ProPharma Group
ProPharma Group

61 Propharma Group Process Validation Engineer Jobs Hiring Near You

We are seeking an experienced Process Validation Engineer to support new pharmaceutical manufacturing projects within a sterile GMP environment. This role will focus on process validation, technology ...

* We are seeking an experienced Process Validation Engineer to support new pharmaceutical manufacturing projects within a sterile GMP environment. This role will focus on process validation, technology ...

* We are seeking an experienced Process Validation Engineer to support new pharmaceutical manufacturing projects within a sterile GMP environment. This role will focus on process validation, technology ...

TSMS - Process Validation Engineer The Technical Services and Manufacturing Sciences (TSMS) Process Validation Engineer will be responsible for supporting all facets of Process Validation, GMP Floor ...

Process Engineer (Process Validation / PPQ Readiness) Location: Sanford, NC (Onsite) Type: Contract | Full-Time (40 Hours/Week) Duration: Approximately 9 Months Position Summary Our client is seeking ...

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Infographic showing various Process Validation Engineer job openings at Propharma Group in the United States as of August 2026, with employment types broken down into 95% Full Time, and 5% Part Time. Highlights an 74% Physical, and 26% Remote job distribution.

Sterile Compounding/Manufacturing Trainer (Columbus, OH)

ProPharma Group

Columbus, OH • On-site

Full-time

Re-posted 3 days ago


Job description

For the past 20 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.
Contract role is onsite in Columbus, OH.
  • New 503A sterile compounding facility in start up mode.
  • Support Training program: Beginning Dec. 1st onsite.

Personnel will need to be trained in sterile compounding activities:
  • Hand hygiene, sterile garbing, gloving
  • Materials Transfer
  • Kitting
  • Cleaning
  • Weighing/Mixing
  • Sterile compounding/transfer
  • Filling/capping

Providing Sterile Compounding Training. Experience in USP <797> compounding is preferred, but experience in aseptic training for 503b or aseptic drug manufacturing could be sufficient.
*Consulting/Contract opportunity lasting 4 to 6+ months
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.
***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***