Jabil
Position Overview
Principal Engineer - Cleanroom SME
at Jabil
Jabil has an exciting opportunity for a Cleanroom and Technical Cleanliness Subject Matter Expert (SME) focused on the manufacturing, technology and/or electronics industry. The SME is responsible for establishing, maintaining, governing and operationalizing cleanliness standards across the organization. You will lead cleanliness activities, conduct cleanliness analyses, and drive continuous technical cleanliness improvements. This includes developing and enforcing contamination control protocols, ensuring compliance with ISO 16232, VDA 19 and ISO 14644, and driving continuous improvement in technical cleanliness for components, assemblies and manufacturing environments. The SME serves as the central authority on cleanliness requirements, bridging engineering, quality and operations to uphold world‑class standards. This role provides expert guidance on contamination control, cleanroom design and operation, and cleanliness validation for components, assemblies and processes.
Key Responsibilities
Develop and maintain cleanroom protocols in accordance with ISO 14644, ISO 16232, IEST‑RP‑CC001/CC002, VDA 19, SEMI E44/F21 and other relevant cleanliness standards.
Develop and enforce SOPs, work instructions and validation protocols for cleanliness‑critical operations.
Develop standards, guidelines and best practices on cleanroom set‑up and operation in Jabil referencing industry standards.
Operationalize cleanliness protocols by integrating them into manufacturing workflows, inspection procedures and supplier requirements.
Maintain and continuously improve cleanliness programs, including documentation, training and audit readiness.
Support the design, layout and specification of cleanroom systems including HVAC, filtration (HEPA/ULPA), airlocks, gowning areas and environmental monitoring systems.
Review and provide support for cleanroom design documents, drawings and change requests across the Jabil enterprise as required.
Provide support for installation and integration of cleanroom systems and ensure construction aligns with defined classifications (ISO 5–8, as required).
Lead contamination control initiatives, including cleanroom design, environmental monitoring and process validation.
Lead technical cleanliness analysis and related activities in the laboratory.
Conduct cleanliness assessments and audits of components, equipment and facilities using ISO 16232‑compliant methods.
Define cleanliness training content and qualification plans for quality specialists, front line workers and other areas regarding cleanliness.
Define resources for cleanliness strategy implementation, including equipment, consumables, headcount and external alternative providers as needed to maintain equipment, ensuring cleanliness and safety standards.
Train and mentor personnel on cleanroom behaviour, cleanliness standards, inspection techniques and cleanliness best practices.
Interface with suppliers to ensure incoming components meet cleanliness specifications and are validated according to ISO 16232, ISO 14644 and VDA 19.
Support root cause investigations and corrective actions related to cleanliness deviations or contamination events.
Collaborate with cross‑functional teams such as engineering and quality to embed cleanliness requirements and controls into product design, development and manufacturing.
Specify and validate cleaning processes for parts and assemblies, including fluid‑carrying components.
Oversee cleanroom certification, monitoring and environmental control systems.
Create a capability tracker of all clean rooms that can be set up for multiple reasons.
Keep abreast of the latest cleanroom requirements and related technologies.
Look for innovative technologies or solutions that support daily activities.
Promote GMPs and baselines in the plant(s).
Develop and implement quality assurance monitoring procedures on particles, temperature, relative humidity and positive pressure.
Ensure cleanroom controls meet local facilities and product requirements.
Establish formal and periodic contact with manufacturing support areas.
Control, verify and maintain compliance with local and international standards as applicable to the business unit.
Support the development and industrialisation of analytical methods to improve cleanliness indicators.
Communicate and record testing results, findings and risks.
Coordinate feasible studies on cleanroom with consultants and propose qualification criteria on service and speed to build the cleanroom.
Maintain control of the files and records of the viable and non‑viable load verification program.
Ensure cleanroom build requirements meet facilities requirements.
Internally coordinate the manufacturing of products and samples necessary to conduct validations and revalidations.
Maintain controlled final reports of cleanroom validations (as built, at rest and operational).
Participate and provide support during client, corporate or third‑party audits.
Participate in the internal audit program as internal auditor and/or leader.
Education & Experience
Bachelor’s degree in Engineering, Chemistry, Microbiology, Industrial Hygiene, Material Science or related technical field (Master’s preferred).
Minimum 5 years of experience in cleanroom operations and technical cleanliness in a regulated industry (e.g., automotive, aerospace, medical device, semiconductor).
Experience with particle measurement techniques, gravimetric analysis and cleanliness inspection tools.
Experience with classification, design, engineering, airflow, wall systems, floors, equipment, hardware, ceilings, quality assurance, viable and non‑viable control systems in cleanrooms.
