Cache of job #14122701

Job Title

Process Development Engineer

Employer

CPL

Location

WESTMEATH

Description

An exciting opportunity has just come up for a Process Development Engineer with an exciting start-up company. The company currently has operations in Dublin West area, but because of demand, they are scaling up their operations and moving to the midlands. This is a fantastic opportunity to become a part of fast-growing start-up company. The Job. Reporting to the R&D Team Leader and Manufacturing Manager, this role is based in supporting the manufacture and supply of medical-grade bioresorbable polymer products for the pharmaceutical and medical devices market place. JOB RESPONSIBILITIES. General Product manufacture and supply. o Manufacture and operational activities within a cleanroom environment including product production, processing, packaging, labelling and cleaning etc. o Quality compliance requirements (testing, record generation. o Reporting to manufacture and quality dept. management as required. o Interacting with other sectors within the company including EHS, risk assessments, additional quality compliance tasks as required. o Interact with suppliers for stock management, co-ordinating deliveries and storage of materials. Interact on a day-to-day basis with manufacturing manager to produce products within a cGMP, ISO 13485 cleanroom environment. General upkeep of facilities. o Cleaning. o Maintenance of equipment. o Calibration co-ordination. Working within the R&D team on product and process developments including overlap in design and development activities, documentation and quality management. Overlapping with teams on design and development of innovative products, including concept development, high-level design feasibility, prototype development, detailed design, test method development, design verification/validation, shelf-life determination and product commercialisation. JOB REQUIREMENTS. An honours Bachelors Degree or related in engineering/science. Chemical Engineering degree is advantageous. Previous qualification/experience relating to quality compliance would be an advantage. Hands-on approach to general working demands. Logical problem-solving approach to challenges. Computer literacy is essential for MS Office programs. Skills with other computer programs may be an advantage. Experience with controlled quality environments would be an advantage. Understanding of medical requirements for products. Strong initiative and follow through in executing responsibilities, overcoming obstacles and balancing multiple priorities effectively. Ability to effectively communicate concepts, ideas and knowledge to all relevant stakeholders. Works well as part of team. Driving license would be an advantage though not essential.

Date Added

1331 days ago

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