What You'll Contribute The Senior Associate, Product Development will play a key part in the ... Comprehensive medical, dental, vision, hospital indemnity, critical illness, pet insurance and more
What You'll Contribute The Senior Associate, Product Development will play a key part in the ... Comprehensive medical, dental, vision, hospital indemnity, critical illness, pet insurance and more
Product Development Process, Receiving Inspection, Complaints & Vigilance, Validation, Device ... the medical device industry. * Minimum 3 years of direct, hands-on experience implementing or ...
Product Development Process, Receiving Inspection, Complaints & Vigilance, Validation, Device ... the medical device industry. * Minimum 3 years of direct, hands-on experience implementing or ...
Lead Design Assurance Engineer
Newark, DE · On-site
$119K - $186K/yr
... in medical device development? At Hologic, we are seeking a Lead Design Assurance Engineer to play a pivotal role in new product development, ensuring that design controls, risk management, and ...
Lead Design Assurance Engineer
Newark, DE · On-site
$119K - $186K/yr
... in medical device development? At Hologic, we are seeking a Lead Design Assurance Engineer to play a pivotal role in new product development, ensuring that design controls, risk management, and ...
Lead Design Assurance Engineer
Newark, DE · On-site
$119K - $186K/yr
... in medical device development? At Hologic, we are seeking a Lead Design Assurance Engineer to play a pivotal role in new product development, ensuring that design controls, risk management, and ...
Lead Design Assurance Engineer
Newark, DE · On-site
$119K - $186K/yr
... in medical device development? At Hologic, we are seeking a Lead Design Assurance Engineer to play a pivotal role in new product development, ensuring that design controls, risk management, and ...
Vice President, Quality Engineering - BSH Division
Newark, DE · On-site
$237K - $422K/yr
... product development to post-market surveillance and product lifecycle management. As a member of ... In-depth understanding of FDA Quality System Regulations, ISO 13485, Medical Device Directive ...
Vice President, Quality Engineering - BSH Division
Newark, DE · On-site
$237K - $422K/yr
... product development to post-market surveillance and product lifecycle management. As a member of ... In-depth understanding of FDA Quality System Regulations, ISO 13485, Medical Device Directive ...
Vice President, Quality Engineering - BSH Division
Newark, DE · On-site
$237K - $422K/yr
... product development to post-market surveillance and product lifecycle management. As a member of ... In-depth understanding of FDA Quality System Regulations, ISO 13485, Medical Device Directive ...
Vice President, Quality Engineering - BSH Division
Newark, DE · On-site
$237K - $422K/yr
... product development to post-market surveillance and product lifecycle management. As a member of ... In-depth understanding of FDA Quality System Regulations, ISO 13485, Medical Device Directive ...
Senior/ Executive Medical Director, Medical Lead IAI, Early Clinical Development
Wilmington, DE · On-site
Facilitates the development of key internal and external documents pertaining to product ... Training in research (wet lab), proven track record of self-directed scientific work (e.g. post doc ...
Senior/ Executive Medical Director, Medical Lead IAI, Early Clinical Development
Wilmington, DE · On-site
Facilitates the development of key internal and external documents pertaining to product ... Training in research (wet lab), proven track record of self-directed scientific work (e.g. post doc ...
Travel Product Development VP
Wilmington, DE · On-site
$125K - $188K/yr
Knowledge of the product development lifecycle including ideation, strategic development ... Citi offers competitive employee benefits, including: medical, dental & vision coverage; 401(k) ...
Travel Product Development VP
Wilmington, DE · On-site
$125K - $188K/yr
Knowledge of the product development lifecycle including ideation, strategic development ... Citi offers competitive employee benefits, including: medical, dental & vision coverage; 401(k) ...
Product Quality Engineer 2
Newark, DE · On-site
$78 - $122/hr
Experience in root cause analysis or product development/R&D is beneficial Skills * Working ... 13485, EU Medical Device Regulation, ISO 14970, Risk Management, GMP, and GDP * Ability to ...