Experience with cleanliness validation in fluid systems or precision assemblies.
Familiarity with cleanroom design and HVAC systems.
Certification in cleanroom or contamination control (e.g., IEST) is a plus.
Must be comfortable with 50% travel globally.
Knowledge, Skills & Abilities
In‑depth knowledge of ISO 14644, ISO 16232, IEST‑RP‑CC001/CC002, VDA 19, SEMI E44/F21 and relevant cleanliness standards.
Certified Cleanroom Professional (CCP or CRCP) or Certified Contamination Control Specialist (CCCS) – preferred.
Good knowledge of laboratory analytical instruments, principles and applications (IR, SEM‑EDX, ICP‑OES, XRF…).
Knowledge of requirements and automotive quality core tools (PPAP, MSA, APQP, SPC, FMEA).
Knowledge of regulatory requirements (FDA, GMP, ISO 13485).
Proficiency in data analysis and reporting tools (Excel, Minitab, etc.).
Strong analytical and critical thinking skills.
Excellent communication and training abilities.
Additional Information
Location: Manufacturing facility in San Jose, CA.
Relocation available.
50% travel required (domestic and international).
Pay range: $151,500 – $272,800.
Eligible for a short‑term incentive based on performance.
Benefits
Medical, Dental, Prescription Drug and Vision Insurance with HRA and HSA options
401(k) Match
Employee Stock Purchase Plan
Paid Time Off
Tuition Reimbursement
Life, AD&D and Disability Insurance
Commuter Benefits
Employee Assistance Program
Pet Insurance
Adoption Assistance
Annual Merit Increases
Community Volunteer Opportunities
Fraud Notice BE AWARE OF FRAUD: When applying for a job at Jabil you will be contacted via official channels with a jabil.com email address. Jabil does not request payments for interviews or at any other point during the hiring process. Jabil will not ask for personal identifying information such as a social security number, birth certificate, financial institution, driver’s license number or passport information over the phone or via e‑mail. If you believe you are a victim of identity theft, contact the Federal Bureau of Investigation’s internet crime hotline ( www.ic3.gov ), the Federal Trade Commission identity theft hotline ( www.identitytheft.gov ) and/or your local police department. Report any scam job listings to the posting website.
#J-18808-Ljbffr
at Jabil
Jabil has an exciting opportunity for a Cleanroom and Technical Cleanliness Subject Matter Expert (SME) focused on the manufacturing, technology and/or electronics industry. The SME is responsible for establishing, maintaining, governing and operationalizing cleanliness standards across the organization. You will lead cleanliness activities, conduct cleanliness analyses, and drive continuous technical cleanliness improvements. This includes developing and enforcing contamination control protocols, ensuring compliance with ISO 16232, VDA 19 and ISO 14644, and driving continuous improvement in technical cleanliness for components, assemblies and manufacturing environments. The SME serves as the central authority on cleanliness requirements, bridging engineering, quality and operations to uphold world‑class standards. This role provides expert guidance on contamination control, cleanroom design and operation, and cleanliness validation for components, assemblies and processes.
Key Responsibilities
Develop and maintain cleanroom protocols in accordance with ISO 14644, ISO 16232, IEST‑RP‑CC001/CC002, VDA 19, SEMI E44/F21 and other relevant cleanliness standards.
Develop and enforce SOPs, work instructions and validation protocols for cleanliness‑critical operations.
Develop standards, guidelines and best practices on cleanroom set‑up and operation in Jabil referencing industry standards.
Operationalize cleanliness protocols by integrating them into manufacturing workflows, inspection procedures and supplier requirements.
Maintain and continuously improve cleanliness programs, including documentation, training and audit readiness.
Support the design, layout and specification of cleanroom systems including HVAC, filtration (HEPA/ULPA), airlocks, gowning areas and environmental monitoring systems.
Review and provide support for cleanroom design documents, drawings and change requests across the Jabil enterprise as required.
Provide support for installation and integration of cleanroom systems and ensure construction aligns with defined classifications (ISO 5–8, as required).
Lead contamination control initiatives, including cleanroom design, environmental monitoring and process validation.
Lead technical cleanliness analysis and related activities in the laboratory.
Conduct cleanliness assessments and audits of components, equipment and facilities using ISO 16232‑compliant methods.
Define cleanliness training content and qualification plans for quality specialists, front line workers and other areas regarding cleanliness.
Define resources for cleanliness strategy implementation, including equipment, consumables, headcount and external alternative providers as needed to maintain equipment, ensuring cleanliness and safety standards.
