Job Title: QC Analyst in Chemistry
We are seeking a highly skilled and dedicated Quality Control (QC) Analyst to join our team at Pfizer's state-of-the-art site in Dublin, Grange Castle.
About the Role:
You will be a member of Pfizer's quality control team, responsible for developing and maintaining quality programs, processes, and procedures that ensure compliance with established standards and agency guidelines. Your expertise will help us identify and mitigate quality risks, ensuring we are prepared for audits and inspections.
You will be recognized as a subject matter expert, adapting standard methods and procedures to meet specific work situations. You will also train others and reinforce behaviors that support our mission to provide the best to patients.
Your Key Responsibilities:
* Perform analysis of quality control samples, including raw materials, in-process, intermediates, stability, and finished products, in line with Current Good Manufacturing Practices (GxP).
* Write up and execute Analytical Method Transfer Exercises for products being transferred to the Grange Castle site, ensuring compliance with site, Pfizer Quality Standards (PQS), International Conference on Harmonization guidance, and Filing requirements.
* Adhere to good laboratory practices and housekeeping standards.
* Assist in the generation and maintenance of Quality procedures and reports.
* Facilitate laboratory investigations and support associated product investigation.
* Analyze both wet chemistry and the use of analytical equipment, including UV, HPLC, FTIR, KF, iCE, ICP, CE, and compendial assays.
* Participate in and seek opportunities for Right First Time, Continuous Improvement, and unburdening activities to facilitate Lean/Agile implementation.
Requirements:
* Third-level qualification in Science, Engineering, or equivalent preferred.
* Strong knowledge of analytical techniques, both theoretical and practical.
* Excellent interpersonal and communication skills.
* Detail-oriented, quick at decision making, self-motivated with good troubleshooting 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.
* Knowledge of computer applications, including MS Office, Excel, Laboratory Information Management System Access, and Track wise.
This job description indicates the general nature and level of work expected of the incumbent. The incumbent may be asked to perform other duties as required.
Candidates who complete the recruitment process and are selected as successful will be offered roles in specific teams within the Chemistry space as QC Analyst depending on their skills, experience, and current vacancy requirements.