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Medical Device Product Development Jobs in Texas

Crown Medical, Inc.

Medical Device Rep

Austin, TX · On-site

$82K - $113K/yr

We are a fully integrated company with internal resources dedicated to the development and promotion of medical supplies and device products. We believe that our proven products and customer focused ...

Astura Medical

Sr. Design Engineer

Irving, TX · On-site +1

Strong background in medical device product development, including design, testing, and manufacturing processes. * Knowledge of materials selection, manufacturing processes (e.g., machining, casting ...

Medivators Inc.

Product Label Design Supervisor

Conroe, TX · On-site

$161K/yr

Technical writing proficiency is highly desirable with emphasis on medical device product labeling development. * Experience in working within a regulated industry. * Software experience with Propel ...

Astura Medical

Sr. Design Engineer

Irving, TX · On-site

Strong background in medical device product development, including design, testing, and manufacturing processes. * Knowledge of materials selection, manufacturing processes (e.g., machining, casting ...

Astura Medical

Sr. Design Engineer

Irving, TX · On-site

Strong background in medical device product development, including design, testing, and manufacturing processes. * Knowledge of materials selection, manufacturing processes (e.g., machining, casting ...

ConsignMed Inc.

Be Seen First

Clinical Specialist Medical Device

Odessa, TX · On-site

$100 - $150/day

Keep current on all product literature and industry developments * Ensure all product issues or ... medical device or Operating Room experience, preferred * Gyn/Surg related experience, preferred

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Medical Device Product Development information

See Texas salary details

$39.6K

$118.3K

$134.6K

How much do medical device product development jobs pay per year?

As of Aug 6, 2026, the average yearly pay for medical device product development in Texas is $118,308.00, according to ZipRecruiter salary data. Most workers in this role earn between $106,700.00 and $133,200.00 per year, depending on experience, location, and employer.

What is a medical device product development?

A Medical Device Product Development job involves designing, testing, and bringing medical devices to market while ensuring compliance with regulatory standards. Professionals in this role work with cross-functional teams, including engineering, regulatory affairs, and manufacturing, to develop safe and effective healthcare solutions. They oversee the entire product lifecycle, from concept and prototyping to clinical validation and commercialization. Strong knowledge of FDA, ISO, and other regulatory requirements is essential.

What are some typical challenges faced in medical device product development roles?

Professionals in Medical Device Product Development often encounter challenges such as navigating complex regulatory requirements, managing cross-functional project teams, and ensuring that products meet both clinical needs and quality standards. Balancing innovative design with safety and compliance can require careful planning and solid problem-solving skills. Additionally, adapting to shifting project timelines and incorporating stakeholder feedback are common aspects of the job. Overcoming these challenges is rewarding and helps ensure the delivery of safe, effective devices to patients and healthcare providers.

What are the key skills and qualifications needed to thrive in medical device product development?

To thrive in Medical Device Product Development, you need a strong background in engineering or life sciences, product design, and an understanding of regulatory requirements like FDA and ISO standards. Proficiency with CAD software, project management tools, and knowledge of quality management systems (QMS) is commonly required, along with certifications such as Six Sigma or PMP being beneficial. Strong problem-solving abilities, collaboration skills, and effective communication are key soft skills for this role. These skills are important to ensure that devices are developed safely, efficiently, and in compliance with industry regulations while fostering innovation and teamwork.

What are the most commonly searched types of Medical Device Product Development jobs in Texas? The most popular types of Medical Device Product Development jobs in Texas are:
What are popular job titles related to Medical Device Product Development jobs in Texas? For Medical Device Product Development jobs in Texas, the most frequently searched job titles are:
What job categories do people searching Medical Device Product Development jobs in Texas look for? The top searched job categories for Medical Device Product Development jobs in Texas are:
What cities in Texas are hiring for Medical Device Product Development jobs? Cities in Texas with the most Medical Device Product Development job openings:
Medical Device Product Development jobs near you
Infographic showing various Medical Device Product Development job openings in Texas as of July 2026, with employment types broken down into 87% Full Time, and 13% Contract. Highlights an 100% In-person job distribution, with an average salary of $118,308 per year, or $56.9 per hour.

