Manager, Quality Salary at Northshore BETA

Director, QA Compliance Our client is a clinical stage biotech that is seeking a Director of Quality Compliance to lead GCP quality systems and ensure compliance with US, EU, and global regulations. This role will oversee quality processes including policies, SOPs, deviations, change control, CAPAs, document control, training, and vendor audits. Responsibilities include building and managing the quality management system, supporting clinical and future commercial activities, leading system implementations, and ensuring inspection readiness. Requirements: Bachelor’s or Master’s in a scientific field with progressive experience in biotech/pharma clinical quality Strong knowledge of GCP QA regulatory requirements and quality systems Experience developing and managing quality processes Risk management, root cause analysis, and inspection support experience Excellent communication, project management, and organizational skills Up to 20% travel Please send resume to sarah.viall@meetlifescien

Director, QA Compliance Our client is a clinical stage biotech that is seeking a Director of Quality Compliance to lead GCP quality systems and ensure compliance with US, EU, and global regulations. This role will oversee quality processes including policies, SOPs, deviations, change control, CAPAs, document control, training, and vendor audits. Responsibilities include building and managing the quality management system, supporting clinical and future commercial activities, leading system implementations, and ensuring inspection readiness. Requirements: Bachelor’s or Master’s in a scientific field with progressive experience in biotech/pharma clinical quality Strong knowledge of GCP QA regulatory requirements and quality systems Experience developing and managing quality processes Risk management, root cause analysis, and inspection support experience Excellent communication, project management, and organizational skills Up to 20% travel Please send resume to sarah.viall@meetlifescien

Director, QA Compliance Our client is a clinical stage biotech that is seeking a Director of Quality Compliance to lead GCP quality systems and ensure compliance with US, EU, and global regulations. This role will oversee quality processes including policies, SOPs, deviations, change control, CAPAs, document control, training, and vendor audits. Responsibilities include building and managing the quality management system, supporting clinical and future commercial activities, leading system implementations, and ensuring inspection readiness. Requirements: Bachelor’s or Master’s in a scientific field with progressive experience in biotech/pharma clinical quality Strong knowledge of GCP QA regulatory requirements and quality systems Experience developing and managing quality processes Risk management, root cause analysis, and inspection support experience Excellent communication, project management, and organizational skills Up to 20% travel Please send resume to sarah.viall@meetlifescien

Job Description Job Description Job Summary Seeking a team member to be an integral part in building a strong quality department and drive quality throughout the company. We are seeking a highly skilled and detail-oriented Quality Engineer / Quality Inspector to ensure our products meet the highest standards of quality and compliance. This role is responsible for performing detailed inspections, utilizing precision measurement tools, managing quality processes, and maintaining compliance with ISO9001/2015 standards. Essential Duties and Responsibilities Inspection and Quality Control Perform detailed inspections using hand tools such as calipers, micrometers, and height gauges. Utilize Coordinate Measuring Machines (CMM), both manual and programmed, for precision measurement. Conduct inspections at various stages: receiving, first article, in-process, and final inspection. Identify defects or discrepancies, report findings to the Quality Manager, and manage Non-Conformance Reports (NCR

Senior Manager of Production Job Summary We are seeking a Senior Manager of Production to lead and optimize operations across our FMT (fecal microbiota transplantation) stool bank, quality assurance, and clean production functions. This role is critical in ensuring the quality, safety, and efficiency of our production processes while maintaining compliance with regulatory and internal standards. The ideal candidate has a strong background in quality assurance, laboratory operations, or production management and is passionate about animal health and microbiome science. This position requires hands-on leadership in donor material management, quality control of incoming products, and clean in-house production. Key Responsibilities 1. Oversight of FMT Stool Bank Donor Testing & Selection: Optimize donor screening and testing to ensure all material meets stringent quality standards. Compliance & Documentation: Maintain detailed records to ensure regulatory and internal compliance. Inventory

Head of Quality San Francisco, CA The Company: Our client is an innovative start-up company that is developing advanced, cloud-controlled robotic systems that enable the production of individualized drugs at scale. Their customers include some of the largest global organizations in the advanced pharmaceutical manufacturing space. Based in San Francisco, California, our client is backed by many top-tier tech and life science investors, including Casdin Capital, Lux Capital, Y Combinator, and more. Position Overview: As the Head of Quality, you will lead the development and implementation of a robust ISO 9001:20XX quality system to ensure compliance with industry standards in a cGMP-regulated pharmaceutical and biopharmaceutical environment. Reporting directly to the CEO, your primary focus will be aligning quality initiatives with customer and regulatory requirements. As the Head of Quality, your role will include the following: Quality Leadership: Build and lead a quality team to devel

The Scientific Team at Russell Tobin & Associates is supporting a Leading Technology Company for hiring a "Documentation Specialist V" Responsibilities: Manage Quality Management System (QMS) documentation and records throughout the product lifecycle. Create and release documents to support product introduction, production, clinical trials, and FDA submissions. Ensure proper document control (management, version control, distribution) and compliance with regulations. Collaborate with Operations, Supply Chain, and Engineering to ensure compliance with medical device standards. Maintain records such as validation and test reports, exit reviews, and results. Support audits for licensure and accreditation. Manage complex projects, solve problems impacting release progress, and support cross-functional teams. Help implement new eQMS and provide end-user support. Qualifications: 5+ years of experience in medical device QMS documentation, preferably in a fast-paced consumer electronics enviro

About Aivres Aivres is a leading global data center and cloud computing solutions provider committed to delivering innovative technologies that propel the world’s leading industries to new frontiers. We deliver and deploy robust, performance-optimized, purpose-built platforms to major data centers around the globe. Primary Responsibilities Manage the quality of L6-L11 manufacturing process, including but not limited to IQC, PQC, OQC, customer complaint handling, outsourcing on-site management, etc.; Led local QC & QE quality assurance work to ensure the quality of outgoing products to reach the standard; Build, optimize, upgrade and localize the quality system to ensure the quality assurance system meets the company and customer requirements; Cooperate with manufacturing, engineering, R&D and other departments to continuously improve product quality and customer satisfaction; Hold local quality activities such as product quality planning, training, product quality improvement activitie