Full-Time Senior QC Analyst
Job Description
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
MINIMUM REQUIREMENTS:
Education:
• Minimum BSc in Science
Experience:
• Minimum 3 years’ experience in a similar role
• Must include role(s) within a QC setting
• Experience of LCMS/MS and GC desirable
• Experience with method validation/ method development
• Pharmaceutical drug/process development experience preferable
How to Apply
Please apply online via the career page at Senior QC Analyst (College Park, Dublin Ireland) (myworkdayjobs.com)103 total views, 0 today