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

SCIENCE IS AT THE HEART OF WHAT WE DO. PEOPLE ARE AT THE HEART OF WHY WE DO IT.

We are now recruiting for a QC Laboratory Analyst to join our diverse Quality teams at AbbVie, Westport Co. Mayo, on an initial fixed-term contract.
As our new Lab Analyst, you will ensure that all raw material, in-process, finished product and method transfer testing is carried out per schedule and records are maintained to appropriate requirements. Working in the quality control labs, you will be equipped with the latest design technology for chemical and microbiological analytical testing to meet customers’ needs.
The right candidate will have the opportunity to grow and develop their skills under the guidance and support of our highly accomplished supervisors and managers. We encourage a nurturing environment where career progression is the driving force for all our analysts many of whom have gone on to more senior roles within AbbVie.

TECHNICAL SKILLS AND EXPERIENCE

• Degree in an analytical science/biochemistry/toxicology is preferred.
• Experience using HPLC/GC analytical methods is essential for Chemistry Lab.
• Strong analytical skills, ability to analyze data and trends and draw conclusions.
• Ability to articulate clearly when dealing with colleagues, peer groups and managers.
• Proven ability to work independently and autonomously when required.
• Excellent oral, written, and presentation skills.
• Excellent attention to detail.
• Ability to plan and schedule workload.
• High drive and energy with a passion for results.
• Ability to work well under pressure and consistently deliver results while demonstrating an action- orientated approach to overcome obstacles.
• Relevant industry experience preferred.
  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.htm

KEY RESPONSIBILITIES:

• Execute analysis of raw materials, in-process material, and finished product in compliance with schedule.
• Complete analysis in accordance with SOP and standard methods.
• Maintain and comply with Laboratory Documentation and Computerized Systems Data Integrity requirements.
• Understand Regulations and business processes required to maintain Laboratory Data Integrity.
• Responsible for the timely completion of chemical testing.
• Ensure that all test equipment is used and maintained correctly. Raise change requests and data verification as assigned.
• Ensure all in-process sampling and testing is completed on time.
• Maintain up-to-date, complete, and precise records of all tests performed.
• Adhere to cGMP and GLP requirements.
• Assist in the resolution of quality problems as required.
• Participation in investigations into failures, out of trends and out of specifications as required.
• Develop in-house laboratory procedures as appropriate.
• Support the transfer of new products.
• Adhere to and supports all EHS standards, procedures, and policies.
• Keep work area clean and tidy, participation in the 6S program.
  Qualifications