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Sr. Regulatory Affairs Specialist

3 months ago

Bothell, Washington, United States Bruker Full time
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

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

Qualifications

Requirements:
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 Qualifications:
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

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.

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