Responsibilities
- Design, implement, and support automation systems in a GMP-regulated pharmaceutical manufacturing environment.
- Ensure automation systems comply with regulatory standards, including computer system validation and electronic batch record or form-fill processes.
- Support data integrity and documentation requirements for all automation and control systems.
- Execute automation commissioning and validation protocols for new and existing systems.
- Troubleshoot and remediate commissioning and validation non-conformances in a timely and thorough manner.
- Support process control and system integration activities to improve automation performance and reliability.
- Collaborate with internal engineers and client teams to improve efficiency, product quality, and profitability of process manufacturing operations.
- Define and implement programmable logic controller (PLC) configurations, with a focus on Rockwell/Allen-Bradley platforms.
- Conduct testing, on-site commissioning, and qualification of control systems in a live manufacturing environment.
- Contribute to continuous improvement initiatives to enhance automation strategies and support highly automated manufacturing processes.
- Work with minimal supervision, managing assignments and priorities independently while maintaining high quality and compliance standards.
Essential Skills
- Bachelor of Science degree in Electrical Engineering, Computer Engineering, Chemical Engineering, or Electrical Technology.
- 28 years of experience in automation or a closely related field.
- Hands-on experience troubleshooting Rockwell PLCs, including Allen-Bradley platforms.
- Proficiency with Allen-Bradley automation systems and Rockwell technologies.
- Strong troubleshooting skills for control systems and automation equipment.
- Demonstrated experience working in a GMP or pharmaceutical manufacturing environment..
Additional Skills & Qualifications
- Experience supporting electronic batch record (EBR) or form-fill processes in regulated environments.
- Knowledge of computer system validation principles and practices.
- Understanding of data integrity and documentation requirements in GMP settings.
- Experience with highly automated manufacturing facilities and large-scale projects.
- Comfort working on long-term projects with opportunities to transition to other projects as needed.
Work Environment The position follows a compressed work schedule, with 4x10-hour shifts that are highly likely to fall on weekend-oriented schedules. Typical shift options include a weekend shift from Thursday to Sunday, 10:00 a.m. to 9:00 p.m., or Friday through Monday, 10:00 a.m. to 9:00 p.m.
Job Type & LocationThis is a Contract to Hire position based out of Concord, NC.
Pay and Benefits The pay range for this position is $60.00 - $65.00/hr.Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:
Medical, dental & vision
Critical Illness, Accident, and Hospital
401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
Life Insurance (Voluntary Life & AD&D for the employee and dependents)
Short and long-term disability
Health Spending Account (HSA)
Transportation benefits
Employee Assistance Program
Time Off/Leave (PTO, Vacation or Sick Leave)
This is a fully onsite position in Concord,NC.
Application Deadline This position is anticipated to close on Jun 15, 2026.About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions.
We help visionary companies advance their engineering and science initiatives through
access to specialized experts who drive scale, innovation and speed to market.
With a network of almost 30,000 consultants and more than 4,500 clients across the U.S.,
Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.
If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email ... for other accommodation options.
San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.
Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.
Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.