Technical Writer

SmartRecruiters, Inc.

Andover (MA)

On-site

USD 34,000 - 58,000

Full time

2 days ago
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Job summary

Global Channel Management in the United States is seeking a Technical Writer with 5 years of experience to create and edit batch records for production of bulk drug substances, using Microsoft Word. You will work with engineers to understand the process at manufacturing scale and draft the batch records using a template as a starting point.

The role involves incorporating comments during review, routing documents for approval through a documentation management system, and collaborating with

Qualifications

  • 5 years of experience as a Technical Writer.
  • Experience creating and editing batch records for pharmaceutical manufacturing.

Responsibilities

  • Create and edit batch records (instructions for production of bulk drug substance) in Microsoft Word.
  • Meet with engineers to understand the process at manufacturing scale and draft batch records using a template.
  • Incorporate comments during record review and route documents for review through a documentation management system.
  • Collaborate with technical project leads, operations staff, and quality assurance on batch record creation.
  • Revise manufacturing procedures as a secondary responsibility.

Skills

Technical Writing

Tools

Microsoft Word

Job description

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job.

Qualifications

Technical Writer needs 5 years experience

Technical Writer requires:

  • technical writing
  • The
    primary job responsibility will be creating and editing batch records
    (the instructions for production of bulk drug substance) in Microsoft
    word.
  • The writer will meet with engineers to gain an
    understanding of how the process will be run at manufacturing scale and
    will then draft the batch records using a template as a starting point.

  • The writer will then incorporate comments as needed during record
    review and route the document for review through a documentation
    management system.
  • Creation of the batch records will require
    close collaboration with technical project leads, operations staff, and
    quality assurance.
  • The secondary job responsibility will be revision of manufacturing procedures.
Additional Information

$42/hr

6 months

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