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Validation Engineer Biomedical Jobs in Connecticut

Minimum 3 years of biomedical equipment experience in a clinical engineering environment * Strong ... Valid driver's license; ability to travel as needed Applicants can expect a compensation range of ...

Utilize product and process controls, risk analysis/management tools, validation, design ... Bachelor's degree in engineering (Electrical, Mechanical, Biomedical) or related field from an ...

New

Senior Quality Engineer

North Haven, CT · On-site

$88K - $119K/yr

Bachelor's degree in Engineering (Chemical, Biomedical, Mechanical, or related discipline); advanced degree preferred. * Strong expertise in process validation across the full validation lifecycle ...

Senior Quality Engineer

North Haven, CT · On-site

$88K - $119K/yr

Bachelor's degree in Engineering (Chemical, Biomedical, Mechanical, or related discipline); advanced degree preferred. * Strong expertise in process validation across the full validation lifecycle ...

Defines and performs verification and validation activities ensuring products meet user needs and ... Bachelor's Degree in Mechanical Engineering, Materials Science & Engineering, or Biomedical ...

Defines and performs verification and validation activities ensuring products meet user needs and ... Bachelor's Degree in Mechanical Engineering, Materials Science & Engineering, or Biomedical ...

Scientist II

Ridgefield, CT · On-site

$35 - $40.05/hr

Validate image-derived biomarkers and ensure analytical accuracy, reproducibility, and scientific ... Proficiency in scientific programming using Python and/or R. * Experience developing and applying ...

Showing results 21-40

Validation Engineer Biomedical information

What does a validation engineer do in biomedical?

A Validation Engineer in the biomedical industry ensures that equipment, processes, and systems used in the production of medical devices or pharmaceuticals meet regulatory standards and function as intended. Their work involves planning and executing validation protocols, documenting results, and troubleshooting any deviations. This role is crucial for maintaining product quality, patient safety, and compliance with regulatory agencies such as the FDA. Validation Engineers often collaborate with quality assurance, manufacturing, and research teams to establish and maintain validated systems throughout a product's lifecycle.

What are the key skills and qualifications needed to thrive as a validation engineer in biomedical?

To thrive as a Validation Engineer in Biomedical, you need a solid background in engineering or life sciences, knowledge of regulatory standards (such as FDA or ISO 13485), and experience with validation protocols. Familiarity with technical tools like statistical analysis software, calibration equipment, and documentation systems is essential, and certifications such as Six Sigma or CQE can be advantageous. Strong problem-solving, attention to detail, and effective communication skills help you excel in cross-functional teams and ensure compliance. These skills are crucial for maintaining product quality, meeting regulatory requirements, and ensuring patient safety in biomedical environments.

What are some typical challenges faced by validation engineers in the biomedical industry and how can they be addressed?

Validation Engineers in the biomedical field often face challenges such as keeping up with evolving regulatory requirements, managing complex documentation, and ensuring equipment or processes meet stringent quality standards. Navigating audits and working cross-functionally with R&D, manufacturing, and quality assurance teams can also be demanding. To address these challenges, staying current with industry regulations, developing strong organizational and communication skills, and maintaining meticulous records are essential for success and career growth in this role.

What is the difference between Validation Engineer Biomedical vs Quality Assurance Engineer Biomedical?

AspectValidation Engineer BiomedicalQuality Assurance Engineer Biomedical
CertificationsGMP, ISO, FDA validation certificationsGMP, ISO, audit and compliance certifications
Work EnvironmentDesign, develop, and execute validation protocols for medical devicesDevelop and maintain quality systems, audits, and process improvements
Industry UsagePrimarily in medical device manufacturing and regulatory validationAcross medical device, pharmaceutical, and biotech industries

Validation Engineer Biomedical focuses on ensuring medical devices meet regulatory validation requirements through testing and protocols. Quality Assurance Engineer Biomedical emphasizes maintaining quality systems, compliance, and process improvements. Both roles are essential in the biomedical industry but serve different functions related to validation versus quality assurance.

What are popular job titles related to Validation Engineer Biomedical jobs in Connecticut?

For Validation Engineer Biomedical jobs in Connecticut, the most frequently searched job titles are:

What job categories do people searching Validation Engineer Biomedical jobs in Connecticut look for?

The top searched job categories for Validation Engineer Biomedical jobs in Connecticut are:

What cities in Connecticut are hiring for Validation Engineer Biomedical jobs?

