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Process Engineer II (Pharmaceutical Manufacturing)

Astrix Technology

Wilmington, OHFull-time$90–115K/yrPosted 5mo agoSeen in employer's feed 1w ago
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At a glance

Compensation
$90–115K/yr
Location
Wilmington, OH
Schedule
Full-time
Work Authorization
US work authorization required

Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

Astrix Technology is hiring a Process Engineer II (Pharmaceutical Manufacturing). The Process Engineer II supports commercial and clinical pharmaceutical manufacturing, focusing on oral solid dosage (OSD) products. This role is responsible for process scale-up and transfer, equipment selection and commissioning, and continuous improvement of manufacturing and packaging operations for a global biopharmaceutical company.

Key focus areas include Troubleshoot and maintain manufacturing systems, processes, and equipment, Support the development or transfer of manufacturing and cleaning processes, and Install and troubleshoot instrumentation and equipment.

Successful candidates bring BS Degree Engineering/Technical, 2-5 Years Manufacturing Experience, and US Work Authorization. Important skills include Troubleshoot Manufacturing Systems, Maintain Manufacturing Systems, Process Scaleup, Process Transfer, Equipment Selection, and Equipment Commissioning. Preferred (not required): OSD Equipment Procurement, cGMP, OSHA, and EPA.

Skills & qualifications

RequiredNice to have

Skills

Troubleshoot Manufacturing SystemsMaintain Manufacturing SystemsProcess ScaleupProcess TransferEquipment SelectionEquipment CommissioningContinuous ImprovementInstall InstrumentationTroubleshoot InstrumentationAuthor Technical ProtocolsAuthor Technical ReportsSpecify Manufacturing SystemsSize Manufacturing SystemsOSD Equipment ProcurementcGMPOSHAEPAFDA Facility RequirementsOSD OperationsStatisticsEquipment DesignProcess ControlProcess Scale-UpOSD Pharmaceutical Process ValidationsOSD Equipment ValidationsSample SizingANOVARegression AnalysisControl Charts

Qualifications

BS Degree in Engineering or Technical Discipline2-5 Years Manufacturing Experience2-5 Years Technical ExperienceAuthorized to Work in US Without SponsorshipMedically Cleared for Respirator Use (PAPR)2-5 Years OSD Pharmaceutical Experience5 Years Pharmaceutical Engineering Experience

Benefits

Relocation Assistance

Full job description

Process Engineer II (Pharmaceutical Manufacturing)

Manufacturing

Wilmington, Ohio, US

  • Added - 23/02/2026

Pay Rate Low: 90000 | Pay Rate High: 115000

Our client is a global biopharmaceutical company seeking a ProcessEngineer II to support commercial and clinical pharmaceutical manuacturing, with a focus on oral solid dosage (OSD) products.

Title: Process Engineer II (Pharmaceutical Manufacturing)

Salary : $90-115K +Bonus

Hours : 1st shift ~8am-5pm M-F

Location : Onsite in Wilmington, OH (Excellent Relocation assistance provided if needed!)

Summary

The Process Engineer supports commercial and clinical pharmaceutical manufacturing, with a focus on oral solid dosage (OSD) products. This role is responsible for process scaleup and transfer, equipment selection and commissioning, and continuous improvement of manufacturing and packaging operations.

Essential Functions

  • Troubleshoot and maintain manufacturing systems, processes, and equipment.

  • Support the development or transfer of manufacturing and cleaning processes for the manufacturing area.

  • "Hands-on" ability to install and troubleshoot instrumentation and equipment.

  • Author high-quality technical protocols/reports (engineering studies, summary reports, equipment specifications, change controls, and investigations)

  • Specify and size manufacturing systems, equipment, and process equipment.

Basic Qualifications:

  • BS degree in Engineering or technical discipline.

  • 2-5 year of manufacturing experience or technical experience.

Preferred Qualification:

  • 2-5 years of OSD pharmaceutical experience or 5 years of pharmaceutical engineering experience.

  • Experience with OSD equipment procurement.

  • Thorough knowledge of cGMP, OSHA, EPA and FDA facility requirements and regulations.

  • Thorough knowledge of OSD operations, statistics, equipment design, process control, and process scale-up.

  • Knowledge of OSD pharmaceutical process and equipment validations.

  • Experience in statistical analysis: sample sizing, ANOVA, regression analysis, control charts, etc

  • MUST be authorized to work in the US without sponsorship

Physical Demands

  • Ability to properly gown and don PAPR for potent controlled substance formulations for extended periods of time

  • Ability to lift/move 40 lbs. overhead. Ability to team lift up to 100 lbs.

  • Must be able to be medically cleared for respirator use (PAPR)

  • Ability to operate different types of production equipment.

  • Ability to gown correctly for clean room manufacturing operations.

  • Ability to stand or sit for extended periods (up to 2 hours at a time).

  • Must be able to work in an office and a manufacturing environment.

INDBH

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We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

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