404 Medical Device Manufacturing jobs in the United States

Job Description

Our Manufacturing Team works as a group to assemble subassemblies and finished goods utilizing workstations and line-assembly operations. We have operations that require the use of hand tools, power tools and fixtures (Assembly Technicians) and industrial sewing machines (Sewing Machine Operators). Though we currently have a full staff, we are always looking for top talent to add to our growing team. If you’re interested in future opportunities at Sentec, please submit an application and we will keep your resume on file when future positions become available.

Essential Duties and Responsibilities

• Uses correct product specifications and assembly procedure/work instructions for each product.
• Assemble medical device components following detailed work instructions and specifications.
• Follows the master production schedule for the facility, while providing adjustments and communication for changes in customer requirements, delays in receiving raw materials, availability of production equipment, etc.
• Working knowledge of standards and regulations as outlined in the Quality Management System (QMS) documentation and structure.
• Conduct in-process inspections to ensure assembled devices meet quality standards and specifications
• Follow all regulatory and company standards, including FDA regulations, ISO 13485, and Good Manufacturing Practices (GMP).

Requirements

• High School diploma or equivalent required.
• Previous Medical Device experience is a plus!
• Previous Industrial Sewing Machine experience is preferred for Sewing Machine Operators.

Benefits

• Meaningful work in a rapidly growing company with opportunity for advancement
• Directly influence the quality of products and make a difference for patients worldwide
• Opportunities for professional and personal growth
• Pay: $18-$20/hr plus bonus

Sentec offers competitive benefits like Medical, Dental, Vision, HSA, FSA, and 401K matching, as well as paid parental leave , a wellness stipend and tuition reimbursement. Sentec emphasizes employee voices and recognizes hard work making it a promising environment for professional growth. Sentec focuses on delivering impactful healthcare products and improving patient care.

By choosing a career at Sentec, you’re not just choosing a job – you’re embracing the chance to make a real impact, contributing to the development of innovative medical solutions that support the wellbeing of individuals worldwide.

Sentec is a Swiss-American medical device company specializing in respiratory care. Since its founding in 1999, Sentec utilizes a deep-tech approach that is founded on advanced science and avant-garde technologies for respiratory patients across care areas. Sentec provides healthcare professionals worldwide with non-invasive, continuous monitoring and effective therapeutic solutions.

Key Responsibilities:
• Assemble and inspect micro-scale components and cartridges using approved procedures.
• Perform mechanical and electronic assembly, including wire harnesses, pin insertion, and microfluidic device integration.
• Operate under a microscope for 5-6+ hours daily to ensure precision and quality.
• Follow gowning protocols including hairnets, shoe covers, and gowns to maintain a contamination-sensitive environment.
• Maintain accurate production records and follow detailed work instructions.
• Use hand tools and basic electronic testing equipment to verify functionality.
• Collaborate with team members to meet production goals and quality standards.

We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy:

Required Skills & Experience

Qualifications:
• High school diploma or equivalent required.
• Experience with microelectronic devices, hearing aids, or nail work is highly transferable.
• Familiarity with wire harnessing, pin assembly, or small-scale mechanical/electronic components.
• Prior work in a production environment with contamination control protocols preferred.
• Strong hand-eye coordination and manual dexterity.
• Ability to work independently under a microscope for
• Basic computer skills for data entry and test documentation.

Nice to Have Skills & Experience

extended periods.
• Experience with Gas Chromatography (GC) columns or microfluidics.

Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.

Title: Engineer III - NPI Manufacturing

Location: Onsite (5 days/wk) in Andover, MA

Duration: 6 months+ (possible extension)

Shift: Monday-Friday (8:00 am- 5pm)

Responsibilities:

• Lead PFMEA activities in coordination with product development, quality, and manufacturing engineering teams.
• Participate in DFM and DFA activities to define manufacturing processes for new product and product enhancement programs.
• Develop manufacturing assembly and test methods to ensure Critical to Quality (CTQ) requirements are met.

Must haves:

• Bachelors Degree at a Minimum
• Only Candidates with a Medical Device Background
• 5+ years of experience working in an FDA/ISO regulated medical device/medical equipment manufacturing environment.
• Must have prior NPI Manufacturing and/or Process Development experience, including disposables and capital equipment.
• Test Method Validation and Verification (TMV, V&V)

Title: Engineer III - NPI Manufacturing

Location: Onsite (5 days/wk) in Andover, MA

Duration: 6 months+ (possible extension)

Shift: Monday-Friday (8:00 am- 5pm)

Responsibilities:

• Lead PFMEA activities in coordination with product development, quality, and manufacturing engineering teams.
• Participate in DFM and DFA activities to define manufacturing processes for new product and product enhancement programs.
• Develop manufacturing assembly and test methods to ensure Critical to Quality (CTQ) requirements are met.