Cities in Connecticut with the most Validation Engineer Biomedical job openings:

Infographic showing various Validation Engineer Biomedical job openings in Connecticut as of July 2026, with employment types broken down into 82% Full Time, and 18% Contract. Highlights an 84% In-person, and 16% Hybrid job distribution.

Senior Process Engineer - North Haven, CT

Medtronic

North Haven, CT

$103K - $133K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 5 days ago


Medtronic rating

7.8

Company rating: 7.8 out of 10

Based on 178 frontline employees who took The Breakroom Quiz

175th of 542 rated manufacturers


Job description

We anticipate the application window for this opening will close on - 24 Aug 2026


Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first - developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.

A Day in the LifeThe Senior Process Engineer is responsible for providing support for multiple product families related to safety, quality, service, product cost, process improvements, and customer feedback across chemical, extrusion, textile, and biomedical manufacturing processes. This role leads and participates in cross-functional teams to achieve project goals, support continuous improvement initiatives, and drive manufacturing performance.
Based at Medtronic's North Haven, Connecticut campus, a major manufacturing and engineering site supporting Surgical Innovations products, the Senior Process Engineer serves as a technical expert for production equipment and manufacturing processes. The role also supports new products transitioning from R&D into manufacturing, helping ensure successful product launch, operational readiness, and long-term manufacturing sustainability.
At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We're working 5 days a week onsite as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary.

The Senior Process Engineer will:

  • Support the day-to-day manufacturing of absorbable and non-absorbable sutures, including polymer development, crystallization, purification, extrusion, annealing, and textile manufacturing processes.

  • Lead cross-functional teams and projects using project management tools to plan, track, and deliver technical, operational, and financial objectives.

  • Provide technical expertise for the specification, procurement, installation, qualification, validation, troubleshooting, and training of chemical, polymer extrusion, textile, and biomedical manufacturing processes and equipment.

  • Identify and lead opportunities to improve process and equipment capability, reliability, and manufacturing efficiency through data analysis, statistical methods, and continuous improvement initiatives.

  • Support new product development, quality improvement, product integration, and capital equipment projects.

  • Execute engineering qualifications and process validations, including IQ/OQ/PQ activities, to support manufacturing, compliance, and operational objectives.

  • Partner with Manufacturing, Quality, Maintenance, Planning, Safety, and other cross-functional teams to investigate production and field issues, perform root cause analysis, and implement effective corrective and preventive actions.

  • Manage engineering change notices, BOM creation and maintenance, ERP/SPAC system activities, and provide technical guidance and mentorship to junior engineering staff.

Required Qualifications

  • Bachelor's degreewith a minimum of 4 years of relevant experience

  • OR Master's degree with a minimum of 2 years relevant experience

  • OR PhD with 0 years relevant experience

  • Experience applying statistical methods and science-based decision making to design experiments and implement process improvements.

  • Experience managing multiple projects and priorities in a manufacturing, engineering, or product development environment.

  • Experience working on cross-functional teams to deliver technical projects and business objectives.

  • Experience using Minitab for data analysis and problem solving.

Preferred Qualifications

  • Experience in the medical device industry.

  • Experience with Design for Reliability (DFR), Design for Six Sigma (DFSS), and/or Lean Six Sigma methodologies.

  • Experience supporting absorbable polymer products or technologies.

  • Experience with polymer development and manufacturing, fiber extrusion, textile manufacturing, and/or material characterization.

  • Lean Six Sigma Green Belt or Black Belt certification.

  • Bachelor's degree or an advanced degree in Chemistry, Chemical, Mechanical, Bio-Medical Engineering, or related

For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. 214.2(h)(4)(iii)(A) is required.

Physical Job Requirements

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.

The physical demands described within the Responsibilities section of this job description 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. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.

U.S. Work Authorization & Sponsorship

At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.

Recruitment Fraud Alert

We are aware of phishing scams targeting job seekers. Please keep the following in mind:


Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses.


Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate.


If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments.


If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at AskHR@medtronic.com.

Benefits & Compensation

Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.

Salary ranges for U.S (excl. PR) locations (USD):$103,200.00 - $154,800.00This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).

The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance,Health Savings Account,Healthcare Flexible Spending Account,Life insurance, Long-term disability leave,Dependent daycare spending account,Tuition assistance/reimbursement, andSimple Steps (global well-being program).

The following benefits and additional compensation are available to all regular employees:Incentive plans, 401(k) plan plus employer contribution and match,Short-term disability,Paid time off,Paid holidays,Employee Stock Purchase Plan,Employee Assistance Program,Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), andCapital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).

Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.

Further details are available at the link below:

Medtronic benefits and compensation plans

It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.


If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can findhere a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.


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