Top 22 Technical writer medical device Jobs

Manufacturing Documentation Specialist
A&Z Pharmaceutical, Inc. —Hauppauge, NY
- $50,000 - $65,000 a year
- Full-time
- English
- Mid-level
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply
10d
Technical Writer
MiniMed —Northridge, CA
- $58,000 - $110,000 a year
- Full-time
- Remote
- Mid-level
- Office
- Bachelor's degree
- Health savings account
- Employee stock purchase plan
Medical Writer (Remote, US)
Maquet Cardiovascular LLC —Boston, MA
- $105,000 - $115,000 a year
- Remote
- Microsoft Excel
- Microsoft Outlook
- 3 years
- Commuter assistance
- Disability insurance
Technical Writer - Product Development (Dental Devices)
Prismatik —Irvine, CA
- $30 - $43 an hour
- Full-time
- Engineering
- Mid-level
- 4 years
Technical Writer
Katalyst Healthcares & Life Sciences —Bothell, WA
- Contract
- Hybrid work
- Mid-level
- Bachelor's degree
- 2 years
Quick Apply
Document Control Specialist - Medical Device #2902
Enhanced Compliance Inc. —Burlingame, CA
- Full-time
- Microsoft Word
- US work authorization
- Senior level
Technical Writer - Operations
Experic LLC —Cranbury, NJ
- $80,000 - $110,000 a year
- Mid-level
- Office
- 3 years
Quick Apply
Sr. Engineer, Production (Technical Writer)
Atrium Medical Corporation —Merrimack, NH
- $95,000 - $120,000 a year
- Extended hours
- 5 years
- Engineering
- Office
- Commuter assistance
- Disability insurance
10d
GMP Technical Writer
Automated Systems Inc. —Madison, WI
- $50 - $70 an hour
- Full-time
- Computer Science
- Mid-level
- Continuous improvement
- Health insurance
- Dental insurance
Quick Apply
11d
Manufacturing Technical Writer
CONFLUENT MEDICAL TECHNOLOGIES INC. —Austin, TX
- Full-time
- Microsoft Word
- Spanish
- ERP systems
6d
Lead Technical Writer, Clinical AI/ML & SaMD
Grant Engine —Remote
- Part-time
- Remote
- English
- Master's degree
- Machine learning
Technical Writer
Perrigo —Eau Claire, WI
- Mid-level
- 3 years
- Analysis skills
Technical Writer - Medical device (Hybrid: Sunnyvale, California) W2 Only
Intuitive —Sunnyvale, CA
- $40 - $70 an hour
- Temporary
- Surgery
- English
- Research
Quick Apply
Technical Writer-Supply Chain (Temporary 6 Months)
Versiti, Inc. —Grand Rapids, MI
- Temporary
- Hybrid work
- Microsoft Excel
- Mid-level
- Office
- Paid holidays
- Disability insurance
CCS Service Engineer
Siemens Healthineers —Knoxville, TN
- $89,220 - $122,672 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Outlook
- Engineering
- Disability insurance
- Health insurance
Quick Apply
Documentation Specialist
Integer Holdings Corporation —Plymouth, MN
- $58,575 - $85,910 a year
- Full-time
- Research
- Mid-level
- Bachelor's degree
- Disability insurance
- Health insurance
Quick Apply
11d
MES Consultant
Katalyst Healthcares & Life Sciences —Manhattan, NY
- Contract
- Remote
- Senior level
Quick Apply
Compliance Documentation Specialist
Quest Global —Phoenix, AZ
- $33 - $36 an hour
- Full-time
- Mid-level
- 3 years
- Bachelor's degree
- Disability insurance
- Health insurance
Quick Apply
11d
Report Writer I, Medical Device Pathology
BRONCO RESEARCH SERVICES LLC —Fort Collins, CO
- $56,000 - $65,000 a year
- Full-time
- Microsoft Outlook
- Computer literacy
- English
- Paid parental leave
- Disability insurance
Quick Apply
11d

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Manufacturing Documentation Specialist

A&Z Pharmaceutical, Inc. -
Hauppauge, NY

Quick Apply

Job Details

Full-time
$50,000 - $65,000 a year
10 days ago

Benefits

Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance
401(k) matching
Life insurance
Referral program

