QC Supervisor Jobs in California

Job Title: Quality Control Supervisor Company: Randstad Location: Benicia, CA Description: Execute company quality control and quality assurance program to ensure all products are manufactured efficiently, with high quality and in compliance to cGMPs and other government regulations. Stay abreast of new regulations and ensure compliance. Support certifications and label compliance. Manage multiple staff members supporting QC functions. Support to Sales, R&D and Operations groups. Conduct off site audits as needed. Main Duties Include:- Update and oversee company quality systems inlcuding execution and monitoring of those systems- Preparation and updating SOPs and overall document control- Oversee Company cGMP training program- Oversee plant environmental monitoring program- Assist in overseeing finished product and raw material chemical and microbial analysis- Ensures label revision process is followed and current revisions are used in production - Address customer and consumer complaints- Supervise staff, interface with department managers, teambuilding- Assist in managing vendor certification program- Support sales in completing customer compliance documents as needed.- Review and audit documents as needed for accuracy- Ongoing label review to ensure compliance - Miscellaneous projects as neededWorking hours: Full-TimeRequirements:--Thorough knowledge of current Good Manufacturing Practices for Foods and Dietary Supplements--Knowledge of Good Laboratory Practices a plus--Excellent interpersonal, organizational and computer skills--Detail oriented with excellent follow up--Excellent problem solving skills--Excellent customer service skills--Leadership skills--Ability to manage multiple projects simultaneouslyQualifications:--5-10 years regulatory and or plant manufacturing experience --Excellent verbal and written communication skills--Knowledge of regulations for label compliance --Position requires interfacing with several departments --Position requires flexibility, careful attention to details, and ability to multi-task --Position requires pro-active and excellent follow-up skills --Chemistry background preferredRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.

Job Title: Quality Control Supervisor Company: Robinson Pharma, Inc. Location: Santa Ana, CA Description: Robinson Pharma, Inc is seeking for a qualified Quality Control Supervisor to join existing team. To overseas Laboratory Operations in order to maintain a “State of Control” over all laboratory testing and reporting systems.  Responsibilities include training, operations, and evaluating the Quality Control staff to ensure that the quality control laboratory is constantly monitored throughout the testing operation.  The Quality Control Supervisor – Chemistry overseas a team of Chemists and Laboratory Technicians and the deployment of procedures, test methods to ensure compliance with regulations and company policy. The Quality Control Supervisor – Chemistry is responsible for enforcing procedures and practices against current 21CFR Part 111 requirements for all Laboratory operations. This is a full-time position and may required extensive long working hours to provide support for the Quality Control Department. Position Purpose: The Quality Control Supervisor - Chemistry is responsible for ensuring compliance with RPI procedures within the laboratory. They oversee the testing, and timely reporting of test results for raw materials, in-process, bulk, finished product, and stability testing. The Quality Control Supervisor – Chemistry acts as a role model of professionalism, ethical behavior, and demonstrates effective decision making at all times. RESPONSIBILITIES This is not intended as a comprehensive list; it is intended to provide a representative summary of the major duties and responsibilities. Incumbent(s) may not be required to perform all duties listed, and may be required to perform additional, position-specific tasks.  Provide feedback to lab management to improve operations for testing, and keep lab management apprise of all aspects involving the release of products. Monitors daily laboratory operations to ensure that the throughput and quality meets cGMP and Regulatory standards. Ensures that excellent documentation, controls and capabilities are in place to maintain data integrity, and ensure timely and effective actions are taken.Prevents any inadvertent release of failed or questionable goods into the market place. Works with manger to builds a team that is skilled and competent to meet the demands of a fast paced compliant culture with a continuous improvement mindset. Responsible for the timely execution of the marketed product stability program, ensuring that tests are conducted according to the Quality System procedures and protocols and failures are investigated and acted upon in a timely manner. Reviews all testing data for accuracy and compliance to company procedures.Authors and/or provides technical approval on all Microbiology and Chemistry SOPs, Specifications, and Test Methods. Evaluate employee’s skills level and provide necessary training to employees to improve their knowledge and ability to bring the Quality Control Department to the next level of technology and professionalism.Monitor outside laboratory test results for correctness and compliance with established standards. Ensure on time reporting of contract laboratories in order to meet aggressive company needs.Ensures all laboratory equipment is validated, maintained, and calibrated according to RPI standards. Will act as a role model of professionalism, ethical behavior, and effective decision making at all times to the employees and customers, both internally and externally. Supervision: Assign and delegate tasks and follow up to ensure tasks are completed in a timely manner. Observing and providing feedback on personnel performance to lab management.  Motivating personnel to perform at high level productivities. Promoting and encouraging personnel development to improve their knowledge and skills. Ensure SOPs are up to date and are indicative of actual work practices.  Ensure the lab area is organized, cleaned, and ‘audit ready’ at all times. Provide training to employees to meet company, cGMP, and FDA requirements. Reports: Complete reports accurately and on time.  Report status of laboratory operations to lab management, using metrics, effectiveness checks, and note current or potential issues with suggested plan of implementation. Planning: Works with Associates, peers, and other Managers to anticipate problems and plan for upcoming events. Sets objectives and ensure they are met using established procedures to maintain and mentor qualified personnel.  Working Relationships: Training and developing personnel through formal training programs, providing both informal (e.g., on-floor coaching) and formal (e.g., written evaluation) job performance-based feedback, delegating and follow-up (i.e., operational control). Communicating and working with all operational areas within Robinson Pharma, Inc. Skills needed: Excellent written and verbal communications skills, as well as detail oriented organizational skills. Strong leadership and interpersonal skills required. Ability to utilize basic computer software such as Microsoft Office, Excel, Power Point, Word, and Outlook. Adept in fast pace work environments and able to deal with multiple critical task/issues. Broad-based experience or combination of experience, in pharmaceutical manufacturing, Quality Operations, Regulatory Compliance or Regulatory Affairs function will be required. Significant knowledge of FDA Regulations, specifically 21 CFR 111. Thorough understanding of QA/QC systems and manufacturing processes are required.  Educational or Experience requirements are: Bachelor Degree or higher in Chemistry or equivalent combination of experience. Five (5) or more years of work experience. Experience with cGMP and GLP regulations.

