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QC Supervisor Jobs
Search all 4,515 QA Jobs for QC Supervisor Jobs|
Job Title: Quality Supervisor
Company: Caroba Plastics, Inc. Location: Englewood, CO Description: Quality Assurance Supervisor Salary: $35,000.00 - 42,000.00
Job Summary: Responsible for all the quality assurance functions in the plant by working closely with the Quality Manager, Quality Inspectors and independently as needed. This position requires the ability to work on multiple projects with changing priorities. Duties and Responsibilities:
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Job Title: Quality Control Asst Manager
Company: Streck Location: Omaha, NE Description: This position is responsible for supervising quality control staff. Other major responsibilities are planning, organizing and implementing activities related to pre-test, vial stability, assay assignment, final release of existing products and directing the implementation of quality control programs. |
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Job Title: QC Supervisor
Company: Confidential Location: Reno, NV Description: Relocation may be paid for the right candidate. Details will be discussed with candidates during the interview process. Only candidates with direct CMM programming experience will be considered. Benefits included. |
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Job Title: QC Supervisor - 2nd shift
Company: Location: Gaithersburg, MD Description: Supervise the daily operations in the QC laboratory product testing group. Provide leadership and supervision for direct reports. Ensure the laboratory meets all GMP requirements Verify data integrity. Promote the career development of junior personnel. Major Duties and Responsibilities: 1. Supervise laboratory personnel. Responsible for daily work assignments and career development of these personnel. Ensures appropriate training is provided. 2. Responsible for the daily operations in the laboratory; review of data, assay trend charts, and equipment logbooks; analyst qualification; performs testing as required, calibrates and maintains laboratory equipment according to standard operating procedures. 3. Responsible for performing routine and non-routine analysis of environmental samples, raw materials, stability, in-process and finished products, as applicable, according to standard operating procedures. 4. Calibrates and maintains laboratory equipment according to standard operating procedures. 5. Conduct and participate in GMP audits. 6. Applies critical thought to solving problems of complex scope. Works on extremely complex problems where analysis of situations or data requires an in-depth evaluation of intangible factors. 7. Acts independently to determine methods and procedures on new assignments. 8. Completes appropriate documentation to support testing procedures including data capture forms, equipment logbooks, electronic systems and inventory forms. 9. Applies knowledge of good manufacturing practices and good laboratory practices on a daily basis. 10. Adheres to Company safety procedures and guidelines on a daily basis. 11. Work with personnel to provide career development. Meet weekly with direct reports in a One on One setting. 12. Investigate and document OOSs and deviations within established timeframes. Business Skills 1. High degree of organization and flexibility with the ability to prioritize responsibilities as needs require. 2. An understanding of the basic business concepts and techniques as they relate to human resource, objectives, appraisals, etc. A working understanding of company goals, strategies and orientation. An understanding of the pharmaceutical industry and its unique business and social responsibilities. 3. The ability to effectively supervise, lead, nurture, discipline and praise subordinates. Technical Skills 1. An understanding of the requirements outlined in Part 211 of the Federal Register cGMP's For Finished Pharmaceuticals, and their practical application during manufacture, testing, and distribution. The ability to evaluate facilities, records, processes, procedures and practices for conformance to these requirements. 2. Identifies and troubleshoots equipment problems. 3. Identifies and troubleshoots adverse assay trends. 4. Identifies technical problems and follows through to find solutions. 5. Prepares validation protocols, executes Experience: Requires at least 5-8 years of laboratory related experience in the biologics industry and at least 1 year of supervisory experience. Experience in a regulated environment is preferred. Educations: Education: Bachelors or Masters degree in the sciences. CLICK HERE TO APPLY |
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Job Title: QC Supervisor
Company: Bio-Rad Laboratories - Clinical Diagnostics Group Location: Hercules, CA Description: Join us at the forefront of scientific discovery! At Bio-Rad Laboratories, you will participate in exciting new developments at the cutting-edge of science and technology. Our teams of dedicated professionals work together in an entrepreneurial atmosphere, providing a broad range of innovative tools and services to the clinical diagnostics and life science research markets. Bio-Rad was founded more than 40 years ago, and we are recognized as a world leader in science and research. Visit us at www.bio-rad.com Position Responsibilities: Supervise 5-7 people in the EIA and QC functional groups. Review and approve Immunoassay in-line testing and final kit batch records. Must have the ability to create and revise EIA procedures and SOP's. Responsible for incoming inspections of raw material, components and kits. Education: BA/BS required. Experience: 2-4 years of direct supervisory experience in a GMP environment. Skills: Basic Knowledge of Immunoassay is required. Excellent written and verbal skills. Ability to interact with various departments and work independently. Knowledge of Excel spreadsheets and Access Databases are required. |
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Job Title: QC Supervisor
Company: Ascendis Location: Miami, FL Description: Job Title: Quality Control Supervisor Summary – Oversee the Quality Control Department on a day-to-day basis to ensure a smooth and timely operation Essential Duties and Responsibilities include the following. Other duties may be assigned to meet business needs. · Guide and direct flow and priority of inventory in and out of Quality Control. · Organize daily inspectors’ workload · Supervise and train QC inspectors · Consult with various departments to establish priorities (Purchasing, Sales, Repair Station) · Work with QC management to solve problems and issues. · Coordinate operations at BMI teardown facility · Oversee inspection of outbound sales and work orders. · Oversee receiving inspection function · Help develop processes and procedures for the department Qualification/Requirements: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. · Must have High School Diploma or equivalent experience · 5 to 8 years experience in a similar position including min 5 years of supervisory experience · Strong customer service orientation · Good communication skills · Ability to network across the company effectively and maintain good working relationship with all departments and employees · Proficient with current software packages such as Microsoft Word, Excel, Outlook · Desire to work in a small firm environment, which requires a broad range of skills CERTIFICATES, LICENSES, REGISTRATIONS A&P license not required, but preferred. WORK ENVIRONMENT Work is normally performed in warehouse work environment What is the expected duration? 90 working days - hire ______ What is the direct labor rate? 38K - $45K Hours: Mon – Fri. 7:00am – 4:00pm. ____________________ Do you anticipate any overtime? Possible Do you perform pre-employment testing? If yes, what? Drug Test and Background What is the break and lunch policy? 1hr lunch and 2 15 min. breaks What is the dress code? Business Casual |
