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Regulatory Affairs Manager Engineer Jobs (NOW HIRING)

The Regulatory Affairs Manager will lead regulatory strategy and submissions for diagnostic ... Bachelor's degree or higher in Biology, Chemistry, Biomedical Engineering, Clinical Laboratory ...

The Regulatory Affairs Manager will lead regulatory strategy and submissions for diagnostic ... Bachelor's degree or higher in Biology, Chemistry, Biomedical Engineering, Clinical Laboratory ...

The Regulatory Affairs Manager will lead regulatory strategy and submissions for diagnostic ... Bachelor's degree or higher in Biology, Chemistry, Biomedical Engineering, Clinical Laboratory ...

Regulatory Affairs Manager Location: Onsite - Atlanta, GA Position Summary: The Regulatory Affairs ... Bachelor's degree in Regulatory Affairs, Life Sciences, Engineering, or a related field required.

Regulatory Affairs Manager Location: Onsite - Atlanta, GA Position Summary: The Regulatory Affairs ... Bachelor's degree in Regulatory Affairs, Life Sciences, Engineering, or a related field required.

Symmetrio is recruiting for our client for a Regulatory Affairs Manager to lead U.S. regulatory ... Collaborate with product development, quality, clinical, and engineering teams to ensure regulatory ...

Regulatory Affairs Manager Location: Onsite - Atlanta, GA Position Summary: The Regulatory Affairs ... Bachelor's degree in Regulatory Affairs, Life Sciences, Engineering, or a related field required.

Regulatory Affairs Manager Location: Onsite - Atlanta, GA Position Summary The Regulatory Affairs ... Bachelor's degree in Regulatory Affairs, Life Sciences, Engineering, or a related field required.

The primary job responsibility for of the Regulatory Affairs Manager is overseeing the day-to-day functions of the Dentsply Sirona Implants and Prosthetics team. This role develops regulatory ...

The primary job responsibility for of the Regulatory Affairs Manager is overseeing the day-to-day functions of the Dentsply Sirona Implants and Prosthetics team. This role develops regulatory ...

Manages Regulatory Risk Assessments per ISO 14971. * Acts as the main primary Person Responsible ... Education Bachelor's degree in Quality, Regulatory Affairs or an applicable science (Engineering ...

Manages Regulatory Risk Assessments per ISO 14971. * Acts as the main primary Person Responsible ... Education Bachelor's degree in Quality, Regulatory Affairs or an applicable science (Engineering ...

Description Harbor Health POSITION OVERVIEW The Regulatory Affairs Manager plays a pivotal role in supporting Harbor Health's health plan business by ensuring regulatory compliance with the Texas ...

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Regulatory Affairs Manager Engineer information

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How much do regulatory affairs manager engineer jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for regulatory affairs manager engineer in the United States is $56.97, according to ZipRecruiter salary data. Most workers in this role earn between $42.07 and $66.59 per hour, depending on experience, location, and employer.

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Infographic showing various Regulatory Affairs Manager Engineer job openings in the United States as of June 2026, with employment types broken down into 53% Full Time, 41% Part Time, 3% Temporary, and 3% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $118,493 per year, or $57 per hour.

Regulatory Affairs Manager

Indianapolis, IN โ€ข On-site

$50 - $53/hr

Other

This job post hasย expired today.ย Applications are no longer accepted.


Key responsibilities

  • Coordinate and compile regulatory submission dossiers to meet planned product registration timelines.

  • Develop and manage parts of comprehensive global regulatory submission and registration plans for complex products or programs.

  • Maintain approvals and licenses through effective regulatory change control across the product life cycle.


Job description


Job Title: US_Regulatory Affairs Manager I_CO


Location: Indianapolis, IN


Duration: Contract - 12 months


Pay Range: $50/hr - $53/hr (W2)


Job ID: 409193


Work Arrangement: Onsite, Hybrid Schedule (3 Days Onsite / 2 Days Remote), 1st Shift Hours


Campus: Indianapolis Indiana Campus


About BCforward


BCforward is a leading global IT consulting and workforce solutions firm providing services and support to Fortune 500 and government clients. Founded in 1998, BCforward has grown with our customers needs into a full-service business solutions provider. With delivery centers and offices across North America and India, we take pride in building long-term relationships and delivering excellence through innovation, collaboration, and integrity.


Job Description


We are seeking a US Regulatory Affairs Manager I to join our team. The ideal candidate will have strong experience in global regulatory submissions, IVDs/medical devices/biopharma regulations, and regulatory change control and a proven ability to secure and maintain product approvals across multiple regions while driving cross-functional alignment and timely registration outcomes.


Responsibilities:



  • Coordinate and compile regulatory submission dossiers to meet planned product registration timelines.

  • Develop and manage parts of comprehensive global regulatory submission and registration plans for complex products or programs.

  • Maintain approvals and licenses through effective regulatory change control across the product life cycle.

  • Partner with internal stakeholders and external bodies (authorities, notified bodies, partners) to resolve issues and advance regulatory strategies.

  • Contribute to audit preparation and participate in audit discussions as needed.

  • Lead adaptation to evolving global regulatory requirements and interpret regulator expectations to guide projects across regions.

  • Create innovative regulatory strategies to avoid obstacles and accelerate worldwide approvals.

  • Influence and negotiate with stakeholders to reach outcomes that align business and regulatory objectives.

  • Exercise sound judgment and timely decision making, escalating or delegating to the appropriate level.

  • Drive problem solving and continuous improvement to ensure compliant, efficient daily operations.

  • Model VACC leadership behaviors, foster inclusion, and mentor junior regulatory staff.

  • Promote data stewardship and effective use of regulatory tools to support digitalization and strategic goals.

  • Facilitate teamwork and clear communication, resolve conflicts constructively, and recognize contributions.


Required Skills & Qualifications:



  • 3-5 years with PhD, 5-7 years with Master's, or 6-8 years with Bachelor's in IVDs, medical devices, pharma, or biopharmaceuticals with significant regulatory affairs experience or equivalent.

  • Proven experience compiling and leading parts of global submissions and managing complex regulatory work.

  • Knowledge of US, EU, and China regulations with the ability to interpret and implement quality and regulatory standards.

  • Strong stakeholder management, negotiation, and cross-functional collaboration skills.

  • Demonstrated decision-making skills and ability to act with limited information while maintaining compliance.

  • Experience with Daily Management and Continuous Improvement best practices.


Preferred Skills:



  • Experience interfacing with health authorities or notified bodies and supporting audits.

  • Background in data stewardship, regulatory information management tools, and digital ways of working.


Why BCforward?


At BCforward, we believe in advancing lives and careers. When you join our team, you gain access to:



  • Competitive compensation and benefits

  • Opportunities for growth with global clients

  • A supportive, inclusive culture that values innovation and people

  • Exposure to cutting-edge technologies and projects


About Our Commitment


BCforward is an equal opportunity employer. We value diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, or veteran status.


Interested? Apply Now!


If this sounds like the right opportunity for you, please apply with your most recent resume.