Global Project Quality Senior Associate

Global Project Quality Senior Associate

Global Project Quality Senior Associate

Thermo Fisher Scientific

7 hours ago

No application

About

  • Work Schedule
  • Standard (Mon-Fri)
  • Environmental Conditions
  • Office
  • Job Description
  • We are currently seeking a remote-based Associate focused on Quality Assurance for Global Projects to join our team. As the sole supplier responsible for delivering all AxMPs and Commercial IMPs for a global project, you will have the opportunity to collaborate with key customers and make a significant impact on approximately 150 Clinical Trials across approximately 70 countries.
  • In this position, you will have a vital role in ensuring the successful implementation of our global sourcing projects. Your contributions will support our mission to enhance global health, cleanliness, and safety.
  • Collaborate closely with the Global Project QA Manager and extended team daily to assist with sourcing strategy for the project, considering both local and global regulatory duties.
  • Serve as the coordinator for strategic and key operational client-related QA communication across multiple sites.
  • Ensure release documentation (certificates, release documentation) is prepared, verified and shared with applicable parties promptly to ensure project timelines are met.
  • Ensure all project documentation is current and accessible to key partners
  • Support situations involving market shortages and country-related challenges, ensuring quick resolution.
  • Support the timely handling of complaints or recalls on multiple sites to ensure client expectations are met.
  • Report or capture important metrics as required.
  • Collaborate with the CRG for AxMP labeling.
  • Ensure key internal team is advised of significant customer relationship issues, needs or developments.
  • Other duties, as assigned to meet business needs.

Keys to Success

To excel in this role, you will need

  • Broad knowledge of GMPs (e.g.: EU, FDA, APJ)
  • QA/regulatory compliance experience in the pharmaceutical, chemical, medical device, or biotech industry.
  • Knowledge of commercial medication sourcing and global labeling requirements for AxMPs and IMPs.
  • Good understanding of global customs requirements and RA submission strategies.
  • Demonstrated ability to lead and work collaboratively with diverse groups.
  • Excellent problem-solving and prioritization abilities to overcome obstacles and achieve key outcomes.
  • The capability to handle competing priorities and adapt to constantly evolving customer requirements.
  • Education
  • Bachelor's Degree, preferably in a scientific field.
  • Experience
  • As mentioned above
  • Knowledge, Skills, Abilities
  • Good knowledge of global supply chain strategies.
  • Good decision-making and negotiation skills.
  • Ability to evaluate potential risks and recommend process improvements.
  • Excellent written and oral communication skills.
  • Ability to prioritize workload and meet customer needs.
  • Remote Office Work environment, Monday-Friday, 8:00 AM- 5:00 PM (additional hours as necessary)