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Quality Control Manager Salary in California, USA

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Quality Control Manager Salary in California, USA

100 000 $ Average monthly salary

Average salary in the last 12 months: "Quality Control Manager in California"

Currency: USD Year: 2024
The bar chart shows the change in the level of average salary of the profession Quality Control Manager in California.

Distribution of vacancy "Quality Control Manager" by regions California

Currency: USD
As you can see on the diagramm in California the most numerous number of vacancies of Quality Control Manager Job are opened in San Diego. In the second place is Los Angeles, In the third is Sacramento.

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Quality Control Inspector
Schneider Electric USA, Inc, Chino
We are looking for a quality-focused and detail-oriented individual to join our growing team. If you are ready to take your logistics career to the next level, we encourage you to apply!What will you do? In this role, you will be responsible for ensure we ship the right product and safeguarding the quality of our logistics operations. You will conduct audits to ensure compliance with company golden rules and best practices. Your work will be influential in minimizing errors, ensuring processes are followed, and maintaining a top customer satisfaction.What skills and capabilities will make you successful? Strong understanding of Quality Control principles Background on Lean methodologies (8D, RCA, Fishbone and 5 Why's) ISO 9001 standard and Quality Management System (QMS) background Excellent analytical and problem-solving skills Proficient in Microsoft Office Suite, including Excel. Excellent written and verbal communication skills. Ability to work independently and as part of a team. Strong attention to detail and accuracy. What's in it for you?Beneficial hands-on knowledge and work experienceValuable mentor relationships and the opportunity to grow your connections within a global, inclusive, and dynamic organization.Create a path to your career goalsWho will you report to?You will be reporting to the Quality ManagerThe U.S. starting rate for this full-time position is $22.0 per hour plus a Performance Award for candidates located within the U.S. Our salary ranges are determined by reviewing roles of similar responsibility and level. Within the salary range, individual pay is determined by several factors including performance, knowledge, job-related skills, experience, and relevant education or training. Schneider Electric also offers a comprehensive benefits package to support our employees, inclusive of paid family leaves, 401(k) + match, well-being programs, holidays & paid time off, military leave benefits, and more. Let us learn about you! Apply today. You must submit an online application to be considered for any position with us. This position will be posted until filled. Why us?At Schneider Electric we're committed to creating a workplace that gives you not just a job but a meaningful purpose in joining our mission to bring energy and efficiency to enable life, progress and sustainability for all.We believe in e mpowering our team members to reach their full potential, fostering a sense of ownership in their work.We embrace inclusion as a fundamental value, ensuring that every voice is heard and valued. We value differences, and welcome people from all walks of life. We believe in equal opportunities for everyone, everywhere.If you want to be part of a company where your contributions truly matter, where you are empowered to make a difference and where inclusivity is valued, we would love to hear from you.Discover your M eaningful, Inclusive and Empowered career at Schneider Electric.€34.2bn global revenue +12% organic growth 135 000+ employees in 100+ countries #1 on the Global 100 World's most sustainable corporationsYou must submit an online application to be considered for any position with us. This position will be posted until filledSchneider Electric aspires to be the most inclusive and caring company in the world, by providing equitable opportunities to everyone, everywhere, and ensuring all employees feel uniquely valued and safe to contribute their best.We mirror the diversity of the communities in which we operate and we 'embrace different' as one of our core values. We believe our differences make us stronger as a company and as individuals and we are committed to championing inclusivity in everything we do. This extends to our Candidates and is embedded in our Hiring Practices.You can find out more about our commitment to Diversity, Equity and Inclusion here and our DEI Policy hereSchneider Electric is an Equal Opportunity Employer. It is our policy to provide equal employment and advancement opportunities in the areas of recruiting, hiring, training, transferring, and promoting all qualified individuals regardless of race, religion, color , gender, disability, national origin, ancestry, age, military status, sexual orientation, marital status, or any other legally protected characteristic or conduct.We are looking for a quality-focused and detail-oriented individual to join our growing team. If you are ready to take your logistics career to the next level, we encourage you to apply!What will you do? In this role, you will be responsible for ensure we ship the right product and safeguarding the quality of our logistics operations. You will conduct audits to ensure compliance with company golden rules and best practices. Your work will be influential in minimizing errors, ensuring processes are followed, and maintaining a top customer satisfaction.
