QC Reviewer - Bioanalytical at Labcorp

Singapore, Singapore, Singapore -

Full Time

Start Date

Immediate

Expiry Date

26 Mar, 26

Salary

0.0

Posted On

26 Dec, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Control, Regulatory Compliance, Data Review, SOP Knowledge, Auditing, Error Tracking, Quality Improvement, Training Development, Documentation, Ligand Binding Assay, GxP Experience, Communication, Problem Solving, Team Collaboration, Attention to Detail, Self-Development

Industry

Medical Practices

Description

Duties and Responsibilities: Assists co-workers and internal customers with interpretation of regulatory requirements (e.g., GLPs), SOP requirements, and other guidance documents, as applicable. Reviews data to ensure quality standards are met and to verify compliance with applicable SOP and regulatory requirements. Maintains working knowledge of client SOPs and requirements as applicable. Ensures that data reviewed meets applicable client SOPs and requirements. Performs regularly scheduled audits of departmental systems and supporting data, as applicable, to ensure proper documentation and maintenance (e.g. training files, client SOP reading lists, logbooks, etc.). Collect error tracking data for items reviewed and reports trends as feedback to the department. Monitors citation trends and performs follow-up actions with respondents, management, or others, if needed, to prevent recurring citations, problems, or errors. Promotes quality and regulatory compliance within the department by working with operations and scientific staff to resolve service/quality issues, serving on a committee, assisting with the development of training programs related to documentation and quality, or other related involvement. Notifies management of observed quality/compliance issues and service failures. Participates in quality improvement opportunities and harmonization efforts to promote best practices. Participates in project debrief meetings as needed. Facilitates changes to SOPs, policies, training materials, and other documents as applicable. Complete self-development opportunities. Performs other related duties as assigned. Requirements: Bachelor of Science/Arts (BS/BA) degree. Ability to efficiently use basic software (e.g., Word, Excel, PowerPoint). Preferably with good knowledge of ligand binding assay and GxP experience. Experience may be substituted for education. For example, a two-year Associate degree plus 2 years applicable experience may be substituted for a BS/BA degree Labcorp is proud to be an Equal Opportunity Employer: Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. We encourage all to apply If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement. We believe in the power of science to change lives. Labcorp is a leading global life sciences company that provides vital information to help doctors, hospitals, pharmaceutical companies, researchers, and patients make clear and confident decisions. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations to improve health and improve lives. Here, you can join our nearly 70,000 employees, serving clients in more than 100 countries, as we work together to transform approaches to patient care.

Responsibilities

The QC Reviewer assists with the interpretation of regulatory requirements and reviews data to ensure compliance with quality standards. They also perform audits, collect error tracking data, and promote quality and regulatory compliance within the department.