Description
Are you a Senior Validation Engineer looking for your next contract opportunity with a leading pharmaceutical company? The Pharma client needs a Senior Validation Engineer to perform equipment and cleaning validation on oral solid dose products, liquids, as well as OTC's.Description: 1 year long contract in New Jersey
- The Senior Validation Engineer will support validation master planning for process, packaging, equipment, computer systems, critical utilities, and equipment cleaning
- Execution, Authoring and/or Review of the above protocols and reports.
- Performs installation, operational, and performance qualification (IQ/OQ/PQ) of manufacturing and packaging equipment, facilities, and utility systems
- The Senior Validation Engineer will be responsible for newly installed equipment and systems, as well as previously qualified equipment and systems which are modified through change control
- Provide support for internal and external compliance and regulatory inspections including FDA, EMEA, and third party inspections to provide information for validated systems
- Writes deviations, CAPAs and change controls as needed to support the validated systems
- Assists Production in problem solving with regard to critical utilities, equipment, and equipment cleaning
- The Senior Validation Engineer will need to plan and manage own work as well as provide support to other validation engineers
- Promotes cGMP compliance within the workplace
- Incorporates cGMP and regulatory compliance into assigned project scope, design & construction work
Qualifications
- B.S. in Engineering, Chemistry, Biology, or Pharmaceutical Sciences with at least 5-8 years of relevant validation experience in the pharmaceutical industry.
- A combination of relevant experience and education will be considered
- Strong verbal and written communication skills; excellent organizational and time utilization skills
To find out more about Real please visit www.realstaffing.com