Regulatory Labeling Expert Pharmaceutical

vor 3 Wochen

Visp, Schweiz Lonza Vollzeit

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 Lonza Visp labeling function, combining knowledge of scientific, regulatory and business issues to ensure compliance with safety and regulatory requirements and Lonza standards. Plans and executes review of safety / non-safety related labeling changes. Demonstrates thorough understanding of applicable international standards and global regulations, communicating across stakeholders. Proactively identifies labeling issues, offering creative solutions and strategies.

Key responsibilities:

  • Develop strategy and oversight process of labeling for CH portfolio.
  • Proactively lead the development, strategic optimization, revision, approval and maintenance of labeling documents via close scrutiny of company data, business strategies and regulatory precedents.
  • Develop workflows for internal /external partners in the labeling process.
  • Support all kinds of product label requirements (incl. outside of the SAP GLM e.g. Supply Chain, warehouses, and toll manufacturer).
  • Ensure timely availability of labels for the site, by checking all data is in order in SAP, checking, and releasing of labels in SAP GLM.
  • Support Master Data Management for labels either within SAP (and related team) or if not possible other systems.
  • Maintain required master data in SAP and associate products with existing Label Template.
  • Liaison with Operations, Program Management, Supply Chain, Quality, Engineering, IT and Regulatory teams to ensure a compliant, lean and cross-functional approach access to labeling.
  • Provide guidance for new products to ensure compliance.

Key requirements:

  • Bachelor’s or Master’s Degree in the areas Chemistry, Regulatory or similar.
  • Working experience in Manufacturing and Supply Chain.
  • Working experience with GMP.
  • First experience with SAP desirable.
  • Fluent English and German required.
  • Assertiveness in interacting with different functions and leadership.
  • Team player and leader able to be working with diverse teams globally.
  • Passion and endurance to challenge processes and overcome hurdles in the labeling environment.
#J-18808-Ljbffr

  • Regulatory Labeling Expert Pharmaceutical

    vor 4 Wochen

    Visp, Schweiz Lonza Group Ltd. Vollzeit

    Regulatory Labeling Expert Pharmaceutical (f/d/m) page is loaded Regulatory Labeling Expert Pharmaceutical (f/d/m) Apply locations CH - Visp time type Full time posted on Posted 18 Days Ago job requisition id R62626 Today, Lonza is a global leader in life sciences operating across three continents. While we work in...

  • Regulatory Labeling Expert Pharmaceutical

    vor 2 Wochen

    Visp, Schweiz Lonza Vollzeit

    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,...

  • Regulatory Labeling Expert Pharmaceutical

    vor 2 Monaten

    Visp, Schweiz Lonza Vollzeit

    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,...

  • Senior Pharmaceutical Automation Specialist

    Vor 3 Tagen

    Visp, Schweiz Randstad - Medium prio Vollzeit

    Job OverviewRandstad - Medium prio is seeking a highly skilled Senior Pharmaceutical Automation Specialist to join their disciplinary team.This role plays a key part in designing, testing, and troubleshooting recipes in Syncade, ensuring compliance with regulatory standards during the design, start-up, qualification, and production phases.

  • Biotechnologist - Pharmaceutical Production Expert

    vor 3 Wochen

    Visp, Schweiz Lonza Vollzeit

    Advance Your Career in Pharmaceutical ProductionAt Lonza, we operate across three continents, pioneering advancements in life sciences. Our success isn't just about cutting-edge science—it's about skilled technical professionals working together to create solutions with impact. We empower our team members to own their careers, fostering an environment...

  • Quality Assurance Specialist for Pharmaceutical Products

    Vor 5 Tagen

    Visp, Schweiz Lonza Vollzeit

    Quality Assurance Role OverviewAbout the Position:The material management team plays a crucial role in supporting projects with informed decisions and addressing material-based deviations. This team ensures that materials are procured and released in line with requirements.We are seeking an experienced Quality Assurance (QA) Specialist to join our...

  • Regulatory Affairs Director

    vor 2 Monaten

    Visp, Schweiz Lonza Vollzeit

    Job SummaryWe are seeking an experienced Associate Director to provide regulatory and strategic guidance to internal and external customers for our Small Molecules business. The successful candidate will partner with stakeholders to prepare high-quality CMC submissions, oversee regulatory aspects of programs, and review change requests for manufacturing...

  • Regulatory Affairs Director for Small Molecules

    vor 3 Wochen

    Visp, Schweiz Lonza Vollzeit

    At Lonza, we're committed to improving lives through science. As an Associate Director, Regulatory Affairs Small Molecules, you'll play a crucial role in providing regulatory guidance to internal and external customers for our Small Molecules business.Key responsibilities include:Partnering with stakeholders to prepare high-quality CMC submissions that meet...

