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Medical Device Associate information

What are some common challenges faced by medical device associates during the product launch phase?

Medical Device Associates often encounter challenges such as coordinating with cross-functional teams to ensure regulatory compliance, managing tight deadlines, and addressing unexpected technical issues during product launch. Effective communication with quality assurance, engineering, and sales teams is crucial to resolve issues quickly and keep projects on track. Additionally, Associates may need to adapt to shifting priorities and provide hands-on support for product training or demonstrations, making organizational and problem-solving skills essential for success in this dynamic environment.

What is a medical device associate?

A Medical Device Associate is a professional who supports the development, testing, regulatory compliance, and marketing of medical devices. They often work with engineering, regulatory, and sales teams to ensure products meet safety standards and reach the market successfully. Their responsibilities can include documentation, quality assurance, coordinating clinical trials, and assisting with submissions to regulatory bodies. Medical Device Associates play a key role in bringing innovative healthcare technologies to patients and providers.

What are the key skills and qualifications needed to thrive as a medical device associate, and why are they important?

To thrive as a Medical Device Associate, you need a background in life sciences or engineering, strong product knowledge, and familiarity with medical regulations, typically supported by a relevant degree. Experience with CRM systems, regulatory documentation tools, and knowledge of FDA or EU MDR guidelines are often required. Excellent communication, problem-solving abilities, and attention to detail help build strong client relationships and ensure compliance. These skills are crucial for effectively supporting healthcare professionals, maintaining regulatory standards, and driving successful product adoption.
What are the most commonly searched types of Medical Device jobs in California? The most popular types of Medical Device jobs in California are:
What cities in California are hiring for Medical Device Associate jobs? Cities in California with the most Medical Device Associate job openings:
Medical Device Associate jobs near you
Infographic showing various Medical Device Associate job openings in California as of July 2026, with employment types broken down into 84% Full Time, 5% Part Time, and 11% Contract. Highlights an 100% In-person job distribution.

Medical Device Packaging Associate

Tucker Parker Smith Group (TPS Group)

Northridge, CA • On-site

$23 - $25/hr

Contractor

Posted 6 days ago

Job description

Packaging Operator (Medical Device)
Location: Northridge, CA (100% on-site)
Pay Rate: $23-25/hr
6-month contract with high potential to extend/convert

Available Shifts:
4 Openings: Monday–Friday Night Shift (3 Crew Schedule) 9:30pm - 5pm 
3 Openings: 12-Hour Rotating Night Shift (4 Crew Schedule) 5pm - 5am 
Candidates with flexible shift availability are strongly encouraged to apply.


Job Overview:
Are you Ready to join an innovative team in manufacturing and packaging advanced transdermal products? This opportunity has great potential for a long-term career advancement in the medical device industry with one of the top Global companies in the US!
Our client is seeking Packaging Operators to join a fast-paced pharmaceutical manufacturing team producing transdermal drug delivery products. This position works closely with Converting Technicians to support packaging and production operations while ensuring compliance with GMP, safety, and quality standards. The ideal candidate is dependable, detail-oriented, and enjoys working in a team environment within a regulated manufacturing facility.



Key Responsibilities

  • Assist Converting Technicians with packaging, filling, and manufacturing operations.
  • Operate production equipment and support packaging line activities.
  • Stage, transport, and replenish raw materials and in-process materials.
  • Perform line clearance, housekeeping, and workstation cleaning to maintain a safe and compliant work environment.
  • Handle and dispose of hazardous waste according to established procedures and safety guidelines.
  • Follow Manufacturing Orders, SOPs, Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and serialization requirements.
  • Accurately complete production documentation, labor reporting, and downtime tracking using basic computer systems.
  • Wear required PPE and follow all environmental, health, and safety procedures.
  • Escalate equipment, quality, or production concerns to leadership when necessary.
  • Participate in training, continuous improvement initiatives, and team production meetings.



Qualifications

Required

  • High School Diploma or GED.
  • Up to 1 year of manufacturing or production experience.
  • Ability to follow written and verbal instructions in English.
  • Basic math and computer skills.
  • Strong attention to detail and commitment to quality.
  • Ability to lift up to 25 lbs. occasionally.
  • Ability to stand for extended periods throughout the shift.
  • Willingness to work a rotating 12-hour night shift schedule and adapt to shift changes as needed.



Preferred

  • 1+ year of experience in an FDA-regulated pharmaceutical, medical device, biotech, or GMP manufacturing environment.
  • Experience working with production, packaging, or assembly equipment.
  • Familiarity with SOPs, GMP documentation, and quality systems.
  • Experience working in a cleanroom or regulated manufacturing environment.

Company Description

The TPS Group, www.tpsmithgroup.com, is a Certified Woman and Disabled Owned Diverse recruiting and staffing firm that is a trusted recruiting partner to top companies.