What are the responsibilities and job description for the Production Manufacturing Technician Supervisor position at INCOG BioPharma Services?
Production Engineering Technician Supervisor Summary
INCOG BioPharma is seeking a highly motivated individual with exceptional mechanical aptitude and subject matter expert (SME) capabilities in the formulation, aseptic filling, inspection, and packaging of sterile drug products. The primary purpose of this role is to provide oversight and leadership to a small team that focuses on:
Essential Job Functions:
At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business.
If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus.
INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics.
By submitting your resume and details, you are declaring that the information is correct and accurate.
INCOG BioPharma is seeking a highly motivated individual with exceptional mechanical aptitude and subject matter expert (SME) capabilities in the formulation, aseptic filling, inspection, and packaging of sterile drug products. The primary purpose of this role is to provide oversight and leadership to a small team that focuses on:
- Asset management of manufacturing equipment (routine and preventative maintenance).
- Troubleshooting, repairing, and resolving mechanical issues to arise in day-to-day manufacturing.
- Supporting routine technical manufacturing processes; changeover, setup, startup, etc.
- Optimization and continuous improvement of manufacturing equipment and technologies.
- Increasing robustness, consistency, and reliability of manufacturing equipment and processing.
- Overseeing various stages of production, identifying potential areas for improvement and implementing measures to enhance the overall efficiency and effectiveness of the manufacturing operations.
Essential Job Functions:
- Lead a small team of Engineering Technicians with strong mechanical aptitude and experience in drug product formulation, filling, visual inspection, and packaging.
- Provide technical support, oversight, team leadership and guidance in technical decision-making related to manufacturing operations.
- Lead technical troubleshooting and investigations of manufacturing processes to support root cause analysis, product impact assessment and effective corrective and preventive actions.
- Implement process improvements based on data analysis and engineering principles; including process design enhancements
- Provide technical guidance and oversight to Operations and Validation groups.
- Collaborate with cross-functional teams to troubleshoot and resolve complex technical issues.
- Own and improve corrective and preventative maintenance strategies, timing, effectiveness, etc.
- Perform GEMBA walks and checks for process improvements.
- 3 years GMP experience with manufacturing processes and equipment in related fields such as biologics, pharmaceutical fill and finish required.
- 1-3 years of experience in people leadership role
- Bachelor’s degree in science, Engineering or related scientific discipline preferred.
- Experience in regulated GMP manufacturing operations preferred.
- Strong communication skill and the ability to build relationships with collegues across all levels of the organization, including business managers, operations leaders, and technical leaders.
At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business.
If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus.
INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics.
By submitting your resume and details, you are declaring that the information is correct and accurate.