Equipment Technical Writer Pharma/Biotech

Job Title: Senior Equipment Technical Writer : Pharma/Biotech
Location : Indianapolis/Lebanon, IN (Onsite)
Duration: 12+ Months
Rate : $60 to $80 Per hour 1099/C2C (all Inc.) - Depends on experience

Job Description:

We are seeking an experienced Equipment Technical Writer to develop and manage documentation for equipment Standard Operating Procedures (SOPs) in a fast-paced pharmaceutical/biotechnology environment. This role requires a deep understanding of purification, chromatography, filtration, cell culture, bioreactor, and mixing equipment to ensure clear, accurate, and compliant documentation.

The ideal candidate will be responsible for authoring, maintaining, and managing timelines for all technical documentation throughout the project lifecycle while adhering to data integrity and compliance standards.

Key Responsibilities:

• Develop, write, and maintain SOPs and technical documentation for biotech/pharma equipment (e.g., purification, chromatography, filtration, bioreactors, mixing systems).
• Ensure documentation aligns with validation requirements, data integrity standards, and industry regulations.
• Manage project timelines and documentation milestones, ensuring deliverables meet quality expectations.
• Format, review, and standardize documentation for completeness, clarity, and compliance.
• Collaborate with cross-functional teams, including engineering, validation, and quality assurance teams, to gather technical information.
• Provide guidance on documentation best practices and mentor junior team members as needed.

Required Skills & Experience:

• 5+ years of experience in pharmaceutical/biotech industries.
• Recent experience in technical writing for Validation SOPs is required.
• Strong understanding of data integrity, completeness, and document formatting standards.
• Ability to independently author, manage, and deliver high-quality documentation in a fast-paced environment.
• Hands-on experience with equipment such as Purification EQ, Chromatography EQ, Filtration Systems, Bioreactors.
• Experience mentoring junior team members is a plus (management experience not required).

This role is ideal for a highly organized, detail-oriented technical writer with a strong background in pharmaceutical/biotech equipment documentation. If you thrive in a fast-paced, quality-driven environment, we encourage you to apply!

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Job Title: Senior Equipment Technical Writer : Pharma/Biotech
Location : Indianapolis/Lebanon, IN (Onsite)
Duration: 12+ Months
Rate : $60 to $80 Per hour 1099/C2C (all Inc.) - Depends on experience

Job Description:

We are seeking an experienced Equipment Technical Writer to develop and manage documentation for equipment Standard Operating Procedures (SOPs) in a fast-paced pharmaceutical/biotechnology environment. This role requires a deep understanding of purification, chromatography, filtration, cell culture, bioreactor, and mixing equipment to ensure clear, accurate, and compliant documentation.

The ideal candidate will be responsible for authoring, maintaining, and managing timelines for all technical documentation throughout the project lifecycle while adhering to data integrity and compliance standards.

Key Responsibilities:

• Develop, write, and maintain SOPs and technical documentation for biotech/pharma equipment (e.g., purification, chromatography, filtration, bioreactors, mixing systems).
• Ensure documentation aligns with validation requirements, data integrity standards, and industry regulations.
• Manage project timelines and documentation milestones, ensuring deliverables meet quality expectations.
• Format, review, and standardize documentation for completeness, clarity, and compliance.
• Collaborate with cross-functional teams, including engineering, validation, and quality assurance teams, to gather technical information.
• Provide guidance on documentation best practices and mentor junior team members as needed.

Required Skills & Experience:

• 5+ years of experience in pharmaceutical/biotech industries.
• Recent experience in technical writing for Validation SOPs is required.
• Strong understanding of data integrity, completeness, and document formatting standards.
• Ability to independently author, manage, and deliver high-quality documentation in a fast-paced environment.
• Hands-on experience with equipment such as Purification EQ, Chromatography EQ, Filtration Systems, Bioreactors.
• Experience mentoring junior team members is a plus (management experience not required).

This role is ideal for a highly organized, detail-oriented technical writer with a strong background in pharmaceutical/biotech equipment documentation. If you thrive in a fast-paced, quality-driven environment, we encourage you to apply!

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.