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Remote Medical Device Technical Writer Jobs in Rochester, NY

SQA Services

Quality Auditor - Pharmaceutical

Avon, NY · Remote

$1.30K/day

... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Assure quality in the supply chains of various clients within the pharmaceutical, medical device ...

Iff

Technical Service Account Manager

Rochester, NY · On-site +1

This role is based in United State and is a remote position. You will be part of a collaborative ... Our benefit package includes medical, dental, vision, 401k, vacation, holidays, 16 weeks paid ...

Info Advantage Inc

IT Support Technician Level 1

Rochester, NY · Remote

$21.25 - $29/hr

Key Responsibilities Remote Support & Service Desk Provide Tier 1-2 remote technical support for ... New user provisioning Device enrollment and configuration Software installation and standardization ...

AppCast

Certified Medical Coder

Rochester, NY · Remote

$35 - $38/hr

Certified Medical Coder - Inpatient (Remote) Pride Health is seeking a Certified Medical Coder ... Under the San Francisco Lactation in the Workplace Ordinance, we will provide written notice of ...

New

Pride Health

Certified Medical Coder

Rochester, NY · Remote

$35 - $38/hr

Certified Medical Coder - Inpatient (Remote) Pride Health is seeking a Certified Medical Coder ... Under the San Francisco Lactation in the Workplace Ordinance, we will provide written notice of ...

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Remote Medical Device Technical Writer information

See Rochester, NY salary details

$13

$38

$57

How much do remote medical device technical writer jobs pay per hour?

As of May 28, 2026, the average hourly pay for remote medical device technical writer in Rochester, NY is $38.12, according to ZipRecruiter salary data. Most workers in this role earn between $25.87 and $48.12 per hour, depending on experience, location, and employer.

What is the difference between Remote Medical Device Technical Writer vs Remote Regulatory Affairs Specialist?

AspectRemote Medical Device Technical WriterRemote Regulatory Affairs Specialist
CredentialsTypically requires a degree in life sciences, engineering, or related field; certifications like RMT or technical writing certifications are commonRequires degrees in life sciences, law, or regulatory fields; certifications like RAC are often preferred
Work EnvironmentPrimarily writes and edits technical documents remotely for medical device companiesFocuses on regulatory submissions, compliance, and communication with authorities, often remotely
Industry UsageUsed across medical device companies, biotech, and healthcare tech firmsCommon in medical device, pharmaceutical, and biotech industries

While both roles require knowledge of medical devices and regulatory standards, the Remote Medical Device Technical Writer primarily creates technical documentation, whereas the Remote Regulatory Affairs Specialist manages regulatory compliance and submissions. Both roles often work remotely and require relevant industry experience, but their core responsibilities differ significantly.

What are the most commonly searched types of Medical Device Technical Writer jobs in Rochester, NY? The most popular types of Medical Device Technical Writer jobs in Rochester, NY are:
What are popular job titles related to Remote Medical Device Technical Writer jobs in Rochester, NY? For Remote Medical Device Technical Writer jobs in Rochester, NY, the most frequently searched job titles are:
What job categories do people searching Remote Medical Device Technical Writer jobs in Rochester, NY look for? The top searched job categories for Remote Medical Device Technical Writer jobs in Rochester, NY are:
What cities near Rochester, NY are hiring for Remote Medical Device Technical Writer jobs? Cities near Rochester, NY with the most Remote Medical Device Technical Writer job openings:
Remote Medical Device Technical Writer jobs near you
Infographic showing various Remote Medical Device Technical Writer job openings in Rochester, NY as of May 2026, with employment types broken down into 63% Full Time, and 37% Contract. Highlights an 100% Remote job distribution, with an average salary of $79,292 per year, or $38.1 per hour.
Quality Auditor - Pharma/Food/Med Device

Quality Auditor - Pharma/Food/Med Device

SQA Services

Avon, NY • Remote

$1.30K/day

Other

Posted 10 days ago

Job description

For nearly 30 years, SQA Services has been a leading provider of managed supplier quality services, offering audits, assessments, remote surveillance, corrective actions, remediation, inspections, and engineering solutions to manufacturers across all industries. We deliver these services by deploying a network of highly skilled associates based throughout the United States and in over 90 countries worldwide, ensuring rapid on-site support at your supplier locations. Our associates are expert quality assurance professionals with extensive experience and local expertise, enabling us to represent our clients on-demand and with greater speed and efficiency than our competitors.
 
We're hiring a Quality Auditor who has direct experience working in both the pharma, medical device, and/or food industries. This is a contract opportunity in which you will perform supplier quality audits at various suppliers in the northeastern region of the US. These audits are generally 1-2 days long. You are given the flexibility to accept or reject these assignments according to your own availability. 
Key Responsibilities
  • Perform supplier audits at various sites within your region of residence
  • Assure quality in the supply chains of various clients within the pharmaceutical, medical device, cosmetics, biologics, and/or animal health industries
  • Coordinate, prepare, execute, and deliver supplier audits based on your own and the client schedule
  • Utilize your regulatory knowledge of various standards from ISO, CFR, FDA, etc...
  • Respond to the Content team in a timely manner regarding edits/questions to your audit report
  • Write audit reports in accordance with client specifications
Required Qualifications
  • 5+ years of hands-on audit experience in pharmaceutical, medical device, and/or biologics industries
  • Has been the lead auditor in at least 10 audits
  • Direct audit experience to 21 CFR part 210/211, EU Vol 4, ISO 13485, 21 CFR part 820, Canada GMP, 21 CFR 111, 21 CFR 117 and/or 21 CFR 121
  • Strong communication and writing skills
  • Proven ability to deescalate workplace conflicts effectively
  • Ability to adapt to new technology and software.
  • Willingness to travel regionally
Preferred Qualifications
  • Direct audit experience to ISO 17025, ISO 15378, 21 CFR 110, 21 CFR 120, 21 CFR 507
  • ISO certifications are a plus but not mandatory
$1,300 - $1,300 a day
Pay Rate: 
 
$1300 for a 1-day audit. Includes: Time spent preparing for the audit, traveling, performing the audit, writing the report, and responding to questions from our Content team of editors and the client until the report is finalized. Does not include: Following up on CAPA for any findings or reimbursement for travel expenses - expenses are reimbursed at cost with receipts per SQA travel policy. Note that SQA helps with the preparation of the audit and proofreads all audit reports.
 
Note: SQA is an Equal Opportunity Employer. Employment is based on merit and qualifications, and is not influenced by race, color, religion, gender, national origin, veteran status, disability, age, sexual orientation, gender identity, marital status, or any other legally protected status.
 
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