What are the responsibilities and job description for the Electrical/Automation SME position at Zachary Piper Solutions, LLC?
Job Details
Piper Companies is seeking a BioPharma Electrical/Automation Subject Matter Expert (SME) to manage the construction and communication of a new facility build for a CDMO out in Bloomington, IN.
The role has an onsite expectation and slated through 2026 and potentially beyond. The SME will provide technical leadership and subject matter expertise throughout the design, construction, commissioning, and qualification of a new pharmaceutical manufacturing facility. This role will be responsible for ensuring all electrical and automation systems are designed and implemented in compliance with industry standards, regulatory requirements, and company objectives.
Responsibilities include:
Qualifications include:
Compensation includes:
This job opens for applications on 4/15/2025. Applications for this job will be accepted for at least 30 days from the posting date.
#LI-KP1 #LI-ONSITE
The role has an onsite expectation and slated through 2026 and potentially beyond. The SME will provide technical leadership and subject matter expertise throughout the design, construction, commissioning, and qualification of a new pharmaceutical manufacturing facility. This role will be responsible for ensuring all electrical and automation systems are designed and implemented in compliance with industry standards, regulatory requirements, and company objectives.
Responsibilities include:
- Serve as the technical authority on all aspects of electrical infrastructure and/or automation systems for the new facility buildout.
- Provide guidance during design reviews, equipment selection, and integration of building and process automation systems (e.g., BMS, BAS, SCADA, PLCs).
- Collaborate closely with engineering, construction, quality, validation, and operations teams to ensure seamless execution from concept to startup.
- Support commissioning, qualification, and validation (CQV) efforts, ensuring systems meet GMP and FDA regulatory standards.
- Oversee contractor and vendor work, ensuring technical compliance, safety, and quality throughout project phases.
- Develop and review technical specifications, SOPs, and protocols related to electrical and automation systems.
- Participate in risk assessments, FAT/SAT activities, and troubleshooting during startup and early operations.
- Stay current with technological advancements and best practices in automation and electrical systems within the pharmaceutical industry.
Qualifications include:
- 7 years of experience in electrical or automation engineering, with a strong background in pharmaceutical, biotech, or GMP-regulated facilities.
- Deep knowledge of automation platforms (e.g., Siemens, Allen-Bradley/Rockwell, DeltaV) and/or electrical systems (medium and low voltage, backup power, etc.).
- Proven experience supporting large capital projects from design through commissioning.
- Familiarity with industry standards (e.g., NFPA, NEC, ISA, GAMP, 21 CFR Part 11).
- Strong problem-solving, communication, and project coordination skills.
- Ability to work effectively in cross-functional teams and under tight timelines.
- Bachelor's degree in Electrical Engineering, Automation, or related discipline; advanced degree or certifications (e.g., PE, ISA, Siemens/Rockwell certifications) preferred.
Compensation includes:
- Commensurate to experience
- Opportunity to influence a major facility buildout from the ground up
- Long term contract with possible extensions/conversions
- Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays
This job opens for applications on 4/15/2025. Applications for this job will be accepted for at least 30 days from the posting date.
#LI-KP1 #LI-ONSITE
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