Supervisor, CONDO
Cincinnati, OH - USA
Posted January 02, 2018

Join us as We Transform How Pharmaceuticals are Made.

Patheon is looking for people who are passionate about making a difference in people’s lives. Patheon is in need of proven leaders to nurture talent, build effective teams and drive engagement in an environment where people are motivated to do their best for the company, its clients and their patients. To inspire collaboration and innovation.

Coordinate and execute production schedule for Condo on the Front of Week Days shift.    Supervise direct and lead employees.  Administer all company policies with respect to GMPs, validation, quality, safety, health, attendance, and environment.  With QA, make quality decisions regarding batches in each manufacturing area.  Develop employees and coordinate training on new equipment.  Improve quality of processes as well as identify safety and efficiency improvements.



Key Requirements
Applicant should have good working knowledge and understanding of GMPs related to dry products manufacturing.  Working knowledge of BPRs, processes, and equipment in all manufacturing areas is required.  Must have demonstrated the ability to motivate, influence and develop team members.  Must have demonstrated ability to solve problems and make decisions independently.  Must work and communicate well with associates in multiple areas.  Responsible for leading the RAPID process including initial response, containment, root cause investigation and determining appropriate CAPA. Responsible for writing the investigation reports in Trackwise.  Responsible for leading RAPID huddle process to achieve timely deviation and CAPA closure to meet departmental goals.  Owner of the Kamishibai audit process for the department. Maintains and continuously improves the audit cards.  Identifies trends and facilitates improvement efforts based upon the audit findings.  Proactively drives quality improvements to achieve department RFT and quality compliance goals.  
Participates in inspection readiness activities and may be involved in inspections by regulatory agencies.  Models effective and constructive communication and interactions with technical departments both orally and in writing; maintain acceptable proficiency in technical and non-technical (e.g. interpersonal) skills.  Requires a passion for problem solving.

Help Us Make a Healthier World.

Patheon provides development and manufacturing services for more than 800 pharmaceuticals, including nearly a fifth of the world’s top selling drugs. We’ve helped our clients earn more than twice as many U.S. FDA approvals than any other CDMO. Are you as committed as we are to exceeding expectations with high-quality solutions to complex problems? If so, we want to talk to you about making a healthier world... together. Join us at

Patheon is an Equal Opportunity/Affirmative Action employer and will consider all qualified applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status.

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