Manager, Regulatory Affairs (Aesthetic Medical Device) (Bothell, WA)

Bausch Health Companies Inc.; Bothell (WA); On-site; USD 115,000 - 158,000; Full time

Job summary

Bausch Health Companies Inc. in Bothell, WA is seeking an EH&S Product Regulatory Compliance Manager to ensure medical devices and medicinal products meet global environmental, health and chemical regulations across product design and lifecycle.

You will integrate requirements into technical documentation, advise on ERA for medicinal products, and partner with development teams to embed environmental compliance into design, while supporting regulatory submissions and audits.

Qualifications

• Bachelor degree in Environmental Science, Chemistry, Toxicology, Engineering, or related discipline.
• Minimum 6 years of experience in regulatory compliance for medical devices or related field.
• Strong knowledge of RoHS, REACH, SVHC, F-gas regulations, EU MDR documentation and audits.

Responsibilities

• Ensure products meet global environmental and chemical regulations.
• Assess materials and substances for regulatory risk.
• Review and approve environmental documentation and SDS.
• Provide regulatory evidence for EU MDR documentation.
• Partner with development teams to embed compliance into design.
• Manage supplier environmental compliance program.
• Respond to inquiries and support audits.
• Monitor regulatory changes and provide guidance.
• Advise on ERA for medicinal products (approx. 20%).

Skills

Regulatory compliance

Environmental compliance

RoHS/REACH

ISO 13485

Regulatory submissions

Education

Bachelor's degree

Job description

Job Location: Bothell, USA

Job Requisition ID: 15763

Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes to our patients. We are all in it together to make a difference. Be a part of a culture that doesn't just wait for change but actively creates it where your skills and values drive our collective progress and impact.

The EH&S Product Regulatory Compliance Manager ensures that the company’s medical device and medicinal products comply with applicable global product-level environmental, health, safety, and chemical regulations, supporting global market access by integrating these requirements into product design, technical documentation, and lifecycle management. The role also advises Regulatory Affairs on Environmental Risk Assessment (ERA) for medicinal products and does not cover manufacturing site or occupational EHS.

Responsibilities

• Ensure products comply with applicable global environmental and chemical regulations, including EU RoHS, REACH (including SVHC), the F-gas Regulation, WEEE, TSCA, and California Proposition 65
• Assess materials, components, and substances used in medical devices for compliance and regulatory risk, and contribute environmental and chemical risk inputs to ISO 14971 risk management
• Review and approve product-level compliance documentation, including material declarations, supplier disclosures, Safety Data Sheets (SDS), and environmental certificates
• Provide product environmental compliance evidence for regulatory submissions and EU MDR technical documentation, in alignment with ISO 13485 design controls and change management processes
• Partner with product development teams to embed environmental compliance requirements into product design and material selection
• Evaluate the regulatory impact of design changes, supplier changes, and material substitutions, and maintain product environmental compliance status throughout the product lifecycle
• Manage the supplier environmental compliance program, including collection and review of RoHS/REACH declarations, and maintain accurate product compliance records and databases
• Respond to customer, notified body, and regulatory authority inquiries on product environmental compliance, and support related audits and inspections
• Monitor changes in global environmental and chemical regulations, assess their impact on products, and provide clear regulatory interpretation and guidance to internal stakeholders
• Advise Regulatory Affairs on Environmental Risk Assessment (ERA) for medicinal products (approx. 20% of role): evaluate product data, determine whether experimental studies are needed or their absence can be justified, and coordinate required studies

Qualifications

• Bachelor Required,minimum 6years of experience
• Relevant field of study, if applicable: Environmental Science, Chemistry, Toxicology, Engineering, Materials Science, or related discipline
• Functional / Technical Knowledge: Product environmental and chemical compliance, preferably in the medical device industry; RoHS, REACH, SVHC, and product chemical regulations applicable to medical devices; F-gas Regulation and fluorinated substances used in medical devices or accessories; EU MDR technical documentation and product compliance annexes; supporting notified body audits or regulatory inspections; PLM and EH&S compliance data management systems; regulated quality system environments (ISO 13485 preferred); regulatory interpretation, technical documentation, and cross-functional collaboration. A background in toxicology and/or ecotoxicology is an advantage

Solta Medical is committed to the health and safety of our employees. We expect that all employees will perform their responsibilities while maintaining a safe, cooperative, and productive work environment, thus ensuring the health and safety of themselves and others.

The range of starting base pay for this role is $115K-$158K. Actual starting pay will be based on a wide range of factors including, but not limited to, relevant skills, experience, qualifications, education and location. In addition to base pay, this position is eligible for participation in either (i) our annual bonus program or (ii) a sales incentive plan.

We are an Equal Opportunity Employer. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates collaboration.