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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, including:
Autoclaves and sterilization equipment
Cleanroom and HVAC & Water systems (e.g., WFI, purified water)
Refrigeration and controlled storage systems
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
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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
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
You bring a positive, professional attitude and can communicate and collaborate with all levels of employees, customers, contractors & vendors.
Comprehensive knowledge of Regulatory and cGMP guidelines, with the ability to contribute to quality records (Deviations, Investigations, CAPA, and Change Control).
Ability to work independently and in a team environment
Thrive in a fast-paced environment and adapt to changing priorities
Detail-oriented individual who understands the importance of accuracy and responsiveness
Ability to work cross-functionally and adapt in a growing environment
Strong attention to detail and ability to thrive in a fast-paced environment
Collaborative mindset and commitment to team success
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 to help you save for the future
Company Paid Life and disability insurance
Access to voluntary insurance options
A generous paid time off program that increases every year
Tuition reimbursement
At Wedgewood Pharmacy, your work has purpose. Every prescription you help prepare, support, or deliver contributes to improving the health and well-being of animals. We are passionate about what we do and proud to build a workplace where people feel supported, included, and valued.
Wedgewood Pharmacy is an equal opportunity employer. We are committed to building a diverse and inclusive workplace where everyone can thrive.
Private U.S. veterinary compounding pharmacy serving veterinarians and animal owners with customized medications.
Visit company websiteJobs and hiring trendsUSD 90000-125000 yearly / year
Full-time
Entry · 1+ years experience
Onsite
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