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Lumen Bioscience

Process Engineer II - GMP Equipment Lifecycle

Seattle, WA; HQUnited States
Mid-level · Production & Development
POSTED 27 AUG
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74 days opentrue age
Posted 27 Aug
Payats field
$80k–110kposted
▼ −36% vs market median $149k
$80k$167k
Market p25–p75
$136k–$167k
Seattle · n=12 · 365d to 6 Nov
CompanyLumen Bioscience →
3open roles
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Closed · 30d
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30d window
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1,699open · Mid-level Software engineering
Opened · 7d
+1127% of open
All software engineering
75,153open
All tracked boards · live 10 Nov · n=1,699

Process Engineer II - GMP Equipment Lifecycle

Lumen Bioscience is seeking a qualified Process Engineer who will be responsible for supporting Lumen's spirulina-based biomanufacturing platform through the lifecycle management of GMP manufacturing equipment.

Role Description

  • GMP Equipment Lifecycle: Owning the onboarding, commissioning, qualification and validation of new GMP process equipment.
  • Preventative maintenance management: Development and improvement of work instructions. Establishing cleaning and sanitization procedures.
  • Manufacturing Process: Partner closely with Engineering and Process Development teams to characterize and optimize manufacturing processes as it is executed on production-scale drug substance and drug product equipment.
  • Team Collaboration: Work closely with manufacturing operations, Quality, and supporting teams to implement procedures, programs, and training to enhance operational efficiency and compliance.

Essential Duties and Responsibilities

  • Serve as the technical owner for manufacturing equipment through its lifecycle: coordinating pre-purchase requirements, safety assessments, training, startup change control, periodic review and eventual decommissioning.
  • Troubleshoot equipment and process failures and lead root cause investigations, corrective and preventative actions (CAPA), and reliability improvements to minimize downtime and improve contamination control.
  • Design, execute and analyze equipment and process-focused experiments – including optimization, scale-up and scale-down studies – to improve yield, throughput, robustness and product quality.
  • Author, revise and continuously improve equipment operating procedures, work instructions, cleaning, set-up and changeover instructions, technical documentation including engineering studies and impact assessments, associated risk assessments and batch records steps to ensure safe, reproducible, compliant processes.
  • Support deviations, change controls, internal and external audits and regulatory inspections as the equipment subject matter expert.

Qualifications & Requirements

  • Educational Background: Bachelor’s degree in an engineering discipline (e.g. Mechanical, Chemical, Biomedical, Industrial) required.
  • Professional Experience: 5+years of relevant process or equipment engineering experience, preferably in a cGMP pharmaceutical, biotechnology, or medical device manufacturing environment.
  • Technical Knowledge: Strong mechanical aptitude and hands-on equipment troubleshooting experience. Experience supporting equipment qualification and validation (IQ / OQ / PQ) and/or developing preventative maintenance programs.
  • Technical Skills: Basic knowledge of food, dietary supplement, biotechnology and biomanufacturing processes per cGMP (21 CFR Part 111 / 117 / 210 / 211). Proficient in Microsoft Office Suite.
  • Personal Attributes: Detail-oriented, highly organized, proactive, with the ability to manage multiple tasks simultaneously in a fast-paced environment. Strong interpersonal skills and commitment to quality and ethical standards.

Physical Requirements

  • Ability to sit, stand and walk for extended periods (2+ hours) in a manufacturing or production environment.
  • Occasionally lift or carry items up to 20 kg.
  • Ability to gown and work in controlled and classified (cleanroom) environments and around production equipment.

Salary & Benefits at Lumen Bioscience

  • $80,000 to $110,000 salary range, depending on experience.
  • Health, Dental, and Vision premiums fully covered by Lumen.
  • 401k match up to 4%.
  • Industry-leading PTO policy, paid refresh days, and paid year-end holiday office closure.
  • Monthly wellness program to support your health and well-being.
  • Free onsite parking or public transportation subsidies.
  • Comprehensive parental leave policies.
  • Life insurance, short & long-term disability, and access to employee assistance programs.

At Lumen Bioscience, we foster a workplace that encourages innovation, collaboration, and professional growth. This role offers an opportunity to enhance your compliance expertise while contributing significantly to advancements in biotechnology and global health solutions.

Source · Lumen BioscienceFirst seen 7 NovOriginal ↗