QC Analyst - ICC
Cpl Group View all jobs
- Dublin
- Contract
- Full-time
- 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.
- Third level Qualification in Science, Engineering or equivalent is 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, and a proficiency in cell culture.
- Excellent interpersonal and communication skills.
- Detail oriented, quick at decision making, self-motivated with good trouble shooting and problem-solving abilities.
- 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
- To be considered for this position you need to be legally eligible to work in Ireland.
- Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
- Due to high volume of applications, we will be contacting successful candidates only.
- We do not offer relocation.