Mechanical Engineer - Pharmaceutical - South Africa
QUALIFICATIONS NEEDED Eng, B.Sc. or BTech degree in Electrical/Mechatronic/Electronic Engineering or equivalent NECESSARY EXPERIENCE & INDUSTRY ACCREDITATION / KNOWLEDGE Min 2 years’ experience within industry, specifically FMCG, dairy, pharmaceutical etc. Sound technical ability and hands on approach Demonstrated technical problem solving and continuous improvement KEY DUTIES & RESPONSIBILITIES OF THE ROLE Responsible for the production equipment and line availability for formulation, fill and finish Establish world class best practice and implement changes to achieve these in the above-mentioned areas Responsible for scoping and execution of engineering projects Responsible for the management of equipment availability to the site Provide guidance and support for commissioning and operational qualification / re-qualification of equipment / system Responsible for environmental and safety aspects within these functions Responsible for maintenance of inventories at optimum level (availability of spare parts and operating supplies) Continually strive to deliver solutions through teamwork that ensures continuous improvement through innovative solutions Achieving / maintaining of the facilities and processes in full compliance with the current regulations and guidelines - both local and international Participating in project teams and supporting other relevant organizational departments Relationship building ability Production support for electrical modules, including electrical wiring harnesses and electronic components: ensuring correct components are loaded to each order and resolving issues that may arise during production Validation updates to electrical modules Maintaining components and BOMs assigned to within the electrical team Interface with the Electronic vehicle control system Support the Engineering Manager in all phases of evolution and customization of products (including design, qualification, industrialisation, and engineering support during production) Support the Production in the development and/or updating of verification plans, test procedures and test environments related to the evolution and customization of products Participating in project teams and supporting other relevant organizational departments Ensures compliance in accordance with (Medicines and Related Substances Act 101 of 1965, Pharmacy Act 53 of 1974) and the organizations policies, procedures, and other applicable laws Continuously build and support a sound quality assurance culture aligned to cGMP within the company
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