Technical Writer (Temp/Hybrid-PA).794.4231

ZipRecruiter; Canonsburg (Washington County); Hybrid; Full time

Job summary

A leading global pharmaceutical corporation is seeking a Technical Writer for a long-term, temporary position in Exton, PA. The successful candidate will author and review technical documents supporting the Analytical Outsourcing team, collaborating across teams to ensure quality documentation. This position offers a hybrid schedule and competitive benefits.

Benefits

ABA-MEC Medical Benefits

PEP 401k

Paid Time Off

Employee Assistance Program (EAP)

Discounts through Working Advantage

FinFit Financial Wellness Program

Qualifications

• 2-3 years of laboratory experience, preferably in protein therapeutics or monoclonal antibody development.
• Proven proficiency in scientific and technical writing.
• Familiarity with GMP/GLP and regulated environments.

Responsibilities

• Authoring and revising technical reports, SOPs, and policies.
• Preparing analytical method validations and regulatory submissions.
• Managing purchase orders and liaising with Finance for budget updates.

Skills

Scientific writing

Technical writing

Analytical skills

Communication

Organizational skills

Education

Bachelor’s degree in Chemistry, Biology, or a related scientific field

Tools

Empower Chromatography Data System

LIMS

Microsoft Word

Excel

SharePoint

SAP/SRM

TrackWise

Veeva systems

Job description

The Opportunity

A preeminent global pharmaceutical corporation seeks a Technical Writer on a long-term, temporary basis for at least twelve months, possibly longer in Exton, PA. The schedule is Monday - Friday, 8:00 a.m. - 5:00 p.m., hybrid (two to three days per week), and may be subject to change. The hourly rate is $30 - $40, plus benefits.

Primary Duties

The Technical Writer should have a strong scientific background to support the Analytical Outsourcing team in the Biopharmaceutical Development sector. Responsibilities include authoring and reviewing technical documents, supporting regulatory submissions, and collaborating across teams to ensure high-quality documentation and data integrity. Additional duties include:

• Authoring and revising technical reports, SOPs, and policies
• Preparing and editing analytical method validations, study protocols/reports, and CMC documentation for regulatory submissions
• Drafting and reviewing deviations, investigations, change controls, and other quality records
• Coordinating with external vendors for testing and sample shipments
• Reviewing and compiling scientific data for completeness and compliance
• Analyzing stability data and supporting shelf-life assessments
• Utilizing LIMS for protocol creation, data entry/approval, and trending
• Managing purchase orders, invoices, and vendor agreements; liaising with Finance for budget updates
• Overseeing review, approval, and archiving of documentation
• Supporting laboratory testing activities as needed

Requirements

• Bachelor’s degree in Chemistry, Biology, or a related scientific field
• 2–3 years of laboratory experience, preferably in protein therapeutics or monoclonal antibody development
• Proven proficiency in scientific and technical writing
• Hands-on experience with Empower Chromatography Data System is REQUIRED
• Familiarity with GMP/GLP and regulated environments
• Strong written and verbal communication skills
• Excellent attention to detail and organizational skills
• Proficiency in Microsoft Word, Excel, and SharePoint
• Advanced Excel skills
• Experience with LIMS, SAP/SRM, TrackWise, and Veeva systems

The Partnership – Benefits

• ABA-MEC Medical Benefits
• PEP 401k
• Paid Time Off
• Employee Assistance Program (EAP), Discounts through Working Advantage, and FinFit Financial Wellness Program

Note: Frink-Hamlett Legal Solutions is an equal employment opportunity employer. All applicants will receive consideration regardless of race, creed, marital status, or citizenship status.