Cleanroom & Lab Manager Job at ICEYE (València)

Senior Facilities Manager

The Senior Facilities Manager is a key leader on the account team who is respons...

Location

United States , Milpitas

Salary:

155000.00 - 185000.00 USD / Year

JLL

Expiration Date

Until further notice

Requirements

10+ years Facilities Management experience, with cleanroom manufacturing and lab space experience preferred
Experience working in union environments and with union work rules
Strong executive presence, effective communication and leadership skills, and ability to build lasting client relationships among a wide variety of stakeholders
Strong organizational, management, interpersonal, and supervisory skills with ability to manage ambiguity and change
effectively delegate
Excellent communications skills, both written and verbal, and an ability to effectively present to large groups
Technology proficiency (MS Office, a wide variety of web-based applications including mobile technologies, and CMMS (Corrigo) supervisory responsibilities)
Strong financial acumen with background in successfully managing P&L outcomes
Working knowledge of skilled trades and building-related systems with demonstrated safety leadership
Familiar with project delivery process and capital planning functions

Job Responsibility

Ensure quality delivery of Facility Management Operations while supporting the Engineering, Project Management, Relocation (MAC), and Occupancy Planning functions
Responsible for the Milpitas HQ campus and outlying facilities, encompassing approximately 1 million SF
Ensure all contract deliverables are met or exceeded, including key performance indicators, operational up time, cost savings initiatives, energy consumption reduction initiatives, service improvements using standardized operating procedures, and introduction of best practices and innovations
Develop operating and capital budgets, control costs, and coordinate service provider and staff activities
Resolve escalated issues, drive continuous process improvement and team development
Provide regular performance feedback, development and coaching to direct reports
Develop and maintain meaningful relationships with all key client stakeholders
Ensure high client satisfaction by continually monitoring performance and delivery
Ensure uptime and proper maintenance of electrical, mechanical, life safety, and critical back-up systems
Understand the engineering design and operational aspects of all critical systems and equipment with strong emphasis on UPS, SEP, MEP systems and cleanroom, lab, and data center environments

What we offer

401(k) plan with matching company contributions
Comprehensive Medical, Dental & Vision Care
Paid parental leave at 100% of salary
Paid Time Off and Company Holidays
Early access to earned wages through Daily Pay

Fulltime

Development, process and engineering technician

Explore a world of opportunities with us. Look ahead with us and help shape inno...

Location

China , Shanghai Xinzhuang

Salary:

Not provided

Evonik Industries

Expiration Date

Until further notice

Requirements

University (First degree)
Experience of R&D and production in medical device company (who produce Class III medical implants device) is preferred
Good experience and skills in processing medical polymers based mainly on bio-resorbable polymers
Good experience and skills in operating and trouble shooting for the process, e.g. single screw extrusion, twin screw extrusion, injection molding etc.
Good experience and skills in producing monofilament, tube, membrane, composite, molding part is preferred
Experienced practitioner able to work unsupervised in project management and execution including evaluating project feasibility and providing technical suggestion, make execution plan, carry out development and production activities including trouble-shooting etc.
Good skills and experience of coordinating, communicating with others in the teamwork
Good skills and experience of coordinating, communicating with external customer and suppliers
Works without supervision and provides work related data, report and records to business objectives under complianced, quality system required, know-how protection regulated way
Good knowledge about cleanroom and lab utilities engineering and management

Job Responsibility

Support RD&production department manager to plan and execute medical device customers' semi-finished product CDMO projects (note: 90% of target end medical implants belong to Class III)
Carry out development and production activities for semi-finished products of medical implants, and assure execution in the ESH and quality system complianced and know-how protected way
Draft SOPs for production and process management when required by RD&production department manager
Support RD&production department manager to manage cleanroom in good way, including cleanliness maintaining, related equipment and utillities routinely monitoring, maintenance reporting, monitoring and feedback.

What we offer

performance-based remuneration
occupational health benefits
hybrid and flexible working environments
attractive career paths
high-quality development programs

Fulltime

R&D Satellite Build & Lab Maintenance Team Lead

In this role, you will support the company's growth as we continue to scale our ...

Location

Finland , Espoo

Salary:

Not provided

ICEYE

Expiration Date

Until further notice

Requirements

BSc degree (or equivalent) in Engineering
Proven track record in team leadership or technical lead roles
Experience with R&D projects
Experience working in cleanrooms
Familiar with Lab standards
Experience working with Electronics & Lab Instruments
Experience using inventory management systems
Hands on experience in complex machines assembly and testing

Job Responsibility

Interpret the team OKRs and delegate tasks in order to achieve the domain goals
Ensure the R&D Labs are well maintained and support the engineering projects
Mentor and support the professional development of team members, helping them grow in their careers and take on new challenges
Help identify development opportunities for team members and support their career growth
Foster a culture of trust, collaboration, innovation, and continuous improvement
Establish and enforce best practices in documentation
Define processes and way of working with stakeholders

What we offer

Occupational healthcare, occupational and accident insurance
A yearly benefit budget to spend as you wish (i.e. on sport, transport, bike benefit, wellness, lunch, etc.)
Phone subscription with iPhone of choice
Relocation support (i.e. flight tickets, accommodation, relocation agency support)
Time for self-development, research, training, conferences, or certification schemes
Inspiring and collaborating offices and silent workspaces enable you to focus
A wide variety of the best coffee, tea, snacks, and sweets to accompany your daily space mission

Fulltime

QA/QC, IMS and Customer Interface Manager

Explore a world of opportunities with us. Look ahead with us and help shape inno...

