MILLENNIUMSOFT
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Clinical Lab Specialist - Urgent Need
role at
MillenniumSoft Inc 11 months ago Be among the first 25 applicants Join to apply for the
Clinical Lab Specialist - Urgent Need
role at
MillenniumSoft Inc Level Of Experience: Mid-Level
Employment Type: Contract on W2 (Need US Citizens or GC Holders Only)
This laboratory-based position will provide input to design, evaluation, execution and reporting for safety and efficacy of new or modified in-vitro diagnostic devices, as well as provide innovative ideas cross functionally with other business units. Possess a technical competence and works with human blood in clinical laboratory disciplines such as phlebotomy, chemistry, hematology, coagulation, urinalysis, point of care and capable operation of numerous instrument platforms. Responsible for managing clinical laboratory studies and complaint testing through a variety of clinical testing methods. Knowledge and expertise demonstrating safety and efficacy of new or modified in-vitro diagnostic devices, as well provide innovative ideas outside of the core business. Develop/implement new testing methodologies in collaboration with R&D. Responsible for understanding product design, function and able to apply quality and regulatory standards. Capable of performing Clinical Software Validations (CSV) and all requirements for new instrument validation/qualification as it relates to best practices for the IQ/OQ/PQ in the clinical lab. Utilizes technical/scientific judgment to resolve technical issues. Works with many different disciplines (manufacturing, marketing, quality, regulatory, etc.), materials, products, and processes in the development of core clinical laboratory and outside the core clinical laboratory products and services. Possesses a strong commitment to quality and continuous improvement.
Position : Clinical Lab Specialist
Location : Franklin Lakes, NJ
Duration : 12 Months
Total Hours/week : 40.00
1st Shift
Client: Medical Device Company
Job Category: Healthcare
Level Of Experience: Mid-Level
Employment Type: Contract on W2 (Need US Citizens or GC Holders Only)
Job Description
This laboratory-based position will provide input to design, evaluation, execution and reporting for safety and efficacy of new or modified in-vitro diagnostic devices, as well as provide innovative ideas cross functionally with other business units. Possess a technical competence and works with human blood in clinical laboratory disciplines such as phlebotomy, chemistry, hematology, coagulation, urinalysis, point of care and capable operation of numerous instrument platforms. Responsible for managing clinical laboratory studies and complaint testing through a variety of clinical testing methods. Knowledge and expertise demonstrating safety and efficacy of new or modified in-vitro diagnostic devices, as well provide innovative ideas outside of the core business. Develop/implement new testing methodologies in collaboration with R&D. Responsible for understanding product design, function and able to apply quality and regulatory standards. Capable of performing Clinical Software Validations (CSV) and all requirements for new instrument validation/qualification as it relates to best practices for the IQ/OQ/PQ in the clinical lab. Utilizes technical/scientific judgment to resolve technical issues. Works with many different disciplines (manufacturing, marketing, quality, regulatory, etc.), materials, products, and processes in the development of core clinical laboratory and outside the core clinical laboratory products and services. Possesses a strong commitment to quality and continuous improvement.
Primary Duties, Responsibilities & Authorities
Provides input to and conducts scientific investigations in areas of considerable scope and complexity. Explores, identifies, and recommends solution, concepts and principles. Adapts methodologies as needed for areas related to the core clinical laboratory. Conducts clinical testing, maintains laboratory instrumentation/reagent test systems and inventory to strategically align with the priorities within the lab and business objectives. Implements and documents Quality Assurance and Quality Control procedures as they pertain to instrumentation and methodology. Conducts instrument verification per CLSI guidelines, assists with updates and preparation of procedures and instrument performance documentation in compliance with GLP and GCP. Performs Clinical Software Validations (CSV) and all requirements for new instrument validation/qualification as it relates to best practices for the IQ/OQ/PQ in the clinical lab. Keeps current in the field of Clinical Laboratory Science through review of technical literature, participation in continuing education via webinars/symposia and or customer visits. Trains new associates (permanent or temporary) on the Laboratory workflow. Senses and monitors trends in laboratory practice and utilizes this information to recommend new projects and influence ongoing projects. Participates in development of the clinical strategy for all client IDS- Specimen Management products and is responsible for generation of scientific and clinical information to support product conceptualization, feasibility, and development. Responsible for scientific integrity and clinical accuracy of all claims and communications made concerning specific PAS products globally. Responsible for management of individual focused projects to complex projects involving multiple internal clinical studies/evaluations. This position provides support from a base of clinical experience and knowledge to resolve customer complaints through clinical investigations. This position will also provide support to guide and implement innovation, product development, clinical testing, manufacturing, and post market surveillance via interfacing with R&D and GCD to insure successful and timely completion of projects.
Knowledge And Skills
Strong working knowledge of clinical laboratory science Excellent verbal and written communications skills Awareness/basic knowledge of GCP/GLP and ISO regulations Clinical Software Validations (CSV) and all requirements for new instrument validation/qualification as it relates to best practices for the IQ/OQ/PQ in the clinical lab Phlebotomy is a plus Experience with human blood specimen collection products Product Trouble shooting as it relates to clinical results Strong computer skills Strong project planning and budget management skills Develop/implement new testing methodologies in collaboration with R&D Proven understanding of clinical laboratory testing, blood collection, Urinalysis, POC and LIS/LIMS systems and an ability to apply knowledge to innovative concepts/projects beyond the core clinical laboratory.
Education AND Experience
BS/BA/MA in Clinical Laboratory Science or Medical Technology, Biology Life Sciences or health related field required. MT/MLT CLS (ASCP) or equivalent experience in a Research environment 5 years+ experience in the Clinical Laboratory environment. Seniority level
Seniority level
Mid-Senior level Employment type
Employment type
Full-time Job function
Job function
Health Care Provider Industries
Staffing and Recruiting Referrals increase your chances of interviewing at MillenniumSoft Inc by 2x Sign in to set job alerts for Clinical Specialist roles.
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Clinical Lab Specialist - Urgent Need
role at
MillenniumSoft Inc 11 months ago Be among the first 25 applicants Join to apply for the
Clinical Lab Specialist - Urgent Need
role at
MillenniumSoft Inc Level Of Experience: Mid-Level
Employment Type: Contract on W2 (Need US Citizens or GC Holders Only)
This laboratory-based position will provide input to design, evaluation, execution and reporting for safety and efficacy of new or modified in-vitro diagnostic devices, as well as provide innovative ideas cross functionally with other business units. Possess a technical competence and works with human blood in clinical laboratory disciplines such as phlebotomy, chemistry, hematology, coagulation, urinalysis, point of care and capable operation of numerous instrument platforms. Responsible for managing clinical laboratory studies and complaint testing through a variety of clinical testing methods. Knowledge and expertise demonstrating safety and efficacy of new or modified in-vitro diagnostic devices, as well provide innovative ideas outside of the core business. Develop/implement new testing methodologies in collaboration with R&D. Responsible for understanding product design, function and able to apply quality and regulatory standards. Capable of performing Clinical Software Validations (CSV) and all requirements for new instrument validation/qualification as it relates to best practices for the IQ/OQ/PQ in the clinical lab. Utilizes technical/scientific judgment to resolve technical issues. Works with many different disciplines (manufacturing, marketing, quality, regulatory, etc.), materials, products, and processes in the development of core clinical laboratory and outside the core clinical laboratory products and services. Possesses a strong commitment to quality and continuous improvement.
Position : Clinical Lab Specialist
Location : Franklin Lakes, NJ
Duration : 12 Months
Total Hours/week : 40.00
1st Shift
Client: Medical Device Company
Job Category: Healthcare
Level Of Experience: Mid-Level
Employment Type: Contract on W2 (Need US Citizens or GC Holders Only)
Job Description
This laboratory-based position will provide input to design, evaluation, execution and reporting for safety and efficacy of new or modified in-vitro diagnostic devices, as well as provide innovative ideas cross functionally with other business units. Possess a technical competence and works with human blood in clinical laboratory disciplines such as phlebotomy, chemistry, hematology, coagulation, urinalysis, point of care and capable operation of numerous instrument platforms. Responsible for managing clinical laboratory studies and complaint testing through a variety of clinical testing methods. Knowledge and expertise demonstrating safety and efficacy of new or modified in-vitro diagnostic devices, as well provide innovative ideas outside of the core business. Develop/implement new testing methodologies in collaboration with R&D. Responsible for understanding product design, function and able to apply quality and regulatory standards. Capable of performing Clinical Software Validations (CSV) and all requirements for new instrument validation/qualification as it relates to best practices for the IQ/OQ/PQ in the clinical lab. Utilizes technical/scientific judgment to resolve technical issues. Works with many different disciplines (manufacturing, marketing, quality, regulatory, etc.), materials, products, and processes in the development of core clinical laboratory and outside the core clinical laboratory products and services. Possesses a strong commitment to quality and continuous improvement.
