Engineering manager
Job Description
General Summary: The Package Engineering Manager will deliver reliably on independent activities within Technical Operations. This role will provide technical support in packaging and process operations, working with internal and external cross-functional teams in a fast-paced environment. The Package Engineering Manager will support completion of project activities and working directly with external Contract Manufacturers. Key Duties And Responsibilities- Maintains effective relationships between Vertex and key suppliers of materials, technology, and manufacturing resources
- Provides technical support on packaging processes to Package Engineering and cross functional teams
- Author and/or review validation and change control documents such as master batch records, protocols, reports and change requests
- Supports packaging projects and process improvement efforts, validations, equipment installation, IQ/OQ/PQ protocol development and execution
- Participates on cross-functional CMC sub-teams
- Evaluates process performance to identify and lead continuous improvement activities for commercial products
- Supports resolution of quality investigations
- Works effectively with multiple stakeholders including Pharmaceutical Sciences, Regulatory Affairs, Project Management, Supply Chain, Quality, and Marketing to meet project timelines and objectives
- Acts as a resource in the assigned technical area
- May lead aspects of technical transfer and process validation activities; responsible for authoring and reviewing packaging qualification and validation documents
- Will require travel to contract manufacturing plants to support process performance or to troubleshoot manufacturing issues
- Supports the responsibilities of the technical operations team in projects related to packaging technology, sustainability, and industry activity
- Experience or certification in LEAN and/or Six Sigma practices is a plus
- Ability to travel domestic and international. (Approximately 25%)
- Good knowledge of cGMP’s and associated CMC regulatory considerations in a pharmaceutical environment
- Fundamental understanding and application of validation processes (IQ/OQ/PQ/PV)
- Ability and flexibility to work globally in a virtual work environment
- Excellent project management experience
- Solid communication, analytical, problem solving and collaboration skills to exchange complex information with others in complex situations
- Demonstrated ability to manage multiple projects concurrently, and flexibility to accommodate changes in responsibilities or project priorities
- Bachelor's degree in Packaging, Chemical, Mechanical, Material or Industrial Engineering, or a related field
- Typically requires 4 years of experience or the equivalent combination of education and experience
- Hybrid: work remotely up to two days per week; or select
- On-Site: work five days per week on-site with ad hoc flexibility.
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