QC Director Jobs in California

Job Title: QC Manager Company: United Pharma LLC Location: Fullerton, CA Description: QC Manager - Vitamin Manufacturer United Pharma LLC is a soft gelatin vitamin and nutritional supplement manufacturing company located in Fullerton, California. Our company is dedicated to offering the highest quality nutritional products on the market today. Our management team has over 20 years of soft gel manufacturing experience, and our state of the art production area reflects our dedication to the quality of the products we manufacture. United Pharma LLC offers a unique environment that fosters individual growth and rewards performance. We offer competitive compensation packages, great benefits, and an enjoyable work atmosphere. We are currently looking for people who want to be a part of a fantastic company. The QC Manager is responsible for overseeing Laboratory Staff and ensuring that laboratory processes are completed properly. Duties and Responsibilities: Develops and recommends inspection and sampling techniques and quality control plans. Participates in the establishment and implementation of quality specifications, testing procedures and standards for raw materials and for process and finished products. Handles complex problems effectively. Separates key issues and generates multiple solutions. Easily analyzes and prioritizes information, distilling it to the critical issues and drawing accurate conclusions. Manages complexities and competing priorities. Coordinates information and activities among groups with differing agendas, across multi-functional areas. Synthesizes all forms of research into clear, thoughtful, actionable deliverables Designs and manages processes to monitor progress and to maximize performance. Successfully manages teams. Excellent people management skills including delegation, giving feedback, promoting teamwork, and performance management. Education and Experience: 2-5 years QC management experience in a food or vitamin mfg environment. Knowledge of GMP and FDA regulations. Experience developing and implementing process improvement initiatives. Experience in operating HPLC, GC, UV. BS in Chemistry. 2-5 years of Laboratory Management Experience.

Job Title: Data Quality Management Lead Company: Apple Location: Elk Grove, CA Description: We are seeking experienced Data Quality Analyst lead. Candidates will be responsible for managing cross-functional and cross-organizational teams to identify, define, build and roll-out data quality initiatives. Candidates should have subject matter expertise of relational databases, familiarity with analysis techniques and statistical packages. Also have the ability to effectively interact with data users, managers, and other stakeholders(owners) of the data. Finally candidates should be able to describe the complex relationship between technology and organizational structure of the data and understand the implications of data quality.Key responsibilities and activitiesData Quality ManagementWork with Business partners in and outside the company to identify Data Quality issues and address them in matter of urgency and priority. Drive improvements of the organization, processes and use of systems and data. Collaborate with direct and indirect team members to create a forward looking Data Quality initiatives roadmap. The role includes:- Understanding future strategies and directions to anticipate needs.Building Internal and external expertise driving Best Practice and innovation.Situation analysis and audit of current processes, data flows and systems.Gap analysis of “as is” vs. “to be”.Proposing and driving new solutions that may be implemented WW or local processes.Develop metrics supporting Quality initiatives and ROI impact.Process Reengineering Through Cross-Functional Projects.Manage Data Quality improvement and process change through projects ensuring:GovernancePlanning of projects.Quality documentation, project management and architecture standards are followed.Organizational alignment.Timely updates to management.Standards and ToolboxDevelop and maintain clear methodology for different components of the job, including use of BPR/BI project methodology as well as other tools to better formulate, justify, prioritize and manage change.Standards and ToolboxDevelop and maintain clear methodology for different components of the job, including use of BPR/BI project methodology as well as other tools to better formulate, justify, prioritize and manage change.Profile:The candidate should ideally have the following skill-set:- Business degree and or engineering degree.- Experience in manufacturing or Data Analysis Leadership Roles.- Experience in blue-chip hi-tech industry.- Proven Team management and cross functional performance- Excellent communication skills and teamwork capability in a Matrixed organization- Business-process and systems / engineering experienceTechnical: - Excellent knowledge of SQL, HTML and XML- Experience with Oracle, MySQL and Teradata- Shell/Perl scripting- Data warehousing knowledge (modeling techniques)- Other technical capabilities is a pro.

