The Fuel / Lube Technician is a developing Maintenance Technician role focused on maintaining equipment, ensuring safe production, and adhering to safety standards.
Locations (2)
Kermit, Texas, United States
Bloomington, Indiana, United States
Responsibilities
Work with employees to ensure a high level of accuracy and engagement on hazard identification and control
Engage crews and leadership to define processes that motivate working towards common goals
Assist with MSHA regulatory training and verify compliance to standards
Assist with training proficiency audits
Involvement in risk assessment processes at various levels of the organization
Own the trending, review, and interpretation of environmental monitoring data for filling lines, identifying adverse trends and emerging contamination risks.
Responsibilities
Own the trending, review, and interpretation of environmental monitoring data for filling lines, including viable and non-viable particulate monitoring, identifying adverse trends and emerging contamination risks.
Ensure environmental and particulate monitoring programmes, limits, sampling plans, escalation processes, and controls remain scientifically justified and aligned with EU GMP Annex 1 and the site Contamination Control Strategy.
Drive risk-based improvements to monitoring programmes, processing controls, filling line practices, and contamination control governance.
Provide microbiological expertise for the development, maintenance, and periodic review of the site Contamination Control Strategy.
Review microbiological excursions, particulate monitoring events, and contamination control failures, ensuring robust root cause analysis, appropriate CAPAs, and effective follow-up.
Requirements
Degree in Microbiology, Biotechnology, or related scientific discipline
Nice to have: Technical interpretation of microbiological and particulate monitoring data
Nice to have: Risk-based problem solving
Nice to have: Clear communication with QC, QA, Manufacturing, Engineering, and Regulatory stakeholders
MedTech Operator focused on washing and packaging activities in a regulated MedTech environment, supporting the production of an innovative product used by patients worldwide.
Compensation
a suitable salary and additional benefits.
Responsibilities
Washing glassware used in the production process according to procedures
Setting up, operating and monitoring the packaging machines
Preparing the packaging line and checking packaging materials
Packaging the product according to procedures, Good Manufacturing and Documentation Practices and the quality standards of the area
Inspecting product quality according to specifications
Filling Line Operator responsible for operational activities within a GMP-regulated production environment, focusing on aseptic Fill & Finish for advanced therapeutics.
Compensation
a suitable salary and additional benefits.
Responsibilities
Preparing, setting up, operating, monitoring and shutting down the aseptic filling line and isolator, including decontamination, glove testing, cleaning and line clearance
Performing or supporting upstream and downstream processing activities where required
Performing routine and non-routine interventions and supporting environmental monitoring and in-process controls
Participating in APS campaigns, qualification activities, water runs, engineering runs and GMP manufacturing campaigns
Supporting material transfers, product handling and reconciliation activities
Ensure quality compliance across manufacturing operations while advancing the mission to make the world healthier, cleaner, and safer, providing essential quality oversight through detailed documentation review, process monitoring, and collaboration with cross-functional teams.
Responsibilities
Provide essential quality oversight through detailed documentation review
Lead and support technical operations in Singapore overseeing complex engineering and construction projects for cleanroom facilities and controlled environments.
Responsibilities
Lead and support technical operations in Singapore
Oversee projects ranging from medium to large-scale greenfield and retrofit projects
Hold full responsibility for all technical matters including engineering, design, construction, commissioning, qualification, project manpower planning, and schedules
Lead and oversee engineering, construction, commissioning, qualification, validation support, and handover of cleanroom facilities
Collaborate with project teams and PMs to ensure sufficient project manpower and resource allocation
Support the development, qualification, and routine execution of analytical methods for RNA, lipids, lipid nanoparticles (LNPs), and related bioconjugates at our Seattle site.
Compensation
Salary range: $65,000 – $80,000 total compensation, including bonus, depending on experience and qualifications.
Responsibilities
Prepare RNA, oligonucleotide, lipid, LNP, antibody, and bioconjugate samples for analytical testing according to established procedures and experimental plans.
Perform HPLC/UHPLC analyses using UV and/or charged aerosol detection (CAD), including sample and standard preparation, instrument sequence setup, chromatogram review, peak integration, and initial data assessment.
Support chromatographic methods for evaluating RNA purity, lipid identity and purity, lipid composition, residual components, and related product-quality attributes.
Assist with preparative chromatography, fraction collection, sample tracking, and evaluation of purification fractions for RNA and related development projects.
Support analytical method development, optimization, troubleshooting, and transfer under the guidance of senior scientists and the group lead.
Requirements
Bachelor's degree in Chemistry, Analytical Chemistry, Biochemistry, Biology, Biotechnology, Pharmaceutical Sciences, or a related scientific discipline.
The Director of Sterility Assurance, Cell Therapy Operations, provides site-level leadership and strategic direction for microbiological and virological control across cell therapy and lentiviral manufacturing at the Raritan facility.
Compensation
The anticipated base pay range for this position is : $154,000.00 - $265,650.00
Responsibilities
Own the Raritan sterility assurance and contamination control program
Develop, implement, maintain, and continuously improve the site contamination control strategy
Provide governance and oversight for microbiological and virological control programs
Lead site risk assessments, gap assessments, mitigation plans, and sustainable remediation activities
Provide strategic input to facility and equipment design, process design, material and personnel flows, cleaning and disinfection, segregation controls, maintenance, environmental monitoring, and microbiological testing
Requirements
Bachelor’s degree in microbiology, pharmacy, engineering, chemistry or a related scientific / engineering discipline
Advanced degree (MS/PHD) preferred
Nice to have: MS/PHD
Nice to have: Aseptic processing in ISO 5 environments
Lead, coach, develop, and hold accountable the Project Engineers and Implementation Specialists assigned to the Data Center practice.
Set clear expectations for technical leadership, execution quality, utilization, communication, behavior, and employee development.
Maintain a current view of PE and IS skills, experience, certifications, readiness, location, availability, and development needs.
Create training, mentoring, succession, and career-development plans that build leadership depth and reduce dependency on individual experts.
Work with Resource Management and delivery leaders to align qualified PEs and ISs to projects based on complexity, technical risk, geography, and customer requirements.
Requirements
Bachelor's degree or equivalent technical, trade, military, operational, and leadership experience.
Nice to have: 10+ years of progressive Data Center field engineering or infrastructure-delivery experience
Nice to have: Experience supporting complex, high-volume, multi-site, colocation, mission-critical, or hyperscale programs
Nice to have: Experience developing technical proficiency frameworks
Nice to have: Experience evaluating and developing national, regional, specialty, or union-capable delivery partners
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