Qualifications

Technical editing
Content creation for technical audiences
Document control experience within pharmaceutical industry
Procedural guides
Technical writing experience within manufacturing
English
Manufacturing standard operating procedures
Bachelor's degree in engineering
Bachelor's degree
Batch records
Technical writing quality assurance
Productivity software
English
Technical writing experience within technology
Standard operating procedures (SOPs)
FDA regulations
Standard operating procedures drafting
Pharmaceutical manufacturing facility experience

Full Job Description

Company Overview:

A&Z Pharmaceutical Inc. is a pioneering leader in the development, manufacturing, and marketing of high-quality pharmaceutical products and nutritional supplements. With over 30 years of industry experience, the company operates globally with dedicated research laboratories and manufacturing facilities committed to advancing health and wellness worldwide.

Job Overview:

We are seeking a dynamic and detail-oriented Technical Writer in the pharmaceutical industry. In this role, you will be responsible for creating, editing, and maintaining high-quality documentation, including Standard Operating Procedures (SOPs), regulatory submissions, batch records, and technical reports. The Technical Writer bridges the gap between complex scientific data and regulatory requirements, ensuring compliance with cGMP (current Good Manufacturing Practices) and FDA guidelines.

Key Responsibilities:

Standard Operating Procedure (SOP) Writing:
Draft, edit, and maintain SOPs, validation protocols, and master batch records.
Ensure all documents adhere to FDA, and other regulatory standards, contributing to submissions and audits.
Regularly review and update SOPs in line with technological or process changes.

Execution of Equipment Qualification (IOPQ):

Assist in the execution of IOPQ protocols for equipment and processes.
Collaborate with senior team members to ensure protocols are followed accurately and completely.
Document results and any deviations, reporting to the Technical Operations Manager.

Technical Document Management:

Organize, store, and manage technical documents in a systematic manner.
Ensure easy access to documents for all relevant departments while maintaining security and confidentiality.
Regularly review and update documents to ensure they are current and compliant.
Identify gaps in current processes and update documentation to reflect improvements or correct deviations.

Equipment Recordkeeping and Maintenance Scheduling:

Maintain an up-to-date list of all equipment, including their specifications, locations, and status.
Collaborate with QA team to schedule and track regular maintenance, ensuring minimal operational disruption.
Collaborate with the maintenance team to preempt potential equipment issues.

Change Control Management:

Collaborate with QA team to understand the implications and requirements of potential changes.
Track and monitor the status of change controls, ensuring relevant stakeholders are kept informed.
Assist in drafting initial change control requests, ensuring all relevant details are accurately captured.

Requirements and Qualifications

Bachelor’s degree in scientific, medical, or technical field (e.g., Chemistry, Biology, Pharmacy) or English/Communications with relevant experience.
1–3+ years of technical writing experience, ideally in pharmaceutical, nutraceutical, biotechnology, or medical device environments.
Strong understanding of cGMP (current Good Manufacturing Practices).
Expertise in MS Office Suite (Word, Excel) and experience with document management systems.
Meticulous approach to reviewing and editing to prevent errors in manufacturing or reporting.

Job Type: Full-time

Pay: $50,000.00 - $65,000.00 per year

Benefits:

401(k)
401(k) matching
Dental insurance
Health insurance
Life insurance
Paid time off
Referral program
Vision insurance

Education:

Bachelor's (Required)

Experience:

Draft, edit SOPs, validate protocols, master batch records.: 1 year (Required)

Location:

Hauppauge, NY 11788 (Required)

Shift availability:

Day Shift (Required)

Work Location: In person

Quick Apply

Refine Your Search

technical writer medical device jobs

Manufacturing Documentation Specialist

Technical Writer

Medical Writer (Remote, US)

Technical Writer - Product Development (Dental Devices)

Technical Writer

Document Control Specialist - Medical Device #2902

Technical Writer - Operations

Sr. Engineer, Production (Technical Writer)

GMP Technical Writer

Manufacturing Technical Writer

Lead Technical Writer, Clinical AI/ML & SaMD

Technical Writer

Technical Writer - Medical device (Hybrid: Sunnyvale, California) W2 Only

Technical Writer-Supply Chain (Temporary 6 Months)

CCS Service Engineer

Documentation Specialist

MES Consultant

Compliance Documentation Specialist

Report Writer I, Medical Device Pathology

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