Job Title: Manager, Quality Control - Microbiology - CA Company: Dendreon Corporation Location: Seal Beach, CA Description: Manager, Quality Control - Microbiology - CAJob Type: Regular Full-TimeLocation: Seal Beach, CAJob Description:Dendreon is seeking a Manager, Quality Control for our California Microbiology Laboratory. This is an exciting position accountable for providing leadership, management and delivery of compliant laboratory data in support of Dendreon's products and in accordance with appropriate regulatory, corporate and scientific guidelines. The successful candidate will manage the Microbiology Laboratory operations on a daily basis, as well as during inspections/audits by the FDA and other regulatory agencies. The ability to function in a fast-paced, highly technical environment, and communicate effectively is essential to success. This person leads, develops and mentors reporting staff at a variety of levels.General Summary:* Responsible for the start-up of the Microbiology Laboratory and providing QC support during the qualification of the California commercial facility.* Manages daily operations in the Microbiology Laboratory.* Responsible for microbiological tests performed during in-process and final product testing of Dendreon products.* Responsible for environmental monitoring sample collection, testing, and data review.* Manages test samples, reagents and reference standards in the Microbiology Laboratory.* Conducts and manages laboratory investigations, and participates as QC representative during investigations into deviations/exceptions and environmental monitoring excursions.* Ensures laboratory data integrity and traceability.* Communicates with Corporate QC and ensures implementation of harmonized laboratory control systems in the CA Microbiology Laboratory.* Participates in planning and process improvement activities at the departmental and inter-functional level.* Sets goals, and conduct performance reviews of direct reports; performs ongoing assessment of development and training needs of reporting staff to ensure continued development of personnel.* Contributes to the development of department budget and monitors expenditures.Job Requirements:* Bachelor's degree in biology, medical technology or equivalent.* Typically 7 years of related experience in a cGMP Quality Control department in an FDA regulated industry (drugs/biologics) with at least 3 years in a leadership role; Commercial phase experience required.* Thorough knowledge of cGMP/ICH/FDA regulations.* Experience with inspections/audits by the FDA and other regulatory agencies.* Experience with LIMS preferred.* Ability to prioritize and successfully manage complex and competing projects.* Proficient in MS Office applications and MS Project.Working Conditions and Physical Requirements:* Limited travel required.* Limited handling of laboratory equipment, chemicals and biological materials.The preceding job description has been designated to indicate the general nature and level of work performed by employees within this classification. Additional and incidental duties related to the primary duties may be required for company business needs from time to time.

Job Title: Manager, QC - Raw Material Company: Dendreon Corporation Location: Seal Beach, CA Description: Manager, QC - Raw Material & Lab Services - CAJob Type: Regular Full-TimeLocation: Seal Beach, CAJob Description:Dendreon is seeking a Manager for our Quality Control department at the Seal Beach, California commercial facility. This is an exciting position accountable for providing leadership, management and delivery of compliant laboratory data in support of Dendreon's products and in accordance with appropriate regulatory, corporate and scientific guidelines. The successful candidate will manage the Raw Material and Lab Services operations on a daily basis, as well as during inspections/audits by the FDA and other regulatory agencies. The ability to function in a fast-paced, highly technical environment and communicate effectively is essential to success.This person leads, develops and mentors reporting staff at a variety of levels.General Summary:* Responsible for providing QC support during the qualification of the California commercial facility, including enrollment and coordination of laboratory equipment qualification across all QC laboratories.* Responsible for the daily management of the Raw Material testing program; provides oversight of contract testing laboratories; ensures timely disposition of test results and issuance of CoA.* Provides technical expertise and collaborates with Corporate Quality Control during development of new material specifications.* Responsible for management of laboratory equipment.* Responsible for the sourcing of laboratory equipment in conjunction with Procurement, Validation and Facilities departments.* Responsible for writing User Requirement Specifications (URS) for new equipment.* Collaborates with Validation and Facilities departments to ensure equipment is adequately maintained in a validated/calibrated state.* Oversees preventive maintenance activities for applicable equipment; coordinates activities with equipment vendors as applicable.* Responsible for conduct and management of laboratory investigations, and participating as QC representative during investigations into exceptions and non-conformance materials.* Participates in planning and process improvement activities at the departmental and inter-functional level.* Sets goals and conducts performance reviews of direct reports; performs ongoing assessment of development and training needs of reporting staff to ensure continued development of personnel.* Contributes to the development of department budget and monitors expenditures.Requirements:* Bachelor's degree in Biology, Chemistry, Biochemistry or equivalent.* Typically 7 years of related experience in a cGMP Quality Control department in an FDA regulated industry (drugs/biologics), with at least 3 years in a leadership role; Commercial phase experience required.* Thorough knowledge of cGMP/ICH/FDA regulations.* Experience with inspections/audits by the FDA and other regulatory agencies.* Proficient in MS Office applications.Working Conditions and Physical Requirements:* Limited handling of laboratory equipment, chemicals and biological materials.The preceding job description has been designated to indicate the general nature and level of work performed by employees within this classification. Additional and incidental duties related to the primary duties may be required for company business needs from time to time.

