Technical Writer

Rise Technical; Newtown (PA); On-site; USD 110,000 - 130,000; Full time

Benefits offered by this job

Annual pay increases

401(k)

Full medical benefits

Tuition & childcare scholarships

Job summary

A growing pharmaceutical manufacturer in Newtown, PA, is looking for a technical writer with experience in pharmaceutical documentation. The role involves preparing and maintaining technical documents to support drug development and manufacturing processes. The company offers competitive pay, annual increases, medical benefits, and a strong emphasis on work-life balance.

Qualifications

• Several years of experience in pharmaceutical manufacturing or R&D.
• Strong background in technical writing and documentation management.
• Solid understanding of drug development and scale-up processes.

Responsibilities

• Write and review SOPs, validation reports, and manufacturing batch records.
• Prepare development protocols and technical transfer documents.
• Support drug development and scale-up activities.
• Maintain document control systems for accuracy.

Skills

Technical writing

Documentation management

Pharmaceutical manufacturing

R&D processes

Oral solid dosage forms

Education

Degree in Chemistry, Chemical Engineering, or related field

Job description

This range is provided by Rise Technical. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$110,000.00/yr - $130,000.00/yr

Newtown, PA

Commute from: Trenton, Levittown, Yardley, Langhorne, and surrounding areas

$110,000 - $135,000 + Annual pay increases, 401(k), full medical benefits, tuition & childcare scholarships, and much more!

Are you experienced in pharmaceutical documentation and looking for a role that offers more ownership, collaboration, and long‑term progression?

Do you want to join a company where your work directly supports new product development and the creation of affordable medicines across the U.S.?

This is a rare chance to join a growing pharmaceutical manufacturer with full in‑house production and a reputation for quality. They’re expanding their R&D team to drive new product launches and technical excellence – and this role is key to ensuring the documentation behind that process is as impressive as the science itself!

In this position, you’ll prepare and maintain technical documentation across R&D and manufacturing. You’ll work closely with scientists, engineers, and production teams to ensure every procedure is clear, compliant, and supports successful scale‑up.

You’ll be based at their Newtown, PA facility, collaborating daily with colleagues in R&D, quality, and manufacturing. The environment is extremely supportive, offering strong stability, genuine development opportunities, and a genuine work‑life balance.

The Role:

• Write and review SOPs, validation reports, and manufacturing/packaging batch records
• Prepare development protocols, technical transfer documents, and process documentation
• Support drug development and scale‑up activities for oral solid dosage forms
• Maintain document control systems and ensure consistent technical accuracy

The Person:

• Several years of experience in pharmaceutical manufacturing or R&D (oral solid dosage experience required)
• Strong background in technical writing and documentation management
• Solid understanding of drug development and scale‑up processes
• Degree in Chemistry, Chemical Engineering, or related scientific field preferred