Perrigo

Vision Engineer

Perrigo$75K — $95K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in engineering discipline
  • 3+ years of experience with Vision Systems troubleshooting
  • Proficiency in AutoCAD and ability to interpret design documents
  • Familiarity with Lean and Six Sigma methodologies
  • Previous experience with electrical troubleshooting is preferred
  • Knowledge of computer system validation in an FDA-regulated context
  • Experience with cGMP standards

Responsibilities

  • Support equipment purchases and modifications to enhance productivity
  • Ensure compliance with cGMP during system lifecycle activities
  • Manage capital projects, ensuring completion within scope and budget
  • Participate in change management to assess impact on control systems
  • Drive quality initiatives through CAPA and technology improvements
  • Identify process improvement opportunities focusing on efficiency
  • Collaborate with cross-functional teams to implement changes and resolve issues

Benefits

  • Comprehensive benefits supporting employee and family health
  • Career development opportunities for professional growth
  • Hybrid work model with flexibility to work from home two days a week
  • Recognition as one of 'America's Best Employers by State 2024'
Full Job Description
Description Overview

The Vision Engineer will provide technical and compliance support to pharmaceutical manufacturing and packaging operations utilizing vision systems. This individual will help lead and assists in the successful development, implementation and completion of vision system and automation related projects across multiple site locations. Explore innovative and alternate solutions to meet business needs while providing a high level of customer service to operations to meet their objectives through timely, professional, and safe practices.

Scope of the Role

  • Supports equipment purchases and modifications, which improve plant productivity or accommodate the manufacturing of new formulations or products.
  • Works closely with others to ensure compliance with FDA current Good Manufacturing Practice (cGMP) regulations during the design, specification, qualification, validation, maintenance, and use of equipment systems.
  • Completes capital and expense projects by meeting agreed upon timelines, scope, and budget, generated with Operations and Engineering, while managing and tracking project costs to complete projects on budget.
  • Participates in the change management program to evaluate the impact of proposed activities on the validation status of control systems.
  • Supports quality initiatives through CAPA activities as well as implementing new technology to solve previously unsolvable problems.
  • Identifies areas of opportunity to improve production processes with an emphasis on detection capabilities and down time reduction.
  • Work closely with other functional areas such as engineering, maintenance, operations, IT, and scheduling to implement changes and to investigate and resolve issues.
  • Respond to emergencies and troubleshoot issues affecting day-to-day machine performance and efficiency.
  • Design and implement new features and technologies to enhance machine operability, efficiency, safety, quality, and data tracking.
  • Provide strategic plans to upgrade aging and obsolete systems.
  • Review technical specifications of new equipment to ensure that automation hardware and software designs align with established standards.


Experience Required

  • Bachelor's degree in an engineering discipline
  • 3 or more years of working with and troubleshooting Visions Systems
  • Working knowledge of AutoCAD software, and the ability to read and understand drawings, flowcharts, schematics, as it relates to system design documentation.
  • Demonstrated understanding of Lean and Six Sigma processes preferred, including experience with the different continuous improvement techniques.
  • Prior electrical troubleshooting skills preferred
  • Flexible schedule with normal working hours of 7am - 4pm.
  • Experience with computer system validation and change management in an FDA regulated environment.
  • Experience and familiarity with current Good Manufacturing Practices (cGMP).
  • Excellent problem-solving skills, sound decision making abilities, and ability to meet deadlines in a team-oriented environment.
  • Demonstrated self-confidence and ability to interface with multiple departments, consultants, and contractors.
  • Experience with PLC programming and troubleshooting preferred.

Benefits
We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.

Find out more about Total Rewards at Perrigo.

Hybrid Working Approach
We love our offices and the setting they provide for in-person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles.

We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more here

Applicants please note: To apply to this position please click the APPLY button at the bottom of the application. (The SAVE button will only save your profile information but not submit an application for this open position.) All application materials, including resumes and CVs, must be submitted in English. Thank you.

About Perrigo

Perrigo Company plc is an Irish–registered manufacturer of private label over-the-counter pharmaceuticals, and while 70% of Perrigo's net sales are from the U.S. healthcare system, Perrigo is legally headquartered in Ireland for tax purposes. The company's shares are traded on the NYSE and the Tel Aviv Stock Exchange; as of 2015, its largest shareholders are the Vanguard Group and BlackRock. Perrigo is the only non-Israeli company listed on the Tel Aviv 100 Index. The company produces a wide variety of products, including generic drugs, infant formulas, and nutritional products. Perrigo is headquartered in Grand Rapids, Michigan.
Learn more about Perrigo
Size
9,900 employees
Market Cap
$4.4 billion
Industry
Net Income
-$162.6 million
Founded
1887
5 Year Trend
-4.8%
Revenue
$5 billion
NASDAQ

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