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.
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
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!
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PharmEng Technology, now part of Efor Group, leader in Compliance Engineering, is a leading provider of technical services and solutions to the pharmaceutical, biotechnology, and healthcare industries. With over 25 years of experience, we specialize in Commissioning, Qualification, and Validation (CQV) services for facilities, utilities, equipment, and processes.
As part of Efor’s global network of 3,000 experts across 12 countries, we are better equipped than ever to deliver innovative and comprehensive solutions tailored to the unique needs of clients worldwide. This integration strengthens our ability to combine global expertise with local proximity, positioning PharmEng as a strategic partner for the industry’s most prominent players.
Our team of highly skilled professionals brings a wealth of industry expertise and knowledge to every project, ensuring that our clients receive the highest quality services and solutions. We pride ourselves on our ability to provide flexible, innovative, and cost-effective solutions that meet our clients' unique challenges.
At PharmEng Technology by Efor, we are committed to delivering excellence in everything we do. We work closely with our clients to understand their goals and objectives, developing customized solutions that deliver measurable results. Our focus on quality, safety, and compliance ensures that our clients can trust us to meet their most critical needs.
Specialties: PharmEng Technology specializes in the planning, design, construction, and validation of Health Care, Laboratory, API Pharmaceutical, and Biotechnology facilities and equipment, including computer systems. We provide professional services that meet both regulatory and business demands, following current Good Manufacturing Practices (cGMP), Good Engineering Practices (GEP), and Good Laboratory Practices (GLP).
