PharmEng Technology has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure that our clients can keep on providing the world with their cost-effective and high-standard healthcare products.

At PharmEng Technology, we strive to cultivate the best working environment where empowerment, passion and perseverance are nurtured while serving our clients to achieve their unique business goals. We are seeking an experienced Automation Instrument Specialist with general manufacturing equipment in Holly Springs, NC.

Objectives of the role:

• Support Manufacturing SME and Tech Transfer engineering for production methods creation and equipment support.
• Provide on the floor operational support as needed.
• Review/revision of Manufacturing related, SOP’s, Batch Records, and work instructions, because of CAPA, equipment/process changes, error prevention activities, etc.
• Support the design and qualification of improvements, changes, or upgrades to this equipment as needed.
• Support the startup of equipment and commissioning plans, User Requirement Specification (URS), Functional Requirement Specification (FRS), Configuration Specification (CS)
• Support the execution of commissioning and qualification activities.
• Automation programming and configuration for corrective and continuous improvement changes
• Maintain and schedule equipment maintenance and historical review.
• Maintain system integrity and identify performance and security improvements.
• Ensures the operations in the manufacturing suites are performed in a manner that secures the safety of his fellow associates and in accordance with the cGMP production standards.
• Assist in the identification of process improvements to enhance ease of operation and reduce errors.
• Work with tech transfer and QA to ensure the adherence to GMP principals in the manufacturing areas.

Required Skills and Qualification:

• Bachelor's Degree is preferred
• Minimum of 3 years in cGMP bio manufacturing or laboratory environment automation. Other industries may be considered
• Background with troubleshooting with Rockwell and Delta V Siemens.
• Strong problem solving and communication skills essential.
• Ability to follow Safety requirements, Standard Operating Procedures, and work under minimal supervision.
• Ability to multitask, time management and prioritize activities.

Why PharmEng Technology?
Our consultants come from different areas of the Pharmaceutical/Biotech/Medical Device industries and have extensive experiences obtained from world-class organizations in North America, Europe, and Asia. At PharmEng Technology, we value everyone’s unique talents and work together to support our clients. We offer continuous career growth, competitive wages, opportunities for travel and a team mentality that sets us apart from our competitors. It is the growth of our staff that continues to grow our company globally.

What We Have:
Comprehensive benefits package & competitive wages
A supportive environment where employee growth is promoted
PTO & paid holidays

Company Response to Covid-19
While we serve industries deemed essential businesses, PharmEng Technology will follow safe business practices and adhere to local, state, and federal guidelines. When possible, PharmEng Technology will allow remote work from home.

EEOC Statement
At PharmEng Technology, we don’t just accept difference — we celebrate it, we support it, and we thrive on it for the benefit of our employees, our clients, and our community. PharmEng Technology is proud to be an equal opportunity workplace.