Delta V Industrial Automation Engineer, II-Senior

About AGC Biologics 

AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners, every step of the way. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells. Our global network spans the U.S., Europe, and Asia, with cGMP-compliant facilities in Seattle, Washington; Boulder and Longmont, Colorado; Copenhagen, Denmark; Heidelberg, Germany; Milan, Italy; and Chiba, Japan. We currently employ more than 2,500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients' most complex challenges, including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more, visitwww.agcbio.com. 

Summary 

The Automation Engineer is a key member of the Engineering team and will be responsible for supporting and maintaining the campus Industrial Automation systems.

PRINCIPAL RESPONSIBILITIES:

• Responsible for the installation, start-up, and maintenance of automation systems.
• Oversees contract resources to ensure all projects are completed on time and within budget and schedule.
• Provides leadership and technical competency to manufacturing and maintenance technicians to operate and maintain automated systems.
• Provides automation technical and training support on new and legacy systems.
• Travel to vendor sites as required during project execution for FATs.
• Oversee SATs for system integration and startup.
• Complete maintenance work orders and engineering change controls within the allotted time.
• Maintain all assigned maintenance records, work orders, and investigations in an orderly and accurate manner in compliance with cGMP's by the utilization of the site CMMS and Document Management Systems.
• Assist in Regulatory and Internal Audits / Inspections.
• Assist in qualification activities related to Automation improvement projects.
• Adheres to all applicable procedures, cGMP's, company policies, and all other quality or regulatory requirements (OSHA, DEA, FDA, EMEA, ANVISA, HS&E, etc.).

KNOWLEDGE, SKILLS & ABILITIES:

• Strong written, verbal, and interpersonal communications skills.
• Strong analytical and problem-solving skills and experience applying these skills to resolve technical problems.
• Strong skills and experience in MS Office products (Word, Excel, Outlook, PowerPoint).
• Computer literate in a CMMS (Computerized Maintenance Management Software) such as Blue Mountain or similar computer-based maintenance program desirable.
• Demonstrated ability to work on assignments that are moderately complex in nature where judgment is required in resolving problems and making routine recommendations to management.
• Knowledgeable of Electrical, Mechanical, Control/SCADA, PLCs, AC / DC drive systems, industrial control system protocols, (controlnet, devicenet, profibus, profinet, BacNet and Ethernet/IP), DCS, (Delta-V), Process Improvement Methodologies, and Root Cause Analysis (RCA).n-depth knowledge of documentation requirements for cGMP manufacturing.
• Demonstrated good interpersonal skills, customer focus, and professionalism.
• Ability to read, interpret, and troubleshoot engineering drawings, P&IDs, and electrical schematics.

EDUCATION/EXPERIENCE:

• Level I: 0-2 Years Experience
• Level II: 2-4 Years Experience
• Level III: 5-7 Years Experience
• Senior 8+ Years Experience
• High School diploma required. cGMP or other FDA regulated operation experience preferred. Bachelors degree in a related discipline highly preferred.
• Experience with Start-Up & Commissioning of cGMP Facility.
• Experience writing reports for senior colleagues outlining new concepts, testing outcomes, and ongoing efficiency.
• Demonstrated ability to develop and maintain clear and accurate documentation of process equipment or manufacturing processes.
• Equivalent education and experience may substitute for stated requirements.

COMPENSATION RANGE:

$94,000 - $170,940

Fluctuations in the job market may necessitate adjustments to pay ranges. Final pay determinations will depend on various factors, including, but not limited to experience levels, knowledge, skills, and abilities.

Benefits available to Team Members include subsidized insurance for the Team Member and designated dependents (medical, vision, dental, life and disability), eligibility to participate in the AGC Biologics 401(k) plan (including a generous matching contribution from the company and immediate vesting), vacation, sick time, and parental leave.

Team Members are also eligible to receive a discretionary annual bonus commensurate to the level of the role. The payout is based on both the company's performance and the Team Member's performance.

AGC Biologics offers a highly competitive compensation package and a friendly, collaborative culture that values personal initiative and professional achievement. AGC Biologics is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sexual orientation, or any other characteristic protected by applicable laws, regulations and ordinances.