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Thermo Fisher Scientific

Global Project Quality Senior Associate

Posted 14 Days Ago
Be an Early Applicant
In-Office or Remote
4 Locations
Mid level
In-Office or Remote
4 Locations
Mid level
The role involves managing quality assurance processes for global projects in clinical trials, ensuring compliance and effective communication with clients across multiple sites.
The summary above was generated by AI

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)

Top Skills

Axmps
Global Customs
Gmp
Imps
Qa
Regulatory Compliance
HQ

Thermo Fisher Scientific Waltham, Massachusetts, USA Office

168 Third Avenue, Waltham, MA, United States

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