What are the responsibilities and job description for the Regulatory Affairs Associate position at Eurofins?
Company Description
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
Job Description
POSITION SUMMARY:
We are seeking an experienced Regulatory Affairs Associate to support our Human Health and Animal Health Diagnostics Groups, specifically focused on regulatory submissions and compliance. This role is ideal for a detail-oriented professional with a strong understanding and experience of global regulatory requirements and a passion for ensuring patient safety.
JOB DUTIES Include But Are Not Limited To
Requirements:
Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
Job Description
POSITION SUMMARY:
We are seeking an experienced Regulatory Affairs Associate to support our Human Health and Animal Health Diagnostics Groups, specifically focused on regulatory submissions and compliance. This role is ideal for a detail-oriented professional with a strong understanding and experience of global regulatory requirements and a passion for ensuring patient safety.
JOB DUTIES Include But Are Not Limited To
- Assist with preparing and review of regulatory documentation for medical devices (e.g. 510(k), CLIA Waivers and Technical Files).
- Ensure compliance with FDA, EU In Vitro Diagnostic Device Regulation, and other international regulatory requirements and appropriate regulatory requirements are provided to support global registrations.
- Utilize checklist, symbol standards, and regulatory guidance’s to ensure label compliance with FDA and global regulatory expectations.
- Collaborate with business partners to assure timely review, approval and processing of regulatory documents.
- Utilize systems for entry and tracking of regulatory activities.
- Manage and communicate accurate timelines for deliverables.
- Assess product changes for potential global regulatory impact.
- Collaborate with the cross-functional development teams to ensure regulatory project needs are met.
Requirements:
- Authorization to work in the United States indefinitely without restriction or sponsorship
- Minimum of BS/BA in a relevant discipline as regulatory and/or biology
- 1-3 years direct human health In Vitro Diagnostics experience and/or Animal Health Diagnostics.
- Preferred: knowledge of SAP, Veeva Vault and Trackwise.
- Strong verbal and written communication and organizational skills:
- High level of competency using Microsoft Office suite, Microsoft Word and Excel and Adobe Acrobat.
- Able to effectively communicate with colleagues at various levels of the organization.
- Attention to detail to ensure all expectations for regulatory documents are met.
- Flexibility and capacity to handle multiple tasks at once.
- Demonstration of a highly effective and deeply committed team player.
- Consistently models behaviors of accountability, approachability, and ownership.
- Ability to work independently, while fostering good working relationships across physical distance.
- Capable of supporting colleagues / teams in a multicultural, dynamic and constantly changing learning environment.
- Position is full-time, Monday to Friday 8:00am - 5:00pm. Candidates currently living within a commutable distance of Kalamazoo, MI are encouraged to apply.
Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.