- Primary responsibility is the preparation of validation protocols (IQ/OQ) and commissioning documents for our clients specilaist equipment and control systems. You will with the companies control system programmers to develop and execute factory acceptance software test documents.
- Interface with equipment manufacturing companies and internal departments to obtain the equipment, controls, and installation support documents necessary for protocol development. You will also specify, obtain, and maintain hardware and software necessary to perform in-house and on-site validation testing.
- As the Validation Engineer you will field execution / testing of approved validation protocols (IQ/OQ) and commissioning documents. This will include (but is not limited to) I/O forcing, alarm testing, sequence testing, PLC diagnostics, and PID loop performance testing.
- Coordinate the efforts of the personnel involved during on-site qualification. This would include the various engineering disciplines from within our client and/or personnel from their equipment manufacturing companies.
- Relevant degree in a engineering discipline with proven experience working in the Pharmaceutical sector as a validation engineer. You need to also hold a valid drivers license as 25%-35% of your time will spent travelling to customer sites to perform key validation activities.
- Proven industry experience in develop validation protocols (IQ and OQ), validation reports, and factory acceptance test documents.
- A working knowledge and practical experience with reading and interpreting electric and pneumatic controls, technical design documents, and PLC code is required as well as an understanding of computer system validation including knowledge of GAMP 5 and CFR 21 Part 11.
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Validation Engineer - Trenton, United States - Hyper Recruitment Solutions Ltd
Description
Job Reference:
J5638077
Status:
Under Offer
Updated:
25/08/2023
We are currently looking for a Validation Engineer to join a leading Pharmaceutical CDMO company based in the New Jersey area.
As the Validation Engineer you will be responsible for a range of activities with opportunities of career development and skill advancement.
Key Duties and ResponsibilitiesYour duties as the Validation Engineer will be varied however the key duties and responsibilities are as follows:
To be successful in your application to this exciting opportunity as the Validation Engineer we are looking to identify the following on your profile and past history:
Key Words:
Pharmaceutical Validation / New Jersey / Validation Engineer / Systems Validation / IQ / OQ / Validation Reporting / Pharmaceutical Engineer
Interested in this job?
Apply for this position now
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for our talent development.
We welcome applications for any applicant who fulfil the role requirements for this position.HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment processionals and scientists.
We look forward to helping you with your next career moves.Sectors:
Pharmaceutical,
Contract Manufacturing Organisation,
Engineering
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