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Visual Inspection Engineer
Visual Inspection EngineerAllergan • Los Angeles, CA, US
Visual Inspection Engineer

Visual Inspection Engineer

Allergan • Los Angeles, CA, US
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Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit abbvie.com.

Job Description

Join our dynamic team at AbbVie in Sligo as a Visual Inspection Engineer! This is an excellent opportunity for a driven engineering or science professional with a passion for quality, continuous improvement, and making a difference in healthcare.

Key Responsibilities

  • Support Visual Inspection operations to meet all safety, regulatory, and organizational standards.
  • Develop and optimize procedures to enhance manufacturing processes.
  • Participate in process, equipment, and facilities validation projects; review and execute commissioning and validation protocols to keep projects on schedule.
  • Support the introduction of new Semi Automated visual inspection equipment on site and associated training.
  • Lead and facilitate FMEAs for Visual Inspection, and drive the certification of technicians.
  • Build and maintain defect libraries and execute trending for defect analysis.
  • Ensure local procedures align with global guidelines and regulatory expectations.
  • Provide technical leadership and guide the development of SOPs for visual inspection.
  • Collaborate with internal and external stakeholders to evaluate particles / defects and support technical transfers for new product introductions.
  • Investigate process deviations and support the production team in achieving output and yield targets.
  • Ensure full compliance with quality, safety, cGMP, and regulatory policies.
  • Supervise external contractors as required.

Qualifications

  • Hold a Level 8 degree (or higher) in Engineering, Science, or a relevant technical discipline.
  • Minimum 3 years' experience in a biotech or pharmaceutical manufacturing environment—experience with biotechnological drug processes, fill finish, lyophilisation, and sterilisation preferred.
  • Strong problem-solving and innovative thinking skills under pressure.
  • Familiarity with Semi Automated Visual inspection equipment.
  • Exceptional attention to detail and commitment to quality.
  • Excellent communication and interpersonal skills; proven ability to work both independently and in cross-functional teams.
  • Leadership qualities with a results-driven mindset.
  • Demonstrate integrity, a strong work ethic, and the ability to work autonomously.
  • Familiarity with cGMP, ISO, FDA regulations, and EHS best practices preferred.
  • Additional Information

  • What We Offer : A collaborative and innovative environment where your work impacts patients lives, opportunities for personal and professional development, and a chance to lead quality improvements in cutting-edge biologics manufacturing.
  • How to Apply : Ready to take the next step in your career? Apply now to join AbbVie and contribute to our mission in delivering best-in-class healthcare solutions
  • AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer / Veterans / Disabled.
  • US & Puerto Rico only - to learn more, visit abbvie.com / join-us / equal-employment-opportunity-employer.html
  • US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more : abbvie.com / join-us / reasonable-accommodations.html
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