Provide technical support to multiple cement plant sites to establish and maintain quality control measures and testing protocols.
Coordinate laboratory testing, analyze results, and drive continuous improvement initiatives to reduce variability and CO2 footprint.
Collaborate with cross-functional teams on root cause analysis, supplier quality management, and data-driven process improvements.
Heidelberg Materials is one of the world's largest integrated manufacturers of building materials and solutions with leading market positions in cement, aggregates, and ready-mixed concrete. We have around 51,000 employees at almost 3,000 locations in more than 50 countries, with a strong focus on sustainability and carbon neutrality.
Manage supplier quality events, including nonconformances, root-cause analyses, CAPAs, and corrective actions.
Support supplier qualification, onboarding, audits, and performance monitoring through scorecards and metrics.
Collaborate cross-functionally with supply chain, regulatory, and operations teams to ensure GMP compliance.
Jobgether is an AI-powered job matching platform that connects candidates with hiring companies. It uses technology to review applications and share top-fitting shortlists with employers, focusing on objective and fair hiring.
Design and develop quality screening strategies, business rules, and disposition plans for centralized quality systems.
Analyze large manufacturing datasets to identify abnormal signatures, trends, and emerging quality risks using statistical methodologies.
Collaborate with cross-functional teams to standardize quality practices, support root-cause investigations, and drive continuous improvement initiatives.
This global quality engineering organization is responsible for centralized quality operations across semiconductor manufacturing sites in Asia and the United States. They focus on safeguarding product quality through automated screening, statistical risk assessment, and data-driven operational controls, offering broad exposure to manufacturing and engineering teams.
Provide end-to-end Product Quality oversight for clinical and commercial programs, including drug substance, drug product, packaging, and labeling.
Lead resolution of deviations, OOS/OOT, change controls, CAPAs, and product quality complaints with risk-based decisions.
Represent Product Quality on CMC and external partner teams to support development, regulatory submissions, and commercialization.
Praxis Precision Medicines is a clinical-stage biopharmaceutical company translating genetic insights into therapies for central nervous system disorders. The company values trust, ownership, curiosity, and results, fostering a culture of diversity and inclusion with a small but dedicated team.
Ensure quality and reliability of components from suppliers specializing in metal casting and mold manufacturing.
Lead supplier qualification, process validation, and quality improvement initiatives.
Conduct audits and support testing to measure compliance with regulatory requirements.
General Dynamics Ordnance and Tactical Systems is a global leader in the design, engineering, and production of munitions, weapons, and missile subsystems. The company fosters a culture of integrity, innovation, and collaboration, offering robust total rewards and a high-performance team environment.
Provide quality oversight and direction to vendors to ensure cGMP compliance for clinical manufacturing.
Lead clinical lot disposition, batch record review, and QP certification for global trials.
Oversee GMP quality systems including deviations, investigations, and audits at contract manufacturing partners.
Pulmovant is a Roivant-backed clinical-stage biotechnology company developing innovative therapies for pulmonary diseases. It is a small, lean organization within the Roivant family, focusing on collaboration and innovation.
Create and maintain SOPs and guidance documents in compliance with ICH-GCP and federal and local regulations.
Conduct internal study reviews to ensure compliance and prepare official reports with findings and corrective actions.
Collaborate with operations teams to remediate noncompliance and participate in quality investigations and audits.
Headlands Research is dedicated to enhancing clinical trial delivery within communities. Founded in 2018, the company operates 20+ clinical trial sites across the US and Canada and is rapidly expanding.
Own and resolve complex L4 support escalations, conducting root cause analysis and collaborating with Engineering and Product teams.
Create and maintain technical documentation, troubleshooting guides, and self-service resources to improve support efficiency.
Analyze support trends and translate findings into actionable recommendations for product quality and customer experience.
They are a global remote-first technology company focused on delivering exceptional customer experiences and scalable solutions. They foster a collaborative environment that values ownership, continuous learning, and innovation.
Lead and develop a world-class Service & Repair Quality organization across multiple international sites, driving continuous improvement and regulatory compliance.
Apply global regulatory requirements to Service & Repair processes, including FDA, GMP, CAPA, ISO 13485, and lead quality support during regulatory inspections.
Develop statistically sound sampling plans, use data analysis to identify trends, and build strong partnerships with site leadership and stakeholders.
