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CQV Engineer
5 months ago
Summary
The successful candidate will primarily be responsible for validating existing manufacturing equipment and processes as the company prepares to begin clinical development. In addition, he/she will plan and implement continuous improvement initiatives, ensure design for manufacturability, and introduce and validate next-generation manufacturing operations. It is also expected that the incumbent will provide engineering support to other groups, including R&D and manufacturing, as required.
Key Responsibilities
- Draft and implement Quality System documentation designed to establish good validation practices within the organization.
- Author URS, IQ, OQ and PQ protocols and execute them in compliance with GDP guidelines and internal quality standards.
- Design validation approaches, supported by appropriate statistical analyses, perform and/or coordinate all validation activities, analyze and assemble results, and draft validation reports.
- Provide input on user and/or functional requirements of current and future processing equipment, and draft appropriate documentation. Additionally, interface with Contract Manufacturers to ensure all relevant user and functional requirements are met.
- Provide support to non-engineering Staff, including those from R&D and Manufacturing, to ensure successful technology transfer and continuous improvement.
- Execute assigned duties on time and pro-actively telegraph delays and other issues to validation manager and other relevant stakeholders.
- Comply with all regulatory, corporate, and Quality System policies
Skills & Qualifications
- B.S. / M.S. in engineering or another relevant discipline.
- Minimum of 5+ years of experience working within a Biotech/Pharma environment or other FDA-regulated environments.
- Experience with device-biologic combination products is highly desirable.
- Experience in the areas of Design Documentation (URS, FRS, DS, and other engineering specifications), Validation (IQ, OQ, PQ, PV, CSV, MVP, etc.), Quality Systems (Change Control, Non-Conformances, Requalification, etc)
- Understanding of c.G.x.P principles and familiarization with ISO 13485, ISO 14971, and 21C.F.R.820
- Working knowledge of Computer Systems Validation lifecycle and documentation.
- Proficient in Microsoft Word, Excel, PowerPoint.
- Must be able to work independently with adequate supervision, multi-task, and support several projects simultaneously.
- Must demonstrate strong communication, interpersonal and teamwork skills.
- A strong understanding of technical writing and presentation skills is required.
The Company
Arcadis DPS Group is a global EPCM firm offering full-service solutions within the Life Sciences (pharmaceutical, biotechnology, and medical technology) and Advanced Technology (semiconductor, data center, and solar) industries. DPS is dedicated to delivering successful projects with a ‘client-first’ mentality and personal touch across a range of market sectors: Project and Program Management, Procurement, Design, Construction Management, Health and Safety Management, Commissioning, Qualification, and Start-up.
Arcadis DPS Group Global is an Equal Opportunity Employer and employment selection decisions are based on merit, qualifications, and abilities. DPS does not discriminate in employment opportunities or practices on the basis of: race, color, religion, gender, national origin, age, sexual orientation, gender identity, disability, veteran status or any other characteristic protected by country, regional or local law.
