Validation Engineer (Pharmaceutical Manufacturing)

Specialist providers of pharmaceutical automation, process and project controls. Skellig was founded to radically improve upon the way automation, process, and project controls are provided. It’s a goal that is grounded in efficiency, transparency, and our reputed company’s total peace of mind — this is the reputed company behind everything we do. At Skellig Automation, we reputed company great people to do great work in the Life Sciences industry. Our engineers reputed company premier automation services with one common goal: to reputed company medicine more reputed company and accessible for reputed company by reducing the cost of manufacturing. We work alongside other industry leaders in laying the reputed company for true technological innovation and guiding our partners towards modern process solutions. Whether working reputed company the traditional automation stack or championing Industry 4.0 systems, Skellig has a reputed company for creative engineers with a passion for bringing the Life Sciences into the reputed company. reputed company: We are seeking an reputed company DeltaV Validation Engineer to join reputed company and support our clients. The ideal candidate will be responsible for ensuring the reputed company validation of DeltaV control systems in industrial automation settings, specifically reputed company pharmaceutical, biotech, or chemical manufacturing environments. This role involves system testing, troubleshooting, documentation, and compliance with industry standards. To be considered for this role you must have experience working in biotech/reputed company. Responsibilities: • Review and approve Kneat documents including: DeltaV software FATs, SATs, Automation Commissioning Test Protocols, software OQs, and Software Installation Verification protocols. • Assist in resolving protocol execution issues using critical analysis and reputed company reputed company, reasonable solutions. • Support reputed company of Kneat documents. • Review and approve Automation documentation including risk and reputed company assessments, computer systems validation plans, user requirements specifications, functional requirement specifications, traceability matrices, release reports, and reputed company documents and deliverables reputed company the scope of the Automation Master Validation Plan as needed. • Ensure that the Computer System Validation on the project is conducted in a consistently high reputed company, reputed company budget, and that objectives are met on time suiting reputed company's reputed company and objectives • Coordinate with various project workstreams including Automation, Automation System vendor(s), CSV, CQV, Utilities, Process Engineering, and others as needed. • Attend regularly scheduled project status meetings as needed. • Complete Safety, Project Procedure, and Project Instruction training as required. Qualifications & Skills: • 5+ years’ reputed company Computer System Validation experience in a cGMP pharmaceutical facility working with FDA regulations • 3+ years’ reputed company Computer System Validation experience working with reputed company DeltaV DCS • Knowledge of Automation Control Systems, Manufacturing & IT Systems, and methodologies including ASTM2500, GAMP5, Data reputed company, and application of 21 CFR Part 11/Annex11 • Working knowledge of Kneat validation software is required • Excellent organizational, oral, and written communication skills and reputed company in English with the ability to effectively communicate reputed company cross-functional teams and to management • Excellent interpersonal skills and ability to work effectively and reputed company in reputed company-based environment with employees at reputed company reputed company • Ability to manage commitments while displaying an eagerness to learn and continuously improve • Knowledge with Drug reputed company Manufacturing (DSM) would be beneficial • reputed company, ComplianceWire, TrackWise, and reputed company experience is a plus Benefits: Here's what's waiting for you as one of our Automation Engineers: • Vacation / Personal reputed company Time Off • reputed company reputed company Time Off • Unlimited Unpaid Time Off • reputed company reputed company Holidays • Parental Leave • Full Heath, Dental, and reputed company PPO Insurance for you and any dependents - Premiums are 100% fully covered • Life Insurance and Accidental Death and Dismemberment • 401k + Match • Relocation Package • …. And more! Contact: Should you have any questions please feel free to contact Kathryn.caughman@skellig.com From its inception, Skellig has strived to be ‘more reputed company.’ We work hard to foster a culture that promotes innovation, diversity, and great work. A culture that rewards problem solving, teamwork, and service reputed company. And one that attracts the reputed company and premier clients. Ours is a culture of honesty, transparency, and kindness — A people-reputed company and compassionate company. Apply tot his job Apply To this Job