Auftragsdetails

Quality Assurance Training - Cumberland, RI (REF11621P) - propharma group

Datum der Veröffentlichung: Nov 11, 2022
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Auftragsdetails

  • Ort:
    Cumberland, Maryland, United States of America
  • Gesellschaft:
  • Typ:
    Full Time/Permanent
  • Shift:
    First Shift (Day)
  • Karrierelevel:
    Experienced Professional
  • Positionen:
    5
  • Erfahrung:
    2 Year
  • Geschlecht:
    Keine Präferenz
  • Grad:
    Bachelors
  • Vorher bewerben:
    Nov 30, 2023

Job Summary

Company Description

ProPharma Group is an industry leading, single source provider for regulatory compliance, pharmacovigilance, and medical information services across the full development lifecycle for pharmaceutical, biotechnology, and medical device companies. Operating around the world with offices in Australia, Canada, Germany, Japan, the Netherlands, Sweden, United Kingdom, and the United States, ProPharma Group’s fully integrated service offerings will provide clients with a comprehensive suite of global support services that are required to be competitive in today’s dynamic markets. We build successful long-term relationships with clients by providing leading industry knowledge, experience, and proven processes.

Detailed Description

Job Description

QA Training Consultant Resource: 

  • 6-month project duration 
  • Initial 1-2 months on-site - then hybrid schedule for remainder of project
  • Build up training plan for mock inspections and QA training
  • Work with a Sr. Quality Specialist to review the current program and look for gaps (curriculum issues, training gaps, etc.) 
  • Based on gaps, work with Quality and Sr. Quality Specialist to implement training program 
  • Develop and execute some trainings as well based on mock inspection findings (Good Document Practices, OOS Writing, Deviation/Investigation Writing, etc) 
  • Develop on-boarding for new employees and consultants/contractors (Including building of training with SMEs about their products) 

Qualifications

Qualified candidates must have:

  • B.S./B.A. in scientific discipline as a minimum. 
  • A Graduate degree in a scientific discipline is preferred.
  • Minimum 7 years’ quality management experience in related industry.
  • Understanding of the criteria for selection for compliance and quality assurance consulting services in the pharmaceutical, medical device and biotech industries. 
  • Proven record with team leadership, problem solving, project tracking and budgeting, and facilitation of efficient communication between the client and the team. 
  • Demonstrated ability to lead people and get results through others.
  • Quality orientation and high attention to detail.

Additional Information

We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.

***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***

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Company Overview

Berlin, Berlin, Germany

ProPharma Group is the leading global, independent, single-source provider of regulatory, clinical, and compliance services serving the pharmaceutical, biotechnology, and medical device companies. Our team of experts brings a comprehensive portfolio... Read More

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