Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
JobTailor Logo

See all jobs on JobTailor

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Perrigo Company plc

Technical Writer – LMS Administrator

Perrigo Company plc

Technical Writer at Perrigo developing controlled GMP documentation and supporting Learning Management System administration. Collaborating with cross-functional teams to ensure accuracy and compliance in documentation.

Posted 5/9/2026full-timeBronx • New York • 🇺🇸 United StatesJuniorMid-Level💰 $75,000 - $80,000 per yearWebsite

About the role

Key responsibilities & impact
  • The Technical Writer is responsible for the development, creation, and revision of controlled documentation using the OpenText System in accordance with Perrigo policies and procedures and current GMP practices.
  • Partner with Quality department, other cross functional managers/supervisors, and engineers to ensure that controlled documents being revised contain the correct information.
  • Provide support for maintaining the Learning Management System (LMS).
  • Support/Train functional departments and subject matter experts in the creation and revision of cGMP documentation to optimize processing and ensure alignment with current practices utilizing the OpenText system: Standard Operating Procedures, Standard Work Instructions, Training Completion Statements, Job Aids, Controlled Forms.
  • Execute tasks associated with LMS administration, including but not limited to the creation and maintenance of: creates and maintains GMP curricula, courses, and items.
  • Enter training records in the LMS system or using the ATA system.
  • Generate and track the audit of each curriculum working with department heads or curriculum owner.
  • Provides training reports, training material and metrics as requested for compliance to support FDA audit, internal/external audit and miscellaneous requests.
  • Recognizes and resolves training discrepancies, reaches out to Global training and communicates corrective action to affected personnel.
  • Review cGMP documentation for standardized formatting, technical accuracy, clarity, grammar, and spelling.
  • Select and edit images/videos (photographs, diagrams, technical drawings) to enhance training materials.
  • Files all training documentation (hard copy) and provides general administrative support for the department as required.

Requirements

What you’ll need
  • Bachelor’s degree.
  • 2 or more years of relevant systems experience required in a regulated industry, preferably in Life Sciences.
  • Learning Management System (LMS).
  • Understands the application of GMP concepts and understands 'why' behind the regulations.
  • Possesses basic technical knowledge and background in the pharmaceutical and biotechnology industry.
  • Comprehensive working knowledge of OpenText, Microsoft suite, including Outlook, Teams, Word, Excel, PowerPoint, SharePoint.

Benefits

Comp & perks
  • 🌐 Worldwide ❌ Jobs You've Hidden ⭐️ Saved Jobs ✅ Applied Jobs ✉️ Email Alerts 👤 Account Perrigo Company plc Website LinkedIn All Job Openings 5001 - 10000 employees ⚕️ Healthcare Insurance 💊 Pharmaceuticals Healthcare Insurance
  • Pharmaceuticals
  • Consumer Products Perrigo Company plc is a global leader in consumer goods with a focus on providing innovative healthcare solutions. The company specializes in over-the-counter pharmaceuticals, dietary supplements, and personal care products aimed at enhancing the health and well-being of consumers. Committed to quality and accessibility, Perrigo strives to meet the diverse needs of consumers by leveraging a talented and inclusive workforce across various functions including sales, marketing, and scientific affairs. Technical Writer – LMS Administrator 🔥 1 hour ago 🏢 Bronx – Onsite 💵 $75k - $80k / year ⏰ Full Time 🟢 Junior 🟡 Mid-level 🔏 Technical Writer Apply Now Find Hiring Managers Customize resume + cover letter Report problem ☆ Save ☑️ Mark as applied ❌ Hide 📋 Description
  • The Technical Writer is responsible for the development, creation, and revision of controlled documentation using the OpenText System in accordance with Perrigo policies and procedures and current GMP practices.
  • Partner with Quality department, other cross functional managers/supervisors, and engineers to ensure that controlled documents being revised contain the correct information.
  • Provide support for maintaining the Learning Management System (LMS).
  • Support/Train functional departments and subject matter experts in the creation and revision of cGMP documentation to optimize processing and ensure alignment with current practices utilizing the OpenText system: Standard Operating Procedures, Standard Work Instructions, Training Completion Statements, Job Aids, Controlled Forms.
  • Execute tasks associated with LMS administration, including but not limited to the creation and maintenance of: creates and maintains GMP curricula, courses, and items.
  • Enter training records in the LMS system or using the ATA system.
  • Generate and track the audit of each curriculum working with department heads or curriculum owner.
  • Provides training reports, training material and metrics as requested for compliance to support FDA audit, internal/external audit and miscellaneous requests.
  • Recognizes and resolves training discrepancies, reaches out to Global training and communicates corrective action to affected personnel.
  • Review cGMP documentation for standardized formatting, technical accuracy, clarity, grammar, and spelling.
  • Select and edit images/videos (photographs, diagrams, technical drawings) to enhance training materials.
  • Files all training documentation (hard copy) and provides general administrative support for the department as required. 🎯 Requirements
  • Bachelor’s degree.
  • 2 or more years of relevant systems experience required in a regulated industry, preferably in Life Sciences.
  • Learning Management System (LMS).
  • Understands the application of GMP concepts and understands 'why' behind the regulations.
  • Possesses basic technical knowledge and background in the pharmaceutical and biotechnology industry.
  • Comprehensive working knowledge of OpenText, Microsoft suite, including Outlook, Teams, Word, Excel, PowerPoint, SharePoint. Apply Now 📊 Check your resume score for this job Improve your chances of getting an interview by checking your resume score before you apply. Check Resume Score 🌐 Worldwide Built by Lior Neu-ner. I'd love to hear your feedback — Get in touch via DM or support@remoterocketship.com Search Search Jobs by country Search jobs by city Search jobs by job title Search entry-level jobs Search junior-level jobs Search senior-level jobs Search jobs by tech stack Search jobs by contract type Search remote internships Search remote part-time jobs Remote jobs Anywhere in the World Companies Hiring Anywhere in the World Companies Hiring Sales People Anywhere in the World Companies Hiring Software Engineers Anywhere in the World Resources Advice Tips for finding remote jobs Interview questions and answers Resume examples Cover letter examples Post a job Affiliates Privacy policy Terms of service Job board SEO course AI Apply Copilot OpenClaw job finder Jobs by Country Remote jobs anywhere in the world (Worldwide remote jobs) Remote jobs United States Remote jobs Australia Remote jobs Brazil Remote jobs Canada Remote jobs France Remote jobs Ireland Remote jobs Germany Remote jobs Netherlands Remote jobs Spain Remote jobs UK Popular Jobs Remote data analyst jobs Remote customer support jobs Remote executive assistant jobs Remote marketing jobs Remote product designer jobs Remote product manager jobs Remote project manager jobs Remote recruiter jobs Remote sales jobs Remote software engineer jobs Jobs by Type Remote full-time jobs Remote part-time jobs Remote contract jobs Remote internship jobs Remote entry-level jobs Remote jobs with no experience required Remote junior jobs (1-3 years of experience) Digital nomad jobs Remote jobs with no degree required Freelance remote jobs Temporary remote jobs Remote jobs hiring now Stay at home mom jobs

ATS Keywords

✓ Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
technical writingGMP documentationLMS administrationcurriculum developmentaudit trackingdocument revisiontraining material creationstandardized formattingimage/video editing
Soft Skills
collaborationcommunicationproblem-solvingattention to detailtraining
Certifications
Bachelor's degree