Job Title: $45-48K Quality Control Manager-Successful Manufacturing Company Company: Company Confidential Location: Anaheim, CA Description: This Quality Control Manager Position Features: Career opportunity Great Pay to $48K Metal fabrication company is seeking an experienced Quality Assurance Manager to implement and oversee QC processes and procedures from start to finish on the production line. This position will manage multiple employees to keep everyone accountable for their particular part of production. Will work closely with other departments such as purchasing, engineering and manufacturing. Candidates must have professional communication skills, proficiency with MS Office Suite and prior management experience with QC. manufacturing industry experience is also needed. Qualified candidates should apply ASAP

Job Title: Director of Quality - In-Vitro Diagnostics - FDA Company: CyberCoders Location: Anaheim, CA Description: Director of Quality - In-Vitro Diagnostics - FDA .body .body h4 .body .section tr.oddRow a, a:link, a:visited Director of Quality - In-Vitro Diagnostics - FDA near Anaheim, CA This job is open as of 2/28/2010. Apply Now! Not a fit for this job? Search other Director of Quality jobs! Are you an employer? Visit us for more info! Email this job to a friend - $1000 Location Anaheim, CA; Irvine, CA Salary $150,000 - $175,000 Education Bachelor of Science Category QA, Quality Control Experience Required At least 2 Years Short Description Director of Quality - In-Vitro Diagnostics - FDA Required Skills Quality Director, In-Vitro Diagnostics, FDA Recruiter Anna Thomas Date Updated 2/28/2010 Skills Required Quality Director, In-Vitro Diagnostics, FDA Job Description Director of QualityIf you are a Directory of Quality with IVD experience, please read on!This is an outstanding career opportunity for a Quality Director to join a leader in the IVD industry.What you need:- Quality Director experience- In-Vitro Diagnostics experience- FDA- ASRsWhat you will be doing:- Management representative for business unit- Serve as keymember of the PAC and provide guidance in product development process and portfolio management- Leverage contract manufacturing of GPR and ASR to drive business and assure compliance within appropriate FDA guidelines- Understand process of reverse integration of LDTs and assist in the conversion of ASRs into IVDs cleared products when financially feasible- Develop and achieve the budgets for the Dx QA/QC, Compliance and Quality SystemsWhat's in it for you:- Competitive pay- Outstanding benefits: Medical, Dental, Vision, 401K, Vacation and much more!- This is a great opportunity to join a leader in the industry- Great work environment and company cultureSo, if you are a great Directory of Quality with IVD experience, please apply today! Are you a fit for this position? Please Click Here to Apply! (your information will be kept strictly confidential!) Not a fit for this position? Click Here to Search Other CyberCoders Jobs! Looking forward to receiving your resume through our website and going over the position with you. Clicking apply is the best way to apply, or you may also: Email your resume in Word to: Register to View **Please do NOT change the email subject line in any way. You must keep the JobID: CC HotJobAp : AT-DirQuality-CA -- in the email subject line for your application to be considered.*** Anna Thomas - Executive Recruiter - CyberCoders Other Jobs FDA JobsIn-Vitro Diagnostics JobsQuality Director Jobs

Job Title: Manager Quality Control Company: Baker Hughes Location: Huntington Beach, CA Description: Establishes installation, inspection and testing procedures for finished products. Establish overall Quality Control program design and implementation for a division or plant. May be responsible for ISO Certification and training compliance. Handles special projects, as assigned.Excellent verbal and written communication skills. Good analytical skills. Sound working knowledge of principles, practices, concepts and theories related to quality control. Comprehensive knowledge of division or plant products. Familiar with a variety of the field's concepts, practices, and procedures.High School Diploma or equivalent. Bachelor's Degree preferred. 7+ years experience in quality operations.

