{"id":38253,"date":"2017-11-21T14:13:39","date_gmt":"2017-11-21T12:13:39","guid":{"rendered":"https:\/\/joblistsouthafrica.com\/?p=38253"},"modified":"2017-11-21T14:13:39","modified_gmt":"2017-11-21T12:13:39","slug":"laboratory-trainee-gsk-2017","status":"publish","type":"post","link":"https:\/\/joblistsouthafrica.com\/laboratory-trainee-gsk-2017.html","title":{"rendered":"Laboratory trainee at GSK 2017"},"content":{"rendered":"
GSK is a science-led global healthcare company on a mission to improve the lives of people all over the world. We have\u00a0career opportunities<\/span>\u00a0at all levels of seniority across the business globally.<\/p>\n Basic\u00a0qualifications<\/span>:\u00a0<\/b><\/p>\n Job Purpose:\u00a0<\/b><\/p>\n Key Performance Area<\/b> 2. Compliance GLP & QMS<\/b> 3.EHS\u00a0<\/b> 4. Operational Excellence<\/b>\n
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\n1. Compliance – Analysis:
\nAnalyses products and materials to ensure compliance to registered\u00a0specifications<\/span>.
\n1.1\u00a0Tests<\/span>\u00a0compliance of products (including routine Stability products) and materials as per documented\u00a0Specifications\u00a0and Analytical Methods.
\n1.2 Analyses a large range of product types \u2013 tablets, capsules, COLs, suppositories and powder formulations.
\n1.3 Performs analysis using wet chemical techniques and instrumental methods of analysis (HPLC, GC) as applicable.
\n1.4 Ensures that applicable SOPs are followed and required records are completed.
\n1.5 Examines samples critically.
\n1.6 Records results as per GLP requirements.
\n1.7 Reviews results for accuracy and reports any anomalies to Supervisor or Manager.
\n1.8 Implements OOS procedure where necessary.
\n1.9 Performs `peer review\u2019 of analytical raw data as required by Manager.
\n1.10 Samples and test compliance of Site systems (Purified water, gasses, steam, etc.) as per documented procedures.<\/p>\n
\nComplies with the requirements of Good Laboratory Practice and the requirements of the applicable GSK QMS Policies..
\n2.1 Ensures cleanliness of working and surrounding area.
\n2.2 Ensures that documentation is performed in the demarcated areas and that chemical analysis is performed on the workbenches.
\n2.3 Ensures that documentation (specifications, etc.) is protected form damage by chemical, water, etc.
\n2.4 Ensures preparation and storage of reagents as per SOPs.
\n2.5 Ensures that chemicals and supplies are ordered timeously.
\n2.6 Ensures that SOPs in use are current and notifies the Manager of any out-of-date procedures.
\n2.7 Prepares SOPs as required by the Manager.
\n2.8 Verifies the calibration status of equipment as required by the Manager.
\n2.9 Performs maintenance of equipment as required by the Manager.
\n2.10 Completes appropriate equipment logs after usage,\u00a0verification<\/span>\u00a0and maintenance.
\n2.11 Assists with the validation of equipment as required by the Manager.
\n2.12 Performs system monitoring (eg. Fridge temperatures, fume cupboard pressures) and completion of appropriate logs as required by the Manager.
\n2.13 Performs area inspections (self-inspections, 6S, EHS) as required by the Manager.
\n2.14 Ensures that laboratory waste is timeously removed as required by Manager.<\/p>\n
\n3.1 Comply with EHS standards and\u00a0guidelines<\/span>\u00a0and Site EHS SOPs.
\n3.2 Complies with SOPs wrt safe use of chemicals\/reagents, glassware, analytical procedures and the use of PPE.<\/p>\n
\nPartakes in continuous improvement activities to reduce costs, increase productivity and improve quality. 4.1 Participates in, projects to continually improve processes \u2013 LeanLab, OE and Lean sigma methodology.
\n4.2 Participates in Manufacturing Technology projects e.g.NIR.
\n4.3 Assists with the delivery of the financial OE benefits.
\n4.4 Participates in \u201cvisual factory\u201d, incorporating 6S.<\/p>\n