Quality Control Research Associate - II*
American Cybersystems, Inc., Santa Monica
Innova Solutions is immediately hiring for a Quality Control Research Associate - II. Position type: Fulltime - Contract Duration: 13 Months Location: Santa Monica, California As a Quality Control Research Associate - II, you will: Job Description: All previous level plus: Conduct non-routine analysis of raw materials, intermediates, and finished product samples. Troubleshoot instrumentation and test methods. Assists in the training of QC staff as needed. Applies knowledge of current Good Manufacturing Practices (cGMPs) and Good Laboratory Working knowledge and proficiency with Microsoft Office software. Writes and executes protocols and reports. Evaluates equipment for purchase and performs installations and qualifications of the new instruments. Thank you! Deeksha Gupta Team Lead - Recruitment (+1) 213-788-7669 [email protected] RANGE AND BENEFITS: Pay Range*: $33-$35/Hour. *Pay range offered to a successful candidate will be based on several factors, including the candidate's education, work experience, work location, specific job duties, certifications, etc. Benefits: Innova Solutions offers benefits( based on eligibility) that include the following: Medical & pharmacy coverage, Dental/vision insurance, 401(k), Health saving account (HSA) and Flexible spending account (FSA), Life Insurance, Pet Insurance, Short term and Long term Disability, Accident & Critical illness coverage, Pre-paid legal & ID theft protection, Sick time, and other types of paid leaves (as required by law), Employee Assistance Program (EAP). ABOUT INNOVA SOLUTIONS: Founded in 1998 and headquartered in Atlanta, Georgia, Innova Solutions employs approximately 50,000 professionals worldwide and reports an annual revenue approaching $3 Billion. Through our global delivery centers across North America, Asia, and Europe, we deliver strategic technology and business transformation solutions to our clients, enabling them to operate as leaders within their fields. Recent Recognitions: One of Largest IT Consulting Staffing firms in the USA - Recognized as #4 by Staffing Industry Analysts (SIA 2022) ClearlyRated® Client Diamond Award Winner (2020) One of the Largest Certified MBE Companies in the NMSDC Network (2022) Advanced Tier Services partner with AWS and Gold with MS Website: https://www.innovasolutions.com/ Innova Solutions is an Equal Opportunity Employer and prohibits any kind of unlawful discrimination and harassment. Innova Solutions is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment on the basis of race, color, religion or belief, national origin, citizenship, social or ethnic origin, sex, age, physical or mental disability, veteran status, marital status, domestic partner status, sexual orientation, or any other status protected by the statutes, rules, and regulations in the locations where it operates. If you are an individual with a disability and need a reasonable accommodation to assist with your job search or application for employment, please contact us at [email protected] or (770) 493-5588. Please indicate the specifics of the assistance needed. Innova Solutions encourages all interested and qualified candidates to apply for employment opportunities. Innova Solutions (HireGenics/Volt) does not discriminate against applicants based on citizenship status, immigration status, or national origin, in accordance with 8 U.S.C. § 1324b. The company will consider for employment qualified applicants with arrest and conviction records in a manner that complies with the San Francisco Fair Chance Ordinance, the Los Angeles Fair Chance Initiative for Hiring Ordinance, and other applicable laws.
