Senior GxP Quality Supervisor

7456-Johnson & Johnson MedTech Colombia S.A.S. Legal Entity

Colombia

On-site

COP 100,000,000 - 150,000,000

Full time

9 days ago
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Job summary

Johnson & Johnson MedTech Colombia S.A.S. Legal Entity is seeking a CQ Sr. Supervisor for the Colombian market.

The role oversees GxP quality systems across commercial and delivery operations, ensuring regulatory compliance and patient safety. You will lead quality analysts and coordinate with stakeholders to drive continuous improvement. The position requires a 5+ year background in medical devices or related quality fields and fluent Spanish/English.

Qualifications

  • Undergraduate degree in pharmacy, engineering, or scientific discipline.
  • Minimum of 5 years’ experience in the Quality area related to Medical Devices, Pharmaceutical or Consumer products
  • Spanish and English proficiency required; strong communication skills in both languages.

Responsibilities

  • Accountable for execution of GxP quality system elements for Commercial and Deliver Operations within Colombian market including NC/CAPA/Change Control/Handling, Storage and Distributions, NPI/Product Lifecycle, Supplier Quality Mgmt.
  • Ensure flawless execution of core GxP processes with focus on product quality, patient safety, and client satisfaction.
  • Act as supervisor of quality analysts to ensure proper execution of quality system elements and warehouse/distribution operations.

Skills

Quality Leadership
CAPA
GxP
Audits
Problem-Solving
Risk Management
Bilingual Spanish/English
People Leadership

Education

Undergraduate degree in pharmacy, engineering, or scientific discipline

Job description

Johnson & Johnson MedTech Colombia S.A.S. Legal Entity is seeking a CQ Sr. Supervisor for the Colombian market.

The role oversees GxP quality systems across commercial and delivery operations, ensuring regulatory compliance and patient safety. You will lead quality analysts and coordinate with stakeholders to drive continuous improvement. The position requires a 5+ year background in medical devices or related quality fields and fluent Spanish/English.

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