About AbbVie
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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
- Support the production schedule according to customer demands from a technical perspective where and when required.
- Work on and lead new projects and problem solving across the business unit to ensure compliance with local procedures and regulations.
- Review, approval and execution of commissioning and qualification activity including FAT’s/SAT’s IQ/OQ/PQ’s.
- Support NPI’s and associated equipment trials and qualifications.
- Technical knowledge in the manufactured products and production equipment used.
- Support lean manufacturing on site by writing/ updating and approving SOPs
- Lead production related product quality investigations in conjunction with Quality Assurance and other cross-functional stakeholders including the assignment and management of corrective and preventive actions. Apply investigational tools like fishbone, 5W, contradiction matrix for root cause analysis.
- Ensure compliance with applicable regulatory agencies by supporting where required, also use knowledge to drive continuity and improvement on an ongoing basis
- Support change management and lead production aspect of CPs as part of a cross-functional team including identification and implementation of relevant tasks in a timely manner.
- Conduct business in compliance with all applicable laws and regulations, company policies and with highest ethical standards.
- Support operations in maintaining a high 5S standard
- Ensure you are fully informed of Shift and Dept performance metrics and have a clear understanding on how they impact overall Site Perfect Index
- BSc in Engineering, Science, a relevant discipline, or equivalent experience required
- 5 + years in a GMP manufacturing environment (equivalent experience considered), aseptic manufacturing experience preferred
- Excellent documentation and communication skills
- Excellent analytical and presentation skills with the ability to work independently
- Ability to work towards strict deadlines
- Ability to build relationships with peers, influence without authority
Closing date for applications: 29th June 2026
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