Company Description
GMP Healthcare Ltd is a consultancy service provider for the pharmaceutical, medical device, and food supplements industry. Our team of over 100 professionals offers support across all GxPs and provides expertise throughout the product life-cycle and manufacturing process. With a diverse range of specialists in various fields, we offer over 400 years of industry know-how to our clients.
Role and Responsibilities
As Validation Engineer you will be responsible for the following:
* Executing validation and qualification activities, authoring and reporting validation activities within the framework of cGMP – Annex 11 & 15 and in compliance with QMS requirements.
* Managing compliance to Business and Engineering Quality standards.
* Ensuring Engineering design meets safety standards for emissions.
* Validating support to project management team.
* Reviewing equipment maintenance history, investigation and audit support, process/component improvement project support, and reliability engineering support.
* Having a good working knowledge of Validation requirements for Equipment / Facilities / Utilities including associated control systems, and understanding EU GMP Annex 11, 21 CFR Part 11, GAMP 5 and associated computerized system validation within the pharmaceutical environment.
* Writing User Requirement Specifications, Design / Installation / Operational / Performance Qualification protocols and reports for validation and/or trial purposes.
* Translating local, corporate and regulatory requirements into validation requirements.
* Managing and coordinating Validation Engineering project activities between key stakeholders.
* Having a detailed understanding of GMP, quality assurance and documentation systems in a pharmaceutical environment.
* Possessing a broad knowledge of validation practices, standards and regulatory requirements/expectations i.e. Annex 11 & 15 and industrial guidelines such as GAMP.
* Providing validation engineering technical support related to the operation, maintenance, installation, start-up/commissioning, testing, and qualification of Lifesciences process equipment and related systems within a manufacturing facility.
* Developing Master Validation Plans and writing Validation Summary Reports.
* Understanding Change Control and Change Reporting as it pertains to validation.
* Providing input to process equipment design, development of start-up documents, commissioning plans, and execution of commissioning plans.
Knowledge, Training & Experience
* Bachelor’s degree in mechanical, electrical, or chemical engineering or related field, or equivalent experience.
* Comprehensive understanding of complex manufacturing processes.
* Working knowledge of Good Manufacturing Practice type systems and practices in a manufacturing environment.
* Ability to communicate and express ideas clearly across all levels of the organization.
* Skilled in Microsoft Office applications including Project, Word, and Excel.
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