Job Title:
QC Analyst in Chemistry Division
About the Role:
In partnership with Pfizer, we are seeking a highly skilled QC Analyst to join our team at their state-of-the-art site in Dublin, Grange Castle.
Key Responsibilities:
* Develop and maintain quality programs, processes, and procedures that ensure compliance with established standards and agency guidelines.
* Contribute to quality risk management, commitment tracking, policy interpretation, site complaints management, and process analysis oversight.
* Ensure quality assurance programs and policies are maintained and modified regularly.
* Adapt standard methods and procedures by applying knowledge, prior work experience, and requirements.
* Train others and reinforce behaviors that contribute to achieving company goals.
Activities:
* Perform analysis of quality control samples, including raw materials, in-process, intermediates, stability, and finished products, in line with Current Good Manufacturing Practices (CGMP).
* Write up and execute analytical method transfer exercises for products being transferred to the Grange Castle site.
* Adhere to good laboratory practices and housekeeping standards.
* Assist in generating and maintaining quality procedures and reports.
* Facilitate laboratory investigations and support associated product investigations.
* Analyze wet chemistry and use analytical equipment, including UV, HPLC, FTIR, KF, iCE, ICP, CE, and compendial assays.
* Participate in Right First Time, Continuous Improvement, and unburdening activities to facilitate Lean/Agile implementation.
Qualifications:
* Third-level qualification in Science, Engineering, or equivalent is preferred though not essential.
* Strong knowledge of analytical techniques, both theoretical and practical.
* Excellent interpersonal and communication skills.
* Detail-oriented, quick decision-making, self-motivated, and good trouble-shooting and problem-solving abilities.
Nice-to-Have:
* Experience in quality control in a biotech, pharmaceutical, or bio-pharmaceutical manufacturing environment.
* Some experience working in a QC Laboratory or production environment is preferred but not essential.
* Knowledge of computer applications, including MS Office, Excel, Laboratory Information Management System Access, and TrackWise.