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Automation EngineerJob Description

This position provides automation guidance and technical support for manufacturing equipment and is responsible for automation and automation infrastructure. The role requires effectively leading the engineering automation function at the Biologic manufacturing facility to ensure product quality and regulatory compliance.

Responsibilities

+ Provide technical mentorship for equipment procurement, including process qualifications to cGMP requirements.

+ Communicate effectively with relevant departments, senior management, and clients.

+ Understand requirements of Equipment Qualification management and craft and review associated technical documents.

+ Quickly assess and evaluate multiple priorities and team resources.

+ Apply outstanding problem-solving skills in situations when manufacturing equipment breaks down, communicating effectively with key employees and site leadership.

+ Work with the capital engineering team during projects to procure and install equipment and processes.

+ Actively involve in the site's Practical Process Improvement (PPI) lean activities.

+ Manage engineering risks effectively and minimize production downtime.

+ Generate, communicate, and keep up-to-date technical documents, procedures, and standards guidelines in accordance with statutory requirements and company policy.

+ Assist with, and lead, continuous improvement initiatives within the function to ensure system and process improvements are implemented effectively and efficiently across the site.

+ Serve as a role model leader, coach, and mentor.

+ Drive safety within the team.

Essential Skills

+ Bachelor’s degree in engineering field, or equivalent experience.

+ 8+ years within a GMP Environment.

+ Proficient with computers, specifically MS Office.

+ Working knowledge of controlled documentation and data systems including SAP.

+ In-depth knowledge of cGMP regulations.

+ 8+ years of experience in pharmaceutical equipment maintenance and GMP manufacturing.

+ 2+ years of supervisory experience.

+ Experience in Automation, GMP manufacturing, Equipment maintenance, Engineering.

+ Expert in managing changes for assessments related to equipment, systems, automation, and processes.

+ Project management, Commissioning, Design, Pharmaceutical manufacturing.

Additional Skills & Qualifications

+ Work attitude that exhibits drive, creativity, collaboration, assertiveness, good judgement, decision-making, and ambition.

+ Excellent interpersonal skills with the ability to build and maintain relationships with internal and external customers.

+ Proven leadership skills with the ability to influence others and lead significant change.

+ Strong proficiency in Microsoft Office Suite, including Word and Excel.

+ Experience with Delta V control systems, network switches & SQL databases.

+ Effective written, interpersonal, and presentation skills.

Work Environment

The work environment is balanced between desk work (60%) and hands-on activities (40%). Minimal travel is required, less than 5%. On-call duties occur occasionally, typically no more than five times a year, and in most cases, physical presence is not required.

Pay and Benefits

The pay range for this position is $69.71 - $75.00/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)

Workplace Type

This is a fully onsite position in Saint Louis,MO.

Application Deadline

This position is anticipated to close on Jul 31, 2025.

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 due to a disability, please email [email protected] (%[email protected]) for other accommodation options.