Senior Engineer
Clitheroe, Lancashire, United Kingdom
Kindeva Drug Delivery
processes, including troubleshooting, and managing improvements. Developing documentation such as SOP's, validation protocols, reports and change controls. Compliance with industry regulations. Maintain the sites 10-year zero lost time accident safety record by actively engaging in a safety-first approach. Skills & Experience: 5+ years' experience working in a manufacturing industry or similar role. Educated to degree level or … equivalent in a Manufacturing, Chemical Engineering, Pharmaceutical Engineering, or related field. Experience of any of the following - GMP working environment, Validation, Project management, ISO 9001 and working within a QMS. Knowledge of lean manufacturing principles, Six Sigma, or other continuous improvement methodologies is a plus. Good understanding of the pharmaceutical industry standards and regulatory requirements (cGMP, FDA, EMA) is … an advantage. Experience in managing multiple projects at the same time. Computer literate, familiar with Microsoft Word and Excel Key Capabilities: Good organisational, interpersonal, and time management skills. Enthusiastic, flexible, conscientious and proactive in approach. Take a positive approach to own training and development. Good decision-making and problem-solving skills. Strong verbal and numerical aptitude skills. Strong More ❯
Employment Type: Permanent
Salary: GBP Annual
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