18,103 Healthcare Products jobs in the United States

About the job Project Manager, Medical Devices

The Project Lead is responsible for providing cross-functional program leadership to ensure projects achieve desired outcomes from product definition through product commercialization.

This leader will help teams define and achieve the objectives and goals required to complete projects on time and within budget. Their focus will be on driving high levels of collaboration and execution across teams. They will ensure effective management of portfolios with a focus on effective design control and risk taking. The successful candidate will possess a high degree of professionalism, maturity and confidentiality.

Responsibilities:

• Provide cross-functional program leadership to drive strategic growth initiatives, innovation portfolio and programs.
• Establish, maintain, and influence program stakeholder relationships, expectations, and communications, both internal and external to the organization.
• Present data and recommend program improvements to senior leaders.
• Execute program plans (quality, risk, communication, staffing, etc.) and capture and communicate program status and data in order to maintain accurate and current program information for the use of stakeholders.
• Originate and drive Project Management Office (PMO) continuous improvement activities. Optimize resource allocation of portfolio in partnership with functional leaders across divisions/site.
• Track overall program progress and provide detailed management status reports. Ensure projects are run in compliance with company, FDA, and ISO procedures.
• Oversee and provide guidance across all phases of the product development life-cycle process from concept to commercialization.
• Drive organizational and program learnings/best practices to continually improve organization to best in class PMO.
• Establish best practices across the company for project management.

• Bachelors Degree required. Masters Degree and/or MBA preferred.
• Program Management Professional (PgMP) or Portfolio Management Professional (PfMP) certification preferred.
• M&A integration experience highly desired.
• 2+ years of experience in the medical device industry.
• 2+ years of experience in a project management role or equivalent experience.
• Experience with project management tools such as MS Project or other.
• Excellent interpersonal skills in addition to having the ability to effectively communicate within the project teams as well as to top level management
• Collaborative leader who excels in leading through ambiguity
• Ability and experience with communicating effectively with executive leaders.
• MS Project software experience
• Understanding ISO and FDA guidelines as they apply to Product Development
• Excellent organization and time management/multi-tasking skills (comfortable in an ambiguous and fast-paced environment, operating at both strategic and tactical levels)

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. Youll also have access to:

• Career development with an international company where you can grow the career you dream of.

• Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.

• An excellent retirement savings plan with a high employer contribution

• Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelors degree.

• A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.

• A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

This position works out of our Pleasanton, CA location in the Heart Failure Division. In Abbotts Heart Failure (HF) business, were developing solutions to diagnose, monitor and manage heart failure, allowing people to restore their health and get on with their lives.

Project Manager for the Supplier Excellence Taskforce aims is to achieve material stabilization through design optimization, improved inspection and process controls, in conjunction with supplier management and component qualifications. You will manage project timelines, budgets, and deliverables, ensuring compliance with regulatory requirements.

What Youll Work On

• Lead cross-functional project teams to drive supplier quality initiatives, ensuring alignment with medical device regulatory standards (e.g., FDA, ISO 13485).
• Develop and manage detailed project plans , timelines, budgets, and deliverables with a focus on supplier performance and risk mitigation.
• Monitor supplier quality metrics and project progress, proactively identifying issues and implementing corrective actions to maintain compliance and minimize delays.
• Coordinate supplier visits, validations, and qualifications , ensuring documentation and processes meet internal and external regulatory requirements.
• Collaborate with engineering, quality, and procurement teams to define technical requirements and ensure suppliers meet product specifications and quality expectations.
• Prepare and present project status reports to stakeholders, highlighting risks, milestones, and quality-related outcomes.
• Manage external contractors and suppliers , ensuring integration into project workflows and adherence to quality standards.
• Drive continuous improvement initiatives across supplier quality processes, leveraging data and feedback to enhance operational efficiency.
• Ensure project documentation (e.g., design history files, CAPAs, change controls) is complete, accurate, and audit-ready.
• Facilitate cross-functional meetings , set priorities, allocate tasks, and guide project staff to meet key deliverables and regulatory milestones.

Required Qualifications

• Bachelors degree in related field or an equivalent combination of education and work experience

• 4+ years of relevant experience

Preferred Qualifications

• Experience in the medical devices or similar field

• A self-directed, efficient individual with excellent analytical and problem-solving skills.

• Must have excellent project and time management skills with the ability to manage multiple projects and tasks.