New
Product Quality Engineer 2
Newark, DE · On-site
$78 - $122/hr
Experience in root cause analysis or product development/R&D is beneficial Skills * Working ... 13485, EU Medical Device Regulation, ISO 14970, Risk Management, GMP, and GDP * Ability to ...
New
Job Summary The Senior Director - Executive Medical Director, Drug Development is responsible for implementing clinical drug efforts for Incyte's oncology products (Phase I though Phase III). ...
Job Summary The Senior Director - Executive Medical Director, Drug Development is responsible for implementing clinical drug efforts for Incyte's oncology products (Phase I though Phase III). ...
Own the global scientific learning strategy across the portfolio, including disease, product, and ... Deep knowledge of the drug development process and stakeholder landscape. * Deep understanding of ...
Own the global scientific learning strategy across the portfolio, including disease, product, and ... Deep knowledge of the drug development process and stakeholder landscape. * Deep understanding of ...
Own the global scientific learning strategy across the portfolio, including disease, product, and ... Deep knowledge of the drug development process and stakeholder landscape. * Deep understanding of ...
Own the global scientific learning strategy across the portfolio, including disease, product, and ... Deep knowledge of the drug development process and stakeholder landscape. * Deep understanding of ...
Own the global scientific learning strategy across the portfolio, including disease, product, and ... Deep knowledge of the drug development process and stakeholder landscape. * Deep understanding of ...
Own the global scientific learning strategy across the portfolio, including disease, product, and ... Deep knowledge of the drug development process and stakeholder landscape. * Deep understanding of ...
Executive Director, Medical Excellence US BBU
Wilmington, DE · On-site
$286 - $429/hr
Own the global scientific learning strategy across the portfolio, including disease, product, and ... Deep knowledge of the drug development process and stakeholder landscape. * Deep understanding of ...
Executive Director, Medical Excellence US BBU
Wilmington, DE · On-site
$286 - $429/hr
Own the global scientific learning strategy across the portfolio, including disease, product, and ... Deep knowledge of the drug development process and stakeholder landscape. * Deep understanding of ...
Lead Compliance Engineer, R&D
Newark, DE · On-site
As the Lead Compliance Engineer, R&D, you will define and execute product compliance strategies ... medical device compliance and safety standards, device manufacturing, and product lifecycle ...
Lead Compliance Engineer, R&D
Newark, DE · On-site
As the Lead Compliance Engineer, R&D, you will define and execute product compliance strategies ... medical device compliance and safety standards, device manufacturing, and product lifecycle ...
Product Quality Engineer 2
Newark, DE · On-site
$78K - $122K/yr
... EU Medical Device Regulation, ISO 14971 (Risk Management), GMP, and GDP. * Familiarity with root ... Familiarity with verification and validation requirements and the development of testable and ...
Product Quality Engineer 2
Newark, DE · On-site
$78K - $122K/yr
... EU Medical Device Regulation, ISO 14971 (Risk Management), GMP, and GDP. * Familiarity with root ... Familiarity with verification and validation requirements and the development of testable and ...
Product Quality Engineer 2
Newark, DE · On-site
$78K - $122K/yr
... EU Medical Device Regulation, ISO 14971 (Risk Management), GMP, and GDP. * Familiarity with root ... Familiarity with verification and validation requirements and the development of testable and ...
Product Quality Engineer 2
Newark, DE · On-site
$78K - $122K/yr
... EU Medical Device Regulation, ISO 14971 (Risk Management), GMP, and GDP. * Familiarity with root ... Familiarity with verification and validation requirements and the development of testable and ...
System Engineers
Newark, DE · On-site
The ideal candidate will have 5-8 years of experience in the medical device industry, with a strong ... product development lifecycle. Key Responsibilities: * Design Controls: Lead efforts to develop and ...