Quality Assurance Manager
The Judge Group Inc., Los Angeles
Location: REMOTESalary: $130,000.00 USD Annually - $150,000.00 USD AnnuallyDescription: Our client is currently seeking a Quality Assurance Manager Quality Assurance Manager will be a pivotal role in ensuring the highest standards of quality and compliance throughout the product development lifecycle. This position involves overseeing and implementing quality management systems, processes, and procedures to meet regulatory requirements and industry standards. The Quality Manager collaborates closely with cross-functional teams, including Chemistry, Manufacturing, and Controls (CMC), Regulatory Affairs, and Quality Assurance and company's GMP suppliers, to drive continuous improvement initiatives and maintain a culture of quality excellence.ROLES & RESPONSIBILITIES:- Identify gaps and opportunities to develop further QMS, including writing and implementing SOPs and work instructions. Maintain electronic systems for training, document control, supplier audit schedule, and files. Review and approve GMP protocols for release and stability testing of company's combination products, analytical method validation protocols and reports, master and executed batch records, product specifications, etc. Experience with analytical testing of combination nasal spray products is preferred. Contribute to out-of-trend and out-of-specification investigations and review executed investigations, ensuring that all documentation, including root causes analysis and applicable CAPAs, are well documented and archived for easy retrieval in Company's electronic file storage system. QUALIFICATIONS:- Minimum of a B.S. degree or equivalent in chemistry, biochemistry, or similar discipline required; Master's degree in scientific discipline preferred. 5+ years in the Quality Assurance role working with internal GMP manufacturing or external GMP suppliers of drug substances, drug products, labeling and packaging, or a combination of the above. (Required) Preferred experience working with combination nasal spray products. Have at least 3-5 years of hands-on analytical chemistry in a GMP laboratory such as quality control or analytical development. Contact: [email protected] job and many more are available through The Judge Group. Find us on the web at www.judge.com
Quality Control Manager
Herman Construction Group Inc (HCG), Sacramento
Herman Construction Group, Inc (HCG) is growing! We are seeking a talented Quality Control Manager to join our dynamic HCG team, a subsidiary of Bristol Bay Construction Holdings LLC (BBCH). As the QC Manager your responsibilities include overall management of the Contractor's Quality Control (CQC) with the authority to act in all CQC matters for the Contractor, Herman Construction. Your duties include maintaining current records of quality control operations, activities, and tests performed, including the work of subcontractors and suppliers. The referenced records shall be on an acceptable form and shall include factual evidence that required quality control activities and/or tests have been performed. Responsibilities Manage and implement the QC Program. Ensure fulfillment of the Contractor's LEED Coordinator duties, as applicable. Coordinate with and support the Government's Commissioning Authority. Attend the partnering meetings, QC Plan Meetings and Coordination and Mutual Understanding Meeting. Perform submittal review. Ensure testing is performed and provide QC certifications and documentation required by the Contract. Manage and coordinate the three phases of control and documentation performed by testing laboratory personnel and any other inspection and testing personnel required by the Contract. Implement and enforce strict QC policies and procedures. Ensure compliance with OSHA and USACE EM385-1-1 regulations. Conduct weekly QC meetings, prepare and submit daily QC reports. Maintain documentation for QC compliance and Maintain record drawings and specifications. Identify, record, track and monitor completion of re-work items. Project Scope of Work Work covered by contract for the Mule Creek State Prison Fire Alarm Replacement Fire Suppression Repair (FARFSR) Project in Ione, CA includes the design and construction to repair or replace the existing non-operational fire alarm system and/or components, to provide a fully operational fire alarm system, as required by the CDCR and Office of the State Fire Marshal. The fire suppression repair consists of the repair of known deficiencies in the sprinkler heads, risers, valves, and switches. It also includes conducting the five-year NFPA 25 inspection, testing, and maintenance of the overhead fire suppression system and providing written reports of the findings. The results of that testing will determine other repairs not covered by the Work needed to bring the fire suppression system into compliance. The DBE will perform this added work through the issuance of change orders approved by the CDCR, funded through the allowance allocated within the Stipulated Sum.Compensation: $105,000 - $125,000 yearly DOEQualifications Minimum five years Construction Quality Control experience of similar size and complexity, OR minimum 10 years construction experience. Previous experience with California Department of Corrections & Rehabilitations or other types of jail/prison systems will be looked at favorably CPR, AED, and First Aid course completed within the last 2 years. As a condition of employment, you may be required to pass a pre-employment drug screening and have acceptable references and background check results. Physical Requirements This position requires the ability to maneuver around work sites, see, hear, and verbally communicate with co-workers and clients. 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The office setting includes exposure to computer screens and requires extensive use of a computer, keyboard, and mouse. Outdoor settings include walking, driving, and carrying supplies throughout all seasons with exposure to heat and cold conditions, and potentially wildlife. Is occasionally exposed to fumes or airborne particles, toxic or caustic chemicals and loud noise. About Bristol Bay Construction Holdings LLC Bristol Bay Construction Holdings LLC (BBCH) is a holding company of Bristol Bay Native Corporation, an Alaska Native Corporation. The BBCH family of companies include 8(a), small, and large businesses operating under the Aerostar, CCI, CSI, Herman, and SES brands. The vision of BBCH is to be best value companies and employers of choice, recognized for our dedication to our unity of purpose, values, employees, clients, and shareholders. For three decades, our best-value companies have provided federal and commercial clients with superior quality and cost-effective, innovative, and sustainable solutions for general construction, restoration services, civil works, fuels systems, environmental services, professional services, and facility support services. BBCH gives hiring, promotion, training, and retention preference to BBCH shareholders, shareholder descendants, and shareholder spouses who meet the minimum qualifications for the job. We are an equal-opportunity employer. All applicants will receive consideration for employment, without regard to race, color, religion, creed, national origin, gender, or gender identity, age, marital status, sexual orientation, veteran status, disability, pregnancy or parental status, or any other basis prohibited by law. We participate in the E-Verify Employment Verification Program. We are a drug-free workplace.
Quality Control Inspector
International Marine and Industrial Applicators, LLC, San Diego
ABOUT THE ORGANIZATION IMIA,LLC is the only national marine surface preparation painting contractor servicing every U.S. Port with a mobile full time workforce that ensures that a quality product is delivered on time every time. IMIA, LLC has the equipment, seasoned deckplate supervision and mechanics, as well as rigorous corporate safety and quality programs and financial strength to support our customer's preservation needs in a truly superior and comprehensive fashion.IMIA, LLC offers a comprehensive benefit package to eligible employees. Eligible employees may enroll in:•Health •Dental•Vision•Life•LTD•Accident•Critical Illness•401kEmployees and their household members are also eligible to participate in the company's Employee Assistance Program.Per Diem OR Dislocation Allowance may be provided to eligible employees to reimburse some or all of the cost an employee might be reasonably expected to incur for lodging, meals, and incidental expenses while traveling out of town for work. EOE STATEMENT IMIA, LLC is an equal opportunity employer and provides equal employment opportunities (EEO) to all employees regardless of race, color, religion, gender, gender identity or expression, national origin, sexual orientation, age, sex, disability status, marital status, status as a covered veteran, genetics, or any other protected groups under state, federal or local Equal Opportunity Laws. This policy applies to all terms and conditions of employment including but not limited to hiring, placement, promotion, termination, layoff, recall, transfer, leave of absence, compensation, and training. JOB TITLE: Quality Control InspectorJOB CODE: Quality ControlREPORTS TO: Quality Assurance Manager. Direct on-site project direction and daily scheduling provided through continuous communication with the applicable IMIA Project Manager and/or Supervisor.Summary of position: Responsible for monitoring quality control/assurance requirements of all preservation preformed onboard commercial and US Navy vessel in accordance with established Navy regulations and industry standards or specific contractual requirements as defined in the Scope of Work. Collaborate with customer QA personnel on necessary aspects of the job.Essential Job Requirements: Produce/create electronic/handwritten Quality Assurance documentation as Objective Quality Evidence for work performed throughout the preservation process. Develop and Maintain Test and Inspection Plan (TIP) for all assigned jobs. Monitor and document all required readings with regard to, but not limited to, metal anchor tooth (profile), paint wet/dry film thickness (DFT), steel temperatures and all required environmental readings using appropriate equipment to include: micrometer, dry film thickness gauge, infrared thermometer, psychomotor. Ensure all assigned equipment is maintained in good working order with within all calibration certification intervals. All of the above requirements shall be completed in a safe and efficient manner so as not to cause injury to self or others.Required Education: High School diploma or equivalentRequired Certification: NACE Inspector and/or SSPC NBPI required.Required Experience: Formal or informal on-the-job training in the marine industry; familiarity with Navy and Society for Protective Coatings standards.Required Skills: Must possess knowledge of Maritime paintings standards with particular emphasis in US Navy ship preservation criterion. Word processing, spreadsheet, email, and database computer skills required. Must be able to accomplish mathematical calculations associated with preservation readings and documentation; must be able to discern and carry out complex written, oral, or diagramed instructions. Must be able to take direction; interact professionally, knowledgeably and cooperatively with supervisors and co-workers and customer representatives.Physical Requirements: Must be physically capable of working an 8-10 hour day requires average use of computer, some physical dexterity, and agility within confined and restricted spaces & tanks.Reasonable Accommodations may be made to enable qualified individuals with disabilities to perform essential job functions.Supervisory Responsibilities: NoneWorking Conditions: Regularly stand for long periods of time; work on scaffolds and ladders; work on top of machinery; work in confined spaces. Regularly exposed to extreme temperatures, high noise levels, toxic or caustic chemicals, fumes, airborne particles, outdoor weather conditions, dusty conditions, wet and/or humid conditions, hazardous machinery, precarious places, close proximity to other employees. Overtime or shift work involved. Travel often required. Must follow strict safety procedures. LOCATION CA, San DiegoEXEMPT/NON-EXEMPT Non-Exempt PI240672354