Apply Now

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at on Facebook at and on Twitter @AbbottNews.

The base pay for this position is $86,700.00 $173,300.00. In specific locations, the pay range may vary from the range posted.

Local manufacturing company needs assembly help to put together plastic medical devices. Work 4 days a week - 10 hours each day. Every weekend off! Essential duties and responsibilities include the following: regularly assembly and packaging in a timely fashion. Complete tasks assigned by group leader, supervisor, or any other manager. All products assembled must be manufactured a.

Summary:

We're seeking a regulatory affairs specialist to join our medical devices compliance team. You will get to work on wearables and Software as a Medical Device (SaMD) applications for the US and worldwide approvals.You will work on cutting-edge wearable technologies, including augmented reality glasses, wrist wearables, and other innovative devices.

Required Skills:

Medical Devices, Regulatory Specialist Responsibilities:

1. Interact directly with FDA and/or indirectly with international regulatory agencies on most projects/products at reviewer level. All significant issues will be reviewed with the manager

2. Support regulatory compliance activities, including site registration, audits, post-market vigilance reporting, product recalls, etc., as needed

3. Prepare FDA, European and Canada submissions for product changes as required to ensure timely approval for market release. Review significant regulatory issues with manager, as necessary, and resolve submission issues with engineering partners, geography regulatory partners, and regulatory agencies as needed

4. Prepare regulatory strategies/plans and compliance requirements. Provide on-going support to project teams for regulatory issues and questions

Minimum Qualifications:

Minimum Qualifications:

1. Bachelor's degree in a scientific discipline or equivalent work experience

2. 3+ years of industry experience in medical device regulatory affairs or related industry

3. Experience working with minimal supervision and under general direction only

4. Experience multitasking, supporting multiple projects, functioning on a global basis, prioritizing, conducting team meetings, and meeting project deadlines

Preferred Qualifications:

Preferred Qualifications:

1. Experience with Food and Drug Administration requirements, guidance documents, Active Medical Device Directive/EU MDR, ISO 14971, ISO 13485, and other global regulatory requirements and quality standards

2. Advanced degree in a scientific discipline (engineering, physical/biological or health sciences) or in Regulatory Affairs

3. Regulatory Affairs Professionals Society Regulatory Affairs Certification

4. Demonstrated experience in negotiation skills, authoring technical reports and submissions, and presenting to cross functional peers and leadership

Public Compensation:

$90,000/year to $137,000/year + bonus + equity + benefits

Industry: Internet

Equal Opportunity:

Meta is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender, gender identity, gender expression, transgender status, sexual stereotypes, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. We also consider qualified applicants with criminal histories, consistent with applicable federal, state and local law. Meta participates in the E-Verify program in certain locations, as required by law. Please note that Meta may leverage artificial intelligence and machine learning technologies in connection with applications for employment.

Meta is committed to providing reasonable accommodations for candidates with disabilities in our recruiting process. If you need any assistance or accommodations due to a disability, please let us know at

We're seeking a regulatory affairs specialist to join our medical devices compliance team. You will get to work on wearables and Software as a Medical Device (SaMD) applications for the US and worldwide approvals. You will work on cutting-edge wearable technologies, including augmented reality glasses, wrist wearables, and other innovative devices.

Medical Devices, Regulatory Specialist Responsibilities

• Interact directly with FDA and/or indirectly with international regulatory agencies on most projects/products at reviewer level. All significant issues will be reviewed with the manager
• Support regulatory compliance activities, including site registration, audits, post-market vigilance reporting, product recalls, etc., as needed
• Prepare FDA, European and Canada submissions for product changes as required to ensure timely approval for market release. Review significant regulatory issues with manager, as necessary, and resolve submission issues with engineering partners, geography regulatory partners, and regulatory agencies as needed
• Prepare regulatory strategies/plans and compliance requirements. Provide on-going support to project teams for regulatory issues and questions

• Bachelor's degree in a scientific discipline or equivalent work experience
• 3+ years of industry experience in medical device regulatory affairs or related industry
• Experience working with minimal supervision and under general direction only
• Experience multitasking, supporting multiple projects, functioning on a global basis, prioritizing, conducting team meetings, and meeting project deadlines

