Pharmaceutical Technical Writer Job at PharmEng Technology in City of Albany

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About the job Pharmaceutical Technical WriterTechnical Writer Engineering & Utilities (Pharma)

Location: Albany, NY (Hybrid One Week Onsite Per Month)

Duration: Long-Term Contract

We are seeking a Technical Writer with experience in engineering documentation for a pharmaceutical manufacturing environment, with a strong focus on utilities and facility systems. The ideal candidate will have expertise in developing, reviewing, and managing technical documents while ensuring compliance with GMP and regulatory standards. This hybrid role requires one week onsite per month to collaborate with stakeholders and gather critical technical information.

Key Responsibilities

Documentation Development: Create, update, and maintain SOPs, technical manuals, work instructions, and engineering documentation related to utilities (HVAC, WFI, compressed air, purified water, clean steam, etc.)

Collaboration & Content Gathering: Work closely with engineering, facilities, validation, and quality teams to collect and document technical requirements

Regulatory Compliance: Ensure all documentation meets FDA, cGMP, and industry standards

Document Workflow Management: Utilize electronic document management systems (EDMS) such as Veeva Vault, MasterControl, Documentum, or OpenText to manage approval workflows

Process Improvement: Assist in standardizing documentation processes, version control, and ensuring consistency across engineering records

Technical Editing & Formatting: Review technical content for clarity, accuracy, and compliance with company style guides

Qualifications & Experience

Experience: 3+ years as a Technical Writer in a pharmaceutical, biotech, or regulated manufacturing setting

Technical Knowledge: Experience documenting engineering processes, utilities, and facility systems

Software & Workflow Management: Proficiency in EDMS platforms such as Veeva Vault, MasterControl, Documentum, OpenText, or similar

Regulatory & Compliance: Familiarity with GMP, FDA 21 CFR Part 11, and industry best practices

Skills: Strong attention to detail, ability to interpret technical concepts, excellent communication, and organizational skills

This is a long-term hybrid opportunity to work in a cutting-edge pharmaceutical manufacturing environment, contributing to critical engineering and utility documentation.

Interested? Apply now or DM for details!

#TechnicalWriting #PharmaJobs #Engineering #Utilities #GMP #Documentation

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Marketing, Public Relations, and Writing/Editing

• Industries

  Pharmaceutical Manufacturing

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