Cache of job #13701738

Job Title

Validation Specialist

Employer

Lotusworks

Location

Mayo, Galway

Description

About Us. A valued and trusted partner to the world’s leading companies. We are committed to service excellence through our talented people who are empowered to be innovative and best in class. Location. Galway is a City and County which caters for everyone. Even though Galway City is one of the fastest growing cities it still retains that friendly feeling! With Culture, Dining, Socialising, Sport, Leisure and a state of the art University and College, there is a fantastic lifestyle on offer if you are relocating. If you already live in Galway, well then lucky you! Join us and work with us to deliver the excellent service we are renowned for with our clients. Be part of something great. Job Purpose. Working with the LotusWorks team as a Validation Specialist you will provide support for the technical/validation documentation activities in engineering ensuring that all compliance issues and requirements of the company’s Validation/Quality Policies and Procedures are addressed. Your Responsibilities: Perform technical writing, research, and related editing functions to prepare documents, test plans, user cases, project manuals, business proposals, reports, briefings, presentations, guidelines, and other written materials. Experience developing User Requirement Specification (URS) for specialist equipment. Responsible for writing,executing and reporting validation documentation (FAT/FRS/DS/IQ/ OQ ) Co-ordinated and participatedwithin development, review and approval of software, equipment and process validations (FAT/URS/DS/IQ/OQ/PQ. Expertise in the use of Microsoft Word, Excel and Power Point. Establishes and manages engagement objectives, expectations, and quality plan. Works independently and/or within team to accomplish job objectives. Establishes and follows priorities. Demonstrates effective and active listening. Inspiring trust, credibility and confidence. Suggest and sometimes may implement innovation and continuous improvement within the technical/validation writing process. Ensure accuracy and consistency of the technical/validation documentation. Ensure all quality/validation documents are authorised and appropriate compliance approval is gained. Requirements: The successful candidate will be qualified in an appropriate discipline (e.g. Engineering, Information Systems, or Life Science with additional IT qualification) with a broad technical/educational skills base with at least 4 years’ experience in a similar role. Understanding of GMP, Compliance, Validation Practices including the system development life cycle and Regulatory expectations. Experience working in a regulated environment would be an advantage. Excellent verbal and written communication skills. Excellent customer service, interpersonal and team collaboration skills are essential. Benefits. Life Assurance. Pension Contribution. Training & Educational Assistance (Engineers Ireland CPD Members. Healthcare Contribution. Annual GP Check-Up. Extra Annual Leave. Healthcare Screening. Not ready to apply, or have some questions? Call our Talent Specialist’s on 07191-69783 or Email jobs@lotusworks.com and we will be happy to help! LotusWorks is proud to be listed in the Best workplaces 2017. Empowering talent we care about for over 27 years. LotusWorks is an Equal Opportunity Employer. This job originally appeared on RecruitIreland.com.

Date Added

2558 days ago

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