Job Title: Quality Control Supervisor Company: Location: Santa Ana, CA Description: Date: March 17, 2010 Position: Quality Control Assistant Supervisor Report to: Quality Control Supervisor Company: $30 MM Cables Manufacturing Salary: Open Company Information: A $30 MM manufacturing company building cable and harness assemblies, with more than 25 years of experience; providing customers with the highest quality products and services available in the Electronic Cables Industry. Position Description: Objectives of the position The Quality Control Assistant Supervisor is responsible for leading, mentoring, coaching the quality control team members. Maintenance of the established Quality Control processes; as well as coordinating, developing and implementing controls to ensure quality on the products and processes with the focus being on continuous improvement. Major Responsibilities ? To maintain order and discipline in the Quality Control Department. ? Resolve employees concerns and issues in a timely matter. ? Ensure that the testing and measurement equipment are used properly and maintained in good condition. ? Maintain Test Fixtures? inventory, which includes classification and maintenance. ? Update work orders (Traveler) with the correct testing information. ? Ensure that product shipments are sent on time and well packaged. ? Make the necessary product movements on the company?s management software. ? Address any problems that arise and make educated decisions in the absence of the Supervisor of Quality. ? Maintain good communication with the Quality Control Supervisor of issues that arise from the second shift. ? Run all necessary employee tracking reports at the end of the day. ? Provide all the paperwork required by the Human Resources Department: attendance list, permits, clarifications, extra time. Experience, education and skills Experience / Knowledge: ? Three years of experience in manufacturing processes and / or technical quality. ? Excellent communication (verbal and writing). ? Able to interact with other people from other departments. ? Self motivated. ? Organized and able to plan time effectively. ? Experience managing small groups of people. Skills: ? Excellent communication (verbal and written), listening and interacting with the rest of the Departments. ? Strong leadership, motivational and presentation skills. ? Organized and plan your time effectively. ? Good judgment and good decision taker. ? Effective in working both independently and in team settings. ? Use of PC: Word, Excel, PowerPoint. ? Attention to detail and follow up to ensure employee?s issues are clearly responded understood and completed. ? Ability to select the best staff for a specific job. ? Flexible and adaptable to company?s changes and needs. ? Achieve activities / responsibilities in time, with the highest quality and efficiency. ? Focus at all times to achieve the objectives and targets set by the company. Education: ? High School, College and / or Technical Education, Quality Control supervision techniques a plus. ? Behaves in an ethical manner and respectful, being a role model and achieving the respect of his co-workers and clients. ? Self started attitude ? Able to speak Spanish (a plus)