Job Title: QA/QC MANAGER Company: Location: San Francisco, CA Description: Our client, a Newark-area based company, is currently seeking Quality Manager. The Quality Manager position requires the individual to possess the skills and work experience to: plan, establish, and maintain a successful quality system. The Quality Manager must have a working knowledge of the ISO9000 essentials. The individual must demonstrate abilities in create, maintain, and ensure compliance to the Quality Management System. This position also requires the candidate to have the background in internal auditing, managing a quality system, and have the experience in trouble-shooting, and root-cause determination and analysis. The individual must create public relations, design policies to improve companyˇ¦s image and status amongst employees, customers, and suppliers in regards to the quality aspect of our business. Quality Manager will review activity reports, production statistics, stated goals, and quality objectives to determine progress in accordance with the companyˇ¦s current quality conditions and status. Hours: Monday ˇV Friday | Dayshift For immediate consideration please Email your resume to Register to View You may also Fax your resume to Register to View . ESSENTIAL JOB FUNCTIONS ?X ISO 9001:200 compliance ?X Responsible for planning, coordinating, and/or conducting internal audits ?X Plan and develop quality policies, objectives, guidelines, and procedures ?X Develop a top-notch quality system, and maintain all specified requirements ?X Conduct employee training which pertains to quality and QMS ?X Be detail oriented and motivated by accomplishment ?X Have a sense of urgency and compliance with stated practices will be essential attributes ?X Posses a high energy level, a sense of commitment to assure that obligations are met ?X Conduct periodic supplier evaluations and surveys ?X Provide daily management and direction to the QA & QC functions of the organization ?X Perform quality inspections and first article reports ?X Develop, maintain, and measure key performances pertaining to quality ?X Monitor inspection tools and equipment calibrations ?X Gather evidence to determine progress toward stated goals and quality objectives ?X Setting an example for the company for following all stated company policies, procedures, guidelines, and safety rules and regulations ?X Performing and collecting Statistical Analysis data to measure trends ?X Looking for ways for continuous improvements in all areas of quality, production, and customer satisfaction NON ESSENTIAL JOB FUNCTIONS ?X Assisting production personnel, and engineering with issues on the floor ?X Safely operating the forklift trucks, cranes, and shop equipment ?X Ensuring that the production personnel have the required tools and equipment to perform their tasks ?X Performing temperature uniformity surveys, if required POSITION REQUIREMENTS ?X Minimum of 5-7 years of experience in managing a quality system related to the brazing industry ?X Excellent organization, communication and management skills ?X Effective leadership skills pertaining to quality ?X Savvy computer skills ?X Critical thinking and problem-solving skills ?X Customer service oriented About Benchmark: Benchmark Staffing is the leader in specialized production and distribution staffing. We represent a variety of professionals, including assembly, shipping, receiving, and inventory control specialists, certified forklift drivers and warehouse professionals. If you're looking for short-term or long-term assignments, competitive pay rates and a variety of shift options, Benchmark Staffing thrives at providing top-quality opportunities that fit your needs. For more information, please visit our website at www.benchmarkstaffing.com. All applicants applying for U.S. job openings must be authorized to work in the United States.

