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Groomfield Recruitment
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Loughborough, Leicestershire
Manufacturing Analyst
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Salary: £12 per hour |
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Overview
Manufacturing Analyst - Loughborough – 12 Months plus FTC - £12ph Groomfield Recruitment are looking for a Manufacturing Analyst to work for our client in the Loughborough area. This is a fantastic opportunity to work within a well-known company that can add to future skills and development. Responsibilities: The successful person will be supporting Manufacturing Technology group in technical document authoring. This will include updating product specifications, Manufacturing batch records, Product Quality Reports and other relevant documents. Supporting supply chain and wider MT group. There are 2 main parts of the role • PQR report writing – this is writing a technical report that requires stats analysis and coordinating multiple groups to input there data into the report. • Document updates – maintaining the documents that instruct the manufacturing process, updating these to ensure they meet the correct standard required Actively raise and support the resolution of APR's, NM and MI's Complete Risk Assessments as required. Coach other team members in the appropriate standards. Effective Root Cause analysis for unplanned deviations using appropriate methodologies and site systems. Maintain training record and LSO. Complete all required training on time. Able to work positively as part of a team and communicate effectively with group and peers. Able to effectively utilise written, electronic, verbal and other communication channels. Able to vary communication styles according to the needs of others. Able to coach other group members in effective communications. The successful Manufacturing Analyst must have: Educated to degree level or equivalent experience in a relevant science/engineering discipline is desirable Must come from a similar background Excellent Excel and Word knowledge Exceptional attention to detail Experience of working within a Pharma, Aerospace OR Food environment is desired. Ideally have worked with GLP, GMP, or ISO accredited organisation Controlled documentation writing and change control process Continuous Improvement techniques including Lean Manufacturing/Six Sigma concepts Experience in GMP within a contract manufacturing environment of the Drug Product industry Familiarity with Drug Product Quality Systems and GMPs for EU, US and ROW, Eudralex/Orange Guide Please submit a copy of your most recent CV to the email address to be considered for the position.