Quality Assurance Manager
Actalent, San Mateo
Description:• Ensures site quality oversight of commercial and/or development products at CMO's.• Oversees the commercial and/or development implementation of the Quality strategy for Gilead development portfolio of products and/or across quality sub functions.• Partners with Development, Manufacturing, Supply Chain, Outsourcing and Drug Substance to deliver on development programs.• Ensures that performance and quality of drug products conforms to established standards and regulatory requirements.• Assure CMO's meet Gilead quality regulatory and compliance standards in order to ensure a sustainable delivery of quality product to patients and maintains a good working relationship.• Reviews regulatory documents and provide expertise and guidance in interpreting governmental regulations agency guidelines and internal policies to assure continued compliance. Participates in regulatory authority inspections.• Collaborates engages and works cross functionally with other Quality groups.• Acts as an escalation contact for complex and high impact quality issues concerns and decisions.• Leads/coordinates investigations and the development and implementation of corrective and preventative action (CAPA)• Quality risk management identifying key risks impacting commercial and development programs• Competent in execution and responsible for translating quality strategy into plans of actions• Anticipates shifts in industry trends and regulatory environment that will impact Gilead's business needs and positions the functions to respond accordingly• Participates in developing controlled documents (e.g. SOPs, validation etc.)About ActalentActalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.Diversity, Equity & InclusionAt Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:Hiring diverse talentMaintaining an inclusive environment through persistent self-reflectionBuilding a culture of care, engagement, and recognition with clear outcomesEnsuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] for other accommodation options.
Quality Assurance Manager
Actalent, San Mateo
Description:• Ensures site quality oversight of commercial and/or development products at CMO's.• Oversees the commercial and/or development implementation of the Quality strategy for Gilead development portfolio of products and/or across quality subfunctions.• Partners with Development, Manufacturing, Supply Chain, Outsourcing and Drug Substance to deliver on development programs.• Ensures that performance and quality of drug products conforms to established standards and regulatory requirements.• Assure CMO's meet Gilead quality regulatory and compliance standards in order to ensure a sustainable delivery of quality product to patients and maintains a good working relationship.• Reviews regulatory documents and provide expertise and guidance in interpreting governmental regulations agency guidelines and internal policies to assure continued compliance. Participates in regulatory authority inspections.• Collaborates engages and works cross functionally with other Quality groups.• Acts as an escalation contact for complex and high impact quality issues concerns and decisions.• Leads/coordinates investigations and the development and implementation of corrective and preventative action (CAPA)• Quality risk management identifying key risks impacting commercial and development programs• Competent in execution and responsible for translating quality strategy into plans of actions• Anticipates shifts in industry trends and regulatory environment that will impact Gilead's business needs and positions the functions to respond accordingly• Participates in developing controlled documents (e.g. SOPs, validation etc.)Additional Skills & Qualifications:Technical skills:Aseptic mfg expExperience in pharmaceutical mfgRoutine skills with quality systemsExcel4-5 years of relevant experience. VeevaVault quality systems experience; or any other quality system TrackWise, MasterControl.QA role that deals internally would be ok. Does not need to be CMO specific.Degree is open.Product knowledge - sterile mfg, aseptic - FDA and European regulations.Experience Level:Expert LevelAbout ActalentActalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.Diversity, Equity & InclusionAt Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:Hiring diverse talentMaintaining an inclusive environment through persistent self-reflectionBuilding a culture of care, engagement, and recognition with clear outcomesEnsuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] for other accommodation options.
