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Dsm Biomedical Jobs (NOW HIRING)

DSM Biomedical information

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$15

$28

$38

How much do dsm biomedical jobs pay per hour?

As of Jun 29, 2026, the average hourly pay for dsm biomedical in the United States is $28.53, according to ZipRecruiter salary data. Most workers in this role earn between $24.28 and $32.21 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Dsm Biomedical position, and why are they important?

To excel at DSM Biomedical, you typically need a background in biomedical engineering, materials science, or a related life sciences field, often supported by relevant degrees or laboratory experience. Familiarity with research and development tools, regulatory compliance systems (like ISO 13485), and quality management frameworks is highly valued. Strong teamwork, problem-solving, and communication skills help candidates coordinate across multidisciplinary teams and adapt to evolving project needs. These skills ensure product innovation, compliance, and successful collaboration in a fast-paced, highly regulated biomedical industry.

What is a DSM Biomedical job?

A DSM Biomedical job typically involves working in the biomedical materials and medical device industry, focusing on innovation, research, and production of advanced biomaterials. Employees in these roles may work in areas such as product development, regulatory affairs, quality assurance, or sales. DSM Biomedical specializes in creating materials used in medical applications like implants, drug delivery systems, and regenerative medicine. Positions can range from engineers and scientists to business development professionals.

What are the typical day-to-day responsibilities for someone working at DSM Biomedical?

At DSM Biomedical, your daily responsibilities may include conducting laboratory experiments, analyzing biomedical materials, and collaborating with R&D teams to develop or test new medical devices and products. You will often participate in project meetings, document findings per regulatory standards, and engage in cross-functional communication with manufacturing and quality assurance departments. Additionally, adhering to strict safety and compliance protocols is an important part of the job. This dynamic environment provides opportunities to work on innovative projects and contribute to advancements in healthcare solutions.

More about DSM Biomedical jobs
What cities are hiring for Dsm Biomedical jobs? Cities with the most Dsm Biomedical job openings:
What are the most commonly searched types of Dsm Biomedical jobs? The most popular types of Dsm Biomedical jobs are:
What states have the most Dsm Biomedical jobs? States with the most job openings for Dsm Biomedical jobs include:
Senior Director, Global Quality & Regulatory - Exton, PA

Senior Director, Global Quality & Regulatory - Exton, PA

DSM

Exton, PA โ€ข On-site

$157K - $225K/yr

Full-time

Posted 11 days ago


Key responsibilities

  • Define and lead the global Quality & Regulatory strategy for Biomedical, aligned with business priorities, innovation objectives, and geographic expansion.

  • Oversee the development, documentation, and implementation of quality procedures and standards across the organization to ensure compliance and continuous improvement.

  • Serve as the senior quality and regulatory interface with customers, notified bodies, and regulatory agencies on matters related to compliance, audits, and product standing.


Job description

Senior Director, Global Quality & Regulatory
Location: Exton, PA/USA
We're building our Biomedical Quality leadership team in Exton, PA - we're hiring for Senior Director, Global Quality & Regulatory This is acritical role at Exton that provides enterprise leadership for the quality and regulatory agenda, ensuring compliance with applicable regulatory requirements, maintaining product integrity and customer confidence, and enabling sustainable business growth through strong quality systems, governance, and performance.
This member of the Global Leadership Team serves as the global head of Quality & Regulatory for Biomedical and is accountable for setting strategy, driving execution, and fostering a culture of compliance, continuous improvement, and operational excellence across all sites and functions. Senior Director, Global Quality & Regulatory operates in a highly regulated environment requiring advanced knowledge of cGMP, ISO standards, ASTM standards, design controls, risk management, change control, and quality system and regulatory requirements.
Local drivers of success rely on your ability to operate in a highly regulated, global environment, where close collaboration with site leadership, operations, R&D, commercial teams, customers, suppliers, and external regulatory bodies occurs. The position is based on-site in Exton, PA and requires regular physical presence at the facility to lead cross-functional decision-making, quality governance, talent development, and site engagement.
We are a leading biomaterials partner to global medical device and pharmaceutical companies, with more than 30 years of expertise in biomaterial science, process innovation, regulatory support, and high-quality manufacturing. The business is recognized for its broad portfolio, proprietary processing capabilities, strong intellectual property, and extensive experience supporting customers worldwide.
At dsm-firmenich people are at the heart of the company. We are committed to equal employment opportunities and value diversity in the workplace.
Your key responsibilities
  • Define and lead the global Quality & Regulatory strategy for Biomedical, aligned with business priorities, innovation objectives, and geographic expansion; Oversee the development, documentation, and implementation of quality procedures and standards across the organization.
  • Ensure the effectiveness, compliance, and continuous improvement of the global quality management system. Ensure compliance with applicable U.S. and international regulatory requirements governing medical devices, biomaterials, and related products
  • Serve as the senior quality and regulatory interface with customers, notified bodies, and regulatory agencies on matters related to compliance, audits, and product standing; Ensure effective supplier engagement and oversight, including performance of required supplier audits.
  • Build, lead, and develop a high-performing global Quality & Regulatory organization, including talent development, succession planning, and organizational capability building
  • Serve as a key member of the Biomedical leadership team, contributing to enterprise risk management, strategic decision-making, and business performance

