Regulatory Affairs Specialist II

Cochlear Ltd

$90K — $95K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree or equivalent work experience; 6+ years of experience in regulatory affairs may substitute degree.
  • 1-3 years of experience in a regulatory role within the medical device or pharmaceutical field.
  • Strong technical writing skills are essential.
  • RAPS certification is preferred.
  • Familiarity with Health Canada and FDA regulations is crucial.

Responsibilities

  • Write and assemble regulatory submissions, ensuring timelines are met.
  • Develop strategies for responding to regulatory inquiries on significant submissions.
  • Collaborate cross-functionally to align on response strategies to regulatory questions.
  • Identify and document improvements for regional and global regulatory processes.
  • Assess impacts of changes to devices, labeling, or manufacturing processes.

Benefits

  • Comprehensive medical, dental, and vision insurance.
  • 401(k) matching with immediate vesting.
  • Paid Time Off and paid parental leave.
  • Tuition reimbursement for continuous learning.
  • Employee Stock Purchase Plan and pet insurance.
Full Job Description
Regulatory Affairs Specialist II

About the role

The role of Regulatory Affairs Specialist II contributes to achieving Cochlear's business outcomes by helping to bring innovative products to our customers and helping ensure that Cochlear is compliant with premarket and post market regulatory requirements for all medical devices. The role of Regulatory Specialist II will work closely with colleagues based at the legal manufacturers and colleagues located in North America. The Regulatory Affairs Specialist II will write and assist in writing submissions for the Food and Drug Administration and Health Canada in order to meet the regional priorities.

Key Responsibilities
  • Write executive summaries, assemble documents, and assist in preparation and creation of regulatory submissions to FDA and Health Canada. Ensure company business goals are met by submitting regulatory applications within agreed timelines.
  • Execute strategies for response to regulatory questions on significant submissions. For minor submissions, independently develop strategy for response.
  • Work cross-functionally with regional colleagues and colleagues at the legal manufacturers to ensure alignment and agreement on answers to any questions.
  • Identify, document and implement improved regional and global regulatory processes
  • Provide initial or final documented assessment of any impacts of changes to devices, labeling, or manufacturing processes.


Key Requirements

To add value to Cochlear in this role you'll be able to meet and demonstrate the following knowledge, skills and abilities in your application and at interview:
  • Bachelor's degree or equivalent work experience
    • 6+ Years of Experience working in regulatory affairs or a related field may be substituted for Bachelor's Degree or equivalent work experience
  • 1-3 Years in a regulatory role (medical devices, pharmaceuticals, etc.)
  • Technical writing skills
  • Ideal candidate will have RAPS certification
  • Knowledge of Health Canada and Food and Drug Administration requirements


Total Rewards

In addition to the opportunity to develop your knowledge and grow professionally, we offer competitive wages and benefits.

  • Pay Range in the United States: $90,000 - $95,000 based upon experience, as well as an annual bonus opportunity of 7.5% of base salary. Exact compensation may vary based on skills, experience, and location.
  • Benefit package includes medical, dental, vision, life and disability insurance as well as 401(K) matching with immediate vesting, Paid Time Off, tuition reimbursement, maternity and paternity leave, Employee Stock Purchase Plan and pet insurance.


Physical & Mental Demands

The physical and mental demands described below are representative of those that must be met to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the individual is regularly required to be in a stationary (seated/standing) position; utilize business technology for work product delivery, communicate orally and in writing with others internal or external to the organization, utilize problem solving/critical thinking skills to discern and convey information. May be asked to occasionally transport/move up to 30 pounds, depending on the position. Specific vision abilities required by this job include ability to adjust focus. The individual is regularly required to utilize comprehension, critical thinking, communication, problem solving, organization reasoning, relating to others and discernment of items such as product specifications, procedures and processes to customers (whether internal or external). Influence, organization/classification of information and planning are also required.

The work environment is an office environment. This is representative of the environment an individual may encounter while performing the essential functions of this job.

Deadline to apply by August 24th, 2026.

Apply now by completing your application form online. Applicants must meet the job specific application criteria to be considered. Visit our careers site at www.cochlear.us/careers to learn more.

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