ASSISTANT MANAGER, CONTINUOUS IMPROVEMENT
Princeton, New Jersey, United States
Job Summary
Occupation
Transportation and Logistics
Specialty
Manager
Location
08520, Hightstown, New Jersey, United States
Visa Sponsorship
No
Job Description
Last Update:
1/11/24
Division Overview:
Eugia is US-based independent specialty pharmaceutical company focused on generic sterile injectables, oncology, hormones, and ophthalmic medicines. Eugia has best-in-class, dedicated manufacturing and R&D capabilities to meet customer needs as they emerge. We are committed to consistently providing our customers with high quality specialty medicines.
Eugias mission is to make the process of buying specialty pharmaceutical products an experience customers look forward to, and our vision is to become synonymous with excellent customer service and continuously improve upon this excellence by being transparent, responsive, and consistent. We are expanding Eugias capabilities to include the manufacture of highly complex injectables to answer that need.
Eugia is the partner of choice to deliver on the promise of generic specialty pharmaceuticals.
Job Overview:
Provide support in achieving the operational productivity targets and identifying Best Practices opportunities. Work to achieve a sustainable continuous improvement site culture and collaborate with the regional network in order to communicate benchmarking methodology.
Responsibilities:
Responsible to plan monthly production schedule as per the cross functional area/personnel availability, raw material and component availability to meet the customer demand.
Source materials to keep up with production goals and meet customer demands.
Manage continuous improvement initiatives to drive gains in quality, flow and output.
Develop new optimal batch sizes as per the business need.
Ensured that SOPs are simplified and easy to understand.
Perform technical review on SOPs, MBRs, Protocols, and Deviations.
Responsible for implementation and closing of Corrective and Preventative Actions (CAPAs) on time.
Responsible to oversee that executed batch records are reviewed on time to support the release of the product into the market.
Provide follow-up and tracking to ensure identified improvement opportunities are completed as planned and teams are accountable to the process.
Perform or assist with all aspects of the Quality Management System: such as corrective/preventive actions, conformance investigation, technical documentation, production reports, regulatory paperwork, deviations, internal audits, validation, and training.
Maintain positive work relationships with members of other teams to communicate effectively, and to ensure compliance with cross-team responsibilities.
Responsible at all times for promoting a safety culture and safety awareness within their area of responsibility.
Qualifications - Skills & Requirements:
Bachelors degree or equivalent work experience of at least five (5) years required.
Minimum of 3+ years experience in a Supply Chain management role, Preferably pharmaceuticals
Experience in business transformation and process improvement roles using proven problem solving/continuous improvement methodologies.
Experience with change management and influencing organizational culture change. 1+ years experience in a project management role.
MS Excel, PowerPoint. Lean Six Sigma
Education & Experience:
Bachelors degree or equivalent work experience of at least five (5) years required.
Minimum of 3+ years experience in a Supply Chain management role, Preferably pharmaceuticals
Experience in business transformation and process improvement roles using proven problem solving/continuous improvement methodologies.
Experience with change management and influencing organizational culture change. 1+ years experience in a project management role.
MS Excel, PowerPoint. Lean Six Sigma
Physical Requirements: OFFICE POSITION - While performing the duties of this job the employee is required to: Stand, sit; talk, hear, and use hands and fingers to operate a computer and telephone keyboard reach, stoop kneel to install computer equipment Specific vision abilities required by this job include close vision requirements due to computer work Light to moderate lifting is required Moderate noise (i.e. business office with computers, phone, and printers, light traffic). Ability to sit at a computer terminal for an extended period of time Sedentary work Exerting up to 10 pounds of force occasionally and/or negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects, including the human body. Sedentary work involves sitting most of the time. Jobs are sedentary if walking and standing are required only occasionally and all other sedentary criteria are met. Additional Physical Requirements: Sitting 1-4 Hours, Standing 4-8 Hours Blood/Fluid Exposure Risk: Category III: Tasks involve no exposure to blood, body fluids or tissues. Category I tasks are not a condition of employment.
Eugia is US-based independent specialty pharmaceutical company focused on generic sterile injectables, oncology, hormones, and ophthalmic medicines. Eugia has best-in-class, dedicated manufacturing and R&D capabilities to meet customer needs as they emerge. We are committed to consistently providing our customers with high quality specialty medicines.
Eugias mission is to make the process of buying specialty pharmaceutical products an experience customers look forward to, and our vision is to become synonymous with excellent customer service and continuously improve upon this excellence by being transparent, responsive, and consistent. We are expanding Eugias capabilities to include the manufacture of highly complex injectables to answer that need.
Eugia is the partner of choice to deliver on the promise of generic specialty pharmaceuticals.
Job Overview:
Provide support in achieving the operational productivity targets and identifying Best Practices opportunities. Work to achieve a sustainable continuous improvement site culture and collaborate with the regional network in order to communicate benchmarking methodology.
Responsibilities:
Responsible to plan monthly production schedule as per the cross functional area/personnel availability, raw material and component availability to meet the customer demand.
Source materials to keep up with production goals and meet customer demands.
Manage continuous improvement initiatives to drive gains in quality, flow and output.
Develop new optimal batch sizes as per the business need.
Ensured that SOPs are simplified and easy to understand.
Perform technical review on SOPs, MBRs, Protocols, and Deviations.
Responsible for implementation and closing of Corrective and Preventative Actions (CAPAs) on time.
Responsible to oversee that executed batch records are reviewed on time to support the release of the product into the market.
Provide follow-up and tracking to ensure identified improvement opportunities are completed as planned and teams are accountable to the process.
Perform or assist with all aspects of the Quality Management System: such as corrective/preventive actions, conformance investigation, technical documentation, production reports, regulatory paperwork, deviations, internal audits, validation, and training.
Maintain positive work relationships with members of other teams to communicate effectively, and to ensure compliance with cross-team responsibilities.
Responsible at all times for promoting a safety culture and safety awareness within their area of responsibility.
Qualifications - Skills & Requirements:
Bachelors degree or equivalent work experience of at least five (5) years required.
Minimum of 3+ years experience in a Supply Chain management role, Preferably pharmaceuticals
Experience in business transformation and process improvement roles using proven problem solving/continuous improvement methodologies.
Experience with change management and influencing organizational culture change. 1+ years experience in a project management role.
MS Excel, PowerPoint. Lean Six Sigma
Education & Experience:
Bachelors degree or equivalent work experience of at least five (5) years required.
Minimum of 3+ years experience in a Supply Chain management role, Preferably pharmaceuticals
Experience in business transformation and process improvement roles using proven problem solving/continuous improvement methodologies.
Experience with change management and influencing organizational culture change. 1+ years experience in a project management role.
MS Excel, PowerPoint. Lean Six Sigma
Physical Requirements: OFFICE POSITION - While performing the duties of this job the employee is required to: Stand, sit; talk, hear, and use hands and fingers to operate a computer and telephone keyboard reach, stoop kneel to install computer equipment Specific vision abilities required by this job include close vision requirements due to computer work Light to moderate lifting is required Moderate noise (i.e. business office with computers, phone, and printers, light traffic). Ability to sit at a computer terminal for an extended period of time Sedentary work Exerting up to 10 pounds of force occasionally and/or negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects, including the human body. Sedentary work involves sitting most of the time. Jobs are sedentary if walking and standing are required only occasionally and all other sedentary criteria are met. Additional Physical Requirements: Sitting 1-4 Hours, Standing 4-8 Hours Blood/Fluid Exposure Risk: Category III: Tasks involve no exposure to blood, body fluids or tissues. Category I tasks are not a condition of employment.