Labeling Operations Lead & Associate Consultant

ClinChoice; Colombia; On-site; COP 42,000,000 - 65,000,000; Full time

Job summary

ClinChoice in Colombia is seeking a Labeling Operations Manager Associate to support initial creation and updates of labeling documents (CDS, USPI, SPC) for EU-registered products, following QRD and PLR formats and internal SOPs. The role coordinates labeling reviews, prepares document renditions, manages workflows, tracks timelines, and ensures timely delivery to meet regulatory deadlines.

You will work with labeling teams, Regulatory Authorities, and the Global Labeling Lead to escalate issues

Qualifications

• Bachelor's degree in science or life sciences.
• 0-2 years of practical labeling experience.
• Strong written and verbal communication skills.
• Fluent English language proficiency.
• Excellent attention to detail and accuracy.
• Experience coordinating with cross-functional teams.

Responsibilities

• Support the review and delivery of labeling documents and patient labeling documents.
• Prepare comparison tables for labeling team discussions.
• Generate renditions (PDF/Word) and bookmark where appropriate.
• Facilitate document management workflows through the DMS.
• Finalize documents after QC and notify stakeholders of availability.
• Ensure compliance with SOPs and submission standards.
• Assist with simple projects and maintain the CDS log.
• Set targets for review timelines and escalate as needed.

Skills

Written & verbal comms

Fluent English

Project management

Attention to detail

Labeling knowledge

Stakeholder liaison

Education

Bachelor's degree in science or life sciences

0-2 years practical experience

Tools

MS Word

Job description

ClinChoice in Colombia is seeking a Labeling Operations Manager Associate to support initial creation and updates of labeling documents (CDS, USPI, SPC) for EU-registered products, following QRD and PLR formats and internal SOPs. The role coordinates labeling reviews, prepares document renditions, manages workflows, tracks timelines, and ensures timely delivery to meet regulatory deadlines.

You will work with labeling teams, Regulatory Authorities, and the Global Labeling Lead to escalate issues