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Advanced Process Design Engineer

Job in Clayton, Johnston County, North Carolina, 27520, USA
Listing for: NNE Inc.
Full Time position
Listed on 2026-02-21
Job specializations:
  • Engineering
    Process Engineer, Pharma Engineer, Manufacturing Engineer, Mechanical Engineer
Job Description & How to Apply Below

Are you passionate about designing the process and mechanical systems that enable pharmaceutical manufacturing? Do you enjoy solving technical challenges in GMP regulated environments and shaping the design of facilities that produce life changing medicines? If so, you’ll fit right in at NNE.

Primary Duties and Responsibilities

We are looking for an Advanced Process Design Engineer with strong experience in pharma or biotech facility design. This role focuses on process and mechanical design engineering across concept, basic, and detailed design phases, ensuring systems meet stringent GMP, regulatory, and industry standards. You will develop design deliverables, perform calculations, support cross‑discipline design coordination, and contribute to technical excellence within our US engineering team.

This is a great role for engineers who enjoy the technical depth of design work and have hands‑on experience with pharma manufacturing processes, mechanical systems, utilities, and equipment.

How You Might Spend Your Days Pharma‑Focused Design Engineering Responsibilities (~80%)
  • Produce process and mechanical design deliverables for pharma/biotech facilities, including but not limited to PFDs, P&IDs, utility flow diagrams, equipment specifications, and mechanical layouts.
  • Perform design calculations such as pump sizing, line sizing, pressure drop, heat transfer, flow rates, and utility loads for cGMP systems.
  • Support the design and specification process for equipment (vessels, bioreactors, mixing tanks, heat exchangers, CIP/SIP systems) used in pharmaceutical manufacturing.
  • Support the development of designs for clean utilities (WFI, PW, clean steam, clean compressed air) and support systems used in GMP environments.
  • Ensure designs meet GMP requirements, pharma industry codes/standards, and regulatory expectations (ASME, ASME BPE, ANSI, API, NFPA).
  • Support design reviews and participate in HAZOPs and other pharma‑specific safety and compliance assessments.
  • Support design activities with automation, electrical, CQV, controls, and other engineering disciplines essential to pharma facility execution.
  • Review vendor documentation—including FAT/SAT packages—for equipment used in pharmaceutical production.
Leadership & Collaboration (5‑10%)
  • Provide discipline oversight for small design packages and support design quality reviews.
Business & Growth Activities (~5%)
  • Contribute technical input for pharma project proposals, scopes of work, basis of design documents, and estimates.
  • Help strengthen client relationships within the pharmaceutical and biotech industry.
Continuous Improvement (~5%)
  • Help develop and refine pharma‑focused design templates, design standards, utility guidelines, and best practices.
  • Participate in technical knowledge sharing communities, especially around pharma process and mechanical design.
Required Qualifications Who You Are:
  • Enjoy designing complex pharma process and mechanical systems and understand how they support GMP manufacturing.
  • Have strong analytical and design skills with a high attention to detail.
  • Can communicate well across cross‑functional pharma project teams.
  • Are organized, proactive, and comfortable managing multiple design tasks in a GMP‑centric environment.
  • Look for ways to improve tools, workflows, and design standards—especially in regulated environments.
The Miles You’ve Walked (Qualifications) Required
  • B.Sc. or M.Sc. in Mechanical, Chemical/Process Engineering, or related field.
  • Strong experience in process mechanical design for pharmaceutical or biotech facilities.
  • Proficiency with P&IDs, equipment design, utility system design, and engineering calculations used in GMP environments.
  • Familiarity with pharma industry standards such as ASME, ASME BPE, API, ANSI, and NFPA.
  • Ability to deliver design work independently and manage small technical priorities.
  • Effective collaboration skills within multi‑disciplinary pharma project teams.
  • Please note:

    NNE is not able to sponsor employment visas for this position. Candidates must have authorization to work in the United States without current or future visa sponsorship.
Preferred / Bonus
  • Experience with clean utilities (WFI, PW, clean steam) and process…
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