Product Integrity Scientist

Swiss American CDMO

Carrollton, TX • On-site

Other

This job post has expired today. Applications are no longer accepted.

Job description

Position Summary: The Product Integrity Scientist will support product safety/integrity related to regulatory affairs for product development, raw materials or finished products. They will provide product integrity support for Swiss American Contract Development and Manufacturing (SA). The person in this role will support sound product safety strategy and follow-through implementation for product, finished good and product compliance in different skin health categories across global regions. As the product integrity personnel in the organization, this role is responsible for supporting product safety and compliance.

Essential Duties and Responsibilities:

  • Responsible for managing product safety and compliance intelligence, policies, and programs of diverse scope across the business for raw materials, bulk products, finished and commercialized goods
  • Responsible for creation of cosmetic ingredient declaration, quantitative and qualitative formulas
  • Review and assess changes to safety and global regulatory requirements and industry best practices and facilitate implementation through new or revised processes.
  • Responsible for evaluating and assessing safety and regulatory compliance of raw materials used at SA
  • Responsible for safety and regulatory documentation for compliance requested by clients on SA formulations
  • Responsible for safety assessments and compliance evaluations for skincare, OTC and medical device products across global regions including but not limited to prop 65, impurities, EU allergens etc.
  • Responsible for working with other employees to ensure adherence to compliance of products, resolve compliance issues, as appropriate, and communicate as required to clients.
  • Develop, plan, oversee and generate clinical, in vitro, in silico studies, and/or technical reviews which will insure the efficacy and safety of Swiss American products or Swiss American contracted formulations
  • Expertise in methodologies used to assess the safety and efficacy of OTC, cosmetic and medical devices
  • Manage client meetings and responses for ingredient and regulatory compliance
  • Responsible for owning and maintaining current formulation system (Formulator Pro) to manage ingredient entry, ingredient compliance etc.
  • Oversee the creation and/or maintenance of technical files as necessary to obtain and sustain product approval.
  • Determine and communicate submission and approval requirements early in the product lifecycle to assure that projects plans are aligned to meet safety and regulatory guidelines.
  • Participate in multidisciplinary project teams with the Client.
  • Responsible for RID product safety compliance metrics for Quality Management Reviews.
  • Responsible for SA quarterly newsletter on compliance based on research and interpretation of compliance guidelines
  • Other duties may be assigned.
Essential Skills and Qualifications:
  • Experienced in leading cross-functional interactions related to product safety matters
  • Bachelor's Degree in Life Sciences or related field.
  • Preferred: Advanced Degree (e.g., Master's, PhD) in a relevant field.
  • Minimum 4+ years of relevant experience in the skincare, pharmaceutical, or OTC industry.
  • Minimum 3 years of experience in a Product Safety/Regulatory function.
  • Proven experience in skincare OTC and medical device product safety and compliance, with a history in clinical studies preferred.
  • Experience interacting with regulatory agencies (e.g., FDA, EMA, Health Canada).
  • Strong understanding of pharmaceutical and medical device R&D, product development, and regulatory environments.
  • In-depth knowledge of global product safety and regulatory requirements for skincare, OTC, and medical devices.
  • Proven ability to lead cross-functional teams and manage complex projects.
  • Excellent analytical, problem-solving, and decision-making skills.
  • Strong written and verbal communication and interpersonal skills.
  • Proficiency in Microsoft Office Suite.
  • Experience with process management and continuous improvement.
  • Demonstrated knowledge of global regulations and compliance requirements.
  • Ability to analyze complex situations, identify risks, and develop effective strategies.
  • Ability to lead teams, build relationships, and effectively collaborate with cross-functional partners.
  • Proven ability to manage multiple projects with aggressive timelines and deliver high-quality results.
  • A proactive approach to identifying and implementing process improvements.
  • May be responsible for supervising a team of 3-6 personnel.
Work Environment:

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The noise level in the work environment Is usually moderate.

Physical Demands:

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions, and perform any other related duties, as assigned by their supervisor.

Candidates selected for employment will be required to complete a pre-employment screening, including a drug test, employment verification, and education verification.

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