Job Description
Cpl is partnering with Pfizer to seek a QC Analyst - ICC team member for an 11-month fixed-term contract at their state-of-the-art site in Dublin, Grange Castle.
This is an on-site role that will involve developing and maintaining quality programs, processes, and procedures to ensure compliance with established standards and agency guidelines.
Your Key Responsibilities
* Perform analysis on QC samples (raw material, In-process tests, intermediates, and finished product) in line with Current Good Manufacturing Practices.
* 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.
* Participate in areas of Right First Time, Continuous Improvement, and 5S.
Qualifications
Must-Have Qualifications
* A third-level qualification in Science, Engineering, or equivalent.
* Some experience working in a QC Laboratory.
* Proven experience with analytical techniques including bioassay/potency testing, ELISA, blotting, flow cytometry assays, PCR, molecular biology techniques.
* Excellent interpersonal and communication skills.
* Detail-oriented, quick decision-making, self-motivated, with good trouble shooting and problem-solving abilities.
Nice-to-Have Qualifications
* Experience in quality control in a biotech, pharmaceutical, or bio-pharmaceutical manufacturing environment.
* Knowledge of computer applications, including MS Office, Excel, Softmax, Laboratory Information Management System (LIMS), and track wise.
* Mammalian cell culture experience.
* Aseptic techniques and sampling handling.
Additional Details
To be considered for this position, you must be legally eligible to work in Ireland. Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation.