Top 23 Technical writer pharmaceutical Jobs

QA Investigations / Technical Writer
KVK Tech —Newtown, PA
- Mid-level
- 3 years
- Master's degree
- Paid holidays
- Dental insurance
Validation Writer
Tjoapack —Clinton, TN
- Full-time
- Background check
- Microsoft Excel
- Engineering
Quick Apply
Technical Writer
CEDENT —Springfield, NJ
- Microsoft Excel
- Mid-level
- Analysis skills
Technical Writer - Tech Transfer and Validation
Adare Pharma Solutions —Vandalia, OH
- Full-time
- Microsoft Excel
- Mid-level
- High school diploma or GED
- Paid holidays
- Disability insurance
Technical Operations Scientist
Lupin Pharmaceuticals Inc. —Somerset, NJ
- $70,000 - $95,000 a year
- Full-time
- Engineering
- Mid-level
- 3 years
Technical Writer II
Thermo Fisher Scientific —Plainville, MA
- $66,000 - $99,000 a year
- Full-time
- 5 years
- Mid-level
- Office
- Commuter assistance
- Paid parental leave
3d
Quality Specialist/Technical Writer
Teledyne Technologies Inc. —Billerica, MA
- $62,800 - $83,700 a year
- Full-time
- Microsoft Excel
- 5 years
- Analysis skills
Regulatory Affairs Technical Writer
Curium Pharma —St. Louis, MO
- Overtime
- Mid-level
- Office
- Microsoft Office
Engineering Technical Writer
INCOG BioPharma Services —Fishers, IN
- Full-time
- Microsoft Word
- Mid-level
- Office
Lead, Technical Transfer
Arrowhead Pharmaceuticals —Madison, WI
- $84,000 - $100,000 a year
- Microsoft Excel
- Bachelor of Science
- Bachelor's degree
MSAT Documentation Scientist II
Thermo Fisher Scientific —Greenville, NC
- Full-time
- Microsoft Excel
- Bachelor of Science
- Mid-level
5d
Deviation Writer - Osmotica Pharmaceuticals
Osmotica —Marietta, GA
- Mid-level
- Microsoft Office
- 3 years
Quick Apply
4d
Architectural Specifications Writer (LSNA-PA Remote)
Jacobs —Conshohocken, PA
- $110,600 - $185,000 a year
- Remote
- 5 years
- Research
- Office
- Paid holidays
- Health insurance
Deviation Writer - Tech Services
INCOG BioPharma Services —Fishers, IN
- Full-time
- Mid-level
- Office
- 3 years
- Health savings account
- Paid holidays
Quality Control Process Writer
AssistRx —Orlando, FL
- $54,000 - $68,000 a year
- Full-time
- Hybrid work
- Background check
- Mid-level
- Office
- Paid holidays
- Disability insurance
Quick Apply
Deviation Writer - Osmotica Pharmaceuticals
Alora Pharmaceuticals —United States
- Mid-level
- Microsoft Office
- 3 years
4d

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Regulatory Writer and/or Regulatory QC/ Editor
Vir Biotechnology —San Francisco, CA
Advanced degree in science or medical field is a plus. Support preparation and inspection‑readiness of technical documents for global regulatory submissions (eg…
$90 - $120 an hour
Quick Apply
Medical Writer
Perceptive —Remote
The Medical Writer will create, research, edit and coordinate the production of clinical documents related to independent review, including independent review…
$65,305 - $93,000 a year
9d

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QA Investigations / Technical Writer

KVK Tech -
Newtown, PA

Apply Now

Job Details

Benefits

Paid holidays
Dental insurance
Tuition reimbursement
Paid time off
Vision insurance
401(k) matching

Qualifications

Content creation for technical audiences
Preventive action implementation
Technical writing experience within manufacturing
Production deviation management
Corrective and preventive actions (CAPA)
Change management
Manufacturing facility experience
Pharmaceutical company experience
Quality assurance experience within pharmaceutical industry
FDA regulations
Pharmaceutical manufacturing facility experience

Full Job Description

KVK Tech is seeking an experienced QA Investigations / Technical Writer to join our team in Newtown, PA.

The QA Investigations / Technical Writer is responsible for supporting site quality systems through the investigation of quality events and the development, review, and maintenance of controlled documentation within an oral solid dosage manufacturing environment. This role ensures deviations, investigations, and quality documentation are accurate, compliant, and aligned with cGMP and regulatory requirements. The ideal candidate will demonstrate strong technical writing skills, experience owning deviations and CAPAs, and the ability to collaborate cross-functionally to support compliant manufacturing and continuous improvement.

This position’s responsibilities will include, but not be limited to the following:

Investigate and document quality events including deviations, incidents, planned deviations, OOS investigations, and customer complaints.

Perform and document root cause analyses and develop appropriate corrective and preventive actions (CAPAs) in alignment with regulatory expectations.

Draft, revise, and maintain controlled documentation such as SOPs, batch records, qualification and validation protocols, technical reports, and risk assessments.

Support change control activities related to manufacturing processes, equipment, facilities, and quality systems.

Collaborate with Manufacturing, Packaging, Engineering, and Quality teams to ensure documentation accuracy and procedural alignment.

Support continuous improvement initiatives through trend analysis, audit observations, and quality system enhancements.

We are looking for applicants with:
Bachelor’s degree in a scientific or technical discipline such as Chemistry, Biology, Pharmacy, or Engineering required; Master’s degree preferred.

Minimum 3–5+ years of experience in a pharmaceutical or regulated manufacturing environment.

Demonstrated experience in technical writing, deviation and CAPA management, and change control systems.

Working knowledge of cGMP requirements (21 CFR Parts 210/211) and FDA quality system expectations.

Strong written communication, analytical, and organizational skills with a high attention to detail.

What we offer:
401(k) with company match

Health, vision, and dental Insurance

Childcare expense reimbursement

Tuition reimbursement

Annual bonus eligibility

Annual merit increases

Paid Time Off and Flexible Holidays

KVK Tech is an affirmative action/equal opportunity employer and does not discriminate in hiring or employment on the basis of age, sex, race, color, religion, national origin, gender identity, veteran status, sexual orientation or any other protected status.

We encourage you to apply if you feel that you are a match! We look forward to hearing from you.

Apply Now

Refine Your Search

technical writer pharmaceutical jobs

QA Investigations / Technical Writer

Validation Writer

Technical Writer

Technical Writer - Tech Transfer and Validation

Technical Operations Scientist

Technical Writer II

Quality Specialist/Technical Writer

Regulatory Affairs Technical Writer

Engineering Technical Writer

Lead, Technical Transfer

MSAT Documentation Scientist II

Deviation Writer - Osmotica Pharmaceuticals

Architectural Specifications Writer (LSNA-PA Remote)

Deviation Writer - Tech Services

Quality Control Process Writer

Deviation Writer - Osmotica Pharmaceuticals

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