Are you a chemistry or biochemistry graduate? Or do you have considerable experience working hands-on in the lab? Are HPLC, and UPLC common your work jargons? Use your expertise in chemical analysis, laboratory techniques, and data interpretation to make a real impact. Apply now and be a part of a giant cutting-edge pharma company.
Job Description:
As a QC Biochemical Analyst, you will mainly support the Qc team in the creation, examination, and validation of analytical techniques used for testing recombinant antibodies for veterinary use during production and upon completion. This position also requires interaction with outside contract testing providers.
Responsibilities:
- Conducting in-process, and final product testing, and examining the stability of drug substances and products.
- Assist in creating, enhancing, and validating analytical test methods, both internally or in partnership with external service providers.
- Perform tech transfer to other sites and vice versa.
- Create protocols, SOPs, and other documentation for analysis under GMP, including data tracking, handling Out of Spec events, and participating in lab investigations.
- Collaborate with the process development team to aid in creating a reliable production process and implementing it in the GMP facility.
- Collaborate with testing companies to maintain partnerships throughout the project.
- Perform raw material testing under GMP standards.
- Aid in identifying equipment needs and collaborating with vendors to complete all requirements, including equipment validation and qualification.
Requirements
- Minimum BSc in science (Chemistry or Biochemistry). Candidates with considerable lab experience will also be considered.
- Experience in the following techniques will be desired: HPLC, UPLC, CE-SDS, and IEF.
- Working under GMP conditions is a pre.
Terms:
- Contract: 12 months.
- Salary: Market conform.
- Working hours: Fulltime.
- Location: County Offaly
