Job Information
Actalent Process Engineer (Pharma Manufacturing) in Saint Louis, Missouri
Process Engineering Opportunity – Floor Support (4×10 Schedule)
On‑Site / 4 Days / 10-Hour Shifts
Are you a hands-on Process Engineer who thrives on the manufacturing floor and wants a schedule that actually gives you work–life balance? This role offers a 4×10-hour shift schedule, real ownership of manufacturing support, and the opportunity to directly impact the production of life‑saving biologic therapies.
We are seeking an experienced Process Engineer II – Floor Support professional to serve as a critical technical bridge between Manufacturing Operations and MSAT in a GMP biologics drug substance facility. This is a floor-facing, non-supervisory role built for engineers who enjoy real-time problem-solving, rapid response, and continuous improvement in a highly regulated environment.
Why This Role Stands Out
4 days on / 3 days off every week (10-hour shifts)
Deep involvement in live manufacturing operations
High visibility and technical ownership on the production floor
Meaningful work supporting therapies for chronic and life‑threatening diseases
Contract-to-hire opportunity with long-term potential
What You’ll Be Doing
Provide real-time technical support to upstream and downstream biologics manufacturing
Troubleshoot process and equipment issues during active manufacturing runs
Perform routine GEMBA walks and observe critical process steps
Ensure adherence to batch records, validated processes, and GMP requirements
Proactively identify potential deviations and support investigations
Author, review, and provide technical input for deviations, CAPAs, and investigations
Partner cross-functionally to standardize unit operation methodologies
Participate in daily tiered huddles to drive communication and continuous improvement
Support implementation of corrective and preventive actions to improve process robustness
What We’re Looking For
Required Experience
Bachelor’s degree in Engineering, Biotechnology, Biochemistry, or a related discipline
Non‑science degrees considered with 8+ years of directly related biopharmaceutical manufacturing experience
Minimum 4 years of experience in GMP-regulated biologics or pharmaceutical manufacturing (Engineering, Operations, or Quality)
Hands-on experience with cell culture, protein purification, or large-scale biologics processing
Experience supporting or participating in deviation and CAPA investigations
Comfort working in cleanroom environments (ISO 5 / ISO 7) with full gowning
Core Technical Skills
Process engineering within biologics manufacturing
Chromatography experience
Strong GMP knowledge and floor-based troubleshooting skills
Work Environment & Schedule
On-site role in a GMP biologics manufacturing facility
Gowning required (ISO spaces): removal of jewelry, cosmetics, hair products, etc.
Internal-facing role (not client-facing)
4 days × 10-hour shifts, with weekend work and on-call rotation as required
This role is a great fit for a process engineer who enjoys working close to the process, making real-time decisions, and driving manufacturing excellence—while also enjoying a schedule with built-in flexibility.
Apply today to take the next step in your biologics manufacturing career.
Job Type & Location
This is a Contract to Hire position based out of Saint Louis, MO.
Pay and Benefits
The pay range for this position is $29.00 - $38.00/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 May 5, 2026.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
Actalent is an equal opportunity employer.
About Actalent
Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day.
Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.