Technical Writer job in Norton, USA

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Job type: Contract

Discipline: Good Manufacturing Practice (GMP)

Location: United States

This vacancy has now expired. Please see similar roles below...

Technical Writer - Contract - Norton, MA

Are you ready to make a groundbreaking impact in the world of biotechnology? Join a growing company that's shaping the future of healthcare and science.

Proclinical is seeking a Technical Writer to join our client's team in Norton, MA.

Primary Responsibilities:

The successful candidate will focus on creating and maintaining essential documentation to support manufacturing operations and quality control processes within the rare disease and biotechnology sector. Your expertise will ensure compliance with regulatory standards and enhance operational efficiency.

Skills & Requirements:

Strong writing and editing skills with attention to detail.
Familiarity with regulatory standards such as GMP, FDA, and EMA.
Ability to work collaboratively with cross-functional teams.

The Technical Writer's responsibilities will be:

Develop and update standard operating procedures (SOPs), batch records, work instructions, and other technical documents.
Ensure all documentation meets GMP, FDA, EMA, and other relevant regulatory standards, as well as internal policies.
Collaborate with subject matter experts from manufacturing, quality assurance, validation, safety, and engineering teams to gather accurate technical information.

If you are having difficulty in applying or if you have any questions, please contact Janelle Jones at j.jones@proclinical.com

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

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