Chile Job Openings
Thermo Fisher Scientific
Quality Supervisor (Pharmaceutical)
FULL TIME
August 28, 2024
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards
Job Description
Leading Quality Assurance team for Andean Region countries
Internal:
Proficiency in English is required for both written and spoken communication in technical conversations.
Availability to travel is required for this role.
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards
Job Description
Thermo Fisher Scientific Inc. is seeking a Quality Supervisor, to join our dedicated team in Santiago de Chile or Bogota, Colombia. As the Supervisor, Quality, you will play a key role in maintaining high-quality services and products by encouraging a Quality Culture that aligns with global policies and processes, c GMP, c GDP, and regulatory requirements. This is an exciting opportunity to contribute to our organization and uphold internal quality standards throughout the Andean Region.
Duties and Responsibilities
- Proactively lead quality processes and policies to ensure compliance with FCS quality standards in Chile, Colombia, and Peru.
- Evaluate and analyse current processes and policies for continuous improvement.
- Drive a quality culture in every sector of the organization through good practices, training, and collaboration with all areas of the organization.
- Carry out batch record approval.
- Ensure that all processes are carried out in accordance with c GMP.
- Responsible for the management of change control activities and planned and unplanned deviations.
- Responsible for the investigation of customer complaints until their resolution, when required.
- Be in direct contact with customers regarding quality issues.
- Conduct internal audits according to SOP requirements and collaborate in regulatory, supplier, and customer audits.
- Promote continuous training of staff in Quality/GMP throughout the company.
- Approve and maintain local SOPs, forms, and policies for Clinical Logistics.
- Approve and support qualification and validation of controlled areas.
- Creation and maintenance of critical metrics.
Education/Requirements
- Pharmacy (Químicos Farmacéuticos TITULADOS )
- Qualification/s or similar experience in the area of quality assurance.
Experience/Skills
- Knowledge of IMP process, preferably with management of protocols, key customers, and business objectives.
- Auditor Experience.
- Up-to-date knowledge of regulatory standards.
- Knowledge of country logistics requirements.
- Ability to analyze problems and define solutions.
- Ability to prioritize and support others.
- Good interpersonal, verbal and written skills
Certifications or licenses
- Preferably a pharmacist (Químicos Farmacéuticos TITULADOS )
Supervisory Responsibilities
Leading Quality Assurance team for Andean Region countries
Internal and external contacts
Internal:
- General Manager, Operations, Client Services, Finance, and Business Development.
- Other FCS sites.
- Global Warehouse Network representatives.
External:
- Client representatives of different areas.
- Suppliers representatives.
Languages
Proficiency in English is required for both written and spoken communication in technical conversations.
Capabilities or skills
- Result focus
- Continuous improvement / Analytical skills
- Partnership with other areas
- Good communication
- Customer interaction
- Decision making
Others
Availability to travel is required for this role.
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