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Manager Biotech Technical Writer Jobs (NOW HIRING)

CEDENT

Technical Writer

Springfield, NJ

Document Management: Assist in the management of controlled documents in document control systems ... biotech, or related industry. * Experience writing technical documentation, including SOPs ...

Integrated Resources INC

Technical Writer

Cambridge, MA · On-site

Excellent communication skills including: technical writing, interpersonal and collaborative skills ... Biotech/Pharma industry, knowledge about FDA regulations is required Some document management ...

Intuitive Surgical

Technical Writer

Sunnyvale, CA

Bring regulatory compliance questions/issues to the attention of management. * Adhere to policies ... biotechnology, or medical environment, including documentation for a highly technical audience.

Intuitive

Technical Writer

Sunnyvale, CA

Bring regulatory compliance questions/issues to the attention of management. * Adhere to policies ... biotechnology, or medical environment, including documentation for a highly technical audience.

Intuitive

Technical Writer

Sunnyvale, CA · On-site

Bring regulatory compliance questions/issues to the attention of management. * Adhere to policies ... biotechnology, or medical environment, including documentation for a highly technical audience.

Lonza

MSAT Process Technical Writer

Portsmouth, NH · On-site

Technical writing in the biotech industry preferred. * Project management skills a plus. * Strong MS Word experience preferred. * Position level and grade determined by level of experience. About ...

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How much do manager biotech technical writer jobs pay per hour?

As of Jun 1, 2026, the average hourly pay for manager biotech technical writer in the United States is $38.94, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $47.12 per hour, depending on experience, location, and employer.

What is the difference between Manager Biotech Technical Writer vs Biotech Technical Writer?

AspectManager Biotech Technical WriterBiotech Technical Writer
ResponsibilitiesOversees writing teams, manages project timelines, ensures regulatory complianceCreates and edits scientific documents, manuals, and reports
Required SkillsLeadership, project management, advanced scientific writingStrong scientific writing, research skills, attention to detail
ExperienceTypically 5+ years, leadership experience preferred2+ years in biotech or scientific writing
Work EnvironmentTeam management, cross-department collaborationIndividual contributor, primarily office-based

The main difference is that the Manager Biotech Technical Writer leads teams and manages projects, while the Biotech Technical Writer focuses on creating scientific content. The manager role involves leadership and oversight, whereas the technical writer role emphasizes writing and research skills.

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What are the most commonly searched types of Biotech Technical Writer jobs? The most popular types of Biotech Technical Writer jobs are:
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Manager Biotech Technical Writer jobs near you
Technical Writer

Technical Writer

CEDENT

Springfield, NJ

Full-time

Posted 6 days ago

Job description

Summary: Reporting to the appropriate department based on area of expertise (Quality Assurance, Quality Control, or Manufacturing). We are seeking a detail-oriented and highly skilled GMP Pharmaceutical Technical Writer to join our team. The ideal candidate will be responsible for creating, revising, and maintaining various controlled documentation that complies with Good Manufacturing Practices (GMP) regulations and industry standards. This role will work closely with internal and client cross-functional teams, including quality assurance, regulatory, production, and project management, to ensure timely delivery, accuracy, and clarity of all technical documents essential for the manufacturing and regulatory processes in a pharmaceutical industry.
Responsibilities:
  • Technical Documentation: Author, edit, and maintain a wide range of documents, including Standard Operating Procedures (SOPs), batch records, validation protocols, technical reports, change control documents, and regulatory submissions in accordance with GMP guidelines.
  • Compliance: Ensure all written materials meet regulatory and GMP requirements, and align with the company’s quality standards, procedures, and policies.
  • Collaboration: Work closely with both Client stakeholders and client stakeholders to establish alignment on deliverables and ensure project timelines are maintained.
  • Document Management: Assist in the management of controlled documents in document control systems (e.g., electronic document management systems), ensuring traceability, version control, and appropriate distribution of approved documents.
  • Process Improvement: Participate in process improvement initiatives related to document control, writing standards, and compliance, ensuring continuous enhancement of documentation practices.
  • Audits & Inspections: Support internal and external audits by preparing relevant documentation and ensuring that all technical writing adheres to current regulatory standards.
  • Change Control: Document and track changes in manufacturing processes, equipment, and methodologies, ensuring updates to procedures and records are properly reflected.
Essential Education and Qualifications:
  • Education: Bachelor's degree in Life Sciences, Chemistry, Pharmaceutical Sciences, Engineering, or a related field. Advanced degree or certification in technical writing is a plus.
  • Experience:
  • Minimum of 2 years of experience in technical writing within a GMP-regulated environment in the pharmaceutical, biotech, or related industry.
  • Experience writing technical documentation, including SOPs, validation protocols, and reports.
  • Knowledge:
  • Solid understanding of GMP regulations (FDA, EMA, ISO, ICH, etc.) and regulatory requirements for pharmaceutical manufacturing.
  • Proficiency with document management systems and Microsoft Office Suite (Word, Excel, PowerPoint).
  • Skills:
  • Exceptional written and verbal communication skills, with a strong ability to translate complex technical concepts into clear, concise documentation.
  • Detail-oriented with strong organizational and project management skills.
  • Ability to work independently, manage multiple projects simultaneously, and meet deadlines in a fast-paced environment.
  • Strong analytical and problem-solving skills, with the ability to work cross-functionally across departments.
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About Cedent

Sourced by ZipRecruiter

CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.

Industry

It services

Company size

11 - 50 Employees

Headquarters location

Plano, TX, US

Year founded

2008

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