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.
Location: Kansas City, KS (onsite)
Duration: 2-3 months
Scope: This consulting role will perform detailed review of manufacturing, environmental monitoring, aseptic processing, deviation, complaint, and visual inspection data to support product impact assessments and retrospective lot evaluations. Duties include:
- Execute lot-review activities in accordance with the approved protocol.
- Review manufacturing, environmental monitoring, aseptic processing, deviation, complaint, and visual-inspection data.
- Perform product-impact assessments and document conclusions.
- Identify recurring trends, adverse quality signals, and potential sterility-assurance concerns.
- Escalate findings requiring additional evaluation.
- Support development of technical justifications and final reports.
Years of Experience: 7 years
Key Experience Required: Sterility assurance, EM, aseptic processing, investigations, batch disposition assessments
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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
- Seven years of relevant experience
- Experience with sterility assurance
- Experience with environmental monitoring
- Experience with aseptic processing
- Experience with investigations
- Experience with batch disposition assessments
ProPharma Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about ProPharma and has not been reviewed or approved by ProPharma.
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Healthcare Strength — Healthcare coverage is considered solid, with medical, dental, vision, and HSA options forming a dependable core. These benefits are often highlighted as a valuable part of total rewards.
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Retirement Support — A 401(k) plan with company matching is viewed as a strong component of the package. This retirement support helps bolster overall compensation when salary levels feel average.
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Leave & Time Off Breadth — Generous PTO, paid holidays, and sick leave are included. Flexible remote or work-from-home options for many roles further reinforce work-life balance.
ProPharma Insights
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