Must haves:

• Bachelors Degree at a Minimum
• Only Candidates with a Medical Device Background
• 5+ years of experience working in an FDA/ISO regulated medical device/medical equipment manufacturing environment.
• Must have prior NPI Manufacturing and/or Process Development experience, including disposables and capital equipment.
• Test Method Validation and Verification (TMV, V&V)

Title: Engineer III - NPI Manufacturing

Location: Onsite (5 days/wk) in Andover, MA

Duration: 6 months+ (possible extension)

Shift: Monday-Friday (8:00 am- 5pm)

Responsibilities:

• Lead PFMEA activities in coordination with product development, quality, and manufacturing engineering teams.
• Participate in DFM and DFA activities to define manufacturing processes for new product and product enhancement programs.
• Develop manufacturing assembly and test methods to ensure Critical to Quality (CTQ) requirements are met.

Must haves:

• Bachelors Degree at a Minimum
• Only Candidates with a Medical Device Background
• 5+ years of experience working in an FDA/ISO regulated medical device/medical equipment manufacturing environment.
• Must have prior NPI Manufacturing and/or Process Development experience, including disposables and capital equipment.
• Test Method Validation and Verification (TMV, V&V)

Job Title: Manufacturing Technician (1st Shift)

Location: Minnetonka, MN 55343

Pay Rate: $22-$24 per hour (W2)

Duration: 1-2 months contract

Schedule: Monday-Thursday, 6:00 AM to 4:30 PM

Position Overview

We are seeking a detail-oriented and dependable Manufacturing Technician to support production and packaging operations for pharmaceutical products in a GMP-compliant facility. This is a hands-on role involving assembly, inspection, and packaging of combination drug-device products. The ideal candidate will have experience working in a cleanroom or controlled manufacturing environment and be familiar with cGMP standards and documentation practices.

Key Responsibilities

• Perform routine and complex assembly, final packaging, and inspection tasks for pharmaceutical products
• Follow Standard Operating Procedures (SOPs) and Work Instructions (WIs) to meet production goals
• Adhere strictly to cGMP and Good Documentation Practices (GDP) standards
• Maintain accurate production records and ensure compliance with internal quality processes
• Handle and distribute materials and supplies in the manufacturing area
• Operate safely and responsibly in a controlled environment with special gowning requirements
• Support team efforts and contribute to continuous improvement initiatives
• Perform other duties as assigned

Qualifications

Education:

• High School Diploma or equivalent required

Experience:

• Prior experience in a manufacturing setting preferred
• Experience in pharmaceutical, biotech, or regulated environments is a plus

Skills & Abilities:

• Strong attention to detail and ability to follow written procedures
• Understanding of cGMP and GDP principles (preferred)
• Comfortable working in cleanroom conditions with specialized gowning
• Ability to lift up to 50 lbs and stand for extended periods
• Good communication and organizational skills
• Able to work independently and as part of a team

Why Apply?

• Great opportunity to gain or grow your experience in pharmaceutical manufacturing
• Consistent weekday schedule with long weekends
• Professional, team-oriented work environment

EQUAL EMPLOYMENT OPPORTUNITY STATEMENT:

Suna Solutions provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

Applicants, with criminal histories, are considered in a manner that is consistent with local, state, and federal laws.

REQUESTING AN ACCOMODATION

Suna Solutions is committed to providing equal employment opportunities for persons with disabilities or religious observances, including reasonable accommodation when needed. If you are hired by Suna Solutions and require accommodation to perform the essential functions of your role, you will be asked to participate in our reasonable accommodation process. Accommodations made to facilitate the recruiting process are not a guarantee of future or continued accommodations once hired.

If you would like to be considered for employment opportunities with Suna Solutions and have accommodation needs for a disability or religious observance, please call us at , send us an email or speak with your recruiter.

PAY TRANSPARENCY POLICY STATEMENT

Compensation for roles at Suna Solutions varies depending on a wide array of factors including but not limited to the specific client, office or remote location, role, skill set and level of experience. As required by local law, Suna Solutions provides a reasonable pay scale to include the hourly or salary range that Suna Solutions reasonably expects to pay for roles that may be hired in California, Colorado, New York City or Washington as set forth below.