Job Title: Quality Control Supervisor Company: AccessClosure, Inc Location: Mountain View, CA Description: Employer Information About AccessClosure, Inc Founded in 2002, AccessClosure is a privately held medical device company that is pioneering innovative access site management products designed to address the complex challenge of vascular closure during interventional and diagnostic procedures. Our first product, the Mynx vascular closure device, is based on a conformable, water soluble polyethylene glycol (PEG) sealant that instantly expands in the tissue tract by rapidly absorbing blood and subcutaneous fluids. The sealant then dissolves....more info View all our jobs Job SUMMARY: Supervise Quality Technicians. Work closely and partner with internal departments to efficiently deliver safe and effective medical device designs for manufacturing in line with AccessClosure’s policies and procedures. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned on an individual basis: • Supervise day-to-day Quality Control functions including scheduling of inspections, line support, lot release testing and reliability testing, including any necessary overtime • Ability to provide hands on assistance to meet department timelines • Develop and train Quality Control personnel including the writing of performance reviews • Assist in resolution of employee issues • Communicate and enforce quality policies • Effective interpersonal skills with cross functional groups • Ability to effectively prioritize and multi-task based on company needs • Initiating action to prevent the occurrence of product nonconformity • Initiating, reviewing and approving modifications to existing documents as required to support Quality Control functions • Manage the QC equipment including, coordinating the calibration and preventative maintenance activities

Job Title: QUALITY CONTROL SUPERVISOR Company: Location: Fresno, CA Description: Expanding International Food Processing Company has an immediate opportunity for Quality Assurance / Quality Control Manager. The QC/QA Manager is responsible for developing, implementing & championing the company?s quality plan as well as engaging the organization to ensure the quality vision is effectively practiced on a daily basis. To work with management & all departments to improve overall effectiveness of company while increasing quality of product manufactured. Key Accountabilities: ? Establish, implement and maintain Quality Management System according to ISO 22000, HACCP, Kosher and Organic protocols/requirements ? Inspect daily returns, ensure their viability, or take all appropriate action from coordinating to participating in the repackaging of product in a manner so they may be returned to inventory without compromise. ? Manage the Document Center to control the quality documents ensuring applicable documents in proper use. ? Follow up customer complaints and take appropriate corrective and preventive actions when poor quality is found. ? Set up and maintain the Production Structure and Production Formulas for mixing items. ? Create and Manage Recipe/Documents to control the quality and ensure applicable documents for proper use ? Review labels and continually update ? Assist in the transfer of Governmental instructions ? Document inspection procedures to ensure product fulfill customer requirements ? Assist Purchasing Department to evaluate suppliers ? Promote the staff awareness of quality control, hygiene and safety through proper training and advising ? Manage Document Centre by ensuring the applicable documents are in proper use ? Supervision of inspection areas & to work alongside department supervisors in increasing quality ? Monitor production?s conformance with quality control standards & procedures ? Suggest methods for improving quality & the quality control process ? Training of all staff in quality control according to identified needs ? Review quality system conformity and take appropriate corrective and preventative actions with management Duties and Responsibilities are but not limited to: 1. Assign the team members on a given day into Goods In and Finished Product depending on experience and volumes involved. 2. Ensure a consistent and accurate approach to quality reporting through all aspects of company, assessing the work, and re-adjusting standards where required. 3. Liaise with appropriate department in discussing staff rotation and shift patterns to ensure appropriate cover for Goods In, Pack house and Dispatch of the QC team. 4. Co-ordinate day to day activities carried out by the QC Team ? daily reporting to sources, stock re-assessments, tests, informal audits, etc. 5. Organize staff training on QA/QC procedures and product knowledge. 6. Plan, develop, co-ordinate, design and implement test strategies for company. Products according to QA/QC guidelines, including determining and managing test environments; 7. To work in conjunction with team members. 8. Develop functional, integration, performance/load, and acceptance test plans for company products; 9. Develop and implement test/use cases with a focus on functionality and performance; 10. Analyze, evaluate, select and introduce industry tools to facilitate testing effort and coordination; 11. Coordinate testing activities to meet overall product release goals and optimize the use of testing environments. Generate project estimations including time frames and staffing efforts. Effectively forecast resource needs while ensuring that project commitments and financial constraints are met; 12. Troubleshoot testing issues and provide guidance to the company and outside entities; 13. Execution of product test cases; 14. Act as a liaison between QA/QC and any other departments within the company.; Your Attributes: Experience in quality control management or equivalent Comprehensive knowledge of quality assurance practices and processes Must have deep product functionality knowledge Highly developed analytical and trouble-shooting skills (the ability to troubleshoot environmental as well as product issues) and the ability to quickly identify and resolve client issues Ability to multi-task and prioritize conflicting demands effectively under tight time constraints Excellent organizational, creativity and perseverance skills Ability to work well in a fast-paced environment, both independently and in a cross-functional team environment Strong interpersonal skills with demonstrated verbal and written communication abilities Excellent management, decision-making and team building skills A positive, ?can-do? attitude and customer focused approach that will enable you to deal with challenging situations with integrity, empathy and sincerity A genuine passion for the creation process and life cycle

Job Title: Quality Control Supervisor Company: Ventura Coastal LLC Location: Ventura, CA Description: Employer Information About Ventura Coastal LLC Ventura Coastal LLC, is a citrus processing company with operations in both Ventura and Visalia, CA. View all our jobs Job Ventura Coastal, a leader in the production of citrus juices and oils, is seeking a Quality Control Supervisor for their Ventura, CA loaction. Will ensure laboratory technicians are correctly performing routine tests including chemical analysis of specified raw materials and finished goods. Also will ensure proper testing and assist in the performance of in-process quality control tests on our products. This position is a working supervisor position meaning that in addition to daily supervision of the lab technicians it is expected this position will be part of the working crew. This would include performance of daily sanitation, GMP and other inspections, microbiological analysis on all products and HACCP compliance. •Train laboratory technicians in the proper means of raw materials, in-process and finished product testing. Follow up to ensure accuracy and reliability of technicians’ work including their input of data into the computer system. •Conduct analysis on all products and ingredients to determine conformance to microbiological standards and advise of potential liability conditions. •Analyze and record all quality attributes for produced and purchased products within the parameters of plant production and/or customer requirements. •Perform necessary calculations required for standardizing products or for adjustment of oil, solids, pulp, and other quality parameters of all blended products. •Clean and calibrate and maintain test equipment. •Evaluate performance of lab technicians and provide positive and constructive feedback on a daily basis to the technicians. Make recommendations and take proper disciplinary actions on employee related matters. •Function as a technical resource in documenting yields for all produced products. •Responsible for the accuracy and documentation of the daily Quality Control production records for all produced products. •If required, collect samples, analyze results and document plant waste effluents and prepare written reports for the City of Ventura Sanitation Department on a weekly or as needed basis. •Interact with sales, customer service, and production departments in a cooperative team effort to achieve the goal of servicing the customers’ needs. Because of the collaborative nature, there may be multiple departments making requests of this position. •Perform daily sanitation, GMP, and other required inspections. Prepare and distribute results; follow up with corrective actions. •Examine production paperwork to verify that the HACCP parameters have been met. •Promote safety in the department and ensure that all technicians adhere to all safety regulations including the wearing of all personal protective equipment. •Ensure that all technicians are following all food safety and personal hygiene practices. •Demonstrate reliable attendance, consistent punctuality and a positive attitude at all times. •Act professionally towards customers, visitors and vendors. •Perform other duties as required and assigned. NOTES: Additional Salary Information: DOE Please forward salary requirements with resume.

Job Title: Laboratory Supervisor - QC/Quarantine Labeling / BIO650 Company: American Red Cross Location: Oakland, CA Description: Position Description:Job Summary:Responsible for the daily operations of Manufacturing. Hire and supervise staff. Participate in education and training activities. Ensure compliance with federal, state, ARCBS directives and regional policy and procedures and regulations. Ensure compliance with safety policies and procedures in the work area and use applicable protective equipment at all times to prevent exposure to potentially infectious blood and body fluids. Comply with the Clinical Laboratory Improvement Amendments (CLIA).Perform all duties and responsibilities in compliance with standard operating procedures, Safety Quality Identity Potency Purity (SQUIPP), regulations outlined in the Code of Federal Regulations (CFR), Occupational Safety and Health Administration (OSHA) and other applicable Federal, state and local regulations.Major Responsibilities:1. Responsible for the supervision of staff including, but not limited to, hiring, training, coaching, evaluating and disciplining to ensure a well-qualified team and to enhance operational success and compliance.2. Responsible for staff training and certification of competency.3. Prepare work schedules and ensure appropriate coverage for assigned shift.4. Assist in the review and update of manufacturing procedures to comply with changes in regulations, ARCBS directives, local and regional policies and procedures and technical advancements.5. Supervise all work processes and ensure work is performed accurately and efficiently.6. Ensure compliance with state and federal regulations, AABB standards, ARCBS directives and regional policies and procedures.7. Perform supervisory review of documents.8. Supervise good inventory management practices.9. Lead suspect product management process.10. Ensure products are suitable for release for distribution and are managed appropriately.11. Ensure monthly product QC requirements are met.12. Ensure quality and quantity of manufacturing and distribution goals are met; including timelines.13. Participate in documenting, investigating, troubleshooting and preventing recurrence of department errors and problems.14. May participate in the validation of hardware, software, instrumentation, test kits, and procedures as directed.15. May perform, review and approve quality control on products, reagents, equipment and various test kits. Maintain the required records and files.16. Communicate with National Testing Laboratory staff when necessary to resolve problems, facilitate sample shipment, and clarify test data transmission issues.17. Ensure accurate electronic and physical inventories location for products are maintained.18. Perform other related duties as necessary.Scope:Responsible for assisting management in maintaining and monitoring area departmental operating budgets. Operate under general guidelines from management.Plan own work and set priorities for assigned area. Actions and decisions based on some degree of established precedent, discretion and judgment.Supervisory responsibility for multiple staff levels, including professional, line, and administrative staff.

