Wedgewood Pharmacy
Pharma
ManufacturingProcessEngineer
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Manufacturing Process Engineer at Wedgewood Pharmacy. Skills: Manufacturing processes, Sterile pharmaceutical production, CGMP compliance. Design manufacturing processes. Develop manufacturing processes”
What You'll Achieve.
Minimize downtime; Ensure production continuity; Increase throughput; Reduce waste; Enhance product quality
Industry & Context.
Troubleshooting; Root cause analysis; Problem-solving
Occasional weekend work, Respond to emergencies, 10-15% travel
What They're Looking For.
Must Have
Bachelor's degree in Engineering, 1–5+ years of experience, Basic understanding of cGMP, Troubleshooting and problem-solving skills, Positive, professional attitude, Ability to work independently, Ability to work in a team environment, Detail-oriented individual, Ability to work cross-functionally, Adapt in a growing environment, Attention to detail, Collaborative mindset
Nice to Have
Experience in a regulated environment, Knowledge of Regulatory and cGMP guidelines
What You'll Do.
Design manufacturing processes
Develop manufacturing processes
Implement manufacturing processes
Support sterile compounding
Support production scale-up
Troubleshoot process issues
Troubleshoot equipment issues
Troubleshoot facility issues
Lead facility startup
Build manufacturing systems
Refine manufacturing systems
Build manufacturing documentation
Refine manufacturing documentation
Build manufacturing processes
Refine manufacturing processes
Partner with Operations
Ensure FDA compliance
Ensure cGMP compliance
Author cGMP documentation
Maintain cGMP documentation
Develop Preventive Maintenance programs
Implement Preventive Maintenance programs
Develop Calibration programs
Implement Calibration programs
Provide engineering support
Drive root cause investigations
Ensure process improvements
Support technology transfer
Evaluate process improvements
Implement process improvements
Enhance product quality
Manage capital projects
Budget capital projects
Execute capital projects
How You'll Work.
Team & Collaboration
Cross-functional teams; Quality, Operations, R&D
Process & Methodology
Capital projects
Full Job Description
At Wedgewood Pharmacy, we are dedicated to improving the lives of animals through customized medication and compassionate care. Every role in our organization contributes to helping pets live healthier, happier lives. We are a team driven by purpose, quality, and a shared commitment to animal health. The Manufacturing Engineer will play a critical role in building and scaling manufacturing operations. This position is responsible for developing, implementing, and continuously improving manufacturing processes, equipment, and systems to support sterile pharmaceutical production. This is a highly hands-on role in a startup environment, requiring the ability to operate both strategically and tactically supporting day-to-day production while establishing scalable, compliant processes aligned with FDA and cGMP requirements. The Basics Location: Albany, Ohio Job Type: Full Time Schedule: Monday - Friday 8:00 am -4:30 pm (Must have the ability to respond to emergencies and be available for occasional weekend work for special projects) Compensation: The base pay range for this position is $90K-$125K base plus an annual bonus commensurate with the individual's experience and qualifications. Benefits: Eligible How You’ll Make an Impact Design, develop, and implement manufacturing processes, tooling, and workflows to support sterile compounding and production scale-up Troubleshoot process, equipment, and facility issues in real time to minimize downtime and ensure production continuity Lead facility startup activities, including equipment installation, commissioning, qualification (IQ/OQ/PQ), and validation Build and refine manufacturing systems, documentation, and processes from the ground up in a fast-paced environment Partner cross-functionally with Quality, Operations, and R&D to ensure compliance with U. S. Food and Drug Administration 503B outsourcing facility requirements and cGMP standards Author and maintain cGMP documentation including SOPs, batch records, validation
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