Manager, QC Salary at Aruba Networks Inc BETA

*Remote* Director, GxP Quality Assurance Remote (West Coast working hours) Our client is a late-stage biologics company focused on treatments for autoimmune diseases and cancer. They are looking for a Director of GxP QA to lead the quality team and help build a scalable quality management system to support their clinical and future commercial efforts. Responsibilities Oversee and enhance GxP compliance across GMP, GCP, and GLP functions Lead development and implementation of the Quality Management System Manage quality processes: deviations, CAPAs, change control, audits, training, and documentation Support regulatory inspection readiness and ensure ongoing compliance Drive continuous improvement and risk-based decision-making across teams Partner cross-functionally on clinical development, tech transfer, and vendor oversight Requirements Bachelor’s or Master’s in a relevant science or engineering field 4–6+ years of QA/GxP experience in biotech, pharma, CRO, or CDMO settings Deep know

Job Description: Working with projects managers on all aspects of a project from bid through project close out Assisting in bidding out projects to subcontractors, estimating for self-performed work and preparing proposals Generate simple estimates and change orders Assisting project manager with prime contract and issuing subcontracts Integral part of the construction team, working on submittals, change orders, RFI’s, project documents, project meetings, invoicing owner, reviewing and approving subcontractor invoices and overall project processes Review and perform minor schedule updates Work with superintendent on a daily basis to resolve conflicts, maintain schedule and perform quality control Manage punch list Oversee closeout process Mentor Project Engineers Liaison between office and field Participate in trade shows and industry organizations Desired Skills and Experience: Bachelor’s degree with a preference in Construction Management or Engineering or equivalent experience Minim

About Glyphic: At Glyphic Biotechnologies, we plan to create the protein revolution for which scientists and researchers have been waiting. We are developing a massively parallel, single-molecule proteome sequencing platform that will transform life science discovery and usher in a new era of insights into human biology and disease. To date, we have raised >$50M from venture partners and non-dilutive grant funding to achieve our vision of next generation proteome sequencing. What we are looking for in you: Glyphic is seeking an experienced quality and analytical development leader who will report to the Chief Operating Officer and anchor a newly formed Quality Control & Analytical Development team focused on establishing an internal core facility to centralize Glyphic's current analytical development activities while building out a phase appropriate Quality Control program in support of a commercial launch. This will be a unique opportunity to design and implement new analytical proces

Neptune Medical is an innovative, venture capital funded medical device startup headquartered in Burlingame, CA. We have already commercialized novel medical devices using our technology. Now the team Triton robotics at Neptune is building something truly unique: a fully flexible medical robot that enables doctors to reach deep into human anatomy. Our Triton robot will disrupt flexible endoscopy. Triton Robotic Endoscopy will set a new standard in outcomes for decades to come. TITLE: Senior/Staff NPI Manufacturing Engineer, Catheters POSITION SUMMARY: The Senior/Staff NPI Manufacturing Engineer will focus on further developing our product and then transferring it into a manufacturing setting. The successful candidate will possess a passion for medical device engineering and a record of successful process, tooling and equipment design. This role will engage in cross-functional collaboration to accelerate the product development process, reduce cost of goods, and enable more complex desi

About Summit Steel Works Corporation With over 23 years' experience as a total service steel trade partner, Summit Steel Works specializes in design, fabrication, and installation. We take pride in professionalism, responsiveness, and quality. Together, we tackle complex projects everyday. Make an impact! Work at a place where you can hone your craft and experience structural steel. QUALITY CONTROL INSPECTOR About The Role The Quality Control Inspector (QCI) is responsible for the accuracy of all items fabricated within the shop. As the QCI, you will act as the gate keeper for all items fabricated. As the QCI you will use a combination of code knowledge (AWS, AISC, RCSC, etc.) and technical expertise to verify that the final product is free of defects and meets the requirements in the contract documents and company fabrication drawings. Responsibilities Candidate Requirements • Conduct inspections for dimensions, fit-up, welds, bolts, and paint. Ensure all aspects meet contract and cod

Director/Associate Director of Quality Control and Analytical Development (QC) We’re partnering with a leading cellular therapy organization that is seeking a highly motivated Director of Quality Control (QC) and Analytical Development with expertise in mAbs, ddPCR, flow cytometry, and cell-based assay methods. This role offers an exciting opportunity to lead quality initiatives supporting cellular therapies within a GMP environment. Key Responsibilities: Conduct GMP In-Process Control (IPC), lot release, and stability testing using ddPCR, flow cytometry, and cell-based methods. Lead method optimization, transfer, qualification, and validation for clinical drug product testing. Prepare detailed and organized reports and presentations describing analytical results. Facilitate cross-functional training and continuous improvement within the QC team. Develop and maintain Quality Control (QC) and Quality Management System (QMS) standards to align with internal and global regulatory requirem

Director, GCP QA Compliance Our biotech partner is a well-established, commercially successful clinical stage biotech that is seeking a Director of Clinical Quality Assurance to lead the CQA function and build/manage a team. This role will oversee CQA strategy across policies, SOPs, deviations, change control, CAPAs, and vendor audits. This is a great opportunity for a Clinical QA leader to help progress a robust pipeline of therapeutics across oncology, neurology, endocrinology, and more areas. This position will be 3 days onsite in Redwood City, CA. Responsibilities: Lead Clinical Quality Assurance as a manager to the CQA team supporting various therapeutic area programs in support of successful clinical studies Lead GCP audit strategy including audits of investigative sites, clinical vendors, internal department, TMF, and study documents Represent QA on clinical teams to provide compliance assessment and advice Manage clinical inspections by regulatory bodies across internal and ext

Staff NPI Manufacturing Engineer Client: Our client is an innovative, venture capital-funded medical device startup in Burlingame, CA. Their team is building something unique: a fully flexible medical robot that enables doctors to reach deep into human anatomy. POSITION SUMMARY: The Senior/Staff Process Development Engineer will focus on further developing our product and then transferring it into a manufacturing setting. The successful candidate will possess a passion for medical device engineering and a record of successful process, tooling and equipment design. This role will engage in cross-functional collaboration to accelerate the product development process, reduce cost of goods, and enable more complex designs through manufacturing improvements. ROLES AND RESPONSIBILITIES Work with product development to design and prototype novel manufacturing processes and equipment Design and prototype novel manufacturing equipment and fixturing Create and maintain necessary Manufacturing Pr