2-year temporary position through AgileOne
This is a remote position. However, you MUST be able to commute to Philadelphia, PA when needed. 25% travel required.
- Must have experience in pharmaceutical / packaging prefilled syringes
This role serves as an essential part of the External Manufacturing & Network Equipment team, overseeing product and technology transfers to Contract Manufacturing Organizations (CMOs). The role involves leading technical interactions with external packaging partners, which are Contract Manufacturing Organizations in the ExM space. The incumbent will work closely with other ExM functions (Quality, Operations, Supply Chain, Procurement) and technology experts within the Centers of Excellence. The engineer will leverage their scientific, technical, and business expertise to lead teams in solving complex packaging issues, optimizing processes, and ensuring compliance, focusing on developing and executing primary and secondary packaging components for Small and Large Molecule assets, assembling Medical Device Combination Products, designing packaging equipment for prefilled syringes, and ensuring packaging process control and efficiency.
Core Responsibilities :
Tasked with leading and implementing technology transfers, qualifications, validations, process enhancements, and change controls for projects involving Small and Large Molecule, medical devices, combination products, and prefilled syringes.Assurance of compliant packaging and assembly process transfer, site readiness and execution excellence.Offer technical expertise in quality and supply investigations with external packaging partners. Lead discussions on packaging processes, equipment, and components to help identify root causes and develop effective corrective and preventive actions.Collaborate with internal packaging teams on project timelines, development of primary, secondary, and tertiary packaging components, testing methods, packaging processes, serialization requirements, and transport / storage systems for the finished product.Collaborating with external packaging partners in weekly meetings to ensure project tasks are executed according to the project schedule.Collaborate with external packaging partners to ensure packaging readiness, including component specifications, operation process, risk assessment (FMEA), testing method transfer, and line qualifications (IQ, OQ, PQ) and validation (PPQ).Oversees Change Control activities for tech transfer workflows to ensure timely task execution.Operating independently while ensuring coordination, communication, and oversight on all technical aspects related to the involved External Packaging partners.Education Minimum Requirement :
A bachelor’s degree in Packaging Science / Engineering, Mechanical Engineering, or a related technical discipline (such as Chemical Engineering or Material Engineering) is mandatory.Required Experience and Skills :
Minimum of 10 years’ experience in the medical device, prefilled syringe packaging, and combination product engineering and pharmaceutical field, with extensive practical knowledge in supporting packaging operations, managing packaging materials and components, and overseeing packaging processesStrong preference for candidates with leadership experience at a pharmaceutical packaging facility or an External Manufacturing site.Extensive experience in handling Capital packaging equipment projects, including technology transfers, designing packaging lines, creating purchase specifications, managing equipment installation and validation, pursuing operational excellence, and troubleshooting on the shop floor.Broad experience with devices, combination products, covering design control to product and technology transfer for both new and existing packaging facilities.Exceptional project management skills, from conception and initiation, through project close-out.Thorough knowledge and proven expertise in GMP application and quality systems, particularly in process and equipment qualification, change control, deviation management, and cleaning qualification.Expert grasp of relevant scientific or technical concepts to handle routine and complex tasks, along with advanced practical knowledge of techniques applicable to these tasks.Experience with key manufacturing change control compliance systems such as Veeva and / or other similar systemsExtensive experience with quantitative decision tools for risk management and options analysis to support risk-based decision making.Exhibited leadership qualities and inclusive practices in managing a diverse, cross-functional team.Familiarity with the regulatory standards of key pharmaceutical markets, such as USFDA cGMPs and EMA guidelines.Demonstrate ability to have a continuous learning mindset and commitment to experiment, learn and embrace informed risk taking and doing things in new ways without fear of failure.Adopt a critical mindset in decision-making to ensure thorough analysis while considering potential impacts on key stakeholders.Ability to serve as a change agent to work collaboratively and act with an enterprise mindset to make appropriate tradeoffs for the project & organization’s greater good.Strong analytical and decision-making abilities, combined with outstanding oral and written communication skills.
