41 Quality Control jobs in San Diego Country Estates

Partner with the project team to understand, plan, and implement the contract drawings and specifications. Collaborate with the owner, design team, and contractors to ensure quality and timeliness of project construction and completion. Implement and Quality Control, Manager, Control, Manufacturing, Construction

3 days ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. This range is provided by Jobot. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range $125,000.00/yr - $50,000.00/yr Direct message the job poster from Jobot Want to learn more about this role and Jobot? Click our Jobot logo and follow our LinkedIn page! Job details Competitive Salary and Benefits for a QC Senior Microbiologist Role for leading Pharma Manufacturer! This Jobot Job is hosted by Jaclyn D'Amore Are you a fit? Easy Apply now by clicking the "Easy Apply" button and sending us your resume. Salary 125,000 - 150,000 per year A Bit About Us Based in the San Diego area, we are seeking a dedicated and meticulous Quality Control Manager to join our dynamic team in the scientific industry. This role is integral to ensuring that our products meet the highest standards of quality, safety, and effectiveness. The successful candidate will be responsible for overseeing all aspects of quality control, from raw material intake to final product release. They will also be tasked with implementing and maintaining Good Manufacturing Practice (GMP) standards throughout our operations. This is a highly collaborative role that requires excellent communication skills, strong leadership abilities, and a keen eye for detail. if you have at least 2 years of GMP microbiologist experience and have managed others, please apply below! Why join us? Excellent health, dental, and vision insurance 401k Bonuses Job Details Responsibilities Oversee the daily operations of the Quality Control department, ensuring all activities comply with regulatory standards. Implement and maintain GMP standards throughout all areas of production. Conduct regular audits to identify potential areas of improvement and ensure compliance with all relevant regulations and standards. Develop and implement quality control protocols and procedures, and ensure they are followed accurately and consistently. Lead and manage a team of quality control technicians, providing training and guidance as needed. Collaborate with other departments to ensure quality control processes are integrated throughout the company. Investigate and address any issues or complaints related to quality. Prepare and present quality reports to senior management. Stay informed about the latest developments in quality control and GMP standards in the scientific industry. Qualifications Bachelor's degree in Science, Engineering, or a related field. A Master's degree is preferred. Minimum of 5 years of experience in a quality control role within the scientific industry, with at least 3 years in a managerial position. Strong knowledge of GMP standards and other relevant regulations. Proven experience in developing and implementing quality control protocols and procedures. Excellent leadership and team management skills. Strong analytical and problem-solving skills. Exceptional attention to detail. Excellent communication and interpersonal skills. Ability to work under pressure and meet tight deadlines. Proficiency in using quality control software and other related technologies. Continuous improvement mindset and dedication to upholding the highest standards of quality. Interested in hearing more? Easy Apply now by clicking the "Easy Apply" button. Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance. Want to learn more about this role and Jobot? Click our Jobot logo and follow our LinkedIn page! Seniority level Seniority level Not Applicable Employment type Employment type Full-time Job function Job function Quality Assurance Industries Biotechnology Research, Research Services, and Nanotechnology Research Referrals increase your chances of interviewing at Jobot by 2x Sign in to set job alerts for “Quality Assurance Manager” roles. Manager / Sr. Manager, Quality Assurance (GxP) - Hybrid Quality Assurance Manager, Precision Sports & Technology Manager, Mobile Applications Software Test Engineering Chula Vista, CA $130 639.57- 160,033.48 5 days ago Sr. Manager - Silicon Test Engineering, Kuiper Silicon Team Staff Design Quality Engineer - Software Test Engineering Manager 3 - Dev Program Lead - R10193213 Associate Project Director, for COWI North America Supervisor, Sterile Processing - Full Time Nights - San Diego Med Ctr Supervisor, Sterile Processing - Full Time Nights - Zion Med Ctr Utility Management Services Business Class Leader Quality Assurance Inspector (All Levels) We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr

1 week ago Be among the first 25 applicants Description Ascential Medical and Life Sciences is a leader in delivering precision engineering and automation solutions for medical devices, diagnostics, and life sciences. We are looking for a Supervisor, Quality Control to join our multidisciplinary team, contributing to cutting-edge projects that drive innovation in healthcare and diagnostics. Position Summary The Quality Control (QC) Supervisor oversees the daily operations of the Quality Control team, ensuring that incoming materials, in-process components, and finished products meet established quality standards, specifications, and regulatory requirements (including FDA QSR, ISO 13485, ISO 9001, and other applicable global regulations). This role involves direct supervision of QC technicians, coordination of inspection activities, data analysis, problem-solving, and driving continuous improvement within the QC function to support the overall Quality Management System (QMS). Job Details Description Ascential Medical and Life Sciences is a leader in delivering precision engineering and automation solutions for medical devices, diagnostics, and life sciences. We are looking for a Supervisor, Quality Control to join our multidisciplinary team, contributing to cutting-edge projects that drive innovation in healthcare and diagnostics. Position Summary The Quality Control (QC) Supervisor oversees the daily operations of the Quality Control team, ensuring that incoming materials, in-process components, and finished products meet established quality standards, specifications, and regulatory requirements (including FDA QSR, ISO 13485, ISO 9001, and other applicable global regulations). This role involves direct supervision of QC technicians, coordination of inspection activities, data analysis, problem-solving, and driving continuous improvement within the QC function to support the overall Quality Management System (QMS). Essential Functions Key Responsibilities: Team Leadership & Supervision Lead, train, mentor, and supervise a team of QC inspectors technicians. Schedule and assign daily/weekly inspection tasks to ensure efficient workflow and timely product release. Conduct performance evaluations, provide feedback, and support the professional development of QC staff. Ensure team adherence to safety protocols, company policies, and Good Manufacturing Practices (GMP). Foster a positive and collaborative team environment focused on quality and compliance. Quality Control Operations Oversee incoming, FAI, in-process, and final inspection and testing activities according to established procedures and specifications. Ensure proper use, maintenance, and calibration of inspection, measuring, and test equipment (IMTE). Oversee all product label issuances and reconciliation. Oversee and maintain all serial number issuances and traceability. Review and approve inspection records, Device History Records (DHRs), and related QC documentation for accuracy and completeness. Manage the identification, segregation, documentation, and disposition of non-conforming materials (NCMRs). Coordinate with Manufacturing, Engineering, Supply Chain, and QA departments to resolve quality issues and ensure smooth production flow. Compliance & Documentation Ensure all QC activities comply with the company's Quality Management System (QMS), FDA 21 CFR Part 820 (QSR), ISO 13485, ISO 9001 and other relevant regulatory requirements. Maintain accurate and organized QC records and documentation. Assist in the development, review, and revision of QC procedures, work instructions, inspection plans, etc. Support internal and external audits (e.g., FDA, Notified Body, customer audits) by providing documentation, explanations, and participating as needed. Process Improvement & Collaboration Monitor QC metrics (e.g., inspection yields, defect rates, turnaround times) and report on performance trends. Implement improvements to inspection methods, equipment, and processes. Identify and implement opportunities for continuous improvement within the QC department to enhance efficiency, accuracy, and compliance. Participate in or lead root cause investigations for quality issues and contribute to the NCMR and CAPA processes. Work closely with Manufacturing to monitor in-process quality and provide timely feedback. Support Supplier Quality Management activities, including the evaluation of supplier materials. Audits & Reporting Prepare the QC department for and participate in internal audits and external regulatory inspections and audits (e.g., FDA, Notified Body, Client). Compile, analyze, and report on QC metrics and trends to senior management. Education, Experience, Skills And Abilities Required Education & Experience: Bachelor's degree in a scientific, engineering, or technical field is preferred. Associate's degree or equivalent technical certification with significant relevant experience may be considered. Minimum of 3-5 years of experience in a Quality Control role within the life science industry. Minimum of 1-2 years of experience in a supervisory or management role within QC. Experience with wide range of life science products and technologies (e.g., instruments, disposables, IVDs). Experience with Lean manufacturing or Six Sigma methodologies. Direct experience managing responses during inspections, Notified Body, client audits. Job Complexity Manages personnel and monitors operations of a unit or sub-unit. Works on issues of broad scope and complexity, and uses judgement to analyze situations based on data and relevant facts. Requires full knowledge of own area of functional responsibility. Establishes policies and procedures with potential impact to other areas of the organization. Supervision Provides direct supervision to a unit or group of employees, assigning tasks, checking work at frequent intervals, and maintaining schedules. A portion of time is normally spent performing individual tasks related to the unit or sub-unit. Generally may supervise semi-skilled and skilled personnel. Normally receives little instruction on day-to-day work; independently manages the coordination of activities of a section or department with responsibility for resources, methods, and results. Responsible for a high level of internal and external partnerships and for interacting in a manner which reflects positively on the department and is consistent with the company’s policies and core values. Knowledge, Skills & Abilities Proven leadership and team management skills. Excellent analytical, problem-solving, and decision-making abilities. Strong attention to detail and organizational skills. Excellent written and verbal communication skills. This is an on-site position in San Diego with an annual salary range of $70,000-$1,000, based on experience and qualifications. Compensation is based on several factors including experience, skills, education, and job-related knowledge. In addition to base salary, Ascential offers a comprehensive benefits package. Technical Knowledge In-depth knowledge of FDA Quality System Regulation (21 CFR Part 820), ISO 13485, and ISO 9001 standards. Knowledge of other relevant regulations (e.g., MDSAP, EU MDR) is a plus. Strong understanding of QC principles, laboratory techniques, testing methodologies, sampling plans (e.g., ANSI/ASQ Z1.4), and statistical analysis. Familiarity with laboratory equipment calibration and maintenance requirements. Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Teams). Experience with Quality Management System (QMS) software and/or Enterprise Resource Planning (ERP) systems is desirable. Effort Required Physical Activities : On a continuous basis, sit at desk for a long period of time; write or use a keyboard to communicate through written means. Intermittently answer telephone. Some walking and lifting up to 20 lbs. may be required. The noise level in the work environment is usually moderate. The physical demands described above are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Travel This position may require limited travel. Qualifications 0" no-style="display: none;"> Skills 0"> 0"> 0" no-style="display: none;"> Behaviors 0"> 0"> : 0" no-style="display: none;"> Motivations 0"> 0"> : 0" no-style="display: none;"> Education 0"> 0"> 0" no-style="display: none;"> Experience 0"> 0"> 0" no-style="display: none;"> Licenses & Certifications 0"> 0"> Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor. Seniority level Seniority level Mid-Senior level Employment type Employment type Full-time Job function Job function Quality Assurance Industries Machinery Manufacturing Referrals increase your chances of interviewing at Universal Balancing (now part of Burke Porter, an Ascential Technologies Company) by 2x Get notified about new Quality Control Supervisor jobs in San Diego, CA . Carlsbad, CA 85,000 - 110,000 3 weeks ago Supervisor, Water Quality (Full-Time, SeaWorld San Diego) Culinary Training & Production Supervisor We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr

Partner with the project team to understand, plan, and implement the contract drawings and specifications. Collaborate with the owner, design team, and contractors to ensure quality and timeliness of project construction and completion. Implement and Quality Control, Manager, Control, Quality, Senior, Manufacturing, Construction

Our client is looking for a Director of Quality who oversees and executes the company's overall quality program. Responsibilities manage a multidisciplinary team, covering food safety, food quality, sanitation, and regulatory compliance at the manufacturing/warehouse level with a focus on continuous improvement. JOB DUTIES AND RESPONSIBILITIES: Ensure manufacturing site is producing safe, quality food that meets the needs and requirements of our customers, stakeholders, and regulatory agencies (audit ready, every day) Ensure sites are maintaining high sanitary standards through the execution of effective Sanitation Operating Procedures and Master Cleaning Schedules. Provide site teams with assistance in managing customer relations including site audit preparation & facilitation as needed Ensure that site teams are effectively managing customer complaints with thorough root cause investigation, effective CAPA plans and timely and meaningful responses Ensure all food safety and quality management programs are effectively implemented and executed Manage team developmental plans and performance issues Develop, manage, and improve key performance metrics Partner cross-functionally to ensure that FSQA is built into all processes Lead change and improve ways of working Mitigate risk through the application of scientific principles, technical experience and employment of Quality and Food Safety Standards Troubleshoot problems associated with product and process industrialization across all facilities; ensure root cause/corrective actions are appropriate and are fully implemented Collaborate with internal functions including Operations, Maintenance/Engineering, Research & Development, Environmental Health and Safety, Operational Excellence, Regulatory, and Commercialization to deliver products to the market that meet company standards Utilize Six Sigma, Lean, and/or other continuous improvement concepts to improve quality, efficiency, and waste Ensure quality teams are effectively testing inbound ingredients to ensure quality, safety and supplier accountability and compliance to established specifications Ensure quality teams are effectively testing finished products to ensure adherence to product specifications and quality standards Stay current with all regulatory and certifying agency guidelines Manage regulatory issues across the company All other duties as assigned REQUIREMENTS: Demonstrated excellence in achieving process improvements and associated operating efficiencies from the application of “LEAN / Six Sigma” operational excellence thinking and toolset Expert understanding of Quality Systems, Food Safety, Quality Assurance and Food Regulations People management experience including coaching, performance reviews, and career development Ability to understand technical and scientific concepts Experience in high-volume, automated food manufacturing Ability to work under deadlines, with multiple priorities Ability to work cross-functionally within the organization Must be adaptable, flexible and comfortable in a change management role Self-driven, results-oriented, and able to work independently Excellent communication/presentation skills Detail-oriented - Excellent record-keeping/documentation skills Able to quickly learn new systems, tools, and programs Experience with 3rd party audits Working knowledge of ERP systems electronic food safety/quality document management systems Compensation: $140,000 plus benefits If this sounds like the position you have been waiting for, please apply using the online application or the link below - all inquiries are strictly confidential. Our focus is to assist you to make your best next career move, and we will not use your information for any other purpose. Kalon Staffing is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. #J-18808-Ljbffr

