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Overview:
ProPharma Group is an industry leader providing validation, compliance and technical services to the pharmaceutical, biotechnology, medical device and related industries. We offer the excitement of a consistently evolving career. Our team is continually learning and working on new and exciting projects in a variety of regions. We look for people who excel in their technical area of expertise, believe in our values of Experience, Integrity and Commitment and thrive in the collaborative, rigorous and entrepreneurial spirit of the company culture.



o Competitive Rates o New Experiences o Evolving Career


ProPharma Group develops long-term relationships with clients across the country to which we provide a wide array of value-added services that complement and support their core business needs.



We are currently looking for Validation Consultants for our Southeastern Region!

Responsibilities:
A Validation Engineer at ProPharma Group will work with our Clients and be responsible for preparing and executing validation documents. Working knowledge of the principles of validation as associated with performance of work for the Pharmaceutical, Biotechnology and/or Medical Device industries. Demonstrate an understanding of GMP. Individuals must represent the company and division at client sites and interact confidently with clients, contractors, management and peers. Protocol development skills will include ability to develop Installation, Operational and simple performance qualification documents. Will work in one or more validation subjects; such as laboratory equipment, facilities utilities, process equipment, packaging equipment, cleaning, computers, HVAC or controls.

Qualifications:
Qualified candidates will possess a Bachelor’s degree in related field along with 5 plus years related industry experience.
Candidates must have excellent verbal communication and technical writing skills.
Experience in executing protocols including complex systems such as Process Validation, computer controlled systems validation, complex utilities, complex manufacturing equipment such as computer controlled filling systems, formulation systems and basic knowledge of laboratory validation (not required but preferred).
Familiarity with many aspects of validation is expected. Depth in one or several areas is critical.
Possess effective skills for developing, performing, evaluating, and/or troubleshooting PLCs and control systems (including SCADA, Delta V, and BMS systems) is a plus.
Experience in Process Qualification execution.
Ability to walk, stand and move about for long periods of time; work with equipment in the field including basic hand tools, lift and manipulate reasonable weights (approximately 35 lbs), ability to sit and type for long periods of time.
Proficient in Microsoft Word, Excel, Power Point and Project.
Ability to plan and manage own work.
Mut be willing to travel regionally and/or nationally throughout the US.
All Applicants must be legally eligible to work in the United States.



We are an equal opportunity employer. M/F/D/V

About ProPharma Group:

ProPharma Group is an industry leader providing validation, compliance and technical services to the pharmaceutical, biotechnology, medical device and related industries. We offer the excitement of a consistently evolving career. Our team is continually learning and working on new and exciting projects in a variety of regions. We look for people who excel in their technical area of expertise, believe in our values of Experience, Integrity and Commitment and thrive in the collaborative, rigorous and entrepreneurial spirit of the company culture.

ProPharma Group, a comprehensive compliance services company serving the pharmaceutical, biotechnology, and medical device industries, on May 13th announced its acquisition of PROSAR, a provider of pharmacovigilance and medical information services. This acquisition brings PROSAR together with international medical information service provider, PI ARM, a wholly-owned subsidiary of ProPharma Group.

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