Job Title: Manager, Quality Control - Microbiology Company: Dendreon Corporation Location: Seal Beach, CA Description: Dendreon is seeking a Manager, Quality Control for our California Microbiology Laboratory. This is an exciting position accountable for providing leadership, management and delivery of compliant laboratory data in support of Dendreon’s products and in accordance with appropriate regulatory, corporate and scientific guidelines. The successful candidate will manage the Microbiology Laboratory operations on a daily basis, as well as during inspections/audits by the FDA and other regulatory agencies. The ability to function in a fast-paced, highly technical environment, and communicate effectively is essential to success. This person leads, develops and mentors reporting staff at a variety of levels. General Summary: Responsible for the start-up of the Microbiology Laboratory and providing QC support during the qualification of the California commercial facility. Manages daily operations in the Microbiology Laboratory. Responsible for microbiological tests performed during in-process and final product testing of Dendreon products. Responsible for environmental monitoring sample collection, testing, and data review. Manages test samples, reagents and reference standards in the Microbiology Laboratory. Conducts and manages laboratory investigations, and participates as QC representative during investigations into deviations/exceptions and environmental monitoring excursions. Ensures laboratory data integrity and traceability. Communicates with Corporate QC and ensures implementation of harmonized laboratory control systems in the CA Microbiology Laboratory. Participates in planning and process improvement activities at the departmental and inter-functional level. Sets goals, and conduct performance reviews of direct reports; performs ongoing assessment of development and training needs of reporting staff to ensure continued development of personnel. Contributes to the development of department budget and monitors expenditures. Job Requirements: Bachelor’s degree in biology, medical technology or equivalent. Typically 7 years of related experience in a cGMP Quality Control department in an FDA regulated industry (drugs/biologics) with at least 3 years in a leadership role; Commercial phase experience required. Thorough knowledge of cGMP/ICH/FDA regulations. Experience with inspections/audits by the FDA and other regulatory agencies. Experience with LIMS preferred. Ability to prioritize and successfully manage complex and competing projects. Proficient in MS Office applications and MS Project. Working Conditions and Physical Requirements: Limited travel required. Limited handling of laboratory equipment, chemicals and biological materials. The preceding job description has been designated to indicate the general nature and level of work performed by employees within this classification. Additional and incidental duties related to the primary duties may be required for company business needs from time to time.

Job Title: Quality Manager (5235BR) Company: Land O'Lakes Location: Tulare, CA Description: AutoReqId: 5235BRJob Title: Quality ManagerCareer Category: QualityLocation of Position - State and City: CA - TulareDepartment Name: Butter OperationsBusiness Unit: Dairy FoodsBusiness Unit Description:Land O’Lakes Dairy Foods division is a leading marketer of a full line of dairy-based consumer, foodservice and food ingredient products across the United States. The LAND O LAKES® brand is recognized and valued by consumers and customers nationwide and internationally.Position Purpose:Provides leadership and guidance in plant level Quality Assurance to ensure compliance with Dairy Foods quality systems for the Butter manufacturing operations. Adherence to these quality systems to ensure compliance with overall product quality and regulatory compliance with the relevant government agencies. Management of GMP and HACCP programsAdministers and facilitates the training and education of butter operation employees with respect to the quality and food safety expectations in the Land O'Lakes Quality Management System. This quality management system will provide effective and long term resolution (food safety, product quality and regulatory hazards (FDA, USDA and CDA)) to successful business performance. Monitor compliance to accepted standards from receipt of raw milk to shipments of finished products. Ensure all quality-auditing functions are being conducted on a daily basis.Provide technical support to plant management regarding process/product improvements including key input regarding butterfat and solids yields. Provide HACCP and GMP training for all employees. Work closely and interacts effectively with production personnel to assist in producing quality products that meet regulatory and customers. Implement and maintain programs to constantly raise the standards for GMP, sanitation, hygiene and safety in all plant areas.Required (Basic) Experience & Education:- BS/BA degree in Food Science or related technical field; Minimum of five to 10 years experience in quality assurance, operations and regulatory responsibilities. Experience will include the development and implementation of quality assurance programs for raw milk, butter, natural cheese and various dried products. Leadership skills and experience managing people including employee development. You must have a thorough knowledge of regulatory requirements (FDA and State), HACCP, GMP and preventative quality systems. Proficient with the concept of risk assessments, root cause analysis techniques.Must have knowledge of trace/recall, critical process measurement, hazard analysis, product design/specifications and systems approach.Required Competencies & Other Skills:-Proven experience in the highly regulated environments of IMS, USDA and wastewater control; Proficient with the concepts of hazard analysis, risk assessments, and system/process applications.-Knowledgeable in quality management techniques of root cause analysis, and preventative quality.-Excellent organizational, communications, interpersonal and team interaction skills; Able to work with cross functional departments within the organization-Highly motivated, self-directed and a self-starter; Good problem solving and corrective action/resolution skillsMust have demonstrated ability to lead change and drive change.Strong analytical problem solving skills are essential.Solid conflict resolution skills.Compiling reports regarding regular inspection, sanitation violations, and taking steps to resolve deficiencies.Commitment to get results through others.