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Job Details
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.
We are currently looking for a Quality Control Analyst for an initial 12 month contract at our site Manufacturing site in Clonshaugh.
The QC Analyst is responsible for conducting raw material, in process, finished product and stability testing according to relevant SOPs and in adherence to the site production schedule and for accurately completing all documentation that supports testing procedures. The QC Analyst identifies issues related to laboratory testing and equipment that requires an in-depth knowledge of scientific methods and techniques. The QC Analyst is responsible for the safe, compliant, and efficient execution of job duties in a team environment. This position reports to the QC Supervisor.
Primary duties and responsibilities of the position are as follows. Other duties may be assigned.
- Conduct chemical and physical laboratory tests and analyze excipients, cleaning samples, raw materials, intermediates, and final products including protocol testing in a timely manner to ensure compliance with standards and production targets.
- Recognize and report to immediate supervisor any issues or deviations from accepted standards.
- Provide status updates on own activities and productivity challenges according to defined procedures
- Maintain data integrity and ensure compliance with FDA, GLP, QSR and cGMP regulations, as well as with company SOPs and specifications.
- Complete and conform to all training requirements for job role, including company-required and job role-specific training.
- Observe all safety and compliance procedures and actively highlighting any safety concerns to help drive the reduction of accidents or near misses.
- Conforming to the safety culture on site on Zero, Believe it, Achieve it.
- Participate in the 6S activities within the QC Laboratory.
- Positively contribute to departmental goals and programs such as Right First Time
- A third level qualification in Chemistry or related Science, preferably a Bachelor’s Degree
- Demonstrate knowledge of cGMP requirements and practices including knowledge of the USP and FDA Guidance Documents relating to the pharmaceutical Quality Control Laboratory.
- Demonstrate knowledge of common analytical instrumentation e.g. HPLC, Dissolution, GC, FTIR, ElectroChemistry (DME), UV/Vis and other USP instrumental and Wet chemistry technologies used in pharmaceutical Quality Control Laboratory.
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:
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