Process Excellence Specialist

Remote: 
Full Remote
Contract: 
Work from: 

Offer summary

Qualifications:

Previous experience managing Pharmacovigilance System Master Files., Experience in quality management system support., Familiarity with managing deviations and CAPAs., Ability to produce standardized quality metrics for PV projects..

Key responsibilities:

  • Manage Pharmacovigilance System Master Files for clients.
  • Produce standardized quality metrics for the UBC Global PV Department.
  • Support the development and maintenance of UBC PV procedural documents.
  • Prioritize and disseminate information related to global PV Safety Regulatory Intelligence.

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UBC Pharmaceuticals Large https://www.ubc.com/
1001 - 5000 Employees
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Job description

As a pharmaceutical support industry leader, UBC is devoted to empowering health solutions for a better tomorrow. We take pride in improving patient outcomes and advancing healthcare. At UBC, we provide services to enhance the entire drug development process and commercialization lifecycle - From clinical trial support to real-world evidence generation. 


Embark on a rewarding career journey with UBC as a Process Excellence Specialist! Grow your career while making a meaningful impact on the world around you. UBC fosters a culture built on our Core Values of Collaboration, Conscientiousness, Curiosity, Compassion and Consultation. We believe in an inclusive workplace that fosters creativity. 


If you are seeking a career that will challenge, inspire, and reward you, join us at UBC!


As a Process Excellence Specialist, you will manage Pharmacovigilance System Master Files for clients and provide support for quality management system aspects. 


Specific job duties: 

  • Management of deviations and CAPAs.
  • Production of standardized quality metrics for the UBC Global PV Department and for PV projects contracted by UBC clients. 
  • Support PV Management in the development and maintenance of the UBC PV procedural documents and for serving as the lead global PV trainer. 
  • Is involved in the prioritization and dissemination of information relating to global PV Safety Regulatory Intelligence.
  • Responsible for the management of Pharmacovigilance System Master files writing and update for European clients, support for quality management system related aspects:

 

Supervisory Responsibility:  

N/A

 

Skills and Qualifications:

  • Previous experience managing the Pharmacovigilance System Master Files, writing and updating.
  • Experience in providing support for quality management system related aspects
  • Previous experience in managing deviations and CAPAs, 
  • Experience in producing standardized quality metrics for the UBC Global PV Department and for PV projects contracted by UBC clients. 
  • Previous experience in supporting PV Management in the development and maintenance of the UBC PV procedural documents. 
  • Ability to prioritize and disseminate information relating to global PV Safety Regulatory Intelligence.

 

UBC is proud to be an equal opportunity employer and does not discriminate because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, and basis of disability or any other federal, state or local protected class.  We are committed to a diverse, equitable and inclusive culture that fosters respect for each other, our clients, and our patients.

 

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Required profile

Experience

Industry :
Pharmaceuticals
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Compassion
  • Collaboration
  • Consulting
  • Curiosity
  • Punctuality

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