Controller Salary at The Santaluz Club BETA

Job Description Job Description About Capricor Therapeutics Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to developing transformative therapies for rare diseases, with a primary focus on Duchenne muscular dystrophy (DMD). We are pioneers in cell therapy and exosome-based technology, leveraging our innovative platforms, including our lead product, deramiocel (CAP-1002), and our proprietary StealthX™ platform, to engineer cutting-edge treatments. Our team is committed to harnessing advanced science and technologies to meet the unmet needs of patients living with DMD and other challenging medical conditions. Join us on our journey as we push the boundaries of medical science and pave the way for a About the Role We are seeking a Manager of Quality Control to join our Quality Control team in San Diego, CA. In this role, you will oversee daily operations of the QC team, support analytical testing of current products, and help define strategies for new product de

Job Description Job Description A-Line Staffing is now hiring a Quality Control Specialist in San Diego, CA. The Quality Control Specialist would be working for a biotechnology leader and has career growth potential. This would be full time / 40 hours per week. If you are interested in this Quality Control Specialist position, please contact Austin Faris at 586-710-7941 or afaris@alinestaffing.com Quality Control Specialist Compensation The pay for this position is $28.00 per hour Benefits are available to full-time employees after 90 days of employment A 401(k) with a company match is available for full-time employees with 1 year of service on our eligibility dates Quality Control Specialist Highlights This position is a contract assignment through 12/20/2025, with potential for extension or hire based on performance and business needs The required shift is 1st shift: Monday–Friday, 8:00 AM – 4:30 PM Interviews will be conducted in person Worksite: 11214 El Camino Real, San Diego, CA

We are looking for a detail-oriented Document Control Specialist to support electric utility programs. This role requires strong organizational skills, experience managing documentation workflows, and a proactive approach to maintaining accurate and up-to-date project records. You will serve as a key support function to ensure documentation is complete, accessible, and compliant with client and regulatory requirements. Responsibilities Maintain and organize project documentation in SharePoint and other systems to ensure easy retrieval and accuracy Track and log the issuance of work orders, ensuring proper documentation of status, timelines, and requirements Support internal and external team meetings by preparing agendas, distributing meeting notes, and updating document repositories Disseminate program communications and document updates to subcontractors and client stakeholders Perform data entry, validation, and file naming to support project tracking and audit readiness Generate re

Net2Source Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth of 300% in the last 3 years with over 5500+ employees globally, with over 30+ locations in the US and global operations in 32 countries. We believe in providing staffing solutions to address the current talent gap – Right Talent – Right Time – Right Place – Right Price and acting as a Career Coach to our consultants. Company: One of Our Clients Job Title: Quality Control Specialist Location: San Diego, CA 92121 Duration: 6+ Months Shift: 8 AM-4:30 PM Pay Range: 26.00-28.00/hour on W2 Job Description: Education BS/BA in a related scientific discipline or some related college coursework with a minimum of 2 years related experience in a biotech lab environment. The QC Associate I is responsible for routine, accurate and timely testing of QC samples according to standard protocols and operating procedures, such as flow cytometry related protocols. The QC

We are seeking a highly experienced and motivated Financial Controller to join our team. This is a critical on-site leadership role responsible for overseeing all accounting operations, accounts payable/treasury, internal controls, system implementations and regulatory compliance. The Financial Controller is an integral part of the overall accounting team (US and MX) and is involved in many cross-departmental and strategic initiatives of the Company. The ideal candidate will have significant experience in both U.S. and Mexico accounting environments, be fluent in English and Spanish, and bring a strong background in SAP ERP systems and U.S. GAAP. Key Responsibilities: Manage the Accounting, Treasury/Accounts Payable and Finance Project Management teams in San Diego and Tijuana offices (as well as foreign bookkeepers/CPAs), including: Accounting Lead the planning, direction, and coordination of all accounting and reporting operations, including general ledger, accounts payable, accounts

Job Description Job Description We are looking for Quality Control Associate for our client in San Diego, CA Job Title: Quality Control Associate Job Location: San Diego, CA Job Type: Contract Job Description: Pay Range: $24hr - $28hr Responsibilities: Trains and becomes proficient in all the required techniques, operation of relevant equipment and software packages associated with testing, data analysis, and data reporting. This may require working with human blood, human or mammalian cell culture and/or animals and animal tissues. Routine, accurate and timely completion of all assigned QC tests under supervision and according to standard protocols or operating procedures. Will prioritize daily workload and develop skills to work independently. Analyze data and report test results including completion of all required documentation and database entries as required by QC protocols or operating procedures. Calibrate and maintain equipment. Report problems to QC Supervisor or Manager. Mai

DIRECT CANDIDATES ONLY, IF INTERESTED APPLY THROUGH JOB POST. NO DIRECT MESSAGES. RECRUITERS: DO NOT CONTACT. Position overview: This position supports creation and/or updates to controlled Quality system procedures and process changes. Collaborates with internal Subject Matter Experts (SMEs) to process document updates in the electronic change control system. Maintains the document control and training modules within the QCBD system.Assists with maintaining company’s training program. Must be able to plan, organize, prioritize and implement multiple concurrent tasks and performs under minimal supervision. Maintains organized and audit ready controlled document storage room. Responsibilities: Document Control Create and coordinate all controlled document files, both electronic and hard copy Manage change order requests as assigned Identify improvements to the Document Control System Works with a variety of SMEs from various departments to quickly update documents while ensuring complia

A brief overview The Director of Quality Control will lead the Quality Control and Analytical functions for release, stability, raw material testing and method validation/transfer functions in compliance with FDA and other international regulatory requirements for research, pre-clinical, clinical and commercial pharmaceutical products at Bachem. What you will do Maintain the quality control laboratories and stability program per FDA cGMP parts 210 and 211, ICH Q7 and Q9 requirements for drug substances and ISO 13485 for raw materials used in device and diagnostics Develop annual master analytical validation plan and ensure validations are conducted per ICH guidelines, including cleaning validations and analytical test method validation Ensure continuous improvement and effectiveness of the quality control labs Oversee and conduct cGMP, ICH and ISO stability programs to comply with regulatory requirements Oversee work of direct reports; distribute workload, and cross-train staff on diff