Senior Engineer
Clitheroe, Lancashire, United Kingdom
Kindeva Drug Delivery
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 … 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 More ❯
Employment Type: Permanent
Salary: GBP Annual
Posted: