Serve as a technical expert for pre-roll manufacturing, driving process optimization and best practices.
Provide training and documentation to ensure consistent operational excellence across sites.
Travel up to 50-75% to support low-performing sites and resolve technical challenges.
Green Thumb is a leading cannabis company involved in cultivation, manufacturing, and retail. The company emphasizes operational excellence and innovation across its network.
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 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.
Provide strategic quality leadership for CMC activities across cell therapy programs.
Lead product quality strategy and lifecycle management with risk-based control strategies.
Oversee QC operations and external partner quality oversight.
BrainChild Bio is a clinical-stage biotechnology company developing CAR T cell therapies for central nervous system tumors. The company prioritizes pediatric brain tumors with a pipeline extending to adult indications, and every team member directly impacts bringing therapies to patients.
Provide strategic pharmaceutical development guidance as CMC lead to cross-functional project teams.
Develop robust formulations and manufacturing processes to support rapid registration of QED products.
Manage CRO relationships, drug forecasts, and regulatory submissions for clinical supply.
BridgeBio is a biotech company pioneering a 'moneyball for biotech' approach to reduce risk and accelerate development of life-changing medicines for rare diseases. They foster a culture of curiosity and experimentation, working alongside respected industry minds to reengineer the future of biopharma.
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.
Manage reprocessing and infection control activities for the endoscopic product portfolio, serving as the primary company resource and subject matter expert.
Work cross-functionally with customers, third-party companies, and internal stakeholders to ensure reprocessing recommendations satisfy US market needs and comply with industry guidelines.
Develop validation programs, technical manuals, and educational tools while representing the company on national committees and keeping leadership informed of trends.
FUJIFILM Healthcare Americas Corporation provides cutting-edge healthcare solutions spanning diagnostic imaging, enterprise imaging, endoscopic and surgical imaging, as well as in-vitro diagnostics. The company is part of Fujifilm, which has over 70,000 employees globally and is guided by a Group Purpose of giving our world more smiles, offering a dynamic and flexible work environment.
Manage analytical development, QC, and stability activities at contract manufacturing sites.
Author and review CMC sections for US and ex-US regulatory filings.
Collaborate with Quality Assurance to close investigations and manage change controls.
BridgeBio is a biotech company that pioneered a 'moneyball for biotech' approach, pooling projects and early-stage research to reduce risk and develop medicines for rare diseases. They foster a culture of curiosity and experimentation with small teams of experts.
Execute analytical strategies for commercial products, ensuring compliance and method lifecycle management.
Lead method transfer, validation, and investigations at CDMOs, supporting regulatory submissions.
Serve as analytical SME, partnering cross-functionally to ensure quality and supply continuity.
Praxis Precision Medicines is a clinical-stage biopharmaceutical company translating genetic insights into therapies for central nervous system disorders. The company fosters a culture of trust, ownership, curiosity, and results with a collaborative team.
Lead extraction and formulation strategy, driving innovation and operational excellence across multi-site facilities.
Oversee compliance with federal, state, and local regulations, maintaining high safety standards.
Build and mentor a high-performing team, fostering a culture of collaboration and continuous improvement.
Green Thumb is a cannabis company that produces and sells cannabis and hemp extracts in Vape, Concentrates, and Edibles categories. It is a multi-state operation with a focus on innovation and quality, fostering a collaborative culture.
Lead clean utilities engineering initiatives across design, construction, commissioning, and startup for large-scale cGMP facility projects.
Serve as technical owner for high-purity water, clean steam, and process gas systems, developing specifications and supporting qualification activities.
Collaborate with cross-functional teams to improve quality, sustainability, productivity, and cost efficiency in pharmaceutical and life sciences environments.
This company provides engineering services for pharmaceutical and life sciences facilities, focusing on clean utility systems and large-scale project support. The team is collaborative and people-focused, offering opportunities to work on high-impact projects with multidisciplinary technical teams.
Leads the most complex product development programs for data center infrastructure, driving products from concept through scaled production.
Defines end-to-end manufacturing strategy, including make-vs-buy decisions, partner selection, and capacity planning.
Drives cross-functional leadership, quality improvements, and operational rigor across internal and external stakeholders.
Tract Capital adopts a unique approach to digital infrastructure investment, leveraging decades of experience to nurture leading-edge digital infrastructure enterprises. Their team of specialized experts acts as a strategic partner and catalyst for innovation within the sector.