Quality Engineering Manager
System Soft Technologies, Los Angeles
Quality Engineering ManagerN. Hollywood, Los Angeles Job DesignationThe Quality Engineering Manager will lead the Quality Engineering team and directs the team objectives while aligning tasks with company policies and procedures. Oversees the Quality Engineering tasks to enhance product quality and to ensure high reliability and proper performance per product requirements. Participates in decision-making that will have a significant impact on product quality.Job Core ResponsibilitiesLed and direct the quality engineering team, ensuring that products or components met design and reliability requirements.Directs quality engineering activities and implements policies and procedures to meet business requirements.Establishes crisis resolution procedures to ensure a continuous flow of products.Oversees Quality audits on various processes to ensure compliance with regulatory requirements.Utilizes expertise and team knowledge to drive improvements and best practices.Leads and directs work for team(s) of employees as defined by business needs.Manages staff selection, performance, development, and training processes to ensure team competencies and capabilities to reach business goals and expectations.Consistent exercise of independent judgment and discretion in matters of significance.Regular, consistent, and punctual attendance is required. May need to work nights and weekends, variable schedule(s), and additional hours as necessary.Job SpecificationsEducation: Bachelor Degree in Quality Assurance, Engineering or related field requiredCertifications: Certified Lead Auditor or equivalent experience in a related fieldYears' Experience: Min 7 years of relevant experience, preferably in aerospace industrySkillsStrong ability to lead, plan, and direct the Quality Engineering Team.Demonstrated engineering expertise and ability to improve products or services by applying professional and business knowledge.We are experienced with making technical and managerial decisions, which will have a significant effect on products.Strong attention to detail, good organizational skills, and the ability to prioritize in changing situations.Solid analytical skills and judgment to proactively identify and solve increasingly complex problems.
Quality Control Manager
Rä Foods LLC, Sacramento
NOTE: To apply for this position, you must be fluent in English and Spanish1. Job Title: Rä Foods is seeking experienced "hands on" Quality (QC) personnel to join our unique and dynamic produce company: https://www.wildaboutsprouts.com/Bilingual candidates (Spanish & English are essential). As QC manager(s), you will play a crucial role in enhancing operational efficiency, product quality, and overall performance within the organization. Your expertise in process improvement methodologies and quality management will be instrumental in driving excellence across all aspects of our innovative produce operations.2. Company Overview: Rä Foods brings great tasting, highly functional foods to market through research, innovation and unrelenting vigilance. It's that commitment that inspired us to invent a revolutionary and safe growing process for sprouts, one of nature's most potent antioxidant, anti-inflammatory nutritional sources. Created as a safe and trustworthy solution to previous pathogen issues associated with the category, Wild About Sprouts (a wholly owned subsidiary or Rä Foods) is a highly successful Controlled Environment Agriculture ( #CEA ) business disrupting the sprouts industry, providing the next generation of highly functional, great tasting sprouts. Using patented COLD GROWN® technology and available in six varieties, these amazing "super veggies" contain specific concentrated phytonutrients, scientifically proven to be of great benefit in preventing and fighting disease. Our Continuous Improvement & Quality Manager will be a key team member for both management, discovery and innovation.3. Job Summary/Objective: The Food Safety & Quality Assurance personnel are responsible for all day-to-day aspects of the facility's food safety and quality programs.4. Key Responsibilities:• Act as liaison with customers, vendors, regulatory agencies and auditing bodies• Maintain and improve overall Food Safety Plan including SOPs, SSOPs, HACCP, recalls, food security and any other relevant GFSI or FDA requirement• Manage SQF programs, relevant meetings, communications, internal audits and annual auditCommunicate quality standards and parameters to plant personnel; track food safety objectives and provide resources where neededAnalyze issues, defects, and other problems, particularly when problems recur in multiple instances; recommend and facilitate solutions to these issuesReview all food safety and quality documentation; create and communicate reports as neededRespond to customer and consumer feedbackOversee new product and process trials; provide feedback and make recommendations to relevant parties Maintain compliance with federal, state, local, and organizational laws, regulations, guidelines, and policiesTraining employees on food safety best practices.Monitoring and evaluating food safety documentation and records.Collaborating with cross-functional teams to address food safety concerns.Managing corrective action plans and continuous improvement initiatives.Keeping up-to-date with industry regulations and best practices.Other duties as assigned5. Qualifications and Requirements: as:Bachelor's degree in Food Science, Food Safety, or a related field (mandatory).SQF certification (desired).4+ years of experience in food safety or SQF compliance (mandatory).Strong knowledge of FDA and USDA regulations (preferred).Excellent communication and leadership skills (preferred).6. Education and Experience:Bachelor's degree in Business, Botony/Horticulture, Engineering, Food Science, or a related field. A Master's degree is a plus.Proven