  • Regulatory Affairs Director for Small Molecules

    vor 4 Wochen

    Visp, Schweiz Lonza Vollzeit

    Join Our Team as an Associate Director Regulatory Affairs Small MoleculesAt Lonza, we're committed to improving lives through innovative life sciences solutions. As an Associate Director Regulatory Affairs Small Molecules, you'll play a crucial role in shaping our regulatory strategy and ensuring compliance with global regulations.Key...

  • Regulatory Affairs Director for Small Molecules

    vor 1 Monat

    Visp, Schweiz Lonza Vollzeit

    Join Our Team as an Associate Director Regulatory Affairs Small MoleculesLonza is a global leader in life sciences, operating across three continents. Our success is built on the creativity and dedication of our people, who devise innovative solutions to help businesses improve lives worldwide.About the RoleWe are seeking an Associate Director, Regulatory...

  • Senior Quality Assurance Expert

    Vor 6 Tagen

    Visp, Schweiz Lonza Vollzeit

    Job Summary:Lonza, a global leader in life sciences, seeks a Senior Quality Assurance Expert to support the qualification of facilities, utilities, equipment, and systems in various projects. This role requires strong decision-making skills and the ability to drive the implementation of new qualification strategies.Key Responsibilities:Represent QA...

  • Small Molecules Expert

    vor 2 Monaten

    Visp, Schweiz Lonza Vollzeit

    Job SummaryWe are seeking an experienced Associate Director to provide regulatory and strategic guidance to internal and external customers for our Small Molecules business. The successful candidate will be responsible for preparing and reviewing high-quality CMC submissions, managing regulatory aspects of programs, and ensuring compliance with regulatory...

  • Senior Quality Assurance Professional

    Vor 6 Tagen

    Visp, Schweiz Lonza Vollzeit

    Join Lonza as a Quality Assurance ExpertTalented professionals who drive progress in life sciences are the backbone of our company. Lonza looks for individuals who can devise innovative solutions that improve the lives of millions of people worldwide.We are seeking a Senior QA Specialist to support our QA team in plant qualification projects. The ideal...

  • Msat Process Expert

    vor 6 Monaten

    Visp, Schweiz Proclinical Vollzeit

    Proclinical are partnering with a pharmaceutical organisation who are recruiting for an individual to join their team. This role is on a contract basis. The opening position currently available recruiting for a MSAT Process Expert. Please ensure that you are eligible for working in the location without any sponsorship or relocation...

  • Associate Director Regulatory Affairs Small Molecules

    vor 5 Monaten

    Visp, Schweiz Lonza Vollzeit

    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,...

  • Process Expert MSAT DSP

    vor 4 Wochen

    Visp, Schweiz Lonza Vollzeit

    Join Lonza's Team as a Process Expert MSAT DSPAt Lonza, we're committed to improving lives around the world through innovative life sciences solutions. As a Process Expert MSAT DSP, you'll play a crucial role in leading cross-functional teams to successfully transfer processes from development to manufacturing scale.Key Responsibilities:Lead technology...

  • Global Data Center Expert

    Vor 7 Tagen

    Visp, Schweiz Lonza Vollzeit

    Data Center Manager Role at LonzaWe are seeking a highly experienced Data Center Manager to join our IT infrastructure team at Lonza in Visp. This role will serve as a technical expert, providing engineering across our region and sites.Key ResponsibilitiesOperations and Maintenance: Ensure the efficiency, reliability, and security of IT/OT infrastructure by...

  • Biopharma Process Expert

    vor 4 Wochen

    Visp, Schweiz Lonza Vollzeit

    Join Our Team as a Biopharma Process ExpertAt Lonza, we're committed to improving lives through innovative life sciences solutions. As a Biopharma Process Expert, you'll play a crucial role in our Manufacturing Science & Technology (MSAT) Team Ibex Visp, driving the successful transfer, scale-up, supervision, and optimization of biopharma processes.Key...

  • Expert in Quality Management

    vor 2 Monaten

    Visp, Schweiz Lonza Vollzeit

    Job Summary:We are seeking an experienced Quality Assurance Specialist to join our team at Lonza. As a Senior Quality Assurance Specialist, you will be responsible for ensuring the quality of our equipment and facilities, particularly in the areas of commissioning and qualification.Key Responsibilities:Owns all quality-related responsibilities for the...

  • Senior Quality Assurance Specialist

    vor 3 Wochen

    Visp, Schweiz Lonza Vollzeit

    Quality Assurance Specialist RoleThe material management team at Lonza supports projects with decisions and takes care of any material-based deviations. Ensuring that materials are purchased and released according to requirements is a key responsibility.To support the strategic growth of the company in Visp, we are looking for an experienced Quality...