Principal Process Engineer

ZipRecruiter; Horsham; Remote; GBP 100,000 - 125,000; Full time

Job summary

An innovative firm is seeking a Principal Process Engineer to support the startup of a GMP biologics manufacturing facility. This role will initially be remote, transitioning to onsite work in Wilson, NC. The ideal candidate will have extensive experience in process engineering within GMP environments, with a proven track record in supporting facility start-ups. You will design and optimize manufacturing processes, ensuring compliance and quality while collaborating across departments. This is a fantastic opportunity to contribute to cutting-edge projects in a dynamic and collaborative environment.

Qualifications

• 8+ years of experience in GMP biologics manufacturing engineering.
• Strong background in GMP compliance and engineering.

Responsibilities

• Design and optimize biologics manufacturing processes.
• Ensure GMP compliance and operational excellence.

Skills

GMP Manufacturing Experience

Engineering Expertise

Project Team Collaboration

Analytical Skills

Problem-Solving Skills

Education

Bachelor's degree in Engineering

Master's Degree, MBA, or Ph.D.

Tools

DeltaV systems

Job description

Principal Process Engineer

Location: Wilson, NC (Remote initially; Onsite once facility opens)
Type: Long Term Contract | Biologics / Pharmaceutical Manufacturing

Job Summary: We are looking for a Principal Process Engineer to support the startup and operation of a GMP biologics manufacturing facility in Wilson, NC. The role will start remotely, but the selected candidate must be within commutable distance to Wilson, NC, as the position will become onsite once the facility is operational.

Key Responsibilities:

1. Design and optimize new/existing biologics manufacturing processes.
2. Lead and support projects involving manufacturing, utilities, automation, and operations.
3. Drive right-first-time start-ups and ensure GMP compliance.
4. Translate business and technical needs into practical solutions.
5. Collaborate across departments to meet project goals and timelines.
6. Apply strong analytical and problem-solving skills.
7. Ensure quality, compliance, and operational excellence.

Must-Have Qualifications:

1. Bachelor's degree in Engineering or a related technical field (required).
2. 8+ years of experience in process or plant engineering within a GMP biologics manufacturing environment.
3. Experience with DeltaV systems.
4. Hands-on experience in Upstream and/or Downstream biologics processes.
5. Proven track record supporting greenfield or brownfield GMP facility start-ups.
6. Strong background in GMP manufacturing and engineering.
7. Ability to work collaboratively in a team environment.

Preferred Qualifications:

1. Master's Degree, MBA, or Ph.D.
2. PE (Professional Engineer) certification.
3. FPX, Six Sigma, or Lean Manufacturing experience.
4. Active involvement in ISPE or ASME BPE organizations.

Top Skills:

1. GMP Manufacturing Experience
2. Engineering Expertise
3. Project Team Collaboration

Work Location: Remote to start, Onsite in Wilson, NC once the facility opens. Candidates must be within commutable distance to Wilson, NC.

For inquiries, please contact: [e-mail]