Quality Assurance Support Consultant

Posted 8 Days Ago
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Hiring Remotely in United States
Remote
Senior level
Healthtech • Consulting • Pharmaceutical
The Role
Provides quality assurance support for quality control laboratories by completing training, reviewing and approving laboratory methods, and communicating barriers to ensure timely approvals. The role requires expertise in method review, approval, transfer, and validation, with LabVantage experience preferred. This is a 12-month contract role supporting pharmaceutical, biotech, or medical device programs.
Summary Generated by Built In

For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.

This is a 12-month contract (multiple roles), beginning in Q4 2026 through the end of Q3 2027 in Indiana. The QA for QC Representatives will focus on approval of lab associated methods.

The QA for QC representatives will go through training with the QA team and be responsible for:

  • Completion of training on time

  • Review of methods

  • Approval of methods

  • Ensuring communication when barriers arise

Requirements

  • The QA for QC Representatives should have a background in Quality Control Laboratories, method review, method approval and method transfer/validation. LabVantage experience is a plus.

  • Personnel are expected to have excellent communication and time management skills to ensure timely reviews and approvals. 

  • 7+ years of relevant experience

  • Position is on-site in Indiana

#LI-EB3

#Quality Assurance

#Quality Control

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.

All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.

Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office.

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

Skills Required

  • 7+ years of relevant experience
  • Background in quality control laboratories
  • Experience with method review
  • Experience with method approval
  • Experience with method transfer and validation
  • Excellent communication skills
  • Strong time management skills
  • LabVantage experience
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The Company
HQ: Raleigh, NC
2,059 Employees
Year Founded: 2001

What We Do

ProPharma is the premier Research Consulting Organization (RCO), delivering fully customizable consulting solutions to empower biotech, med device, and pharmaceutical organizations of all sizes to advance scientific breakthroughs confidently and introduce new therapies. With over 20 years of expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma partners with clients across the complete product lifecycle through an advise-build-operate model. Our end-to-end suite of consulting solutions de-risk and accelerate high-profile drug and device programs, ultimately improving patient health and safety. Discover how ProPharma can help you inspire the future of science

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