Quick apply
System Engineers
Newark, DE · On-site
The ideal candidate will have 5-8 years of experience in the medical device industry, with a strong ... product development lifecycle. Key Responsibilities: * Design Controls: Lead efforts to develop and ...
SR Electrical Engineer, R&D, NPD
Newark, DE · On-site
$105K - $136K/yr
Experience in an FDA regulated medical device industry is beneficial. Skills * Advanced knowledge ... Knowledge and experience working through full product lifecycle. * Proficiency with laboratory test ...
SR Electrical Engineer, R&D, NPD
Newark, DE · On-site
$105K - $136K/yr
Experience in an FDA regulated medical device industry is beneficial. Skills * Advanced knowledge ... Knowledge and experience working through full product lifecycle. * Proficiency with laboratory test ...
Systems Engineer
Newark, DE · On-site
$78K - $122K/yr
Support concept development, specification, and design of new medical imaging products. * Implement ... Knowledge of medical device regulations and standards, including: FDA QSR, ISO 13485, ISO 14971 ...
Systems Engineer
Newark, DE · On-site
$78K - $122K/yr
Support concept development, specification, and design of new medical imaging products. * Implement ... Knowledge of medical device regulations and standards, including: FDA QSR, ISO 13485, ISO 14971 ...
Director Medical Device Product Development information
What is the difference between Director Medical Device Product Development vs Product Manager Medical Devices?
| Aspect | Director Medical Device Product Development | Product Manager Medical Devices |
|---|---|---|
| Responsibilities | Oversees entire product development lifecycle, manages teams, sets strategic direction | Focuses on product planning, feature definition, and market analysis |
| Required Credentials | Engineering or life sciences degree, experience in medical device development, regulatory knowledge | Background in engineering, marketing, or life sciences, familiarity with medical device regulations |
| Work Environment | Leadership role in R&D or product development departments, cross-functional teams | Collaborates with engineering, marketing, and sales teams, often in a more tactical role |
The main difference is that the Director Medical Device Product Development leads and manages the entire development process and teams, focusing on strategic oversight, while the Product Manager Medical Devices concentrates on product planning and market needs. The director role involves higher-level management and regulatory oversight, whereas the product manager handles day-to-day product features and customer requirements.
What are popular job titles related to Director Medical Device Product Development jobs in Delaware?
For Director Medical Device Product Development jobs in Delaware, the most frequently searched job titles are:
What job categories do people searching Director Medical Device Product Development jobs in Delaware look for?
The top searched job categories for Director Medical Device Product Development jobs in Delaware are:
- Remote Quality Engineer Medical Device
- Contract Quality Engineer Medical Device
- Quality Manager Medical Device
- Director Pharmaceutical Manufacturing
- Medical Device Quality Consultant
- Remote Director Engineering Medical Device
- Medical Device Finance
- Manager Post Market Surveillance Medical Device
- Pharmaceutical Asset Management
- Quality Director Medical Device
What cities in Delaware are hiring for Director Medical Device Product Development jobs?
Cities in Delaware with the most Director Medical Device Product Development job openings:
Full-time
Medical, Dental, Vision, Life, PTO
Re-posted 14 days ago
Job description
When you join Sallie Mae, you become a champion for all students.
We're on a mission to power confidence as students begin their unique journey. To help them plan their higher education, successfully finish, and prepare for life after school. To help them Start smart. Learn big.
Students need guidance navigating this important time in their life. They need someone who acknowledges that their education path is unique. They need a partner willing to evolve and not only meet but surpass their expectations. We're changing. Because students need a better way.
We're looking for people who are excited to drive this transformation. To break barriers and think of new ways to adapt, help, and create better experiences for students-and for each other.
This is where diverse backgrounds, beliefs, and perspectives matter. It's where you're empowered to bring your authentic self to work.