• Experience with Food and Drug Administration requirements, guidance documents, Active Medical Device Directive/EU MDR, ISO 14971, ISO 13485, and other global regulatory requirements and quality standards
• Advanced degree in a scientific discipline (engineering, physical/biological or health sciences) or in Regulatory Affairs
• Regulatory Affairs Professionals Society Regulatory Affairs Certification
• Demonstrated experience in negotiation skills, authoring technical reports and submissions, and presenting to cross functional peers and leadership

This range is provided by Maxonic Inc. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range $65.00/hr - $70.00/hr Direct message the job poster from Maxonic Inc. Maintains a close and long-term relationship with our direct client. We are looking for a Project Manager (Medical Devices) for this hybrid position in Sunnyvale, CA. Responsibilities The Project Manager is responsible for providing cross-functional project management within the Global Services Business Unit (GSBU), supporting new product development and strategic initiatives. The role serves as the primary liaison between ISI's Engineering teams / Engineering PMO and the Field Service, Technical Support, Customer Success, and Service Operations teams for each product. The Project Manager will identify service strategies, requirements, risks, and schedules, driving the cross-functional effort to ensure Global Services readiness aligned with the project plan. They will closely coordinate with upstream/downstream business partners across assigned product lines. The success of the Services Program Management (SPMO) team is critical to the global success of the GSBU. This role is ideal for someone with leadership experience, a passion for robotics, and the ability to lead change in a complex, regulated environment. Provide strategic and tactical leadership to project teams for new product launches or ongoing product support, ensuring proper planning, communication, risk management, and readiness in line with development and commercialization timelines. Create and maintain project schedules and budgets, and communicate status and risks to GSBU stakeholders. Collaborate with Engineering to ensure service requirements are integrated during product development, influencing product design for better serviceability. Regularly review service strategies, assumptions, and opportunities throughout the project lifecycle. Manage a portfolio of projects, organize design review meetings, and foster strong partnerships with internal and external teams, including marketing and engineering, to align development processes and cultures. Work with partner groups to align priorities and lead staffing, organizational, and strategic planning to anticipate future needs. Lead continuous improvement initiatives in project management and product development efforts for the Services BU. Maintain comprehensive knowledge of product lifecycle and engineering best practices, including handling complex tasks autonomously, applying innovative engineering methods, and influencing design and development processes. Communicate effectively with diverse audiences, including internal teams, suppliers, and leadership, using tailored messaging. Proactively identify risks, assess root causes, and implement solutions under pressure. Prioritize tasks effectively, seek relevant information proactively, and demonstrate strong analytical and problem-solving skills. Required Skills and Experience Proven track record of managing products from conception to market, particularly in field service or service operations roles. Minimum 4+ years experience with complex capital equipment, such as medical devices or robotics, including mechanical, electrical, and software components with many SKUs. Experience supporting field service or technical support teams. Knowledge of Design for Serviceability/Maintenance (DFS/DFM) principles. Strong ability to influence, build relationships, and promote ideas persuasively. Autonomous thinker with innovative mindset, quick to respond, and capable of linking information to insights. Excellent organizer, communicator, and presenter, capable of simplifying complex ideas for technical and non-technical audiences. Required Education and Training Bachelor's degree in Engineering or a related scientific field is preferred; equivalent experience in business, finance, or other fields will be considered. Additional Details Seniority level: Mid-Senior level Employment type: Contract Job function: Project Management Industries: Medical Equipment Manufacturing #J-18808-Ljbffr

We're seeking a regulatory affairs specialist to join our medical devices compliance team. You will get to work on wearables and Software as a Medical Device (SaMD) applications for the US and worldwide approvals. You will work on cutting-edge wearable technologies, including augmented reality glasses, wrist wearables, and other innovative devices.

• Interact directly with FDA and/or indirectly with international regulatory agencies on most projects/products at reviewer level. All significant issues will be reviewed with the manager
• Support regulatory compliance activities, including site registration, audits, post-market vigilance reporting, product recalls, etc., as needed
• Prepare FDA, European and Canada submissions for product changes as required to ensure timely approval for market release. Review significant regulatory issues with manager, as necessary, and resolve submission issues with engineering partners, geography regulatory partners, and regulatory agencies as needed
• Prepare regulatory strategies/plans and compliance requirements. Provide on-going support to project teams for regulatory issues and questions

• Bachelor's degree in a scientific discipline or equivalent work experience
• 3+ years of industry experience in medical device regulatory affairs or related industry
• Experience working with minimal supervision and under general direction only
• Experience multitasking, supporting multiple projects, functioning on a global basis, prioritizing, conducting team meetings, and meeting project deadlines

