Senior Regulatory Affairs Specialist, (Hybrid)

Stryker Employment Company, LLC
Portage, Michigan
Full-time

Work Flexibility : Hybrid

Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better.

The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes.

Alongside its customers around the world, Stryker impacts more than 130 million patients annually. More information is available at .

We are currently seeking an Senior Regulatory Affairs Associate to join our Acute Care business unit , Hybrid, to be based in Portage, Michigan .

Who we want

  • Self-directed imitators. People who take ownership of their work and need no prompting to drive productivity, change, and outcomes.
  • Strategic thinkers. People who enjoy analyzing data or trends for the purposes of planning, forecasting, advising, budgeting, reporting, or sales opportunities.
  • Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, data and insights to drive continuous improvement in functions.
  • Dedicated achievers. People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations.
  • Goal-oriented developers. Keeping the customer and requirements squarely in focus, people who deliver safe and robust solutions.

What you will do

As the Regulatory Affairs Specialist, you will support Stryker’s Acute Care portfolio for our global market. You will be responsible for maintaining global market access by analyzing the impact of device modifications and emerging regulatory intelligence.

You will help identify global regulatory requirements to support new product development. You will enable global product sales in new markets by liaising with global Stryker teams to execute registrations in accordance with health authority requirements.

  • Evaluate device modifications and takes appropriate action to ensure global product compliance.
  • Support new product development in submitting registrations and subsequently support registration renewals in global markets.
  • Analyze and advise on the impact of emerging regulatory intelligence.
  • Provide regulatory input and technical guidance on global regulatory requirements to product development teams.
  • Determine requirements and options for global regulatory submissions, approval pathways, and compliance activities.
  • Prepare and submits regulatory submissions according to applicable regulatory requirements and guidelines in global markets.
  • Participate in preparation and execution of audit required to enable of maintain market access.
  • Identify the need for new regulatory procedures, SOPs, and participates in development and implementation.

What you need

  • A minimum of a Bachelor’s Degree (B.S. or B.A.) in Science, Engineering or equivalent focus required.
  • A minimum of 2 years of experience in an FDA or highly regulated industry required.
  • A minimum of 1 2 years in a Regulatory Affairs role required.
  • Previous experience with Class II / III medical devices preferred.
  • Previous experience drafting 510(k)s preferred.
  • RAC certification or Advanced Degree (Masters in Regulatory Affairs) preferred.
  • Experience authoring regulatory submissions for product approval preferred.
  • Experience interacting with regulatory agencies preferred.
  • Ability to comply with constantly changing regulatory procedures and prioritize work effectively.
  • Ability to analyze and resolve non-routine regulatory issues using independent judgment.
  • Excellent analytical and writing skills.
  • Excellent interpersonal, written and oral communication skills.
  • Effective organizational skills.
  • Advanced PC skills with proficiency in Microsoft office Suite, including Excel.

Travel Percentage : 10%Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status.

Stryker is an EO employer M / F / Veteran / Disability.Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant.

However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.

30+ days ago
Related jobs
Stryker Employment Company, LLC
Portage, Michigan

As the Regulatory Affairs Specialist, you will support Stryker’s Acute Care portfolio for our global market. Provide regulatory input and technical guidance on global regulatory requirements to product development teams. Prepare and submits regulatory submissions according to applicable regulatory r...

Stryker Corporation
Portage, Michigan
Remote

Principal Regulatory Affairs Specialist. Principal Regulatory Affairs Specialis. Minimum 9 years of experience in Medical Device Regulatory Affairs. Ability to provide regulatory judgement for products and QMS's and with BD targets and active integrations. ...

Stryker Employment Company, LLC
Portage, Michigan

Senior Staff Regulatory Affairs Specialist. Senior Staff Regulatory Affairs Specialist. Assesses regulatory intelligence to assist in the development of local, regional, and global regulatory strategies. Assists in the development of regulatory strategy and updates strategy based upon regulatory cha...

Promoted
PFES
MI, United States

Project Managers will oversee the construction project from start to finish, and often be responsible for multiple projects at once. Project Managers will take ownership of the entire project performance including safety, quality, schedule, budget, and client satisfaction. PFES has multiple openings...

Promoted
DTE Energy
MI, United States

Associate PM: (4+years) Capital PM:(6+years) Senior Capital PM: (7+years) managing projects using Project Management Body of Knowledge (PMBOK) project methodologies including Project Integration, Scope, Scheduling, Cost, Quality, Resource, Communications, Procurement, Risk, and Stakeholder Managemen...

Promoted
The ELTA Group
MI, United States

In this role, you'll be able to manage a variety of projects and manage the project team in the Water and Wastewater Treatment market. Do you have Water/Wastewater Treatment project management experience? If yes, come join our team where you can enjoy growth, collaboration and advancement. Minimum o...

Promoted
Metric Geo
MI, United States

Building Enclosure Commissioning Project Manager - Grand Rapids, MI. Must have worked with on the following projects:. ...

Promoted
Consumers Credit Union
Kalamazoo, Michigan

The Compliance Specialist also provides critical support to other employees; in this role you will assist other individuals and teams by responding to individual inquiries as well as through your support of compliance and risk-related training initiatives. The Consumers Credit Union team is looking ...

Promoted
DLZ
Kalamazoo, Michigan

Senior Project Manager in the Water and Municipal Services Group in the Western Michigan area. Business and project fee development for site-civil, water, storm water and wastewater projects at treatment plants, distribution and conveyance systems. Our staff of experienced engineers and environmenta...

iboss
Michigan

The IT Governance, Risk, and Compliance Specialist will play a key role on the iboss team by aligning security initiatives with enterprise programs and business objectives. The IT GRC Specialist will make an impact on iboss’ security program and services through experience with various areas includi...