Job Title: Strawberry QC Supervisor Company: Dole Food Company Location: Watsonville, CA Description: This position is responsible for ensuring that Dole's quality standards and customer specifications are met, and for reporting on quality at the harvest point. It is also responsible for developing and communicating harvest estimates and for coordination of daily volumes and special packs. 1. Grade product and document findings for strawberries, raspberries, and blackberries. Will maintain documentation and communicate findings to the Manager of Cooling/Quality Control on all quality issues. 2. Will provide copies of inspection sheets to crew forepersons and communicate findings to ranch managers. 3. Will assist with coordinating special trials regarding packaging materials, shelf life, etc. 4. Communicates with the Cooler and Sales regarding harvest estimates and the condition of the product. Works with the Cooler on special picks/packs and relays appropriate information to field forepersons. 5. Ensures that quality standards are presented and implemented at independent grower locations, and works with field forepersons and ranch management on training. 6. Advises field forepersons on product issues, pack, pallet stacking, box marking, traceability, etc. Will communicate information to them and coordinate training if necessary to ensure proper implementation. Will also communicate with outside growers and assist with recommending training for field forepersons. 7. Other duties as assigned. REQUIREMENTS OF THE POSITION: EDUCATION: High School diploma or equivalent combination of education and experience specifically dealing produce quality. SKILLS: Ability to communicate in both English and Spanish, verbal and written preferred. Ability to use a computer. OTHER: Must have the ability to make decisions, maintain regular and acceptable attendance, follow directions, interact well with co-workers, understand and follow posted work rules/procedures and to accept constructive criticism. Must have valid CA Driver's License. Must be available for regular travel and seasonal relocation (North/South) as required by the business.

Job Title: Supervisor, Quality Control Company: TRD USA Inc Location: Costa Mesa, CA Description: TRD USA, Inc. is involved in the design, development and support of racing engines and chassis technologies to the US racing industry. TRD currently has a vacancy for the following position in our Costa Mesa , California office. Supervisor, Quality Control – Reference #HJ031810 This is a unique opportunity for a talented individual to be involved in the daily supervision of a small quality control department. The ideal candidate will have at least 5 years in a similar position with strong knowledge and understanding of all quality concepts as well as excellent written and verbal skills. Prior experience involving the inspection of high performance parts to ensure all products meet the specifications and superior quality levels is required. We prefer a candidate with a BS in Quality Assurance, Mechanical Engineering or equivalent work experience. We offer a competitive compensation package with excellent benefits. For immediate consideration, please email or fax your resume with salary history to: TRD U.S.A. , Inc. Attn: Human Resources Department 335 East Baker Street Costa Mesa, CA. 92626 Fax: Register to View Register to View No Phone Calls Please An Equal Opportunity Employer

Job Title: Quality Control Supervisor Company: Location: Sacramento, CA Description: Benicia food manufacture is in search of experienced Quality Control Supervisor. This individual will execute company quality control and quality assurance program to ensure all products are manufactured efficiently, with high quality and in compliance to current GMPs and other government regulations; stay abreast of new regulations and ensure compliance; support certifications and label compliance; manage multiple staff members supporting QC functions including training; providing support to Sales, R&D and Operations groups and conduct off site audits as needed; prepare and update SOPs and overall document control; oversee plant environmental monitoring program; update and oversee company quality systems including execution and monitoring of those systems; preparation and updating SOPs and overall document control; oversee Company cGMP training program; assist in overseeing finished product and raw material chemical and microbial analysis; ensure label revision process is followed and current revisions are used in production; address customer and consumer complaints; supervise staff, interface with department managers, teambuilding; assist in managing vendor certification program; support sales in completing customer compliance documents as needed; review and audit documents as needed for accuracy; ongoing label review to ensure compliance; miscellaneous projects as needed. The qualified candidate will have 5-10 years regulatory and/or plant manufcaturing experience, preferrably with a chemistry background. Email a confidential resume today for consideration!