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API Maintenance Lead

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Sligo, SO

  1. Operations
  2. On-Site
  1. Full-time
R00139905
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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 us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.


Job Description

We have an exciting opportunity for a Maintenance Lead to join our engineering team in Sligo. This position reports to the Drug Product Engineering Manager. The successful candidate will lead and manage a team of plant support engineers and technicians to support manufacturing continuously, efficiently, and effectively.

Roles and Responsibilities

  • Ensure continuity across shifts throughout the week, including a.m. handovers.
  • Complete timecard review and approval for all PSEs.
  • Responsible for adherence to training schedule, delivery of toolbox talks, WO coordination, WO reviews.
  • Complete weekly review/accuracy/completeness of PH sheets.
  • Arrange shift cover for Annual Leave, approve Annual Leave and other requests.
  • Set goal, manage performance and development activities for all direct reports.
  • Input to weekly planning meeting.
  • Represent Engineering shift support at Tier 1 morning meetings.
  • Resolve manufacturing escalations in a timely manner.
  • Coordinate resources and assign tasks and activities.
  • Work closely with Technical Shift Leaders/Operation Supervisors to ensure interdepartmental activities are planned and executed safely.
  • Ensure Engineering compliance with all safety, environmental and quality related BOPs.
  • Document all activities in line with cGMP requirements.
  • Cross train team members and train new team members.
  • Maintain the overall cGMP of the pharmaceutical processing areas.

Qualifications

  • Diploma/Trade qualification in suitable science/engineering course and/or suitable experience.
  • 3+ years’ experience in a highly regulated industry performing an equivalent position.
  • Detailed functional knowledge required of a wide range of manufacturing equipment is essential.
  • Proven instrumentation/troubleshooting ability.
  • Good knowledge of procedures, policies and guidelines required to comply with cGMP and HPRA/FDA guidelines.
  • Must be flexible and support the business through working shift and adhering to the standby schedule.

Additional Information

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 https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

Recruitment Fraud Alert

We have recently become aware of various recruitment phishing scams targeting job seekers. Please be advised:



  • AbbVie will never request sensitive personal information (such as bank account details, social security numbers, or payment of any kind) during the recruitment process.
  • If you suspect you have received a fraudulent offer or communication claiming to be from AbbVie, please do not respond, open any attachments, or click on any hyperlinks.


If you have any questions or concerns regarding the authenticity of a communication alleged to have been made by or on behalf of AbbVie, please contact us immediately.


Protect yourself by verifying job offers and communications. Your safety is important to us.

Pay Range: $

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