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QA Specialist I


Job Location:

Santiago - Chile

Monthly Salary: Not provided by the employer
Posted: 11 July 2026 (30+ days ago)
Application Deadline: 8 October 2026
Vacancies: 1 Vacancy

Job Summary

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards Office

Job Description

As part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the worlds toughest challenges like protecting the environment making sure our food is safe or helping find cures for cancer.

DESCRIPTION:
Join our high-performing team at Thermo Fisher Scientific where youll ensure quality compliance across manufacturing operations while advancing our mission to make the world healthier cleaner and safer. As a Quality Specialist I youll provide support to the Quality Assurance sector performing support tasks in the management of SOPs product release monitoring of processes filing and updating of documentation in order to ensure that CTD Andean Region operates within standards of good storage and distribution practices as well as the functions interconnected with the various Third Party Depot in Chile Colombia and Peru. All these activities shall be carried out in accordance with the specifications and IT/administrative tools required by the Company and/or clients.

REQUIREMENTS:
Bachelors Degree required

At least 1 year in the area and preferably in similar tasks in the pharmaceutical industry CROs or similar logistics companies
Preferred Fields of Study: Pharmacist Chemistry Biology Engineering or related scientific field.
Thorough knowledge of GMP standards and local regulations.
Proven ability to review and approve GMP documentation batch records and quality records.
Strong understanding of quality management systems and tools (e.g. CAPA change control learning systems.)
Ability to work independently and collaborate effectively across functions
Commitment to maintaining a quality-focused culture and driving continuous improvement
Intermediate level oral and written English.


Required Experience:

IC


About Company

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Electron microscopes reveal hidden wonders that are smaller than the human eye can see. They fire electrons and create images, magnifying micrometer and nanometer structures by up to ten million times, providing a spectacular level of detail, even allowing researchers to view single a ... View more

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