Analytical Scientist - Contract - Life Sciences - County Meath This is a fantastic opportunity to be part of a fast-paced, €400 million project; with lots of opportunities to work with and learn about cutting-edge technologies, in addition to developing your own skills.
This is a truly exciting project, which when complete will contribute to the manufacturing of a life-changing treatment.
Responsibilities:
Execution of analytical method validations and transfers and write technical protocols and report Execution of analytical testing of drug substance release, stability and characterization for biologics under GMP/GDP Support equipment maintenance, calibration and qualification work Preparation of analytical methods, SOPs and other documents as required Other analytical activities in consultation with the Supervisor Works in accordance with applicable internal company regulations: safety, health and environmental protection.
Train new analysts Requirements:
Experience with analytical testing with Ultrahigh Pressure Liquid Chromatography (UPLC)/High Performance Liquid Chromatography (HPLC), Capillary Electrophoresis, or other large molecule characterization technique Strong oral and written communication skills Ability to work in a team environment with cross-functional interactions is essential GMP working experience Perform supporting activities for general lab operations, training, new product introduction, method verifications and method transfers.
Execution and review of analytical method validations and transfers (among different sites, and between the company and CROs) Execution and review of analytical testing of drug substance release, stability, method qualification, incoming goods, ID testing, and characterization for biologics under GMP/GDP.
Cross-train Scientists within the department for new and existing technologies.
Ability to organise and establish testing schedules and adhere to deadlines.
Support equipment maintenance, calibration and qualification work Perform periodic review of instrument systems Generate instrument data in support of SDLC Validation.
Initiate, review, and support deviations, CAPAs, and risk assessments, and change records as required.
Preparation of analytical methods, SOPs and other documents as required.
If this role interests you, apply today
Seniority level Entry level
Employment type Contract
Job function Research, Analyst, and Information Technology
Industries Staffing and Recruiting
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