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Planet Pharma
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Manufacturing Technical Procedure Writer
Posted: 05/06/2025
2025-05-06
2025-06-11
Employment Type:
Contract
Job Category: Scientific
Job Number: 619403
Is job remote?: No
Country: United States
Job Description
Job Summary:
The Manufacturing Technical Procedure Writer is responsible for creating, revising, and maintaining clear, accurate, and compliant standard operating procedures (SOPs), batch records, and other technical documentation for pharmaceutical manufacturing processes. This role ensures all documentation adheres to Good Manufacturing Practices (GMP), regulatory requirements (e.g., FDA, EMA), and internal quality standards. The ideal candidate is detail-oriented, has strong technical writing skills, and possesses a deep understanding of pharmaceutical manufacturing processes.
Key Responsibilities:
• Develop and Update Documentation: Write, edit, and maintain SOPs, batch records, work instructions, and other technical documents to support manufacturing operations, equipment use, and quality control processes.
• Ensure Regulatory Compliance: Ensure all documentation complies with GMP, FDA, EMA, and other relevant regulatory standards, as well as internal policies.
• Collaborate with Subject Matter Experts (SMEs): Work closely with manufacturing, quality assurance, validation, safety, and engineering teams to gather technical information and ensure accuracy and clarity in documentation.
• Streamline Processes: Translate complex technical processes into concise, user-friendly instructions to enhance operational efficiency and reduce errors.
• Document Control: Manage document lifecycle, including version control, reviews, approvals, and archiving, using electronic document management systems (EDMS).
• Training Support: Assist in developing training materials based on SOPs and provide support to ensure effective implementation of procedures.
• Continuous Improvement: Identify opportunities to improve documentation processes, readability, and usability, incorporating feedback from end-users.
• Audit Preparation: Support internal and external audits by ensuring documentation is accurate, up-to-date, and readily accessible.
Qualifications:
Education: Bachelor’s degree in Technical Writing, Pharmaceutical Sciences, Chemistry, Biology, Engineering, or a related field.
Experience: 2+ years of technical writing experience in a pharmaceutical, biotechnology, or regulated manufacturing environment. Familiarity with GMP and regulatory requirements is highly preferred
Skills:
Exceptional technical writing and editing skills with a focus on clarity, accuracy, and conciseness
Strong understanding of pharmaceutical manufacturing processes, equipment, and terminology.
Proficiency in document management systems (e.g., Veeva, Trackwise, MasterControl, Documentum) and Microsoft Office Suite.
Ability to work collaboratively with cross-functional teams and manage multiple projects under tight deadlines.
Knowledge of regulatory guidelines (e.g., 21 CFR Part 211, ICH Q7).
Certifications (Preferred): Certification in Technical Writing (e.g., AMWA, STC) or GMP training.
Work Environment:
Primarily office-based with occasional time spent in the manufacturing cleanroom or production areas.
May require adherence to gowning and safety protocols when entering manufacturing zones.
Key Competencies:
Attention to detail and commitment to quality.
Strong organizational and time-management skills.
Ability to simplify complex technical concepts for diverse audiences.
Problem-solving mindset with a focus on continuous improvement.
Pay ranges between $38-42.50/hr based on experience
The Manufacturing Technical Procedure Writer is responsible for creating, revising, and maintaining clear, accurate, and compliant standard operating procedures (SOPs), batch records, and other technical documentation for pharmaceutical manufacturing processes. This role ensures all documentation adheres to Good Manufacturing Practices (GMP), regulatory requirements (e.g., FDA, EMA), and internal quality standards. The ideal candidate is detail-oriented, has strong technical writing skills, and possesses a deep understanding of pharmaceutical manufacturing processes.
Key Responsibilities:
• Develop and Update Documentation: Write, edit, and maintain SOPs, batch records, work instructions, and other technical documents to support manufacturing operations, equipment use, and quality control processes.
• Ensure Regulatory Compliance: Ensure all documentation complies with GMP, FDA, EMA, and other relevant regulatory standards, as well as internal policies.
• Collaborate with Subject Matter Experts (SMEs): Work closely with manufacturing, quality assurance, validation, safety, and engineering teams to gather technical information and ensure accuracy and clarity in documentation.
• Streamline Processes: Translate complex technical processes into concise, user-friendly instructions to enhance operational efficiency and reduce errors.
• Document Control: Manage document lifecycle, including version control, reviews, approvals, and archiving, using electronic document management systems (EDMS).
• Training Support: Assist in developing training materials based on SOPs and provide support to ensure effective implementation of procedures.
• Continuous Improvement: Identify opportunities to improve documentation processes, readability, and usability, incorporating feedback from end-users.
• Audit Preparation: Support internal and external audits by ensuring documentation is accurate, up-to-date, and readily accessible.
Qualifications:
Education: Bachelor’s degree in Technical Writing, Pharmaceutical Sciences, Chemistry, Biology, Engineering, or a related field.
Experience: 2+ years of technical writing experience in a pharmaceutical, biotechnology, or regulated manufacturing environment. Familiarity with GMP and regulatory requirements is highly preferred
Skills:
Exceptional technical writing and editing skills with a focus on clarity, accuracy, and conciseness
Strong understanding of pharmaceutical manufacturing processes, equipment, and terminology.
Proficiency in document management systems (e.g., Veeva, Trackwise, MasterControl, Documentum) and Microsoft Office Suite.
Ability to work collaboratively with cross-functional teams and manage multiple projects under tight deadlines.
Knowledge of regulatory guidelines (e.g., 21 CFR Part 211, ICH Q7).
Certifications (Preferred): Certification in Technical Writing (e.g., AMWA, STC) or GMP training.
Work Environment:
Primarily office-based with occasional time spent in the manufacturing cleanroom or production areas.
May require adherence to gowning and safety protocols when entering manufacturing zones.
Key Competencies:
Attention to detail and commitment to quality.
Strong organizational and time-management skills.
Ability to simplify complex technical concepts for diverse audiences.
Problem-solving mindset with a focus on continuous improvement.
Pay ranges between $38-42.50/hr based on experience
The staffing industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly and never provide banking information during the application process. Candidate safety is a top priority at Planet Pharma.
Planet Pharma is an equal opportunity employer. It is our practice not to discriminate against any employee or applicant based on any criteria, condition or basis protected by laws or regulations in the locations where we do business. All qualified applicants are encouraged to apply. We celebrate diversity and are committed to providing an environment of mutual respect. We believe that diversity, equity and inclusion enable us to better meet our mission and values while serving our clients across the globe. If you have a disability or handicap and would like us to accommodate you in any reasonable way, please inform your recruiter, or contact us, so that we can discuss the appropriate alternatives available.
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