The salary scale provided reflects the pay range dsm-firmenich expects to pay the successful candidate for the position. Individual pay offered will be based on the applicant's job-related skills, experience, relevant education or training, and primary work location. Salary $157,200-$225,000.
We bring
  • A culture that prioritizes safety and well-being, both physically and mentally
  • A firm belief that working together with our customers is the key to achieving great things
  • A space to grow by encouraging and supporting curiosity and an open mindset
  • The opportunity to work for a company where sustainability is much more than a claim and is core to our strategy and purpose
  • Barrier-free communities within our organization where every employee is equally valued and respected - regardless of their background, beliefs, or identity
  • An eagerness to be one team and learn from each other to bring progress to life and create a better future

You bring
  • Minimum of 15 years of experience in Quality Assurance and/or Regulatory Affairs, preferably within medical device manufacturing, biomaterials, or another regulated life sciences environment required
  • Minimum of 10 years of progressive leadership experience in quality systems and processes within a regulated and internationally operating environment
  • Deep knowledge of quality management systems and regulatory frameworks applicable to medical devices and related products for a Class III medical device operation (21CFR 820, ISO 9001, 13485, 14001, 45000); experience with clean room theory and operation is a plus
  • Demonstrated experience in change management, team leadership, and organizational development. Global quality experience and experience in the pharmaceutical industry a plus.
  • Experience and success with Lean Manufacturing implementation and working knowledge of tools such as 5S, Kanban, Kaizen events, visualization, standardized work
  • Bachelor's degree required with preference for a degree in Engineering or a related technical discipline. Auditing certification is preferred

Our recruitment process
Interested in this position? Please apply online by uploading your resume in English via our career portal by July 3, 2026.
Inclusion, belonging and equal opportunity statement
At dsm-firmenich, we believe being a force for good starts with the way we treat each other. When people feel supported, included, and free to be themselves, they do their best work - and that's exactly the kind of culture we're building. A place where opportunity is truly equal, authenticity is celebrated, and everyone has the chance to grow, contribute, and feel they belong.
We're proud to be an equal opportunity employer, and we're serious about making our hiring process as fair and inclusive as possible. From inclusive language and diverse interview panels to thoughtful sourcing, we're committed to reflecting the world we serve.
We welcome candidates from all backgrounds - no matter your gender, ethnicity, sexual orientation, or anything else that makes you, you.
And if you have a disability or need any support through the application process, we're here to help - just let us know what you need, and we'll do everything we can to make it work.
About dsm-firmenich
As innovators in nutrition, health, and beauty, dsm-firmenich reinvents, manufactures, and combines vital nutrients, flavors, and fragrances for the world's growing population to thrive. With our comprehensive range of solutions, with natural and renewable ingredients and renowned science and technology capabilities, we work to create what is essential for life, desirable for consumers, and more sustainable for the planet. dsm-firmenich is a Swiss-Dutch company, listed on the Euronext Amsterdam, with operations in almost 60 countries and revenues of more than โ‚ฌ12 billion. With a diverse, worldwide team of nearly 30,000 employees, we bring progress to lifeโ„ข every day, everywhere, for billions of people.
www.dsm-firmenich.com
Agency Note
Please note this is a direct search led by dsm-firmenich. We only accept applications from candidates, not from agencies nor subject to agency's fees, percentages or similar.