Laboratory Manager
Applus+ Laboratories
Position Summary Applus+ Keystone Compliance, a regulatory compliance test, is currently seeking candidates for a Lab Manager position. The successful candidate will possess a strong work ethic, excellent character, and a commitment to producing high-quality work. We are looking for someone who can work independently, is self‑motivated, and can manage their time effectively. Key Responsibilities Lead day‑to‑day operations of the Product Safety laboratory, ensuring safe, efficient, and compliant execution of testing activities. Ensure accurate application and interpretation of applicable product safety standards (e.g., IEC, UL, EN, CSA, and other national/international safety standards). Review and approve test plans, test setups, and final test reports to ensure technical accuracy and consistency. Oversee equipment utilization, maintenance, calibration status, and capital planning for Product Safety test systems. Quality & Accreditation Ensure ongoing compliance with ISO/IEC 17025 requirements as they apply to Product Safety testing activities. Support internal and external audits, including accreditation body assessments and customer audits. Collaborate with the Quality Manager to address nonconformances, corrective actions, and continuous improvement initiatives. Maintain technical documentation, procedures, and work instructions related to Product Safety testing. Supervise, mentor, and develop Product Safety technicians and engineers. Assign workloads, manage priorities, and ensure adequate staffing to meet customer commitments. Identify training needs and support technical competency development for laboratory personnel. Foster a culture of safety, accountability, and continuous improvement within the laboratory. Customer & Business Support Serve as a technical escalation point for customers regarding Product Safety testing requirements, results, and compliance pathways. Support Sales and Project Management teams by providing technical input during quoting, test planning, and customer consultations. Participate in customer meetings to clarify requirements, explain test outcomes, and support mitigation strategies when issues arise. Contribute to service development and process improvements that enhance customer experience and operational efficiency. Safety & Compliance Ensure laboratory safety procedures are followed at all times, including proper handling of test samples, high‑voltage equipment, and environmental hazards. Promote and enforce Keystone Compliance’s safety policies and best practices. Required Qualifications Bachelor’s degree in Electrical Engineering, Mechanical Engineering, or a related technical field (or equivalent experience). Minimum 5–7 years of experience in Product Safety testing or a related compliance laboratory environment. Demonstrated experience interpreting and applying product safety standards (IEC, UL, EN, CSA, etc.). Prior experience working in an ISO/IEC 17025–accredited laboratory. Proven leadership or supervisory experience in a technical or laboratory setting. Strong technical writing skills with experience reviewing and approving formal test reports. Preferred Qualifications Experience serving as a Technical Manager or acting technical authority under ISO/IEC 17025. Familiarity with combined Product Safety and EMC testing environments. Experience supporting customer product mitigations and design consultations. Exposure to multiple industries such as industrial equipment, laboratory instruments, household/commercial appliances, or similar regulated products. Key Competencies Strong technical judgment and attention to detail. Effective people leadership and communication skills. Ability to manage multiple priorities in a fast‑paced lab environment. Customer‑focused mindset with the ability to explain complex technical concepts clearly. Commitment to quality, safety, and continuous improvement. What We Offer Opportunity to lead a critical technical function within a growing compliance and testing organization. Collaborative environment with cross‑functional exposure to Sales, Quality, and Engineering teams. Competitive compensation and benefits. Professional development and advancement opportunities within Keystone Compliance and the broader Applus+ organization. Applus+ Laboratories is an equal opportunity employer. We welcome and encourage applications from individuals of all backgrounds and provide accommodations at all hiring stages. If you require accommodations, please let us know in advance. #J-18808-Ljbffr Applus+ Laboratories
$93.1k - $232.8k
...solutions and trusted partnerships that help bring breakthrough treatments to patients faster.We are seeking a US-based Clinical Project Manager with proven experience in Immuno-oncology and Cell & Gene Therapy clinical trials to join IQVIA Biotech.OverviewAs a Clinical...SuggestedFull timePart timeLocal areaImmediate startWorldwide$93.1k - $232.8k
...delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. Clinical...SuggestedFull timeContract workPart timeLocal areaImmediate startWorldwide$93.1k - $232.8k
...expertise in the Healthcare Industry or a related field, at least 5years of prior relevant experience including > 1 year’s project management experience.Conceptual and practical knowledge of Product Development and basic knowledge of Clinical Operations or related areas....SuggestedFull timeTemporary workPart timeImmediate startWorldwide$93.1k - $232.8k
Senior Clinical Project Manager - Global Study LeadershipAt IQVIA, our Senior Project Managers play a pivotal role in bringing innovative medicines to patients worldwide. You'll provide strategic leadership for complex global clinical trials, partnering directly with sponsors...SuggestedFull timePart timeImmediate startWorldwideFlexible hours$93.1k - $232.8k
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$61.03k - $101.96k
...data collection and entry, participant compensation, study monitoring activities, etc.), and will work with the lead coordinator to manage regulatory tasks (such as study start up and close out, IRB tasks, etc.). You will have an essential role in the recruitment and...ApprenticeshipWork experience placementWork at officeFlexible hours$61.03k - $101.96k
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...while serving as a trusted resource for research teams, sponsors, and investigators. Clinical Trial Operations Coordinate and manage complex clinical research studies, including drug, device, and procedural trials involving randomization, blinding, crossover...Full timeContract workWork experience placement- ...oriented, highly skilled Clinical Research Coordinator (CRC) to manage and conduct clinical trials from study startup through site... ...ECGs, and vital signs. Collect, process, package, and ship laboratory specimens in accordance with study protocols, local laws, and IATA...Full timeContract workWork at officeLocal areaMonday to Friday
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$59.83k - $99.96k
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$25 - $30 per hour
...supports the successful implementation of clinical research studies by assisting investigators, research associates, and project managers with day-to-day study operations. This role focuses on participant recruitment and consent, data collection and management, and administrative...Contract workTemporary work$59.83k - $99.96k
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$66.27k - $107.1k
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$63.69k - $102.94k
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$64.97k - $105k
...involving human participants Experience working with oncology patient populations Strong organizational skills with the ability to manage multiple, complex clinical trials simultaneously Experience using electronic health records (EHR), Electronic Data Capture (...Full timeWork experience placement- ...methodologies for monitoring data collection. Ability to take a leadership role in implementing changes in design of clinical research management. Ability to problem solve and resolve quality control issues by changing processes. Strong written and verbal communication...Work at officeWeekend work
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$25 per hour
...Laboratory General Supervisor - Wake Forest, NC MainStreet Family Care operates over 60 fast-growing urgent care clinics across Alabama... ..., HIPAA, and infection control standards ~ Prepare and manage specimens for internal and external testing as needed ~...Shift workRotating shift- ...methodologies for monitoring data collection. Ability to take a leadership role in implementing changes in design of clinical research management. Ability to problem solve and resolve quality control issues by changing processes. Strong written and verbal communication...Work at office
$66.27k - $107.1k
...in these policies and processes. Participates in or leads the development of institutional policies and guidance documents about managing investigational product (IP). Serves as expert resource and trainer to implement and comply with systems for managing and documenting...Full timeWork experience placementWorldwide$55k - $70k
...pediatric populations are supported by the CRI Pediatric Clinical Research Unit (PedsCRU), which provides infrastructure such as program management, regulatory support, data management, sample processing, training, and space for study visits. The primary purpose of this...Permanent employmentFull timePart timeH1bLive inWork at officeLocal areaMonday to FridayFlexible hoursNight shiftWeekend workAfternoon shift$64.97k - $105k
...and impactful role where you will combine your clinical expertise with research coordination, contributing to study development, managing regulatory requirements, and helping bring new treatments to patients. You will also serve as a mentor and resource to colleagues...Temporary workWork experience placementWork at office
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