PharmEng Nordic ApS is hiring: Pharmaceutical Technical Writer in Albany

About the job Pharmaceutical Technical Writer Technical 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! #J-18808-Ljbffr