- Review labeling/promotional/advertising materials, and other documents to ensure regulatory compliance
- Represent and/or lead Regulatory affairs in project team meetings throughout the lifecycle of large-scale projects
- Assist in the interpretation and submission of domestic and international regulatory registrations, testing and certifications
- Assist regulatory initiatives for compliance and risk management
- Interpret Regulatory Affairs policies and guidance and correctly apply them as regulatory activities
- Manage for the successful execution of regulatory plans
- Participate in internal and external Quality and Regulatory audits
- Maintain current knowledge of relevant regulations and trends, including proposed and final rules
- Use excellent time management, verbal and written communications
- BA/BS degree is required
- Previous in vitro diagnostic (IVD) nucleic acid experience, a plus
- 2-5 years of (hands on) experience in Regulatory Affairs
- Working knowledge of FDA QSR, ISO 13485 and ISO 9001 regulations
- Experience in a Molecular Biology research environment, a plus
- Excellent interpersonal skills with the ability to influence others in a positive and effective manner
- Strong organizational skills and the ability to support multiple projects
- Proven ability to work on product development teams
- Intellectual curiosity and an ability to digest complex technical data
- Preferred education/experience includes bioengineering, biological, physical, clinical and regulatory sciences. Advanced degrees (MS, MBA, PhD., etc.) a plus
- Strong intellectual capacity and curiosity desired
- Previous in vitro diagnostic (IVD) nucleic acid experience highly preferred
- Certifications: RAC, CQA, CQM preferred
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Sr. Regulatory Affairs Specialist - Bothell, United States - Bruker
Description
Sr. Regulatory Affairs Specialist
Job Locations
US-WA-Bothell | US-WA-Seattle
ID
# of Openings
1
Job Function
Quality & Regulatory
Overview
The Senior, Regulatory Affairs Specialist is responsible for acting as the regulatory representative on product development teams aiming to achieve and maintain regulatory compliance for NanoString's products, with a particular focus on instrument/software development and manufacturing.
Responsibilities
Essential Functions:
- Maintain Regulatory Affairs documents, policies, plans and procedures to support compliance with regulatory requirements
Qualifications
Requirements:
Preferred Qualifications:
At Bruker, base salary is part of our total compensation. The estimated base salary range for this full-time position is between $$87,000 and $120,000 and provides an opportunity to progress as you grow and develop within a role.The base salary for the role will depend on a several job-related factors, including, but not limited to education, training, experience, the geographic location of the successful candidate, skills, competencies, job-related knowledge and travel requirements for this position. Full-time employees may also be eligible for a performance-related incentive in addition to a full range of benefits including 401(k) with company match, an employee stock purchase plan, medical and dental plans, life insurance, short-term and long-term disability insurance, employee assistance program and paid time off including vacation, sick time and holidays, and more.
Bruker is an equal-opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.
Certain positions at Bruker require compliance with export control laws and as a result, all interviewed candidates for all positions will be screened pre-interview to determine their eligibility in light of export control restrictions.