• Responsible for the efficient and effective performance of testing in conformance with regulations and standards.
• Responsibilities include inspection (Visual), analysis of results, determining final disposition of some product and detecting nonconforming conditions.
• Works within clearly defined SOPs and/or scientific methods at the Final Inspection Area.
• Adheres to quality guidelines.
• Complies with regulations and standards.
• Identifies basic non-compliance within regulations and standards.
• Maintains appropriate licenses / training / certifications, as needed.
• One (1) to two (2)years' experience is desirable.
• Proven ability to correctly interpret drawings and geometric dimensions and tolerances.
• Able to use standard measuring equipment including calipers, Random-Access memory (RAM) optic, micrometers, pin gauges, gage blocks, etc. is a plus.
• Previous experience participating in continuous improvement activities.
• Demonstrated understanding in the use of calibrated equipment and ability to follow equipment maintenance repair procedures.
• High school diploma Is desirable but not a must and if the person has experience it should also be enough.

JOB DESCRIPTION/SUMMARY The CQC Manager will be assigned to Department of Defense (DoD) construction project(s) located in various regions. This individual will be responsible for all aspects of quality control (QC) and must be onsite during all phases of the construction work. While at the jobsite, the CQC Manager works with the customer and other contractor staff to ensure QC objectives are met in accordance with the contract requirements and high standards of service delivery are maintained. DUTIES AND RESPONSIBILITIES Prepare and update the QC Plan. Attend coordination meetings with the Client, subcontractors, and vendors. Implement the “Three Phases of Control” for all definable features of work. Perform inspections to ensure work is completed in compliance with contract requirements. Stop work that does not comply with the contract plans and specifications and direct the removal and replacement of any defective work. Prepare and submit daily quality control reports. Conduct weekly QC meetings at the jobsite. Oversee the review and approval of design and construction submittals. Ensure As-Built drawings are updated daily. Coordinate onsite and offsite testing. Maintain a testing log. Review invoices prior to approval to ensure all relevant work has been completed in accordance with the contract requirements. Perform punch-list and pre-final inspections. Perform other duties as requested by supervisors and senior level managers in support of successful performance on all projects. MINIMUM QUALIFICATIONS, SKILLS, AND EDUCATIONAL REQUIREMENTS A Bachelor’s of Science degree from an accredited school in engineering or sciences with a minimum of seven (7) years’ experience (within the last ten (10) years), as a Superintendent, Project Manager, or Project Engineer and at least five (5) years field experience as a CQC Manager with repairs to DoD petroleum, oil, and lubricants (POL) facilities, tank rehabilitation, tank cleaning and repairs and emergency inspection. Familiar with requirements of USACE EM-385-1-1, and experience in the areas of hazard identification, safety compliance, and sustainability. Knowledge and experience with POL industry standards including API Std 650, API Std 653, API RP 2016, and API Std 2015 and procedures an applicable DoD criterion. Completion of course entitled Construction Quality Management for Contractors must be completed prior to fieldwork. INTER-PERSONAL RELATIONSHIPS Must work effectively with employees, subcontractors, and clients at all levels. WORKING CONDITIONS The position requires working at the construction jobsite for extended periods of time. The position may require working during weekends and extended hours in order to meet deadlines. #J-18808-Ljbffr