Manufacturing Process Engineer

Wedgewood Pharmacy; Albany (OH); On-site; USD 90,000 - 125,000; Full time

Benefits offered by this job

Opportunities for growth and career development

Comprehensive benefits including health and dental

Generous paid time off program

Job summary

Wedgewood Pharmacy is seeking a Full Time Engineer in Albany, Ohio. The role involves designing and implementing manufacturing processes, troubleshooting equipment issues, and leading facility startups while ensuring compliance with cGMP standards.

The ideal candidate holds a Bachelor's degree in Engineering or Life Sciences and has 1–5+ years of experience in manufacturing. Wedgewood offers a comprehensive benefits package including health, dental, and a 401(k) retirement plan.

Qualifications

• 1–5+ years of experience in manufacturing or a regulated environment.
• Practical hands-on experience with solid oral dose manufacturing.
• Basic understanding of cGMP or regulated industry practices.

Responsibilities

• Design, develop, and implement manufacturing processes.
• Troubleshoot process, equipment, and facility issues.
• Lead facility startup activities for equipment installation.

Skills

Troubleshooting and problem-solving skills

Ability to travel up to 10-15%

Comprehensive knowledge of regulatory guidelines

Detail-oriented and accurate

Education

Bachelor’s degree in Engineering, Life Sciences, or related field

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.

Basics

Location: Albany, Ohio
Job Type: Full Time
Schedule: Monday - Friday 8:00 am - 4:30 pm (must be available for occasional weekend work for special projects)
Compensation: Base pay range $90K-$125K plus annual bonus commensurate with 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 protocols, and technical reports
• Develop and implement preventive maintenance and calibration programs for critical manufacturing and facility equipment
• Provide engineering support for critical systems such as autoclaves, sterilization equipment, cleanroom and HVAC & water systems (e.g., WFI, purified water), refrigeration, controlled storage, filling, compounding, and packaging equipment
• Drive root cause investigations, deviations, and CAPAs to ensure sustainable process improvements
• Support technology transfer and scale‑up of new products into manufacturing
• Evaluate and implement process improvements to increase throughput, reduce waste, and enhance product quality
• Manage capital projects, including vendor selection, budgeting, and execution
• Operate with a high sense of urgency and adaptability in a startup environment with evolving priorities

What We’re Looking For

• Ability to travel up to 10‑15% dependent on business needs
• Bachelor’s degree in Engineering, Life Sciences, or related technical field
• 1–5+ years of experience in manufacturing, engineering, or a regulated environment (internships/co‑ops considered)
• Practical hands‑on experience with solid oral dose manufacturing
• Basic understanding of cGMP or regulated industry practices
• Strong troubleshooting and problem‑solving skills
• Positive, professional attitude and ability to communicate and collaborate with all levels of employees, customers, contractors, and vendors
• Comprehensive knowledge of regulatory and cGMP guidelines, with ability to contribute to quality records (deviations, investigations, CAPA, and change control)
• Ability to work independently and in a team environment
• Thrives in a fast‑paced environment and adapts to changing priorities
• Detail‑oriented, accurate, and responsive
• Works cross‑functionally in a growing environment
• Strong attention to detail and commitment to team success

What You’ll Love About Wedgewood

• Opportunities for growth and career development
• A supportive, team‑first culture where your work matters
• The ability to make a real impact on animal health every day
• A comprehensive benefits package that includes health, dental, and flexible spending accounts
• 401(k) retirement plan with a generous company contribution
• Company paid life and disability insurance
• Access to voluntary insurance options
• A generous paid time off program that increases every year

Our Commitment to Inclusion

Wedgewood Pharmacy is an equal‑opportunity employer. We are committed to building a diverse and inclusive workplace where everyone can thrive.