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Perrigo
Associate Continuous Improvement Engineer
Entry-Level JobVerifiedNo experience needed
Career Insights for Process Quality Engineer
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Based on Michigan data
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What they do
A Process Quality Engineer evaluates production processes and performance in manufacturing. Develops engineering to improve the quality of existing production processes or develops new processes to improve quality and efficiency.
$85,059 / year median in Michigan
-4% projected decline
Job Description
At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill(R), Compeed(R), Solpadeine(R), NiQuitin(R), and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging. Join us on our One Perrigo journey as we evolve to win in self-care. Description Overview The Continuous Improvement Engineer provides technical support as it relates to incident/deviation investigationsfor all commercialized products at Perrigo facilities within Michigan. Scope of the Role
- Provide technical expertise and support to identify root causes of incidents and deviations
- Develop and implement corrective and preventive actions to prevent reoccurrence of incidents and deviations
- Collaborate with cross-functional teams to coordinate investigations and ensure timely resolution of issues
- Conduct risk assessments to identify potential areas of improvement in manufacturing processes Utilize Lean Six Sigma methodologies and tools to drive continuous improvement initiatives
- Collect and analyze data to identify trends and areas for improvement
- Stay updated with industry best practices and technological advancements to enhance continuousimprovement efforts.
- Support ODR activities by helping define base equipment conditions, inspection points, and lubrication standards.
- Partner with operations and maintenance to identify and eliminate sources of contamination and hard to access areas.
- Provide technical guidance to ensure ODR routines strengthen equipment reliability and align with continuous improvement objectives.
- Experience Required
- Bachelor's degree preferably in engineering, chemistry, pharmaceutical sciences or related field.
- Knowledge of principles, concepts and practices in pharmaceutical sciences and manufacturing processes.
- Well-developed interpersonal, organization and communication skills, ability to work effectively with staffmembers at all levels, strong technical writing skills, familiarity with cGMP and FDA regulations.
- Experience with operator focused reliability programs (ODR, Autonomous Maintenance, TPM) preferred.
- Familiarity with c
GMP, FDA
regulations, including experience with investigations and/or developing andrecommending process improvements.- Computer literacy with a working knowledge Microsoft Office (Excel and Word), and SAP experience preferred.
- Ability to work independently on multiple concurrent projects with minimal guidance and to meet project deadlines.