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Freelance Contract Medical Device Jobs (NOW HIRING)

SGS

Contract Opportunity - Medical Device Auditors

We are looking for Contract Medical Device Auditors with: * Non-active cardiovascular, vascular, and neurovascular implants (2+ years) * Non-active, non-implantable ophthalmologic devices (2+ years)

Astrix Inc

Medical Device Assembler

Santa Rosa, CA · On-site

$21 - $24/hr

Monday-Thursday, 5:00 AM-3:30 PM | Optional OT Fridays Type: 6-month contract with potential for ... Qualifications * 1+ year of manufacturing experience; medical device experience is a plus.

System One

Medical Device Assembler

Lakewood, NJ · On-site

$16/hr

Contract To Hire Compensation: $16.00 / hr. Contractor Work Model: Onsite Hours: 7:00 AM-3:00 PM Monday-Friday Medical Device Assembler Responsibilities: * Use various machinery to assemble medical ...

Astrix Inc

Medical Device Assembler

Trumbull, CT · On-site

$17.75 - $21.50/hr

Mon-Thu 3:45pm-2:15am Type of Job : 3-6 Month Contract w/ Potential to convert permanently Location : Trumbull, CT Benefits Offered: * Medical/dental coverage! * Weekly pay! Medical Device Assembler ...

Marquee Staffing - OC

Be Seen First

Medical Device Packaging (Cleanroom)

Lake Forest, CA · On-site

$20 - $21/hr

Medical Device Assembler - Packaging Job Type: Full-Time, Contract-to-Hire Pay & Schedule: * 1st Shift: $19-$20/hr | Monday-Thursday, 5:00 AM-3:30 PM * 2nd Shift: $19-$21/hr | Monday-Thursday, 3:30 ...

Aerotek

Medical Device Assembler

Irvine, CA

$19.50 - $21/hr

Now Hiring Medical Device Assemblers Location: Irvine, CA Pay: $19-21/hr Shifts Available: * Monday ... Job Type & Location This is a Contract position based out of Irvine, CA. Pay and Benefits The pay ...

Pride Global

Medical Device Engineer

San Diego, CA · On-site

$82.66 - $96.43/hr

We are seeking a Senior Medical Device Engineer to join our Research & Development team. In this ... Contract Length: 06 Months with the possibility of extensions Pay range: $60 to $70 per hour on W2 ...

VOLT

Medical Device Assembler

Plymouth, MN · On-site

$17.50 - $19.25/hr

... is a full time, contract opportunity. Schedule: 1st Shift : 5:00 AM - 3:30 PM Monday through ... Experience as a Medical Device Assembler or Production Assembler. * Strong attention to detail ...

Astrix Inc

Medical Device Assembler

Santa Rosa, CA · On-site

$22 - $24/hr

Pay Rate Low: 22 | Pay Rate High: 24 A medical device manufacturer is seeking a Production/Assembly ... Onsite in Santa Rosa, CA | Type : 6-month contract with possibility for conversion or extension ...

VOLT

Medical Device Assembler

Irvine, CA · On-site

$18 - $19.75/hr

This is a full time, contract opportunity. Schedule: 1st Shift: 5:00 AM to 1:30 PM Monday to Friday ... Prior experience as a Medical Device Assembler or Production Assembler preferred. * Previous ...

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Freelance Contract Medical Device information

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How much do freelance contract medical device jobs pay per hour?

As of Aug 26, 2026, the average hourly pay for freelance contract medical device in the United States is $47.71, according to ZipRecruiter salary data. Most workers in this role earn between $24.28 and $61.78 per hour, depending on experience, location, and employer.
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Freelance Contract Medical Device jobs near you
Infographic showing various Freelance Contract Medical Device job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, and 6% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $99,230 per year, or $47.7 per hour.

Medical Writer

Maple Grove, MN • On-site

Three Point Solutions, Inc.
Recruiting and Staffing Services • 11 - 50 employees
Learn more about Three Point Solutions, Inc.external

Full-time

Re-posted 24 days ago

Job description

Job Title: Medical Writer
Client: Medical Device Manufacturing Company
Duration: 12 Months
Location: Maple Grove, MN, 55311
**Mandatory- Must be US Citizen or Green Card Holder Only
Key Words:
  • CER (Clinical Evaluation Review/Report) Writing
  • MDR (Medical Device Regulations)
  • EU (European Union)
  • Literature Review (e.g., PubMed)

Responsibilities:
  • Write and review scientific manuscripts, congress abstracts, and scientific meeting presentations aligned with journal and congress guidelines.
  • Prepare clinical content for study investigator meetings, interim data analyses, and other internal/external meetings related to clinical studies.
  • Create symposia (non-CME), speaker decks, post-meeting slide decks, topical slide decks, and other Professional Education modules as needed.
  • Collaborate extensively with internal medical leadership, clinical research scientists, clinical trial managers, medical affairs managers, statisticians, and other medical writers as part of publication teams.
  • Develop partnerships with study investigators, external authors, and interact externally with journals, conference organizers, and freelance/contract medical writers.
  • Ensure clinical data is represented accurately in published literature, slide sets, and other materials.
  • Lead and organize document production meetings and related activities.
  • Review documents related to clinical evidence for proper evaluation and presentation of data, methodology, and interpretation.

Required Qualifications:
  • Degree in Life Sciences (Advanced degree preferred).
  • Experience in Medical Device or Pharmaceutical Industry with a focus on Medical Writing or Clinical Research.
  • Extensive experience in writing, editing, and submitting publications to journals and congresses.

Preferred Qualifications:
  • 5-7 years of relevant experience.
  • Therapeutic area knowledge in peripheral interventions is desired.
  • Excellent written, analytical, verbal, and communication skills.
  • Ability to manage multiple projects independently and meet deliverables on time.
  • Capable of working effectively in a matrix environment.
  • Ability to develop strategic solutions to significant business issues.
  • Commitment to patient safety and product quality by adhering to the Quality Policy and documented quality processes and procedures.

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