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Other
high school, associate degree, bachelor degree
Development opportunities, Employee resource groups, Flexible working environment, Competitive total rewards, Wellness incentives, Recognition and performance awards
Posted 1d ago
~40 hrs/week
Responsibilities
The Medical Writing Specialist independently authors regulatory clinical documents such as CEPs, CERs, and SSCPs while ensuring traceability and compliance. They also execute literature strategies, perform data analysis, and collaborate with cross-functional teams to maintain audit-ready documentation.
Requirements
Candidates must have a Bachelor's degree in Health or Life Sciences with at least 2 years of relevant experience, or equivalent education and experience combinations. Strong scientific writing skills, knowledge of medical device regulations, and the ability to manage multiple deadlines are required.
Full job description
At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.
As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.
What You Can Expect
Independently authors standard sections of regulatory clinical documents with limited supervision. Executes literature strategies, execute National Joint Registry (NJR) data analysis, ensures traceability and compliance, and collaborates cross functionally to deliver audit-ready documentation.
How You'll Create Impact
Independently authors standard sections of Clinical Evaluation Plans (CEPs), Clinical Evaluation Reports (CERs), Post Market Surveillance (PMS), Post-Market Clinical Follow-up (PMCF), and Summary of Safety and Clinical Performance (SSCP) documents
Executes NJR analysis and literature search strategies and documents appraisal outcomes
Drafts clinical safety and performance summaries and benefit–risk analyses
Ensures traceability across data sources and regulatory requirements
Maintains template compliance and audit-ready documentation
Coordinates with Regulatory, Clinical, and Development partners to finalize drafts
Supports methodological consistency across product lines
Participates in internal peer reviews
Manages timelines for assigned deliverables
Follows established procedures
Performs quality control checks for formatting, references, and traceability
Ability to escalate and resolve compliance or risk concerns
What Makes You Stand Out
Strong scientific and technical writing skills
Basic working knowledge of medical device clinical and regulatory documentation
Ability to execute literature strategies and appraise evidence
Ability to analyze National Joint Registry (NJR) data
Understanding of global medical device regulations and post-market obligations
Strong analytical and data synthesis skills
Effective cross-functional communication
Ability to manage multiple documents and deadlines
High attention to detail and commitment to accuracy Willingness to learn regulatory requirements
Organizational skills and ability to manage multiple deliverables
Awareness of audit/inspection readiness and compliance expectations
Your Background
Bachelor's Degree in Health, Life Sciences or related field and 2 years of relevant experience, or Associate's Degree and 4 years of relevant experience, or High School Diploma or Equivalent and 6 years of relevant experience
Preferred: Degree in Health, Life Sciences or related field
Preferred: 2+ years experience in medical or regulatory writing
Travel Expectations
EOE/M/F/Vet/Disability
Related keywords
Medical WritingRegulatory AffairsClinical Evaluation PlanClinical Evaluation ReportPost Market SurveillancePost-Market Clinical Follow-upSummary of Safety and Clinical PerformanceNational Joint RegistryData AnalysisComplianceAudit ReadinessTechnical WritingMedical DevicesQuality ControlTraceabilityScientific Writing
Zimmer Biomet is a global medical technology leader with a comprehensive portfolio designed to maximize mobility and improve health. We advance our mission to alleviate pain and improve the quality of life for patients around the world with our innovative products and suite of integrated digital and robotic technologies leverage data, data analytics and artificial intelligence. Founded in 1927 and based in Warsaw, Zimmer Biomet has operations in more than 25 countries and sales in more than 100 countries. We maintain world-class scientific facilities and resources and collaborate with leading clinicians and researchers around the world.
Awards and Recognitions
• Forbes: America's Best Companies 2026
• Workhuman: Luminary Award 2025 & Innovator Award 2024
• TIME: America's Best Companies [Mid-Size] 2024
• Great Place to Work - Best Workplaces: Switzerland & Poland 2025
• Great Place to Work Certified 2025 - 2026: USA, Poland, India, Colombia, Ireland, Puerto Rico, Kingdom of Saudi Arabia, Switzerland
• MedTech: Breakthrough Award Best New Technology Solution in Orthopedics 2025
• Top Employers Institute: China 2025
• VETS Indexes: 4 Star Employer 2025
Offices: 345 East Main Street, P.O. Box 708, Warsaw, Indiana 46580, US · 455 Riverside Dr, Palm Beach Gardens, Florida 33410, US · 1520 Tradeport Dr, Jacksonville, Florida 32218, US · 10225 Westmoor Dr, Westminster, Colorado 80021, US · 10 Pomeroy Rd, Parsippany, New Jersey 07054, US
How many Science & Research jobs are open in Bogota, Colombia right now?
There are currently 39 open science & research positions in Bogota, Colombia listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Science & Research roles in Bogota, Colombia?
Companies currently hiring include SGS, Anyone App, Zurich Canada, AgileEngine, Arthrex, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Science & Research jobs in Bogota, Colombia?
Yes — 17 of the 39 open science & research positions offer remote or hybrid work (11 remote, 6 hybrid).
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