Location

Thailand , Saraburi

Salary:

Not provided

Evonik Industries

Expiration Date

Until further notice

Requirements

Bachelor’s degree / Master’s degree in chemistry or chemical engineering
15-20 years working experience in chemical/pharma/FMCG industries as Quality Control Manager
Strong communication, collaboration, and networking abilities
Fluency in English, both written and spoken
Proficiency in Microsoft tools, Minitab, Six Sigma., etc.
Analytical and problem-solving skills
Ability to work effectively in a global, multicultural environment

Job Responsibility

Building safety awareness & observing safety adherence in all operations of QA/QC to ensure zero incidence by regular safety talks & safety rounds with team members
Reviewing and controlling raw materials’ quality compliance to ensure the right raw material input into the production process
Raw material new vendor development to reduce dependability on single supplier by assessing new vendor’s specification & process capabilities, sample analysis, trials at lab/plant
Reviewing and controlling FG quality in compliance to ensure the right product is produced as per customers’ requirements by evaluating FG quality, its consistency & process capabilities
Planning, executing all improvement activities for product development, quality improvement of all grades of H2O2 & PAA by conducting lab trials & coordinating with plant team for plant modifications, plan trials & ending with commercial production
Train & guide team for SPC analysis, identifying improvement opportunities & implementation
Identify areas for improvement and develop strategies to achieve quality KPIs
Collaborate with cross-functional teams, suppliers and internal & external stakeholders to address quality issues and drive continuous improvement initiatives
Product specific regulatory approvals as per customer need and application
Evaluate the annual performance of direct reports, identify gaps/OFIs for individuals help them overcome and develop people. Drive quality culture and develop people

What we offer

hybrid and flexible working environments with #SmartWork
performance-based remuneration
occupational health benefits
attractive career paths
high-quality development programs

Fulltime

Critical Environments Manager

We are seeking an experienced and technically proficient Critical Facilities Man...

Location

United States , Mountain View

Salary:

143600.00 - 249000.00 USD / Year

JLL

Expiration Date

Until further notice

Requirements

7-10 years of experience in critical facilities operations and management, preferably in laboratory, cleanroom, pharmaceutical, or semiconductor manufacturing environments
Bachelor's degree in Mechanical or Electrical Engineering, or a related technical field
equivalent professional experience will be considered
In-depth, system-level knowledge of critical MEP systems including UPS, generators, power distribution, HVAC (chillers, cooling towers, AHUs), and fire/life safety systems
Proven experience managing vendor relationships, contracts, and on-site performance
Strong understanding of and experience with change management controls, MOPs, SOPs, and risk mitigation in a critical environment
Excellent leadership, problem-solving, and communication skills with a proven record of providing excellent customer service
Candidates must be authorized to work in the United States without sponsorship

Job Responsibility

Supervise and direct all preventative and corrective maintenance performed by equipment vendors on critical lab support systems
Develop, review, and approve all Method of Procedures (MOPs) for work on critical systems to ensure risk is minimized
Manage the site's change management control process for all planned maintenance
Oversee the activities of contractors working within the building
Serve as the subject matter expert on the lab's critical MEP infrastructure
Maintain a comprehensive understanding of system capacity, load, and redundancy
Ensure the 24/7 reliability and operation of all building systems supporting labs
Develop, implement, and maintain disaster recovery and business continuity plans for critical facility operations
Lead root cause analysis (RCA) investigations for all facility-related incidents
Ensure all lab utility infrastructure complies with local, state, and federal laws and regulations

What we offer

401(k) plan with matching company contributions
Comprehensive Medical, Dental & Vision Care
Paid parental leave at 100% of salary
Paid Time Off and Company Holidays
Early access to earned wages through Daily Pay

Fulltime

Safety Specialist

The Safety Specialist will ensure safe operation, maintenance, and integration o...

