Description:

　　Assists with administration, development and coordination of Quality System based on the current Pennsylvania Chapter 252 and Chapter 109 standards and all applicable accrediting authorities.

　　Assists with completing accreditation applications for all applicable accrediting authorities.

　　Develops, reviews, modifies, and maintains SOPs for analyses and supporting activities in accordance with regulatory requirements and laboratory policies.

　　Administers lab training records including but not limited to Demonstration of Capability and Method Detection Limits.

　　Assists with the review of laboratory data to ensure that regulatory and client requirements are met.

　　Assists with reporting of results to regulatory agencies.

　　Assist with scheduling and conducting internal audits of each laboratory department and supporting areas.

　　Documents and follows up on Corrective Actions in the laboratory departments and supporting areas.

　　Assists with Proficiency Test scheduling, ordering, and reporting.

　　Assists with the scheduling, tracking, and coordination of compliance samples

　　Assists with preparation of requested documentation for laboratory assessments and responses to laboratory assessments.

　　Provides day-to-day support for laboratory and other staff and assistance with special monitoring projects, i.e. UCMR and subcontracting of samples.

　　Administer Quality Management System (QMS) Software

　　Develop and maintain knowledge and understanding in the following areas: Laboratory methods, technology, capabilities and capacity; Laboratory Accreditation, Quality Assurance, and Quality Control; Regulatory Programs applicable to Aqua drinking water and wastewater; Client-specific needs and expectations; Subcontract laboratory capabilities and accreditations.

　　Skills:

　　Quality assurance, Gmp, Quality control, Inspection, Sop, Chemistry, Batch record, Capa, Audit, Batch record review, Document control, corrective action, lab data, quality systems management

　　Top Skills Details:

　　Quality assurance, Gmp, Quality control ,Inspection, Sop ,Chemistry, Batch record, Capa, Audit, Batch record review, Document control, corrective action, lab data, quality systems management

　　Additional Skills & Qualifications:

　　Bachelor’s Degree in chemistry, microbiology, or environmental science

　　3+ years of experience in laboratory testing and/or QA/QC.

　　Must be familiar with basic laboratory principles, analytical techniques, instrumentation, and methodology

　　Must be experienced in use of LIMS, computer spreadsheets, database, and word processing programs.

　　Mathematical or statistical knowledge or background is a plus

　　Excellent written and verbal communications skills; communicate effectively (clearly, concisely and professionally) with internal customers

　　Experience Level:

　　Intermediate Level

　　Diversity, Equity & Inclusion

　　At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

　　Hiring diverse talent

　　Maintaining an inclusive environment through persistent self-reflection

　　Building a culture of care, engagement, and recognition with clear outcomes

　　Ensuring growth opportunities for our people

　　Actalent is an equal opportunity employer.

　　About Actalent

　　Actalent connects passion with purpose. We help visionary companies advance their engineering and science initiatives through access to specialized experts that drive scale, innovation, and speed to market. With a network of almost 30,000 engineering and sciences consultants and more than 4,500 clients across the U.S., Canada, Asia, and Europe, Actalent serves many of the Fortune 500. An operating company of Allegis Group, the global leader in talent solutions, Actalent launched as a new specialized engineering and sciences services and workforce solutions brand in 2021.