The Labeling Specialist supports the development of labeling activities for all regulatory submissions. This individual works cross-functionally with internal and external departments on Regulatory Af...

Works with personnel in other departments including Marketing, CMR, Legal, and counterparts in NNAS Regulatory Affairs. Works with manager to compose letters incorporating NN position on external regu...

Implement regulatory strategies for launching new products and maintaining existing products. Anticipate regulatory obstacles and emerging issues throughout the product lifecycle and develop solutions...

Req: Masters in Pharmacy Administration and Regulatory Affairs or rltd + 3 months exp in the use of SOPs.

The Senior Regulatory Affairs Specialist will work in BD – Specimen Management providing regulatory leadership to cross-functional project teams from early development to new product launches in vario...

They engage in correspondence, meetings, and interactions with the FDA to address regulatory inquiries, respond to requests for additional information, and seek clarification on regulatory matters und...

Integration liaison role between Global/Regional/Local RA and cross-functional team members to streamline, manage and track all integration projects and coordinate post- integration RA activities such...

The Labeling Specialist supports the development of labeling activities for all regulatory submissions. Effective collaboration with Regulatory Affairs, CMR, Supply Chain, and HQ colleagues regarding ...

Implement regulatory strategies for launching new products and maintaining existing products. Anticipate regulatory obstacles and emerging issues throughout the product lifecycle and develop solutions...

Our client is looking to fill the role of Regulatory Affairs Specialist. The primary responsibility is writing regulatory submissions by successfully coordinating with the Regulatory Consultant and Ma...

Our client is looking to fill the role of Regulatory Affairs Specialist. The primary responsibility is writing regulatory submissions by successfully coordinating with the Regulatory Consultant and Ma...

Participates in the preparation, planning, coordination and oversight of planned and unplanned regulatory survey and reporting by The Joint Commission, New York State Department of Health, CMS and oth...

Coordinates the collection of documents, records, reports, and data from the Development, Clinical Affairs, Quality, and Operations Departments for inclusion in regulatory documents. Responsible for t...

Provides administrative support for regulatory affairs manager. Minimum 1-3 years' experience in Regulatory Affairs in the medical device industry. Conducts regulatory assessments and determines need ...

The Regulatory Affairs Specialist will review and approve Dietary Supplement/Food labels for technical accuracy and compliance to all mandated regulatory requirements, provide information to rectify l...

Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society. Provide strategic input and technical guidance on regulatory requirements to development teams. Anticipate regul...

Maintains advanced and current knowledge of relevant regulations, policies, and guidelines and acts as Regulatory Affairs Subject Matter Expert in assigned areas. Provides guidance/direction within th...

Hiring - Senior Regulatory Affairs Specialist. Assess applicable change requests for regulatory impact and follow-up on related regulatory action items. Support marketing, R&D and Lonza BU in ad hoc p...

Determine appropriate regulatory requirements and strategies for new product development projects including both domestic and foreign activities and provide regulatory consultation to other internal a...

Regulatory expert support IVDR teams, implements regulatory strategies for IVDR activities; provides regulatory leadership; collaborates with the regulatory staff from other business units, companies,...