About the Role
Cpl, in partnership with our Client Pfizer, are seeking a highly skilled QC Analyst - ICC to join their team at their state-of-the-art site in Dublin, Grange Castle, for a contingent 11-month fixed-term contract. This is an on-site role.
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, and seek opportunities, in the areas of Right First Time, Continuous Improvement and 5S.
Requirements:
* Third-level qualification in Science, Engineering or equivalent preferred though not essential.
* Some experience working in a QC Laboratory.
* Demonstrate 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 at decision-making, self-motivated with good trouble-shooting and problem-solving abilities.
Desirable 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 TrackWise.
* Mammalian cell culture experience.
* Aseptic techniques and sampling handling.