QC Analyst

Job Description

An experienced QC analyst is required for a global pharmaceutical company based in North Dublin. This is a fantastic opportunity to gain significant Validation, Development and Transfer experience.

The main areas of responsibility of this role are as follows:

• Testing of routine release of raw materials, intermediates, finished product and stability as requested
• Draft and review documentation - SOPs, protocols, training modules, investigations, reports and QMS documents
• Actively participate in analytical method transfers and method validations as required
• Conduct and document out-of-specification/out-of-trend result investigations
• Responsible for the day to day running of the QC laboratory
• Experience with wet chemistry, GC, HPLC and a willingness to learn new analytical techniques as the laboratory evolves
• Work within the test schedule for the facility and the stability programmes
• Day to day activities required for running of the laboratory

Skills/Competencies:

• Self-starter with strong work ethic
• Good interpersonal skills are required, as is the ability to communicate well, both verbally and written.
• Must be able to function effectively in a teamwork environment
• Ability to identify, execute and prioritize work tasks/projects and know when to escalate
• Excellent problem-solving, decision-making and communication skills
• Good computer skills, including proficiency with business and technical software (Word, Access, Excel, PowerPoint, SAP, Empower)
• Ability to plan, organize, and prioritize effectively
• Good technical and compliance-based writing skills
• High levels of integrity and trustworthiness

Requirements

• Minimum BSc in Science
• Minimum 3 years' experience in a similar role
• Experience of LCMS/MS and GC preferred
• Experience with method validation/ method development desirable
• Pharmaceutical drug/process development experience desirable

Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative.

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