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An established industry player is seeking a skilled Automation Engineer to join their team in Durham, NC. This role involves overseeing the design and configuration of the DeltaV platform, ensuring compliance with industry standards, and providing technical leadership to a team of system integrators. The ideal candidate will have extensive experience in Biopharma engineering, particularly with DeltaV control systems, and will play a crucial role in maintaining high-quality standards and effective communication across teams. This position offers a unique opportunity to contribute to impactful projects in a dynamic and supportive environment.
Job Description
PharmEng Technology is a global ISO certified Pharmaceutical Compliance Consulting Firm with projects around the world providing quality services to the manufacturers of pharmaceutical and health care products for over 25 years.
Our 300+ global consultants have expertise in Commissioning & Qualification, Validation, Quality Systems, Engineering, Medical Devices, Modular Cleanrooms, Thermal Mapping, Training, Toxicology and Regulatory Affairs.
PharmEng Technology is a cGMP compliant leader with international offices in Canada, Spain, France, Germany, Austria, Switzerland, Italy, Belgium, Singapore, Malaysia, Indonesia, Taiwan, Ireland, Denmark, Brazil and USA and maintains strategic partnerships for extended capabilities internationally.
PharmEng Technologies is seeking a full-time experienced Automation Engineer in Durham, NC.
The Automation Hardware Engineer will oversee the system integrator design, construction, and configuration of the DeltaV platform. This includes but is not limited to:
The specifications and testing are being executed by a System Integrator (SI), and this role is to provide technical oversight of the SI, review and approve documents the SI produces, and in general represent the client’s interests.
The platform engineer is also responsible for establishing standard work practices with the SI, such as configuration management practices, and testing practices, and will have responsibility for reviewing, evaluating, and impact assessments of changes.
Responsibilities
Qualifications