Quality Controller at Thermo Fisher Scientific

The Job:

The purpose of a quality controller is to ensure our quality management system remains up to date and adhered to through our quality policies/procedures and to ensure they are maintained to Fisher Clinical Services Global quality and/or our client's standards at all times, The holder of this position is independent in carrying out assigned tasks listed below and is expected to practice continuous improvement and self-training on our quality management system.

What will you do:

• Adhere to Good Manufacturing Principles and Good Wholesale Practice Principles.
• Offer expertise and assistance on quality-related matters to ensure a cohesive team effort.
• Assist Quality Management in all document control activities and ensure compliance with policies and procedures throughout the business. Stay updated on industry standards and legal requirements to ensure compliance.
• Handle administrative tasks related to quality system management, including but not limited to document control (writing procedures, creation of forms, etc., ), data analysis, and report generation.
• Participate in the management of non-conformances and corrective actions.
• Encourage and support initiatives aimed at improving quality standards consistently.
• Participate in ensuring the effectiveness and efficiency of the quality management system in place.
• Set and strive to meet quality performance goals.
• Collaborate with operational teams to develop and implement effective quality procedures.
• Conduct training sessions to enhance employees' understanding of quality standards and practices. Ensure training compliance and timelines are adhered to throughout the business.
• Participate in self-inspections as per the approved program.
• Lead the management of Supplier Training and supplier tasks.
• Perform Quality Control checks in the execution of pharmaceutical secondary packaging jobs for clinical trials.

How will you get here?

• A minimum of 2 years experience in the pharmaceutical/health industry.
• Experience in Pharmaceutical Regulatory Requirements will be advantageous.
• Experience with ISO: 13485 will be advantageous.

Knowledge, Skills, Abilities

• Ability to work independently and be self-motivated with a positive demeanor.
• Ability to perform tasks under pressure and meet tight target timelines.
• Passion for providing training to employees.
• Effective time management and prioritization skills.
• Meticulous with outstanding accuracy.
• Strong digital literacy (Microsoft Office skills) with the ability to learn new software and tools quickly.