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
More than a job - It's a chance to make a real difference
Working at AbbVie is more than a job. It’s a career with meaning. A chance to make a difference, in the world and in your life.
We are now recruiting Visual Inspection Operator join our diverse Packaging team in Westport, on a fixed term contract. As our newest operator, you will ensure the highest quality and safety compliance standards while gaining exposure to new and advanced technology in our packaging area. This role would suit career changers or anyone wishing to gain valuable experience within the pharmaceutical industry. You will operate high-speed equipment for the manual and/or automated assembly and packaging of pharmaceutical products, ensuring adherence to specifications.
Is this a team you want to be part of? Then read on…
Key Responsibilities:
Core duties include:
- Perform all assigned duties in accordance with SOP’s and cGMP’s.
- Operate Core lines which includes coding and inspection.
- Operate Inspection and vacuum equipment.
- Complete in process check.
- Ensure all samples are handled as per procedure.
- Ensure line clearances are completed diligently and in accordance with department procedures and cGMP every time.
- Complete batch documentation associated with activity in compliance with cGMP
- Maintain a clean and organized workstation with good housekeeping.
- Complete all assigned duties according to departmental SOP’s and cGMP.
- Remain current on effective procedures relating to the job through eLMS and on the job training.
- Complete and remain current with all required cGMP and safety training.
- Engage and be proactive in departmental incentives for safety, quality and BBI program.
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Perform other duties as assigned.
Qualifications
What you will need:
- Leaving cert or equivalent qualification required.
- Previous experience in Pharma OR GMP regulated industry
- Ability to build strong relationships and work within cross-functional teams.
- Strong communication and presentations skills, both written and oral. Articulate the quality requirements in a clear, concise and persuasive manner.
- Aptitude to Plan & Organise work schedules with an analytical mindset.
- Good decision making to identify and understand issues, problems and opportunities whilst providing a viable solution.
- Adaptability to work in a fast, dynamic environment whilst adjusting readily to meet unexpected constraints.
- Drive, high energy, maturity, and ability to work under pressure, deliver results, and overcome obstacles.
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
