Regulatory Compliance Coordinator

Job Description:Innovative Regulatory Compliance RoleWe are seeking an experienced Compliance Specialist to join our team in Device Development at Novo Nordisk A/S. As a key member of our Technology & Processes team, you will play a vital role in ensuring compliance with health authorities' regulations on our marketed product portfolio.Your primary...

Senior QC Team Member in Regulatory ComplianceAs a Senior QC Team Member in Regulatory Compliance, you will play a vital role in maintaining the highest standards of quality assurance at FUJIFILM Diosynth Biotechnologies. You will work closely with our Analytical Development team to ensure that all method transfer activities are carried out in accordance...

About Novo Nordisk A/S\At Novo Nordisk, we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world. Our vision is to make a difference by delivering innovative solutions that improve the lives of people living with chronic diseases.\The Job Description\We are seeking a...

Job OverviewThe Global Lead for IT Compliance will set the overall strategy and delivery support methodology for the computerized system validation team. This role ensures appropriate validation and vendor assurance, as well as customer/regulatory audit coordination.This position provides guidance and mentorship to the CSV team and the broader IT...

Job DescriptionWe are seeking a skilled Pharmaceutical Process Engineer - Regulatory Compliance Specialist to join our team at Novo Nordisk A/S. As a key player in the Validation Support team within the Project Quality Management (PQM) department, you will be responsible for ensuring that validation structures and processes are robust and effective.In this...

At FUJIFILM Diosynth Biotechnologies, we are seeking a highly skilled Contract Coordinator to join our Technical Planning & Control department.The successful candidate will be responsible for managing and maintaining external maintenance/service contracts for the Technical Operation and Support organization.As a key member of our team, you will work closely...

About the RoleWe are seeking a highly motivated and organized professional to support our department in maintaining compliance with current Good Manufacturing Practice (cGMP) regulations.Key ResponsibilitiesCollaborate with the team to identify continuous improvement opportunities and implement process enhancements.Drive transparency initiatives for key...

AccountabilitiesDevelop and implement a global validation strategy.Support the organization's compliance with regulatory requirements.Provide mentorship and guidance to the CSV team.Continuously improve CSV delivery methodologies and internal processes.Effective communication and interpersonal skills are required to communicate with technical and...

Job Overview:Compliance Specialist - Device DevelopmentWe are looking for a highly skilled Compliance Specialist to work in our Device Development team at Novo Nordisk A/S. The successful candidate will be responsible for analysing and guiding the implementation of health authorities' regulations on our marketed product portfolio. This is a challenging and...

We are currently expanding our automated and digitalized facilities across all production phases, both locally and globally. Our team at FPMSAT QA sets the compliance direction for operations in transportation, intralogistics, laboratories, testing equipment, testing methods, digital solutions, robotics, and automation.Key Responsibilities:Establish and...

About the RoleThe GMP Coordinator will be responsible for maintaining a high level of compliance with cGMP and Novo Nordisk's Quality Management System. This involves supporting the department in developing and maintaining a robust quality management system, ensuring that all processes and procedures are in place to meet regulatory requirements.Key...

Job Overview\At Novo Nordisk A/S, we are committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve, and the communities we operate in. As a senior compliance coordinator, you will play a key role in driving quality-related improvements and ensuring compliance with regulatory...

Fujifilm Diosynth Biotechnologies Denmark is expanding its Quality Control department, and this presents a fantastic opportunity to join our vibrant team as a Quality Assurance Specialist for Compliance and Process Improvement.Located in Hillerød, our Quality Control department comprises approximately 230 employees across five testing teams and five support...

We are looking for a highly skilled GMP Coordinator Lead to join our team in API Manufacturing 4, 25K Multi-Product Facilities. This is an exciting opportunity for a seasoned professional with expertise in Good Manufacturing Practice (GMP) to drive quality-related improvements and lead audit and inspection setup within the four...

About the RoleThe Director of Operational Excellence will be responsible for overseeing the daily operations of our laboratory, ensuring that all tasks are completed efficiently and effectively. This includes managing a team of chemists and laboratory technicians, as well as developing and implementing processes to improve operational efficiency.Key...

About the CompanyFujifilm Diosynth Biotechnologies is a leading Contract Development and Manufacturing Organization (CDMO) that enables the success of innovative biotech and biopharma companies. We have a strong commitment to diversity, inclusion, and sustainability, and we strive to foster a collaborative and rewarding work environment.About the RoleWe are...

We are seeking a Senior Manager of Process Execution to join our team in Denmark. In this role, you will be responsible for driving process execution across various projects, ensuring timely completion and budgetary adherence.About the RoleThe successful candidate will have extensive experience in project management, specifically in cGMP...

About the Department:

At Fujifilm Diosynth Biotechnologies, we are committed to developing and manufacturing innovative biological products. As a leading Contract Development and Manufacturing Organization (CDMO), our goal is to provide high-quality services that meet the needs of our clients.About the RoleWe are seeking a dedicated Quality Assurance specialist to join our audit...

Job SummaryWe are seeking a highly skilled Manager for Quality Control and Improvement to join our team. The successful candidate will be responsible for leading the development and implementation of process improvements, as well as maintaining a high level of quality control and compliance with regulatory requirements.Key responsibilities will...