Laboratory Systems Administrator 2
jobdivaPortsmouth, NH
Laboratory Systems Administrator 2
jobdivaPortsmouth, NH
yesterday
Occupations
Quality Control Systems ManagersMedical and Clinical Laboratory TechnologistsMedical and Clinical Laboratory TechniciansIndustries
Testing Laboratories and ServicesPharmaceutical Preparation ManufacturingResearch and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)About the role
Summary:
Responsible for the accurate setup and loading of master data into the gLIMS according to global guidelines and data principles. This role plays a crucial part in ensuring data integrity and establishing local support structures for ongoing data management.
Key Accountabilities:
Perform local master data setup and load in alignment with global guidelines and data principles.
Build and input all initially required master data into the global LIMS system, including consumables, sampling plans, specifications, parameter lists, test methods, and LES templates.
Conduct local data cleansing to ensure data quality and accuracy.
Develop local work instructions to detail the execution of global processes at site level.
Proficiency in using Lab Vantage LIMS or similar systems and familiarity with quality standards and regulatory requirements.
Ability to work independently and with the team with little guidance.
Qualifications:
Experience in data management and familiarity with master data setup and loading processes.
Strong attention to detail and analytical skills to ensure data accuracy and quality.
Ability to develop clear and concise local work instructions.
Knowledge of QC lab operations and related data requirements.
Proficiency in using LIMS or similar data management system Skills Advanced technical knowledge of Quality control and manufacturing operations.
Working knowledge and experience with Quality Systems including deviations, change controls, CAPAs, OTNs, deviations; both the system (Track Wise) and the practical applications in operations
Knowledgeable in process, equipment, cleaning, and computer system validations to the extent of being able to effectively review and approve protocols and reports and support implementation of new equipment.
Demonstrated ability to manage medium to large sized projects within required timeframes.
Demonstrate ability for effective Planning, Organizing and Controlling competency
Demonstrate sound decision making.
Ability to work inter-departmentally and with customers.
Demonstrates role model behaviors for GMP and Safety behaviors Education Bachelor of Science, Science related discipline or relevant experience in the field. Work ExperienceQC, Enterprise systems, Validation, Highly Experienced - 10+ years
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JOB OVERVIEW
Experience level
Mid
Location
Portsmouth, NH
Occupation
Quality Control Systems Managers
Industry
Testing Laboratories and Services
Posted
yesterday
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