Feeling your best allows you to do your best. Our benefits take care of the whole you-from physical and mental to financial and professional. You'll get opportunities to further your education and career, support for you and your family (including your pets!), paid time off to volunteer for the things that matter to you, and more.
We're obsessed with impact and making a real difference. For us, that means putting relationships first, asking "why not?" when tackling challenges, and continuously learning new skills.
Come do more than join something, change something. For students, for future generations, for the future of education.
What You'll Contribute
The Senior Associate, Product Development will play a key part in the product development process, supporting the successful execution of projects from concept to launch for Customer Communications.
What You'll Do
- Assist in managing the product development lifecycle, including requirements gathering, design, development, testing, and launch, ensuring projects are delivered on time and within scope.
- Collaborate with product managers, engineers, and designers to translate product requirements into actionable tasks and project plans.
- Support the execution of product development projects, ensuring adherence to project schedules, milestones, and quality standards.
- Contribute to the creation and maintenance of product documentation, including specifications, design documents, and user manuals.
- Assist in coordinating and facilitating product testing, gathering feedback, and identifying areas for improvement or refinement.
- Assist in monitoring and tracking project progress, identifying and escalating risks or delays as necessary.
The above information is intended to describe the general nature and level of work performed by employees assigned to this job; it is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees in this role.
What you have
- Strong organizational skills, with the ability to effectively prioritize tasks and manage multiple projects simultaneously.
- Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and stakeholders at various levels.
- Detail-oriented mindset, with a focus on delivering high-quality work and ensuring accuracy in documentation and project execution.
- Proficient in project management methodologies and tools, with the ability to contribute to project planning, tracking, and reporting.
- Analytical and problem-solving skills,
- Bachelor's degree in a relevant field such as engineering, computer science, business administration or related discipline.
Preferred:
- 3+ years of experience in product development or a related field, demonstrating a solid understanding of the product development lifecycle.
- Salesforce Marketing Cloud experience
- Experience with Visio, Figma, and Microsoft Office tools.
The Americans with Disabilities Act
The Americans with Disabilities Act of 1990 (ADA) prohibits discrimination by employers, in compensation and employment opportunities, against qualified individuals with disabilities who, with or without reasonable accommodation, can perform the "essential functions" of a job. A function may be essential for any of several reasons, including: the job exists to perform that function, the employee holding the job was hired for his/her expertise in performing the function, or only a limited number of employees are available to perform that function.
Feeling your best helps you do your best:Our benefits take care of the whole you-so you can build your work around your life (not the other way around!).Competitive base salaries
Bonus incentives
Generous PTO, Floating Holidays and 12 Federal Holidays observed
Support for financial-well-being and retirement401k with employer match
Comprehensive medical, dental, vision, hospital indemnity, critical illness, pet insurance and more
Employer paid short-term/long-term disability and basic life insurance
Flexible hybrid working arrangements.
Paid parental leave and adoption reimbursement programs
Free access to on-site staffed fitness centers (in Delaware) and gym subsidy (for locations outside Delaware)
Confidential counseling support (EAP), Health Advocacy services and Wellness program with financial incentives
Tuition Reimbursement and Family Scholarship Programs
Career development and training opportunities
Not the right fit? Let us know you're interested in a future opportunity by clickingIntroduce Yourselfin the top-right corner of the page or create an account to set up email alerts as new job postings become available that meet your interest!
Sallie Mae is proud to be an equal opportunity (EEO) employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender, sexual orientation, national origin, age, genetic information, gender identity, disability, Veteran status or any other characteristic protected by federal, state or local law. Click hereto view the U.S. Pay Transparency Policy, here for federal job applicant notices, and here to view the California Employee Privacy Notice.Reasonable accommodations are available for applicants with disabilities in all phases of the application and employment process. To request an accommodation please call (855) 756-2007 and choose option 9. All information you provide will be kept confidential and will be used only to the extent required to provide needed reasonable accommodations.