Quality Control Analyst - AbbVie
AbbVie is seeking a QC Analyst for our manufacturing site in North Dublin. The QC Analyst is responsible for conducting raw material, in-process, finished product and stability testing in accordance with relevant SOPs and 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 require in-depth knowledge of scientific methods and techniques. The QC Analyst is responsible for the safe, compliant, and efficient execution of duties in a team environment. This position reports to the QC Supervisor.
Responsibilities
* 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 the 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 highlight any safety concerns to help drive the reduction of accidents or near misses.
* Participate in the on-site safety culture and 6S activities within the QC Laboratory.
* Contribute to departmental goals and programs such as Right First Time.
Qualifications
* A third-level qualification in Chemistry or related Science, preferably a Bachelor’s Degree.
* Demonstrate knowledge of cGMP requirements and practices including USP and FDA guidance documents related to pharmaceutical Quality Control Laboratory.
* Demonstrate knowledge of common analytical instrumentation (e.g., HPLC, Dissolution, GC, FTIR, Electrochemical methods, UV/Vis) and other USP instrumental and wet chemistry technologies used in pharmaceutical Quality Control Laboratory.
Employment details
* Employment type: Full-time
* Seniority level: Entry level
* Job function: Quality Assurance
* Industries: Pharmaceutical Manufacturing and Biotechnology Research
Equal Opportunity
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.
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