System Manager Laboratory Information Systems Job at American Nursing Care (Phoenix)

Microbiology Product Testing Laboratory Manager - 14 Month FTC/Secondment

We are seeking an experienced and capable QC Release Laboratory Manager, Microbi...

Location

United Kingdom , Barnard Castle

Salary:

Not provided

GSK

Expiration Date

Until further notice

Requirements

Higher National Certificate (HNC)/Higher National Diploma (HND) in a scientific or related discipline (e.g., Microbiology, Pharmacy, or other relevant science fields)
Experience in regulatory and technical knowledge of GMP requirements and GSK quality regulations
Experience in supervising teams or leading activities within GMP/GLP operations or quality functions
Experience to analyse complex information and makes decisions based on defined risk criteria, using structured communication and established mentoring process
Experience compiling technical information into structured documentation, present data and conclusions clearly to relevant stakeholders, and provide coaching using predefined materials and standardized processes
Experience planning, organising, and managing defined workloads, including the use of specified IT systems to meet operational timelines
Degree in a scientific or related discipline, such as Microbiology, Biomedical Sciences, Applied Biology, Quality Assurance, or other STEM fields, with experience working in regulated environments
Practical working knowledge of GPS principles, including PPM, problem solving, CI, and LSW and knowledge to improving GPS Maturity Scores

Job Responsibility

Oversee the performance of the QC Release Microbiology Team to deliver finished product testing and batch release requirements
Ensure robust, validated, and compliant microbiological methodologies in line with regulatory and company quality standards
Drive continuous improvement, deviations, root cause analysis, process improvements within the team
Train and develop team members, creating structured development plans along with stretch objectives, and fostering a safe and efficient working environment
Support microbiology testing-related project activities, ensuring adherence to schedule, including New Product Introduction (NPI) requirements
Lead preparation activity and represent the department during external regulatory inspections and company internal audits
Provide technical leadership, supervise lab investigations, and address GMP microbiological issues in collaboration with production and quality teams
Drive resource planning, monitor team workload, compliance metrics and training status
Prioritisation to meet workload demands effectively
Support the QC improvement plan aligned to the 6 QC KPIs

What we offer

Competitive base salary
Annual bonus based on company performance
Flexible working options available for most roles
Learning and career development
Access to healthcare & wellbeing programmes
Employee recognition programmes

Fulltime

Manager Laboratory Services

As a Manager, Laboratory Services, you will oversee daily operations and strateg...

Location

United States , Little Rock

Salary:

40.06 - 59.59 USD / Hour

CommonSpirit Health

Expiration Date

Until further notice

Requirements

Bachelors Of Science in biological or chemical sciences, as defined by CLIA.
International Medical Laboratory Scientist
Blood Banking
Chemistry - ASCP
Clinical Laboratory Scientist
Clinical Laboratory Technologist
Technologist in Molecular Biology
Medical Laboratory Scientist - Med Technologist
Medical Technologist AAB
Technologist in Microbiology

Job Responsibility

Oversee daily operations and strategic development of the clinical laboratory
Manage and mentor staff, monitor test quality, ensure regulatory compliance, and collaborate with pathologists and clinical teams to optimize workflows and integrate new technologies
Responsible for the overall administration of all laboratory operations
Monitors employee and departmental performance to ensure adherence to policies and procedures, timelines and regulatory requirements
Remains knowledgeable on new technologies, methods and approaches within the laboratory community
Stays informed on and quickly ensures compliance with changes to regulatory and state requirements
Ensures ongoing compliance with federal and state regulations
Responsible for development, implementation and compliance with policy and procedures
Develops monitoring systems to improve quality
initiates corrective action plans, and monitors results

What we offer

medical
prescription drug
dental
vision plans
life insurance
paid time off
tuition reimbursement
retirement plan benefit(s) including 401(k), 403(b), and other defined benefits offerings

Fulltime

Manager Laboratory Services

As a Manager, Laboratory Services, you will oversee daily operations and strateg...

Location

United States , Little Rock

Salary:

40.06 - 59.59 USD / Hour

American Nursing Care

Expiration Date

Until further notice

Requirements

Bachelors Of Science in biological or chemical sciences, as defined by CLIA.
International Medical Laboratory Scientist
Blood Banking
Chemistry - ASCP
Clinical Laboratory Scientist
Clinical Laboratory Technologist
Technologist in Molecular Biology
Medical Laboratory Scientist - Med Technologist
Medical Technologist AAB
Technologist in Microbiology

