QA/MLR Specialist – Medical Content Compliance

Apolis; Bogotá; On-site; COP 109,521,027 - 164,281,541; Full time

Job summary

Apolis is seeking a talented MLR / QA Specialist in Bogotá, Colombia. The candidate will support the Medical, Legal and Regulatory review process for U.S. content and market access materials. Responsibilities include ensuring compliance with regulations, guiding teams based on feedback, and maintaining high output quality.

The ideal candidate will have medical education, experience in the pharmaceutical industry, strong communication skills in Portuguese, and be detail-oriented. Join Apolis for an opportunity to leverage your expertise in a multi-national setting.

Qualifications

• Intermediate understanding in the field of Respiratory & Immunology, cardiovascular, renal & metabolic, oncology and rare diseases.
• Ability to respond to a multi-brand volume of requests.
• Experience working in a big multi-national company.

Responsibilities

• Ensure compliance with US legislations and regulations.
• Guide the copy writing and design teams based on feedback.
• Maintain standard output quality through timely reviews.

Skills

Medical education

Up to 3 years of experience in pharmaceutical industry

Strong written and verbal communication skills in Portuguese

Detail oriented

Client-oriented attitude

Job description

Apolis is seeking a talented MLR / QA Specialist in Bogotá, Colombia. The candidate will support the Medical, Legal and Regulatory review process for U.S. content and market access materials. Responsibilities include ensuring compliance with regulations, guiding teams based on feedback, and maintaining high output quality.

The ideal candidate will have medical education, experience in the pharmaceutical industry, strong communication skills in Portuguese, and be detail-oriented. Join Apolis for an opportunity to leverage your expertise in a multi-national setting.