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Grifols

Engineer III – Utility and Automation GMP

Grifols

. Serve as counsel within areas of engineering expertise, including Mechanical, Electrical, Chemical, Facilities and Process .

Posted 10/6/2026full-timeEmeryville • California • United StatesMid-LevelSenior💰 $97,340 - $146,010 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in engineering disciplines such as Mechanical, Electrical, and Chemical, with a strong focus on compliance with FDA Good Manufacturing Practices. Proven ability to lead teams, solve complex problems, and support the design and implementation of manufacturing facilities and systems.

Highest-signal resume keywords
Bachelor's Degree In EngineeringFDA Good Manufacturing Practice ComplianceTechnical Writing SkillsBiotech Or Chemical Industry ExperienceProject Management In Manufacturing

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Engineering Project SupportManufacturing Technology DesignQuality Control SupervisionProblem-Solving SkillsRegulatory Expertise
Soft Skills
Interpersonal SkillsCommunication SkillsTeam LeadershipAdaptabilityFlexibility
Certifications & Qualifications
Professional Engineering License
Industry Keywords
Manufacturing EnvironmentBiotech IndustryChemical IndustryEnvironmental Safety RequirementsPersonal Safety Requirements

About the role

Key responsibilities & impact
  • Serve as counsel within areas of engineering expertise, including Mechanical, Electrical, Chemical, Facilities and Process
  • Make decisions on designated assignments that influence department goals
  • Produce results contributing to business or technical goals
  • Develop alternative solutions and handle complex problems independently
  • Provide engineering project support for the design and implementation of new and upgraded manufacturing facilities, systems and equipment
  • Sustain facilities in compliance with FDA Good Manufacturing Practice Regulations and environmental and personal safety requirements
  • Work in one or more engineering areas in a manufacturing environment: Project, Plant & Reliability, and/or Utilities
  • Collaborate with Engineering, Manufacturing, Quality, Regulatory and other functional areas
  • Design and operate manufacturing technology for the organization
  • Supervise quality control and oversee fulfillment of FDA regulations
  • Train entry-level personnel

Requirements

What you’ll need
  • At least a bachelor’s degree in engineering or related field
  • Professional certifications and licenses as appropriate
  • At least 4 years of experience
  • Biotech or Chemical industry experience preferred
  • Excellent interpersonal, technical writing and communication skills
  • Strong technical and problem-solving skills in a manufacturing environment
  • Strong technical and/or regulatory expertise
  • Ability to adapt to changing circumstances
  • Flexibility with assignments in different units/plants
  • Ability to complete assignments in more than one business unit or functional area
  • Ability to communicate effectively and promptly at all levels of the organization
  • Ability to lead teams and promote a team approach
  • Directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements

Benefits

Comp & perks
  • Up to 5% of the company bonus pool
  • Medical insurance
  • Dental insurance
  • Vision insurance
  • Life insurance
  • PTO
  • Paid holidays
  • Up to 5% 401(K) match
  • Tuition reimbursement
  • Opportunities for professional growth and career progression