Job Responsibility

Oversee daily operations and strategic development of the clinical laboratory, ensuring accurate, timely, and high-quality diagnostic testing
Manage and mentor staff, monitor test quality, ensure regulatory compliance, and collaborate with pathologists and clinical teams to optimize workflows and integrate new technologies
Responsible for the overall administration of all laboratory operations
Monitors employee and departmental performance to ensure adherence to policies and procedures, timelines and regulatory requirements
Remains knowledgeable on new technologies, methods and approaches within the laboratory community
Stays informed on and quickly ensures compliance with changes to regulatory and state requirements
Ensures ongoing compliance with federal and state regulations
Responsible for development, implementation and compliance with policy and procedures
Develops monitoring systems to improve quality
initiates corrective action plans, and monitors results

What we offer

medical
prescription drug
dental
vision plans
life insurance
paid time off (full-time benefit eligible team members may receive a minimum of 14 paid time off days, including holidays annually)
tuition reimbursement
retirement plan benefit(s) including, but not limited to, 401(k), 403(b), and other defined benefits offerings

Fulltime

Manager Laboratory Services

As a Manager, Laboratory Services, you will oversee daily operations and strateg...

Location

United States , Bryan

Salary:

41.97 - 62.43 USD / Hour

American Nursing Care

Expiration Date

Until further notice

Requirements

Bachelors Of Science in biological or chemical sciences, as defined by CLIA
International Medical Laboratory Scientist
Blood Banking
Chemistry - ASCP
Clinical Laboratory Scientist
Clinical Laboratory Technologist
Technologist in Molecular Biology
Medical Laboratory Scientist - Med Technologist
Medical Technologist AAB
Technologist in Microbiology

Job Responsibility

Oversee daily operations and strategic development of the clinical laboratory, ensuring accurate, timely, and high-quality diagnostic testing
Manage and mentor staff, monitor test quality, ensure regulatory compliance, and collaborate with pathologists and clinical teams to optimize workflows and integrate new technologies
Demonstrate strong leadership, expert technical knowledge, and strategic management skills, driving continuous quality improvement and fostering a collaborative team for essential diagnostic support
Responsible for the overall administration of all laboratory operations
Monitors employee and departmental performance to ensure adherence to policies and procedures, timelines and regulatory requirements
Remains knowledgeable on new technologies, methods and approaches within the laboratory community
Stays informed on and quickly ensures compliance with changes to regulatory and state requirements
Ensures ongoing compliance with federal and state regulations
Responsible for development, implementation and compliance with policy and procedures
Develops monitoring systems to improve quality

What we offer

medical, prescription drug, dental, vision plans, life insurance, paid time off, tuition reimbursement, retirement plan benefit(s) including, but not limited to, 401(k), 403(b), and other defined benefits offerings

Fulltime

Information System Security Officer

Astrion has an exciting opportunity for an SE-3 Information System Security Offi...

Location

United States , Eglin Air Force Base

Salary:

Not provided

Astrion

Expiration Date

Until further notice

Requirements

Bachelor's Degree and 3- 10 years of relevant experience. Additional experience may be substituted for education
Active Top Secret Clearance is required
Must be able to obtain and maintain a DoD TS/SCI clearance (i.e. DCID 6/4 eligibility)
Eligibility for access to Special Access Program (SAP) Information
US Citizenship required
In-depth knowledge of RMF with the ability to write all supporting documentation
Able to produce Assess and Authorize (A&A) packages with extensive experience in building, configuring, and adapting DoD Information System (IS) RMF documentation to meet test requirements
Well-versed in National Institute of Standards and Technology (NIST) security control guidance to build Security Control Traceability Matrix (SCTM) features and to assess the vulnerability of various operating systems within the physical operating environment
Self-starter, able to multi-task and perform effectively in a highly-dynamic, fast-paced environment with very little supervision
Able to deploy CONUS/OCONUS and possess a strong ability to work independently

Job Responsibility

Will primarily perform duties of an Information Systems Security Officer (ISSO) in an Advanced Programs Developmental Test, and Evaluation laboratory
Requires the production of a high volume of written documentation throughout the Risk Management Framework (RMF) life cycle for a numerus systems in multiple operating locations
Conducts technical and non-technical reviews and audits as prescribed by the Information System Security Manager (ISSM)

What we offer

Competitive salaries
Continuing education assistance
Professional development
Multiple healthcare benefits package options
401K with employer matching
Competitive time off policy along with a federally recognized holiday schedule

Ict Systems Analyst (Laboratory Infrastructure)

Our client has a long term contract opportunity for a highly accomplished ICT Sy...