Primary Duties, Responsibilities & Authorities
Provides input to and conducts scientific investigations in areas of considerable scope and complexity. Explores, identifies, and recommends solution, concepts and principles. Adapts methodologies as needed for areas related to the core clinical laboratory. Conducts clinical testing, maintains laboratory instrumentation/reagent test systems and inventory to strategically align with the priorities within the lab and business objectives. Implements and documents Quality Assurance and Quality Control procedures as they pertain to instrumentation and methodology. Conducts instrument verification per CLSI guidelines, assists with updates and preparation of procedures and instrument performance documentation in compliance with GLP and GCP. Performs Clinical Software Validations (CSV) and all requirements for new instrument validation/qualification as it relates to best practices for the IQ/OQ/PQ in the clinical lab. Keeps current in the field of Clinical Laboratory Science through review of technical literature, participation in continuing education via webinars/symposia and or customer visits. Trains new associates (permanent or temporary) on the Laboratory workflow. Senses and monitors trends in laboratory practice and utilizes this information to recommend new projects and influence ongoing projects. Participates in development of the clinical strategy for all client IDS- Specimen Management products and is responsible for generation of scientific and clinical information to support product conceptualization, feasibility, and development. Responsible for scientific integrity and clinical accuracy of all claims and communications made concerning specific PAS products globally. Responsible for management of individual focused projects to complex projects involving multiple internal clinical studies/evaluations. This position provides support from a base of clinical experience and knowledge to resolve customer complaints through clinical investigations. This position will also provide support to guide and implement innovation, product development, clinical testing, manufacturing, and post market surveillance via interfacing with R&D and GCD to insure successful and timely completion of projects.
Knowledge And Skills
Strong working knowledge of clinical laboratory science Excellent verbal and written communications skills Awareness/basic knowledge of GCP/GLP and ISO regulations Clinical Software Validations (CSV) and all requirements for new instrument validation/qualification as it relates to best practices for the IQ/OQ/PQ in the clinical lab Phlebotomy is a plus Experience with human blood specimen collection products Product Trouble shooting as it relates to clinical results Strong computer skills Strong project planning and budget management skills Develop/implement new testing methodologies in collaboration with R&D Proven understanding of clinical laboratory testing, blood collection, Urinalysis, POC and LIS/LIMS systems and an ability to apply knowledge to innovative concepts/projects beyond the core clinical laboratory.
Education AND Experience
BS/BA/MA in Clinical Laboratory Science or Medical Technology, Biology Life Sciences or health related field required. MT/MLT CLS (ASCP) or equivalent experience in a Research environment 5 years+ experience in the Clinical Laboratory environment. Seniority level
Seniority level
Mid-Senior level Employment type
Employment type
Full-time Job function
Job function
Health Care Provider Industries
Staffing and Recruiting Referrals increase your chances of interviewing at MillenniumSoft Inc by 2x Sign in to set job alerts for Clinical Specialist roles.
Science Laboratory Assistant (Part Time)
Laboratory Technician - Newark, DE, 19702
Laboratory Technician 3 - Newark, DE, 19702
Laboratory Technician 2 - Newark, DE, 19702
New York, NY $50,000.00 - $70,000.00 1 week ago Laboratory Technician 2 - Newark, DE, 19702
Laboratory Technician 3 (Tuesday --Saturday) _ Newark, DE, 19702
Clinical Lab Specialist (No Microbiology, No Covid testers, No Chemical lab)
White Plains, NY $39,000.00 - $58,488.64 1 week ago Research Assistant | Laboratory of Molecular Genetics and Immunology
White Plains, NY $39,000 - $58,488.64 1 month ago Science Laboratory and Department Assistant
Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr