Job Description

Job objective

xe2x9cx93 Coordination of projects of a technical nature aimed at:

o Developing new products/processes from conception through to realisation.

o Modifying existing products to improve quality, fitness for use and generate cost savings.

xe2x9cx93 Execution of process and product in line with regulatory requirements and contributes to the Device Master Record (DMR) by compilation of product development and manufacturing documentation

xe2x9cx93 Equipment Qualification

xe2x9cx93 To establish product ageing regimes & analysing data generated from these stability trials

Main tasks / responsibilities

xe2x9cx93 Planning and co-ordination of trials is in accordance with business requirements.

o Production trials on new or existing products / packaging in the factories.

o Process or product validations on new or existing products / packaging in the factories

xe2x9cx93 Co-ordination of assigned projects in accordance with company policies/regulatory requirements

xe2x9cx93 Compilation and execution of qualification protocols and reports (SLIA, IQ/OQ).

xe2x9cx93 Execution of Performance Qualification

xe2x9cx93 Establishment/compilation of stability protocols/Report

xe2x9cx93 Creating of new versions R&D technical and manufacturing documents (DIOS, UOUP, DMR, IPRS, PMCC, etc,)

xe2x9cx93 Compiles cost estimates and feasibility studies of projects/products.

Performance indicators

xe2x9cx93 Accuracy of work (documentation, cost estimates)

xe2x9cx93 Meeting Project Deadlines.

xe2x9cx93 Displays the culture (care, commitment, courage, collaboration) of Essity.

Non-Negotiables

xe2x9cx93 A bachelor's degree Industrial/Process Engineering

xe2x9cx93 3-5 years working experience in a production environment preferably within a medical device/pharmaceutical environment.

xe2x9cx93 Proficiency in Microsoft packages, specifically MS Excel, MS Word, PowerPoint.

Remuneration for the role is between R35-45k basic salary p/m

Please email your CV to kendall@proppoint.co.za

Pro Talent