroughly read the job description for the Pharma Labelling Compliance Expert position. Understand the key responsibilities and required qualifications, as this will help you tailor your application.
Highlight Relevant Experience: In your CV and cover letter, emphasize your experience in Chemistry, Biology, or Life Sciences, as well as any relevant work in Manufacturing, Product Safety, or GMP. Use specific examples to demonstrate your expertise.
Showcase Your Skills: Clearly outline your skills related to regulatory compliance, risk management, and collaboration with diverse teams. Mention any experience you have with FDA regulations, EU directives, and other international standards.
Craft a Strong Cover Letter: Write a compelling cover letter that not only summarizes your qualifications but also expresses your passion for life sciences and your commitment to ethical practices. Make sure to connect your personal values with Lonza's mission.
Wie du dich auf ein Vorstellungsgespräch bei public.client.lonza.display.name vorbereitest
✨Understand Regulatory Requirements
Make sure you have a solid grasp of the relevant regulatory requirements, such as FDA regulations and EU directives. Be prepared to discuss how your experience aligns with these standards and how you can ensure compliance in your role.
✨Showcase Your Collaborative Skills
Since the role involves working closely with various teams like Product Safety and EHS, highlight your ability to collaborate effectively. Share examples from your past experiences where teamwork led to successful outcomes.
✨Demonstrate Risk Management Awareness
Be ready to talk about how you identify potential risks related to regulatory changes. Discuss any strategies you've implemented in the past to minimize risks and ensure compliance, showcasing your proactive approach.
✨Prepare for Technical Questions
Expect technical questions related to labeling regulations and compliance processes. Brush up on your knowledge of ADR, ICH, GHS, and CLP standards, and be prepared to explain how you would apply this knowledge in your work.