Location

United States , San Jose

Salary:

122000.00 - 135000.00 USD / Year

Archer Aviation

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Mechanical, Electrical, Safety Engineering, or a related field
5+ years of experience in laboratory safety, facilities engineering, or EHS within a technical or research environment
Experience with lithium-ion battery safety, including handling, storage, and risk mitigation
Knowledge of applicable standards and codes (e.g., OSHA, NFPA, ANSI, ISO, ASHRAE, EPA)
Knowledge of lab and building infrastructure systems (ventilation, compressed gas systems, electrical panels, etc.)
Experience working with fire alarm control panels, suppression systems, smoke control systems, and emergency power systems
Strong communication, project management, and organizational skills
Comfortable working hands-on in a dynamic, cross-functional lab environment

Job Responsibility

Conduct hazard analyses and safety assessments for laboratory equipment, infrastructure, and facility systems (e.g., HVAC, gas delivery, power distribution)
Support the design, setup, and relocation of lab equipment, ensuring compliance with safety standards and best practices
Monitor and maintain safety systems, including ventilation (fume hoods, cleanrooms), emergency power, fire suppression, gas detection, and containment systems
Partner with EHS, Facilities, and Lab Managers to identify, mitigate, and track risks related to equipment use, electrical loads, chemical storage, and space layout
Investigate safety incidents and equipment failures
perform root cause analysis and drive corrective actions
Lead or support internal audits, regulatory inspections, and routine safety walkthroughs
Develop and deliver safety training for lab personnel on topics such as proper equipment use, emergency procedures, and PPE
Maintain documentation including safety data sheets (SDS), equipment logs, calibration records, and compliance reports
Support emergency preparedness planning, including drills, response coordination, and business continuity planning

Fulltime

Calibration and Maintenance Engineer

C12 develops reliable & application-specific quantum computers, to solve highly ...

Location

France , Paris

Salary:

Not provided

C12 Quantum Electronics

Expiration Date

Until further notice

Requirements

Bachelor or Master’s degree in Nanotechnology, Nanoscience, Quantum Physics, Experimental Physics, Vacuum Engineering, Electrical Engineering, Mechanical Engineering or a related field
Previous experience (> 12 months) of performing maintenance of cleanroom tools and other systems: Evaporator, dry etch, e-beam lithography, SEM (at least 1)
Cryopumps, turbopumps, primary pumps, dry pumps
Chillers, filters, air compressors
Previous experience (> 6 months) of performing nanofabrication autonomously in a cleanroom with the following processes or tools is desired: Dry etch
Wet processes (cleaning, resist spinning and wet etch)
Metrology tools (SEM, AFM)
Metal evaporation
Meticulous attention to detail
Good English language and written skills

Job Responsibility

Calibrating nanofabrication equipment on a regular basis
In charge of the maintenance of nanofabrication equipment hosted in our cleanroom
Calibration of tools (dry etch, e-beam, evaporator) and monitoring of this calibration by using metrology tools (AFM, SEM, EDX)
Regular maintenance of the cleanroom’s main equipment (e-beam, evaporator, SEM, ICP, etc.) with the assistance of our lab manager and the help of tool manufacturers
Creating, developing and maintaining the user manual, maintenance guideline and checklist, calibration log file and process data sheet

Fulltime

Supervisor, QC Microbiology, Second Shift

Life changing therapies. Global impact. Bridge to thousands of biopharma compani...

Location

United States , Bedford

Salary:

Not provided

PCI Pharma Services

Expiration Date

Until further notice

Requirements

Master’s degree in Microbiology, Biology, or related life science (preferred)
Bachelor’s degree with 5+ years of progressive GMP QC Microbiology experience
1–3+ years in a leadership role within a QC Microbiology lab
Hands-on experience with aseptic processing, environmental monitoring, and USP microbiological testing required
Skilled in data analysis and report writing
Must be able to work across NH PCI sites, including remote locations
Ability to gown for ISO-classified cleanroom work
Ability to lift up to 20 lbs
Occasional off-shift support may be required

Job Responsibility

Lead daily lab operations—including oversight of environmental monitoring, microbial testing of utilities (USP <61>, <62>, <85>), and in-process/final product testing
Supervise, mentor, and develop a high-performing team of microbiologists and lab personnel
Manage scheduling, workloads, and ensure timely testing and release of all microbiological samples
Perform risk assessments and investigations (EM excursions, aseptic incidents) and implement effective CAPAs
Perform data trending and statistical analysis
author quarterly reports on environmental and utility data
Oversee testing for endotoxins, bioburden, growth promotion, EM sampling, and clean utility sampling
Collaborate cross-functionally with Operations and Facilities to protect aseptic integrity
Support and coordinate equipment validation, calibration, and maintenance
Drive compliance with cGMP, FDA, EU, and international microbiology regulations

What we offer

Opportunities for growth and advancement within a science-driven, patient-focused organization
A collaborative, team-oriented environment with cross-functional exposure
The chance to make an impact on public health by ensuring the safety of every batch
Ongoing training and development to keep your skills sharp in a fast-evolving industry

Fulltime

Cleanroom & Lab Manager

ICEYE

Location:
Spain , València

Category:
Manufacturing

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
January 26, 2026

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ICEYE

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Job Description:

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Job Posted:January 26, 2026

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January 26, 2026