Overview
EMO Process Engineer (Salt Lake City, UT, US, 84101)
We are Reckitt
Supply
About the role
The External Manufacturing Organisation (EMO) Process Engineer will be responsible for all functions applicable to the EMO Technical team.
Providing expertise to ensure Reckitt NPD’s and EPD’s are developed and delivered to plan.
This will cover validation/qualification of new and existing processes and equipment with NA EMOs.
Provides process engineering support for improvement efforts for the Manufacturing, and Packaging areas of the EMO plants, as well as new processes, and new capital equipment installations.
Your responsibilities
• Provides leadership in managing behavior relative to policy, procedures and functionally assigned tasks.
• Drive work practices, policies and procedures that support meeting or exceeding safety, quality and supply goals.
• Develops and maintains interdepartmental and intradepartmental relationships to effectively work with all functional areas and external manufacturing parties.
• Support the development and implementation of NPD’s. Identify issues that prevent scale up of new formulations.
• Organize and co-ordinate EMO industrial trials as required during the technology transfer process. Supporting where possible on site at EMO facilities.
• Participate in and drive continuous improvement projects with EMOs.
• Assures compliance with all cGMPs.
• Liaise with cross functional teams to support key strategic site to site transfer projects from Reckitt facilities or EMOs, into new or existing EMOs.
• Manages interactions and relationships with external parties, as required.
• Lead and support supply planned projects, delivering key material BCPs or PPV benefits.
• Drives root cause analysis for failures and implements all corrective and preventative actions.
• Effectively applies knowledge of FDA, and DEA guidelines.
• Assists in the development, improvement and implementation of the EMO supply plan.
• Ensure that the elements or functions that are regulated by the cGMPs for equipment, facilities, computer systems, manufacturing processes and packaging processes meet the regulatory requirements.
• Support the Reckitt change management process by assessing the impact of changes via Quality One.
The experience we're looking for
- Beneficial to have a bachelor’s degree in a scientific field such as, but not limited to, Chemical Engineering, Computer Science/Information Technology, Chemistry, Biology, or Biochemistry, or at least three years’ experience in Process Engineering, Validation, Quality Assurance or Quality Control in an FDA regulated manufacturing or processing environment.
- Must have a minimum of 3 years of professional experience, ideally within healthcare or consumer goods industries
- Ability to work over eight hours a day when needed.
- Computer Literacy, especially with the Microsoft Office Suite products.
- Strong communication skills in both a written and verbal manner
- Superior ability to analyze data and generate conclusions based upon the data
- Excellent interpersonal and problem-solving skills in dynamic environment.
- Strong organizational skills.
- Strong capability in the use of statistical tools to develop sampling plans.
- Ability to manage multiple priorities within established project deadlines.
- Ability to lead meetings, managing stakeholders, timelines and deadlines to meet project milestones.
- Ability to travel to EMOs when required for visits and/or industrial trials.
The skills for success
What we offer
Salary ranges
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