Leads quality compliance, risk management, and vendor oversight programs to support late-stage development.
Manages inspection readiness, data integrity assessments, and regulatory authority interactions across GxP.
Provides senior-level quality judgment and drives risk-based decisions in a dynamic environment.
Braveheart Bio is a clinical-stage biopharmaceutical company developing therapies for hypertrophic cardiomyopathy and other cardiovascular diseases. It has a proven leadership team, strong financial foundation, and a high-value late-stage asset, offering an opportunity for mission-driven professionals.
Lead the implementation of manufacturing improvements and standardization in the Forming discipline across the country group.
Provide technical leadership and training to build factory capability and drive continuous improvement in process, productivity, and quality.
Partner with engineering, mold design, and other functions to resolve complex manufacturing issues and support new equipment introductions.
O-I is a leading producer of glass bottles and jars worldwide, with over 120 years of experience and more than 1,800 patents. As a global company, they are dedicated to sustainability and innovation, providing high-quality glass packaging for top food and beverage brands.
Lead the strategy, execution, and continuous improvement of systems and processes for end-to-end network service delivery.
Oversee technology capabilities that translate network infrastructure into customer-facing services with a focus on automation and operational excellence.
Drive cross-functional collaboration to ensure seamless order-to-service delivery and proactive monitoring.
TDS Telecom provides high-speed internet, TV entertainment, and phone services to communities across the U.S. With over 1 million connections and 50+ years of experience, they foster a culture of innovation and excellence.
Define and manage product requirements, user stories, and backlog in collaboration with engineering and business stakeholders.
Validate features against requirements, coordinate QA triage and UAT, ensuring release readiness.
Track delivery schedules, communicate updates across teams, and support go-to-market efforts with release notes and documentation.
OneStudyTeam specializes in accelerating clinical trials through its cloud-based platform, StudyTeam, which digitizes research site workflows and improves collaboration among sponsors, sites, and stakeholders. Trusted by the largest global biopharmaceutical companies, the platform is used in over 6,000 research sites across 100+ countries, fostering a culture of one team and one mission.
Set the strategic direction for Compliance Operations, transforming regulatory requirements into scalable practices that enable growth.
Partner with Product and Engineering to build tech-first, automated solutions that reduce manual effort and scale operations.
Lead state licensing audits, develop key compliance metrics, and build a high-performing team of 5-10 professionals.
Honor Technology is changing how society cares for older adults by providing technology, tools, and services that empower them to live life on their own terms. With over 100,000 Care Pros and a global franchise network, the company delivers over 50 million hours of personalized care annually, fostering a culture of innovation and compassion.
Serve as TMF subject matter expert, partnering with study teams to ensure documentation is complete and inspection ready.
Lead the setup, maintenance, and quality review of electronic Trial Master Files, monitoring health and driving issue resolution.
Collaborate with clinical operations and vendors to improve TMF processes and support regulatory inspections.
Praxis Precision Medicines is a clinical-stage biopharmaceutical company developing therapies for central nervous system disorders. With a focus on trust, ownership, curiosity, and results, they foster a collaborative, inclusive culture.
Lead and empower the Technical Operations team to ensure seamless execution of testing, provisioning, and service requests.
Oversee device testing, certification, and provisioning workflows, maintaining high accuracy and adherence to SLAs.
Drive process improvements and automation, including GenAI solutions, to create a more scalable and efficient operational environment.
Trustonic makes smartphones affordable for the many by providing the world's most secure smartphone locking technology. They partner with mobile carriers, retailers, and financiers across 30+ countries, powering device financing solutions that drive economic inclusion and growth. They pride themselves on a culture code that celebrates diversity and recognizes that great working environments are essential to success.
Lead and scale the Computer System Validation capability across IT, defining validation strategy, operating model, and risk-based approach while building the CSV team.
Author, review, and execute validation lifecycle deliverables including validation plans, requirements, risk assessments, and test protocols.
Collaborate with Quality, IT, business owners, and vendors to translate compliance needs into practical, scalable validation strategies.
Praxis Precision Medicines is a clinical-stage biopharmaceutical company translating genetic insights into the development of therapies for central nervous system disorders. It is a lean and growing organization guided by core values of Trust, Ownership, Curiosity, and Results, with a commitment to diversity, equity, and inclusion.