• Experience with Food and Drug Administration requirements, guidance documents, Active Medical Device Directive/EU MDR, ISO 14971, ISO 13485, and other global regulatory requirements and quality standards
• Advanced degree in a scientific discipline (engineering, physical/biological or health sciences) or in Regulatory Affairs
• Regulatory Affairs Professionals Society Regulatory Affairs Certification
• Demonstrated experience in negotiation skills, authoring technical reports and submissions, and presenting to cross functional peers and leadership

$90,000/year to $137,000/year + bonus + equity + benefits

Individual compensation is determined by skills, qualifications, experience, and location. Compensation details listed in this posting reflect the base hourly rate, monthly rate, or annual salary only, and do not include bonus, equity or sales incentives, if applicable. In addition to base compensation, Meta offers benefits. Learn more about benefits at Meta.

Meta is proud to be an Equal Employment Opportunity employer. We do not discriminate based upon race, religion, color, national origin, sex (including pregnancy, childbirth, reproductive health decisions, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetic information, political views or activity, or other applicable legally protected characteristics. You may view our Equal Employment Opportunity notice here.

Meta is committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans in our job application procedures. If you need assistance or an accommodation due to a disability, fill out the Accommodations request form.

Our client, a leading organization in the medical device industry, is seeking a Quality Inspector to join their team. As a Quality Inspector, you will be part of the Quality Assurance department supporting inspection and compliance teams. The ideal candidate will have attention to detail, strong communication skills, and a commitment to quality, which will align successfully in the organization. Job Title: Quality InspectorLocation: Salt Lake City, UTPay Rate: $20.33/hrWhat's the Job? Perform accurate mechanical, physical, and visual inspections of raw materials, components, and sub-assemblies. Conduct PCI activities for NA Notifications at the US Regional Service Center. Follow procedural requirements to maintain compliance with Quality System Regulations (e.g., cGMP). Support document archival processes including scanning and pallet preparation. Initiate Non-Conformance reports and support NC and CAPA activities.What's Needed? High School Diploma or GED equivalent (AA or Technical Degree preferred). Basic computer skills for documentation and data access. Ability to read and comprehend written instructions and engineering drawings. Familiarity with medical device regulations and FDA standards (preferred). Must be at least 18 years of age.What's in it for me? Medical insurance Dental insurance Disability insurance Life insurance Weekly paymentIf this is a role that interests you and you'd like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you!About ManpowerGroup, Parent Company of:Manpower, Experis, Talent Solutions, and Jefferson Wells ManpowerGroup® (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We develop innovative solutions for hundreds of thousands of organizations every year, providing them with skilled talent while finding meaningful, sustainable employment for millions of people across a wide range of industries and skills. Our expert family of brands - Manpower, Experis, Talent Solutions, and Jefferson Wells - creates substantial value for candidates and clients across more than 75 countries and territories and has done so for over 70 years. We are recognized consistently for our diversity - as a best place to work for Women, Inclusion, Equality and Disability and in 2022 ManpowerGroup was named one of the World's Most Ethical Companies for the 13th year - all confirming our position as the brand of choice for in-demand talent.

• Bachelor's degree in computer science, Cybersecurity, or related field
• 8+ years of combined experience in software development, security engineering and security regulatory and compliance, with at least 5 years of experience in security engineering
• Strong understanding of security principles, threat modeling, and risk assessment
• Experience with secure coding practices, vulnerability remediation, and security testing
• Familiarity with regulatory requirements for medical devices (e.g., FDA, CE)
• Experience with mobile application security domain and issues (both Android and iOS)
• Experience with embedded systems/IoT devices a plus Should be hands-on with Open Web application security project - OWASP procedures
• Hands-on with Static code analyzer tools like Valgrind to trace Buffer overflow, Stack overflow, memory leaks, API testing
• Hands-on with code reviews to identify potential issues
• Fluent with code injection attacks - SQL, NoSQL, OS command, Object Relational Mapping (ORM), LDAP, and Expression Language (EL) or Object Graph Navigation Library (OGNL) injection
• Identify risks during firmware update
• Identify risks in Cryptography signature
• Able to guide and hands-on with Toolchain hardening
• Able to identify Identity and Access management attacks
• Data collection, storage, privacy
• Transport layer security