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Biomedical Product Manager Jobs in Delaware (NOW HIRING)

Clinical QA Specialist

Newark, DE · On-site

$85K - $133K/yr

... product portfolio. * Familiarity with post-market surveillance requirements, adverse event ... Biomedical Engineering, Electromedical Engineering, or a related field. Risk Managers will also be ...

Clinical QA Specialist

Newark, DE · On-site

$85K - $133K/yr

... product portfolio. * Familiarity with post-market surveillance requirements, adverse event ... Biomedical Engineering, Electromedical Engineering, or a related field. Risk Managers will also be ...

... product portfolio. * Familiarity with post-market surveillance requirements, adverse event ... Biomedical Engineering, Electromedical Engineering, or a related field. Risk Managers will also be ...

$85K - $137K/yr

Manage configuration for PACS/RIS/VNA, including routing rules, hanging protocols, display sets ... Monitor radiology volumes, modality productivity, turnaround times, and repeat/reject trends.

Showing results 21-25

Biomedical Product Manager information

What does a biomedical product manager do?

A Biomedical Product Manager oversees the development, marketing, and lifecycle management of biomedical products such as medical devices or diagnostic equipment. They act as a bridge between engineering, regulatory, marketing, and sales teams to ensure products meet market needs and comply with industry regulations. Their responsibilities include market research, product strategy, and communicating product value to internal and external stakeholders. Ultimately, they play a key role in bringing innovative biomedical solutions to market.

What are some common challenges faced by biomedical product managers when bringing new medical devices to market?

Biomedical Product Managers often face the challenge of navigating complex regulatory requirements, such as FDA approval, which can be time-consuming and require meticulous documentation. They must also coordinate closely with cross-functional teams—including R&D, quality assurance, and marketing—to ensure products meet both clinical needs and business objectives. Balancing innovation with compliance, managing project timelines, and adapting to rapidly changing technologies are all typical hurdles. Effective communication and a strong understanding of both technical and market demands are essential for success in this role.

What are the key skills and qualifications needed to thrive as a biomedical product manager, and why are they important?

To thrive as a Biomedical Product Manager, you need a solid background in biomedical engineering or life sciences, combined with experience in product development and project management. Familiarity with regulatory requirements (such as FDA or CE Mark), product lifecycle management software, and quality management systems is typically required. Outstanding communication, leadership, and problem-solving skills help you collaborate effectively across cross-functional teams and drive product success. These competencies are crucial for ensuring biomedical products meet market needs, comply with regulations, and achieve commercial goals.

What are popular job titles related to Biomedical Product Manager jobs in Delaware?

For Biomedical Product Manager jobs in Delaware, the most frequently searched job titles are:

What cities in Delaware are hiring for Biomedical Product Manager jobs?

Cities in Delaware with the most Biomedical Product Manager job openings:

Clinical QA Specialist

Hologic

Newark, DE • On-site

$85K - $133K/yr

Full-time

Re-posted yesterday


Hologic rating

8.0

Company rating: 8.0 out of 10

Based on 25 frontline employees who took The Breakroom Quiz

176th of 489 rated machine equipment manufacturers


Job description


Are you passionate about ensuring compliance and patient safety in the medical device industry? At Hologic, we are seeking a Clinical QA Specialist to play a critical role in the investigation and reporting of potential and actual adverse events, as well as other regulatory reporting activities. In this role, you'll collaborate with cross-functional teams, including Technical Service, Marketing, Sales, and Regulatory, to ensure timely and thorough documentation, analysis, and reporting. If you thrive in a fast-paced, collaborative environment and have a strong background in regulatory compliance and quality assurance, this is your opportunity to make a meaningful impact on healthcare innovation.
Knowledge:
  • Comprehensive understanding of FDA Quality System Regulations, ISO 13485, EU Medical Device Regulation, and ISO 14971 for risk management.
  • Strong knowledge of medical procedures and the expected and potential outcomes related to Hologic's product portfolio.
  • Familiarity with post-market surveillance requirements, adverse event reporting, and health risk assessments.
  • Awareness of regulatory reporting processes, including MedWatch reports, notified body communications, and external notifications.

Skills:
  • Proven ability to independently collect, analyze, and assess information associated with adverse events and determine appropriate next steps.
  • Effective communication skills to interact with internal teams, sales personnel, customers, patients, and regulatory agencies.
  • Strong organizational skills to ensure timely documentation, reporting, and follow-up of adverse events and regulatory submissions.
  • Analytical skills to support and lead investigations, including CAPAs, nonconformances, and other quality system processes.
  • Experience in developing metrics and quality reports related to reportable events and identifying potential excursions.
  • Ability to innovate and improve processes to enhance efficiency and compliance with post-market surveillance requirements.
  • Proficient in leading or participating in internal and external audits, inspections, and assessments.

Behaviors:
  • Proactive and detail-oriented, ensuring compliance with regulatory requirements and internal procedures.
  • Collaborative and team-oriented, fostering strong relationships across functions to support investigations and reporting activities.
  • Customer-focused, ensuring communications and responses are timely, accurate, and aligned with patient safety goals.
  • Resilient and adaptable, thriving in a fast-paced and evolving environment.
  • Problem-solving mindset, with a commitment to driving resolution and continuous improvement in quality processes.

Experience:
  • Bachelor's degree in Medicine, Nursing, Biomedical Engineering, Electromedical Engineering, or a related field. Risk Managers will also be considered.
  • 5+ years of experience in a similar role, preferably within the medical device or healthcare industry.
  • Hands-on experience with adverse event reporting, regulatory communications, and health risk assessments.
  • Proven track record in supporting or leading CAPAs, nonconformances, and quality investigations.

Why join Hologic?
We are committed to making Hologic the destination for top talent. For you to succeed, we want to enable you with the tools and knowledge required and so we provide comprehensive training when you join as well as continued development and training throughout your career.
The annualized base salary range for this role is $85,200 - $133,300 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, education, business needs and market demand.
Agency and Third-Party Recruiter Notice
Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition, Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered.
Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans.
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