Technical Writer (Pharmaceutical) Job at Piper Companies in Frederick

Piper Companies is seeking a Technical Writer to support a well‑established biopharmaceutical client out of Frederick, MD. The Technical Writer will be responsible for supporting documentation efforts for critical facility operations. Responsibilities of the Technical Writer: Create, revise and maintain controlled documentation in support of Facilities operations, including SOPs, Work Instructions, and Risk Assessments (and other technical documentation) Format using Microsoft Word and Excel to produce clear, consistent and compliant documentation Facilitate document routing, review, and approval activities within the electronic document management system (Veeva / eDMS / ECMS) Partner with facilities personnel and subject matter experts to capture accurate technical content and translate it into well‑structured documentation Ensure all documentation complies with GMP requirements, safety standards, and regulatory guidelines Qualifications of the Technical Writer: 3+ years of hands‑on experience working as a technical writer and creating, revising, and maintaining controlled documentation Experience with document management systems such as Veeva, EDMS, ECMS, LIMS, LMS, etc. Must have prior experience working with GMP (Good Manufacturing Practices) – regulated facilities documentation Experience supporting manufacturing, facilities, or engineering teams in a biotech/pharmaceutical environment Strong written communication skills and organizational skills Proven ability to interpret technical processes and translate them into compliant written procedures Strong attention to detail and organizational skills Experience working within document control systems and formal approval workflows Proficiency in Microsoft Word and Excel for professional document formatting Bachelor’s degree in related field Compensation of the Technical Writer: Salary Range: Between $75,000 - $110,000 based on years of relevant experience Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Paid Holidays, Sick Leave as required by law This job opens for applications on 1/6/2026. Applications for this job will be accepted for at least 30 days from the posting date. Keywords: Technical Writer, Tech Writer, Technical Operations, Manufacturing, Engineering, MSAT, biotech, biopharmaceutical, pharmaceutical, GMP, good manufacturing practice, document management system, veeva, veevavault, EDMS, ECMS, LIMS, LMS, technical trainer, CAPA, SOP, standard operating procedure, facilities management, facilities, writing, science writing, technical writing, risk assessment, protocol development, revisions, editing, Microsoft office, excel, word, formatting, regulatory, electronic document management system, work instructions, policies and procedures, procedures, templates, document control, document management, controlled technical documentation, version control, revision, approval workflow, document archival, retrieval, mastercontrol, electronic content management system, digital content, manual, document, training material, PDF, controlled documentation, life sciences, quality assurance, QA #J-18808-Ljbffr