Process Engineer II

Process Engineer – Biopharmaceutical ManufacturingAbout the Role

Are you passionate about advancing biopharmaceutical manufacturing? We’re seeking a Process Engineer to join our dynamic team and play a pivotal role in the development, scale-up, validation, and transfer of biologics manufacturing processes. This is a rare opportunity to contribute to cutting-edge clinical and commercial production in a rapidly expanding facility with newly opened suites and increased capacity.

As a Process Engineer, you’ll collaborate across departments to ensure seamless technology transfer and continuous process improvement - all while maintaining strict compliance with GMP standards. You’ll be a key technical contributor, helping shape the future of biologics manufacturing.

Key Responsibilities

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  Provide scientific and engineering input into process development, scale-up, and validation.

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  Lead and support technology transfer and continuous improvement initiatives.

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  Collaborate with cross-functional teams including Operations, QA, and Process Development.

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  Ensure compliance with cGMP and regulatory standards (US/EU).

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  Apply chromatography techniques (training available if needed).

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  Draft and review technical documentation including batch records, validation protocols, and process flow diagrams.

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  Participate in internal and client-facing meetings, audits, and CAPA implementation.

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Required Qualifications

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  Bachelor’s degree in Chemical Engineering, Biochemistry, or a related field.

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  Minimum 3 years of experience in GMP-regulated biologics or pharmaceutical manufacturing.

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  Strong understanding of cGMP and regulatory requirements.

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  Proficiency in Microsoft Word and Excel.

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  Knowledge of chromatography.

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  Excellent communication, documentation, and teamwork skills.

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  Ability to work independently and within cross-functional teams.

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Preferred Skills

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  Experience with upstream and downstream processing.

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  Familiarity with statistical methods for process analysis.

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  Knowledge of Chemistry, Manufacturing, and Controls (CMC) principles.

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  Experience mentoring junior engineers or technicians.

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Work Environment

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  Regular gowning into ISO-classified cleanroom spaces is required.

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  Must be comfortable removing personal items (e.g., earrings, cosmetics, hair products) at least once a week.

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  Client-facing role with opportunities to present and collaborate externally.

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Why Join Us?

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  Be part of a growing team with expanded manufacturing capacity and exciting commercial programs.

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  Work in a collaborative, innovation-driven environment.

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  Contribute to meaningful projects that impact global health.

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  Opportunity for long-term growth and transition to a permanent role.

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Ready to make a difference in biopharmaceutical manufacturing? Apply now and help us shape the future of biologics production, or send your resume directly to

Pay and Benefits

The pay range for this position is $29.00 - $35.00/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 Oct 14, 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 (% ) for other accommodation options.