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Role: Staff Quality Engineer Contract W2 Only Location: San Diego, CA The Sr. Staff Quality Engineer is a contract role that will be responsible for leading a project to improve the Quality and compliance of the Dispensing Implementation process. This role will work with the Dispensing Implementation teams to document and suggest compliance-related improvements or changes to that process. The intent of this role is to bring the Dispensing Implementation process to a state of compliance that would pass an external regulatory agency inspection. Duties include: • Evaluating the Dispensing Implementation process against regulatory requirements associated with CFR 820.200 and international regulatory requirements. • Leading a cross-functional effort to develop and execute the plan to improve the compliance state of the process. • Communicate weekly status to the Quality and SDS leadership teams. • Compliance to all service record documentation requirements. Job Family Summary: Quality Engin

Join Our Team at Dirt King Fabrication! Are you looking for an exciting role to put forth your skills with the best of the best in the off-road industry? Dirt King Fabrication has been at the forefront of off-road excellence since 2008. We specialize in top-tier suspension systems, innovative off-road parts, and precision engineering that caters to every off-road enthusiast! Why Work with Us? The Core Values at Dirt King Fabrication: ● Respect: Everyone is a priority. ● Personal + Professional Growth: Support each other’s individual growth so we grow as a team. ● Teamwork: We contribute & collaborate positively. ● Clear + Honest Communication: Our effective communication leads to our success. ● Work/Life Balance: We work to live, not live to work. Employee Benefits: ● Competitive pay ● Comprehensive benefits package including health insurance ● Dental and vision plans ● 401K with a generous company match ● Holiday, vacation, and paid sick time ● Casual work environment ● And much more!

Job Description Job Description Shifts Available: 1st Shift Position Summary: We are seeking an ambitious and detail-oriented Manufacturing Lab Technician to join our team. This position is crucial in supporting lab operations. The ideal candidate will thrive in a laboratory environment that requires critical thinking and adhere to strict safety protocols. Recent college graduates with a science background are encouraged to apply! (biology or chemistry preferred, must have taken lab classes) Key Responsibilities: Perform accurate pipetting and manual handling of liquids to prepare reagents, samples, and formulations. Operate and maintain various liquid handling machines and laboratory equipment to ensure optimal performance and quality output. Conduct routine and specialized quality control tests to verify product consistency and integrity. Maintain a clean, organized, and safe laboratory environment in compliance with all safety protocols and standard operating procedures. Manage the

Job Summary Mauricio Ducassi is looking for a Sr. Quality Assurance Associate for a biopharmaceutical client. The Sr. Quality Assurance Associate will be responsible for supporting site management ensuring the site performs in a state of compliance by supporting all Quality Compliance and Inspection Management oversight activities while fostering an empowered culture of quality across all functions. Responsibilities Author, review and approve SOPs, protocols, reports, and other quality and regulated records for accuracy and compliance with all applicable regulations, international standards. Assists with continually evaluating Quality Systems and procedures while independently identifying areas for improvement and assisting in the implementation of new practices Assists with preparing and providing GMP training to cross-functional departments Assists with executing and maintaining internal/external audit programs Assists with maintaining the customer audit process Assists in the manage

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. Grifols Diagnostic Solutions is seeking a Senior Quality Assurance Specialist. The Sr Quality Assurance Specialist manages nonconformances, Out-of-Tolerance Reports, and CAPA records, ensuring timely corrective actions and comprehensive documentation. They lead quality meetings, represent QA in daily meetings, and drive quality improvements through operational analysis and compliance audits. The role involves improving procedures, conducting risk assessments, preparing for audits, managing metrics, mentoring junior staff, and

ASSISTANT DIRECTOR-ANALYTICAL DEVELOPMENT & QUALITY CONTROL Seeking an experienced analytical chemist to join our QC & Analytical Development group at the Assistant Director level. The ideal candidate will be a self-starter, familiar with a broad range of analytical techniques, possess a strong work ethic, have good communication skills, and have experience working in a GMP environment. The successful candidate will be able to perform the following responsibilities with a high degree of independence and attention to detail. RESPONSIBILITIES: Coordinate and execute testing of drug substance intermediate, drug substance, and drug product samples Develop drug substance specifications ensuring efficient integration across Chemistry, Manufacturing, and Controls (CMC) and other relevant disciplines such as Clinical and Toxicology Author scientific reports and portions of the CMC section of regulatory filings Manage the analytical activities for therapeutic development projects May develop an

Job Summary: The Production Chemist will be responsible for manufacturing complex bulk formulations, sub-assembly preparation, and in-process testing of diagnostic kit reagents. The role includes handling raw materials, maintaining detailed records, operating lab equipment, and ensuring compliance with safety and regulatory standards (cGMP, QSR, ISO). The technician will also manage ERP transactions and assist with equipment and supply ordering. Key Responsibilities: Manufacture and formulate diagnostic reagents and bulk solutions. Perform in-process testing and maintain device history records. Handle hazardous/bio-hazardous substances safely. Operate, calibrate, and maintain lab equipment. Complete ERP transactions and manage materials. Ensure compliance with laboratory safety and cGMP practices. Qualifications: Bachelor’s Degree or equivalent; 0-1 years of related experience. Basic computer skills, proficiency in Microsoft Office. Knowledge of laboratory practices, record keeping, an

We are a leading partner to the worlds major cloud providers. The formation of Accenture Cloud First, with a $3 billion investment over three years, demonstrates our commitment to deliver greater value to our clients when they need it most. Our Cloud First multi-service group of more than 70,000 cloud professionals delivers a full stack of integrated cloud capabilities like data, edge, integrated infrastructure and applications, deep ecosystem skills, culture of change along with pre-configured industry solutions to shape, move, build and operate our clients businesses in the cloud. We combine world-class learning and talent development expertise; deep experience in cloud change management; and cloud-ready operating models with a commitment to responsible business by design with security, data privacy, responsible use of artificial intelligence, sustainability and ethics and compliance built into the fundamental changes Accenture helps companies achieve. Are you ready to step up to the