Execute and ensure intermediate complexity test work is completed as required, with minimal guidance.
Review and ensure job request, relevant MSDS and fully understand requirements is in accordance with laboratory SOPs, without guidance.
Review and ensure documents prepared appropriately using datasheets or laboratory notebooks, with minimal guidance. Review and ensure test apparatus are readily available and suitable, with minimal guidance.
Ensure and operate, understand and be able to troubleshoot all equipment/instrumentation necessary to support testing, with minimal guidance.
Execute test work is completed according to laboratory request requirements. Ensure raw data is recorded into laboratory notebook (or similar). Immediately notify laboratory management of any test delays, problems, or deviations.
Reqirements :
MSc in Biochemistry, Chemistry with 1-5 years of experience in the Pharmaceutical Industry.
Hands-on experience with Handling, maintaining, and trouble-shooting Balance, pH meter, UV and HPLC equipment’s.
Basic understanding of Analytical equipment validation.
Hands on Experience with handling, maintaining and troubleshooting ICP-MS, LCMS-QToF, GCMSMS.
Knowledge of Veeva QMS, Smartsheet & ValGenesis.
At Cytiva, we see a world where people's health is transformed by access to treatments that can change their lives. Our extensive portfolio, deep heritage, vast technical experience, first-rate service, and broad and deep portfolio support researchers and biopharma in advancing therapies at every step of the process, from discovery to delivery.
With the goal of accelerating and improving therapies as our compass, Cytiva has a sustainable plan to meet its impacts on people and the environment while expanding its business.