Location

Australia , Sydney

Salary:

Not provided

Randstad

Expiration Date

June 27, 2026

Requirements

Demonstrated experience (minimum of 3 years) supporting the delivery of IT enhancement projects. Such experience may relate to instrument control software, data mapping and storage, workflow management or information management systems
Demonstrated self-motivation and organisational skills, combined with well-developed analytical and problem-solving skills, working autonomously under very broad direction
The ability to work collaboratively in a team and demonstrated experience of negotiation and influence to establish and maintain productive working relationships with management as well as operational staff and vendors
Excellent communication skills, particularly for engaging with a diverse range of laboratory staff, report and technical writing
Tertiary qualifications in either chemistry/biology/physics/engineering/ICT areas are desirable
Must hold an active Baseline security clearance

Job Responsibility

Engage with testing laboratories to develop and implement work practices and associated procedures to leverage the air gapped Local Area Network. Support will be provided for business change management activities
Mapping of data flows and storage, developing a current state understanding of where and how data is stored
Report and present on solution uptake and issues to management and staff user forums. This includes contributing to ICT project governance reporting
Interact with laboratory users and software vendors to create and maintain a register of current software and licences to allow for planning and supporting procurement activities

!

Laboratory Programme Manager

Laboratory Programme Manager – Fugro Location: UK (office-based laboratory envi...

Location

United Kingdom , Wallingford

Salary:

Not provided

Fugro

Expiration Date

Until further notice

Requirements

Degree (or equivalent) in project/programme management, geotechnical, civil engineering, or a related field
Experience in project or programme management (typically 3–8 years) within a technical or engineering environment
Strong organisational and communication skills, with the ability to manage multiple priorities and stakeholders
Commercial awareness, with the ability to monitor budgets and contribute to financial performance
Confident using project management and standard office software tools

Job Responsibility

Develop and manage laboratory testing schedules, ensuring all project requirements are clearly defined and delivered on time
Act as the primary point of contact for clients and internal teams on complex projects, building strong, trusted relationships
Monitor testing progress and proactively address risks, delays, or changes to maintain delivery targets
Coordinate information flow between laboratory teams and project stakeholders, ensuring clear and timely communication
Support financial and contractual processes, including budget tracking and revenue recognition
Drive continuous improvement by monitoring laboratory utilisation and supporting process and system enhancements
Champion quality, safety, and compliance, promoting QA/QC best practices and adherence to Fugro's QHSSE standards

What we offer

Extensive career & training opportunities both nationally and internationally
Competitive salary
Contributory pension scheme
Private medical insurance
Health cash plan
Group life assurance
Group income protection
Discounted gym membership
Discounts platform
The Fugro Card (pre-paid virtual visa card, which earns cash back automatically when money is spent at any participating retailers)

Fulltime

Clinical Laboratory Study Manager

Location

United States

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Minimum of 6 years clinical research experience with academic, Contract Research Organization, pharmaceutical or biotech industry
Working knowledge of clinical drug development process and clinical databases, as well as ICH, GCP guidelines, and US FDA and/or local country regulations as applicable
Requires bachelor degree in life sciences or equivalent (i.e., science, technology, engineering, or mathematics) or relevant work experience. Biology or equivalent major preferred.
Strong project management and organization skills in a matrix environment
Analytical and problem-solving experience
Excellent written and verbal communication skills
Effective communication and interpersonal skills, with proven ability to build relationships internally and externally
Fluent in speaking/writing English
Proficiency in Microsoft Office applications, including strong excel knowledge, as well as relevant role specific systems
Proficiency in Python, R, Perl, SQL or other programming languages, as well as familiarity with APIs and Linux/Unix environments, if acting as programming lead for supplies and laboratory operations

Job Responsibility

Participates in cross-functional study team meetings and workstreams to support the delivery of the precision medicine strategy for the assigned studies
Supports clinical study teams as subject-matter expert for technical and operational matters related to sample management and testing, including anticipating challenges, managing risk across projects and responding queries from internal and external stakeholders
Works with clinical study teams on the development and review of sample-related sections of study-specific documents such as the clinical protocol, Informed Consent Forms (ICFs) and sample management guidelines
Supports project management and study set-up teams in the creation and validation of specialty laboratory databases for data collection and sample kit tracking
Manages all activities related to biosample process planning and execution, including storage, shipping, and data transfer throughout the study lifecycle
Oversees the acquisition and testing of clinical trial samples designated for biomarker research (including human tissue, whole blood, plasma, serum, etc.), liaising with relevant stakeholders to assess biosample vendors, review proposals/bids, and define contractual scope
Forecasts operational costs and timelines, and manages budgeting, invoicing and reporting for study-related operations
Works closely with data management and biostatistics leads to determine how biomarker data will be captured, blinded, transferred and reported for clinical trials
Develops and reviews data transfer specifications and related documents
Provides guidance and training to clinical teams and investigative sites regarding collection, storage and shipment of biospecimens to ensure compliance with the clinical protocol

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System Manager Laboratory Information Systems

Job Description

Job Responsibility

Requirements

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