Wedgewood Pharmacy

Pharma

ManufacturingProcessEngineer

$90–125k Albany, Ohio, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid+ candidates.

The Brief

“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.

Pharma
Problems you'll solve

Troubleshooting; Root cause analysis; Problem-solving

Eligibility Requirements

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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