Train and mentor personnel on cleanroom behaviour, cleanliness standards, inspection techniques and cleanliness best practices.
Interface with suppliers to ensure incoming components meet cleanliness specifications and are validated according to ISO 16232, ISO 14644 and VDA 19.
Support root cause investigations and corrective actions related to cleanliness deviations or contamination events.
Collaborate with cross‑functional teams such as engineering and quality to embed cleanliness requirements and controls into product design, development and manufacturing.
Specify and validate cleaning processes for parts and assemblies, including fluid‑carrying components.
Oversee cleanroom certification, monitoring and environmental control systems.
Create a capability tracker of all clean rooms that can be set up for multiple reasons.
Keep abreast of the latest cleanroom requirements and related technologies.
Look for innovative technologies or solutions that support daily activities.
Promote GMPs and baselines in the plant(s).
Develop and implement quality assurance monitoring procedures on particles, temperature, relative humidity and positive pressure.
Ensure cleanroom controls meet local facilities and product requirements.
Establish formal and periodic contact with manufacturing support areas.
Control, verify and maintain compliance with local and international standards as applicable to the business unit.
Support the development and industrialisation of analytical methods to improve cleanliness indicators.
Communicate and record testing results, findings and risks.
Coordinate feasible studies on cleanroom with consultants and propose qualification criteria on service and speed to build the cleanroom.
Maintain control of the files and records of the viable and non‑viable load verification program.
Ensure cleanroom build requirements meet facilities requirements.
Internally coordinate the manufacturing of products and samples necessary to conduct validations and revalidations.
Maintain controlled final reports of cleanroom validations (as built, at rest and operational).
Participate and provide support during client, corporate or third‑party audits.
Participate in the internal audit program as internal auditor and/or leader.
Education & Experience
Bachelor’s degree in Engineering, Chemistry, Microbiology, Industrial Hygiene, Material Science or related technical field (Master’s preferred).
Minimum 5 years of experience in cleanroom operations and technical cleanliness in a regulated industry (e.g., automotive, aerospace, medical device, semiconductor).
Experience with particle measurement techniques, gravimetric analysis and cleanliness inspection tools.
Experience with classification, design, engineering, airflow, wall systems, floors, equipment, hardware, ceilings, quality assurance, viable and non‑viable control systems in cleanrooms.
Experience with cleanliness validation in fluid systems or precision assemblies.
Familiarity with cleanroom design and HVAC systems.
Certification in cleanroom or contamination control (e.g., IEST) is a plus.
Must be comfortable with 50% travel globally.
Knowledge, Skills & Abilities
In‑depth knowledge of ISO 14644, ISO 16232, IEST‑RP‑CC001/CC002, VDA 19, SEMI E44/F21 and relevant cleanliness standards.
Certified Cleanroom Professional (CCP or CRCP) or Certified Contamination Control Specialist (CCCS) – preferred.
Good knowledge of laboratory analytical instruments, principles and applications (IR, SEM‑EDX, ICP‑OES, XRF…).
Knowledge of requirements and automotive quality core tools (PPAP, MSA, APQP, SPC, FMEA).
Knowledge of regulatory requirements (FDA, GMP, ISO 13485).
Proficiency in data analysis and reporting tools (Excel, Minitab, etc.).
Strong analytical and critical thinking skills.
Excellent communication and training abilities.
Additional Information
Location: Manufacturing facility in San Jose, CA.
Relocation available.
50% travel required (domestic and international).
Pay range: $151,500 – $272,800.
Eligible for a short‑term incentive based on performance.
Benefits
Medical, Dental, Prescription Drug and Vision Insurance with HRA and HSA options
401(k) Match
Employee Stock Purchase Plan
Paid Time Off
Tuition Reimbursement
Life, AD&D and Disability Insurance
Commuter Benefits
Employee Assistance Program
Pet Insurance
Adoption Assistance
Annual Merit Increases
Community Volunteer Opportunities
Fraud Notice BE AWARE OF FRAUD: When applying for a job at Jabil you will be contacted via official channels with a jabil.com email address. Jabil does not request payments for interviews or at any other point during the hiring process. Jabil will not ask for personal identifying information such as a social security number, birth certificate, financial institution, driver’s license number or passport information over the phone or via e‑mail. If you believe you are a victim of identity theft, contact the Federal Bureau of Investigation’s internet crime hotline ( www.ic3.gov ), the Federal Trade Commission identity theft hotline ( www.identitytheft.gov ) and/or your local police department. Report any scam job listings to the posting website.
#J-18808-Ljbffr