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Technical Writer | Validation

Masis Professional Group -
Bethlehem, PA

Quick Apply

Job Details

Temporary
$40 - $50 an hour
12 days ago

Qualifications

Microsoft Excel
Content creation for technical audiences
Microsoft Outlook
Document control experience within pharmaceutical industry
Pharmaceutical regulatory compliance
Document control experience within engineering industry
Word embeddings
Technical writing experience within manufacturing
GMP
Quality reports
Manufacturing facility experience
Quality assurance standard operating procedures
Scientific protocols
Compliance documentation
Process validation (IQ/OQ/PQ)
Cross-functional collaboration
Standard operating procedures (SOPs)
Production documentation
Quality control records management
Cross-functional communication
FDA regulations

Full Job Description

Technical Writer | Validation
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?

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!

#MPGAll

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).

Quick Apply

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