This is a senior quality leadership opportunity within a global medical technology environment focused on delivering safe, reliable, and innovative healthcare solutions. The company is a partner of Jobgether, with operations across the US, Germany, and Japan, and emphasizes a collaborative, ethical, and inclusive culture.
Serve as an agency expert on our quality assurance program
Monitor quality reporting to identify trends and problems
Collaborate with the Director of Quality & Compliance on strategies to improve focus areas
Trellis is rewriting the insurance experience by building a tech-powered insurance agency. We are a profitable, fast-growing Series A startup backed by top venture firms, with a remote-first culture that values speed, experimentation, and intentional building.
Lead customer-flow validation initiatives by partnering with Support and Field teams to translate real-world customer use cases into comprehensive testing and validation strategies.
Define end-to-end test strategies for major features, architectural changes, and complex cross-component workflows, acting as a quality gatekeeper to identify and address potential gaps.
Own release-readiness activities for key unified endpoint management modules, including test pipelines, risk assessments, quality evaluation, and technical Go/No-Go recommendations.
Our partner is a fast-growing company focused on delivering secure, resilient, and enterprise-ready technology through a digital work environment. They offer remote, hybrid, or onsite working options in India with a collaborative culture emphasizing technical excellence, inclusion, and growth.
Own the systems that keep Daymark's clinical quality and safety program credible as it scales, including audits and incident investigations.
Partner with clinical leadership to embed quality standards into daily workflows, not layered on top.
Manage external audits and regulatory reviews, and provide clear-eyed analysis when issues arise.
Daymark Health is a value-based oncology company redefining the cancer care experience for patients, providers, and health plans. It is a growing company backed by leading venture capital firms, with a collaborative culture focused on transforming cancer care.
Manage and oversee the GCP Quality Management System for global clinical operations, including decentralized trials.
Lead quality investigations, CAPAs, and audits to ensure compliance with regulatory standards.
Provide strategic quality advice and drive continuous improvement across the organization.
WEP Clinical partners with biopharmaceutical sponsors to bring treatments to patients through clinical trial delivery and home health services. With over 15 years of global experience, the company fosters a collaborative, innovative culture focused on improving patient outcomes.
Develop and execute instrumentation engineering designs, specifications, and sizing calculations.
Coordinate with manufacturing, vendors, and project teams for technical compliance.
Support installation, testing, commissioning, and documentation of instrumentation systems.
The company specializes in complex instrumentation and field engineering projects, providing technically advanced solutions. The culture emphasizes collaboration and continuous improvement, with a focus on multidisciplinary teamwork.
Lead internal audits, gap assessments, and action item closure for periodic QMS reviews
Manage and maintain design and development files for FDA regulated products
Build and refine quality systems and SOPs in line with cGxP, ISO 13485, and other applicable standards
UpDoc builds the first clinically validated, physician-supervised AI agents that manage chronic diseases. Founded by Stanford physicians, it is an early-stage startup focused on bringing its AI-powered platform to patients and providers.
Own GTI's QA/QC policies, SOPs, and quality management system across a multi-state network, driving consistency and continuous improvement.
Direct company-wide sanitation and QC practices ensuring product purity, consistency, and compliance with regulatory standards.
Manage nonconformance records, CAPA processes, and complaint investigations to drive systemic improvements and regulatory compliance.
Green Thumb Industries is a multi-state cannabis operator involved in cultivation, manufacturing, and production of cannabis products. The company emphasizes a culture of quality, food-safety, and compliance excellence across its network.
Provide independent support for quality, safety, and compliance initiatives across client assignments and internal programs.
Develop, monitor, and improve program performance metrics, objectives, and targets to enhance operational outcomes.
Plan, lead, and support internal and client audits, assessments, and compliance reviews to evaluate program performance.
Our partner supports critical government missions by strengthening quality, safety, and compliance programs within highly regulated environments. They are a federal contractor seeking experienced professionals to contribute to meaningful work with a culture of safety, accountability, and innovation.
Support supplier qualification and approval through documentation review and audits.
Maintain approved supplier records and ensure compliance with food safety and regulatory standards.
Travel up to 50% to conduct supplier audits and drive corrective action resolution.
Niagara Bottling is a family-owned bottled water manufacturer supplying major retailers across the US. With incredible growth and a fast-paced, collaborative culture, the company offers competitive benefits and career advancement opportunities.