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Validation Technical Writer | Pharmaceutical Manufacturing 

  • Temp
  • Temp
  • PA
  • Bethlehem

Job ID:103560

Not Ready

Important Notice About the Application Process

This position offers use of our AI screening tool as part of the initial candidate review. While completing the AI screening is optional, please note:

  • Candidates who complete the AI screening are reviewed first—daily.
  • We strongly encourage you to complete it promptly to ensure early consideration (first come, first served).
  • Expect to receive a prompt from our AI screener shortly after applying.

The AI screener helps us streamline the Candidate intake process, but rest assured—you’ll still work directly with a Masis recruiter throughout the rest of your hiring journey.

Validation Technical Writer | Pharmaceutical Manufacturing 
Bethlehem, PA Onsite
$40-$50/hr. DOE
Long-Term Contract (6-12 Months)
US citizens or Green Card holders
No C2C

Love technical writing? Know cGMP inside and out?

#MPGAll 

A well-established pharmaceutical manufacturing company is looking for an experienced Validation Technical Writer to support major validation initiatives, capital projects, and quality documentation.

You'll partner with Engineering, QA, QC, and Operations to create audit-ready documentation supporting equipment, utilities, manufacturing processes, and validation activities.

Must have experience with:

  • IQ / OQ / PQ Protocols
  • Validation Reports
  • SOP Authoring
  • cGMP Documentation
  • FDA-Regulated Manufacturing
  • API or Chemical Manufacturing (highly preferred)
  • Document Control
  • Cross-functional collaboration with Engineering & Quality

Requirements

  • Bachelor’s degree in a scientific, engineering, quality, or related technical field
  • Minimum 3 years of technical writing experience in pharmaceutical, API, or regulated chemical manufacturing
  • Proven experience with qualification and validation documentation in a cGMP environment
  • Strong understanding of cGMP principles and data integrity requirements
  • Experience authoring IQ OQ PQ protocols and validation reports
  • Excellent written communication skills with strong attention to detail and accuracy
  • Ability to manage multiple priorities in a fast paced manufacturing environment
  • Proficiency in Microsoft Word, Excel, Outlook, and document management systems

This is an outstanding opportunity to join a respected pharmaceutical manufacturer on a long-term project with the potential for additional extensions!

Masis Staffing is committed to providing a workplace free of discrimination, harassment, and retaliation. We are an equal opportunity employer. Applicants, employees, and former employees are protected from employment discrimination based on race, color, religion, sex (including pregnancy, sexual orientation or transgender status), national origin, age (40 or older), veteran status, disability and genetic information (including family medical history).

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