... 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 ...

61 Propharma Group Process Validation Engineer Jobs Hiring Near You
... 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 ...
We are seeking a Process Validation Engineer to support validation and qualification activities in a GMP-regulated manufacturing environment. The ideal candidate will have experience with process ...
We are seeking a Process Validation Engineer to support validation and qualification activities in a GMP-regulated manufacturing environment. The ideal candidate will have experience with process ...
Process Validation Engineer
Concord, NC · On-site
Process Validation Engineer Location: North Carolina Duration: Long Term Job Overview We are seeking a Process Validation Engineer to support process validation activities for sterile pharmaceutical ...
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Process Validation Engineer
Concord, NC · On-site
Process Validation Engineer Location: North Carolina Duration: Long Term Job Overview We are seeking a Process Validation Engineer to support process validation activities for sterile pharmaceutical ...
Process Validation Engineer
Raleigh, NC · On-site
Process Validation Engineer Location: North Carolina (Onsite) Duration: Long-Term Contract Job Overview We are seeking an experienced Process Validation Engineer to support new pharmaceutical ...
Quick apply
Process Validation Engineer
Raleigh, NC · On-site
Process Validation Engineer Location: North Carolina (Onsite) Duration: Long-Term Contract Job Overview We are seeking an experienced Process Validation Engineer to support new pharmaceutical ...
We are seeking a Process Validation Engineer to support validation and qualification activities in a GMP-regulated manufacturing environment. The ideal candidate will have experience with process ...
We are seeking a Process Validation Engineer to support validation and qualification activities in a GMP-regulated manufacturing environment. The ideal candidate will have experience with process ...
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 ...
Process Validation Engineer
Newark, NJ · On-site
* 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 ...
Process Validation Engineer
Newark, NJ · On-site
* 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 ...
Process Validation Engineer
New Haven, CT · On-site
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 ...
Process Validation Engineer
New Haven, CT · On-site
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 ...
Process Validation Engineer
Enola, PA · On-site
* 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 ...
Process Validation Engineer
Enola, PA · On-site
* 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 ...
Process Validation Engineer
Concord, NC · On-site
Process Validation Engineer Location: North Carolina Position Overview We are seeking an experienced Process Validation Engineer to support multiple pharmaceutical manufacturing projects, with a ...
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Process Validation Engineer
Concord, NC · On-site
Process Validation Engineer Location: North Carolina Position Overview We are seeking an experienced Process Validation Engineer to support multiple pharmaceutical manufacturing projects, with a ...
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 ...
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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 Validation Engineer
Fishers, IN · On-site
Description TSMS - Process Validation Engineer The Technical Services and Manufacturing Sciences (TSMS) Process Validation Engineer will be responsible for supporting all facets of Process Validation ...
Process Validation Engineer
Fishers, IN · On-site
Description TSMS - Process Validation Engineer The Technical Services and Manufacturing Sciences (TSMS) Process Validation Engineer will be responsible for supporting all facets of Process Validation ...
Process Validation Engineer
Fishers, IN · On-site
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 Validation Engineer
Fishers, IN · On-site
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 ...
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 ...
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 ...
Chemence Medical Inc. seeks Sr. Process Validation Engineer in Alpharetta, GA to develop IQ/OQ/PQ protocols, coordinate and perform equipment qualifications, and ensure that automated process ...
Chemence Medical Inc. seeks Sr. Process Validation Engineer in Alpharetta, GA to develop IQ/OQ/PQ protocols, coordinate and perform equipment qualifications, and ensure that automated process ...
The Senior Process Validation Engineer is a key member of the Technical Services organization, responsible for leading and supporting validation activities for sterile injectable manufacturing ...
The Senior Process Validation Engineer is a key member of the Technical Services organization, responsible for leading and supporting validation activities for sterile injectable manufacturing ...
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 ...
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 ...
The Senior Process Validation Engineer is a key member of the Technical Services organization, responsible for leading and supporting validation activities for sterile injectable manufacturing ...
The Senior Process Validation Engineer is a key member of the Technical Services organization, responsible for leading and supporting validation activities for sterile injectable manufacturing ...
ProPharma Group Jobs Information
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Full-time
Re-posted 3 days ago
Job description
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.***
About ProPharma Group
Sourced by ZipRecruiter
Industry
Business management consulting
Company size
51 - 200 Employees
Headquarters location
Overland Park, KS, US
Year founded
2001