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| Firma: |
The Barron/Carlington Group |
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| Job-Titel: |
Principal Engineer/Validation |
| Job Kategorie: |
Pharma/Biotech |
| Arbeitsort: |
Rochester - NY New York - USA Vereinigte Staaten |
| Ref.-Nummer für Ihre Einträge: |
4466 |
| Stellen-Beschreibung: |
4466 - Principal Engineer - Validation Location: Rochester, Ny
This is a Retained Executive Search, our client is a Major health products organization with the oldest, best known and most respected healthcare brands in the world. We are searching for a Principal Engineer – Validation If you are interest please forward your resume and I will respond back Asap.
Position Details
Salary Range: $84K - 105K w/15% bonus
US Citizen or Permanent Resident [Green Card Holder] only
Best Industry- Healthcare
Department : Quality Assurance , Research & Development
4 Year Degree
5-10 years exp
Up to 10% Travel
Relocation allowance of one (1) month’s salary.
Individual will be responsible for leading validation activities to the Process Development Department, a R&D aseptic processing facility, in support of FDA compliance. Activities include: preparation and execution of validation strategies, FAT, IQ, OQ, PQ & PV validation protocols, and reports for equipment and processes. You will be responsible for the design, preparing specifications, design review, installation and startup of new equipment, design changes and modifications to existing equipment and utilities that support the equipment for aseptic processing in Process Development.
Job Duties:
Prepare IQ, OQ, PQ & PV validation protocols and final reports for Process Development. Provide guidance for troubleshooting during validation activities as warranted, and review and analyze data generated during a validation.
Coordinate validation and revalidation activities on a routine basis per Process Development schedule for maintaining equipment & processes in a validated state.
Assist in the selection of appropriate vendors for Process Development equipment purchase and modifications.
Prepare plans, timing estimate, scope of work and bid documents as necessary for equipment purchase/modifications and utilities installation for the Process Development organization with internal maintenance facilities and/or external contractors. Work with selected vendors and affected parties to schedule work for minimum business impact.
Provide cleaning and sterilization validation strategies for Process Development.
Maintain an annual validation strategy and a validation archive for Process Development.
Act as an engineering technical resource for equipment trouble-shooting and problem-solving as necessary to maintain schedules in the Process Development department.
Candidate Must Have:
Bachelor’s degree, preferably in Engineering or Microbiology
Minimum of 8 years experience in an engineering or equivalent position in a pharmaceutical or medical device manufacturing or research environment
Experience with Purified Water Systems, Clean Steam Systems, Autoclave, Cleanrooms, HVAC Systems and aseptic processing are highly desirable
Knowledge of cGMPs for medical devices and pharmaceutical
Good interpersonal, organizational, communication and execution skills |
Sprachkenntnisse: |
Englisch-Sehr Gut |
| Beschäftigungsart: |
Vollzeit |
| Jahresgehalt: |
95000 USD |
| Eintragsdatum: |
2008-07-22 |
| Grad der Ausbildung: |
Studium |
| Ihre Erfahrung in Jahren: |
5 to 7 Years |
| Firma: |
The Barron/Carlington Group |
| Kontakt-Name: |
The Barron/Carlington Group |
| Kontakt-Telefon: |
2126431111 |
| Bevorzugte Kontaktmethode: |
E-mail |
| Preferred Language of Resume/Application: |
English |
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