Process Engineer

We are Reckitt

​Supply​

About the role

The Process Engineer will be responsible for all functions applicable to the Process Engineering team.Providing expertise to ensure Reckitt NPD’s and EPD’s are developed, scaled up and delivered to plan. This will cover validation/qualification of new and existing processes and equipment. Provides process engineering support for improvement efforts for the Manufacturing and Packaging areas of the plant, 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.
• Participate in the protection of the facility and physical assets of the plant.
• Drive work practices, policies and procedures that support meeting or exceeding safety, quality, and production goals.
• Develops and maintains interdepartmental and intradepartmental relationships to effectively work with all functional areas.
• Support the development and implementation of NPD’s. Identify issues that prevent scale up of new formulations.
• Organize and lead industrial trials as required during the technology transfer process. Both on site and at co-packer facilities.
• Participate in and drive continuous improvement projects.
• Assures compliance with all cGMPs.
• Liaises with process development, technical service, operations, maintenance, engineering, and planning to ensure expeditious validation/qualification of equipment, process improvements, and new processes/products introduced into the plant. 
• Manages interaction with governmental agencies and customers, as required.
• Participates in the coordination and implementation of the capital planning projects from a process engineering / validation perspective.
• Drives root cause analysis for failures and implements all corrective and preventative actions.
• Effectively applies knowledge of FDA, MHRA and DEA guidelines.
• Support the overall validation and compliance efforts for the Salt Lake site.  Generating and executing protocols, such as Installation, Operational, and Performance Qualifications (IOPQs), Process Validations (PVs) and Cleaning Validations (CVs).
• Assists in the development, improvement, and implementation of the Salt Lake validation master 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 site change management process by assessing the impact of changes on the validation status of the equipment.  

The experience we're looking for

• Must 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.
• Desired 2+ years of professional experience

• 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
• Must be able to read, write and speak English fluently
• This role is not currently sponsoring visas or considering international movement
• Relocation services are not being offered for this role

What we offer

US salary ranges

US pay transparency

Equality