Mechanical Engineer - Pharmaceutical

Details of the offer

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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