experience (4+ years) in continuous improvement and quality management within the produce industry.GFSI training• HACCP training• PCQI certification• In-depth knowledge of Microsoft Excel and reporting7. Skills and Abilities:• Excellent verbal and written communication skills; Conversant in both English and Spanish• Excellent interpersonal and customer service skills• Excellent organizational skills and attention to detail• Excellent time management skills with a proven ability to meet deadlines• Strong analytical and problem-solving skills• Strong supervisory and leadership skills• Proficient with Microsoft Office Suite or related software• Very detail oriented and comfortable filling and maintaining daily paperworkStrong knowledge of Lean Manufacturing, Six Sigma, and other process improvement methodologies.Experience with statistical analysis and data-driven decision-making.Familiarity with relevant food safety regulations and quality standards, with #CEA a plus.Excellent leadership, communication, and interpersonal skills.Ability to drive change, influence stakeholders, and manage projects effectively.Supplier Management:Collaborate with procurement and supply chain teams to ensure quality standards are met for all incoming produce.Assess and monitor supplier performance and implement improvement plans where necessary.8. Company Benefits: Company health, dental, vision, and life insurance, and professional development opportunities.9. Salary Range: Commensurate with experience.10. Company Culture: Join our innovative portfolio of companies and be part of a highly integrated and exceptional team dedicated to delivering innovative high-quality products while continuously improving our processes and practices. If you meet the standards outlined in this job description and thrive in a fast-paced, challenging environment and have a passion for excellence, and innovation, we welcome you to apply for the Continuous Improvement & Quality Manager position.11. How to apply: email: [email protected]
Quality Assurance Manager
Voluspa, Irvine
Company Profile:An introduction to Voluspa unveils stunning packaging design coupled with rare exotic fragrances, as the brand invites fans to seek everyday chic illumination. Founded in 1999, Voluspa is an industry leading luxury home fragrance brand. Voluspa designs, markets, manufactures, and distributes its products worldwide. About our Culture:Voluspa attracts the most talented, innovative, and creative minds in the luxury goods industry. We offer a collaborative and family-oriented environment, uncapped growth possibilities, and lucrative benefits focusing on the well-being of every employee.About the Role:The Quality Assurance Manager is responsible for developing, implementing, and managing quality control programs across Voluspa's manufacturing and business operations.Key Accountabilities:Manage and develop the company's quality control program and foster an environment of continuous improvement across Manufacturing and Supply Chain.Lead the Quality team to conduct consistent and efficient audits/inspections of incoming raw materials, in-process manufacturing, and finished goods.Responsible for writing and maintaining documentation for Quality, Manufacturing, Regulatory, etc. to ensure that processes are accurately documented, personnel is trained, and documentation is periodically reviewed and revised - including Standard Operating Procedures (SOPs), Work Instructions, Forms, etc.Responsible for training the production team on quality control measures to improve product excellence.Manage the Quality test lab and evolve its testing capabilities to deliver best-in-class capability.Develop test methods for the thorough evaluation of home fragrance products - fragrances, waxes, raw materials, and packaging which impact product performance and consumer experience.Communicate proactively with vendors to define raw material and product quality characteristics during development, ensure specifications are met during production, and identify opportunities for improvement over time.Lead communication to vendors regarding Quality topics - through product development, production, and Shipping - any issues, corrective actions, and ongoing improvements.Manage internal and external corrective actions through use of root cause analysisManage key quality management system processes including document control, record management, training, audits, and complaint handling.Support the Product Development team by creating prototypes and initial samples of new launch products for testing and evaluation, as well as managing the inventory for those products.Physical Demands and Working Conditions: Bending, lifting, squatting and standingEducation:Bachelors of Science degree requiredExperience/Skills:5 + years in quality with extensive experience running formal quality programsExcellent problem solving skills with design of experiments knowledgeDemonstrated ability to lead in a collaborative environment with a positive leadership styleExcellent interpersonal skills and a record of creating enthusiasm amongst the team for quality improvementStrong Project Management skillsExcellent oral & written communication skillsIn-depth knowledge of quality control procedures and legal standardsExcellent organization and record keeping skillsKnowledge of ASTM standards, product safety and CPSC requirements, knowledge of GHS and IFRA preferredExperience with manufacturing candles, fragrance, or cosmetics a plusProven ability to provide leadership designing, implementing, and managing QC systems to meet the business goals of the companyExperience with equipment calibration and troubleshooting errorsFamiliarity with ISO 9000 document structureKnowledge of Kaizen/Lean Manufacturing principlesBenefits:Medical, Dental/Ortho, Vision InsuranceLife Insurance401k with matching incentivesPiad Holidays and Accrued PTOTuition ReimbursementSalary:Depending on Experience