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Job Title: Senior Supervisor, Quality Control - Microbiology
Company: Location: Boston, MA Description: Job Title Senior Supervisor, Quality Control - Microbiology Location Cambridge,MA Requisition Number RUSABIO155-599225 Job Description Broad Function: Oversee Microbiological testing of water systems and environmental monitoring to support production timelines. Participate in cross-functional teams with Manufacturing, Quality Engineering, Validation, and Manufacturing Engineering Key responsibilities: - Direct supervision of daily operations of QC Microbiology facility support group - Mentoring and career development of direct reports - Represent Microbiology at tech transfer meetings - Perform complex data analysis and trending - Scheduling of daily activities - Scheduling and coordinating of water validations and environmental certifications - Completion of performance appraisals and goals for direct reports - Provide technical support to manufacturing for investigations - Ensure documentation is generated in accordance with cGMP - Performance of complex investigations in support of OOS, deviations, invalid assays, and alert action exceptions. - Author SOPs, method development protocols, and validation protocols. - Audit vendors and contract test facilities - Assist in validation of new instrumentation - Assure overall cGMP compliance in the laboratory Qualifications Minimum of 8 years of cGMP industry experience. Prior supervisory experience a must. Bachelors Degree in Microbiology or related field. About Biogen Idec: Transforming Discovery into Care With operations across the Americas, Europe, and Asia, Biogen Idec (NASDAQ:BIIB) is one of the world's leading biotechnology companies, creating new standards of care in oncology, neurology, and immunology. Every day, employees of Biogen Idec make a difference in people's lives, through pioneering research and development, manufacturing, and our worldwide commercial capabilities. Learn more at www.biogenidec.com/careers Biogen Idec is proud to be an equal opportunity employer |
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Job Title: QC Supervisor, Chemistry (2008138)
Company: Lonza Location: Hopkinton, MA Description: Provide guidance and mentoring for staff. Maintains timelines for all testing and work within labs. Sets up a testing schedule to meet the timelines and communications these timelines to his/her staff, (i.e. in-process testing, stability testing, raw materials sampling, inspection, testing, product change over and other ongoing manufacturing support, safety). Participoates in cross-functional teams. Creates and revises SOP's, Monographs, and perfoirms the needed training to the QC Chemistry/Raw Materials personnel. Leads investigation to OOS results. Demonstrates competency in instrumentation knowledge: knows how to use, clean, and maintain equipment. Troubleshoots problems within the labs equipment, assays, or procedures and reports them to his/her management. Maintains cGMP of the labs (QC Chemistry and Raw Materials), and follows the actions and rules of all compliance proigrams. Proivides guidance to his/her staff so that this is maintained. Lead person for audits (FDA, EU, and Client based). Required Experience BS in a scientific discipline; Chemistry preferred. 8-10 years experience working in a cGMP Chemistry lab setting. Must know compendial (USP, EP) test method. Must know FTIR testing as well as othertesting apparatus. ~cb~ |
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Job Title: QC Supervisor-Fab
Company: ATR International, Inc. Location: Santa Clara, CA Description: ATR Professional, a division of ATR International, has been a leader in the staffing industry since 1988, placing professionals in the industry's most innovative companies. We currently have an exciting opportunity for a QC Supervisor-Fab with one of our important clients. Position Information: Job Title: QC Supervisor-Fab Location: Santa Clara, CA Duration: Temp-Permanent Compensation: Open/doe Job description: We are looking for a QC Supervisor-Fab Engineer who has experience as a FAB Process Engineer, and/or FAB QE, and/or FAB QC/QA Manager. Performs the duties of the Fabrication (bare board) QC Supervisor. Trains, evaluates, and provides work direction for FAB QC and Test operators. Performs QC inspection and test as a back up for employees with a focus for On-Time-Delivery. Trains employees per IPC 600, IPC 6012, IPC 2221, IPC 4101 and MIL-PRF-55110/31032, and assures that all FAB operations are in accordance with the latest published specifications/standards; looks for and procures latest specification/standards and makes sure that the changes in the new publications are implemented throughout all FAB processes. Assures that QC and Test operators are cross-trained on all QC and Test operations, and coordinates cross-training of FAB QC/Test operators in the Company's Assembly processes for continuity of the company and reduction of overtime and temporary worker costs. Collects Yield and defect data and publishes Yield reports with paretos and action items. Conducts root cause failure analysis for RMAs, internal DRs, and continuous improvement goals. Requirements: The ideal candidate will assure that work areas and storage areas are neat and clean at all times, ready for customer walkthroughs. Supports On-Time-Delivery by making sure the through put in QC and Test are optimized and supported via overtime, as required. Performs personal overtime in support of daily shipment and training off shift personnel. T o be considered for this position, please click the "Apply Now" button or contact the following recruiter directly: Name : Van Nguyen Phone : Register to View Email : Register to View Visit our website at www.myatr.com for an up-to-date listing of opportunities. |
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Job Title: 2nd Shift QC Supervisor
Company: Optimum Nutrition, Inc. Location: Aurora, IL Description: Optimum Nutrition, Inc., an exciting entrepreneurial manufacturing company enjoying double digit growth in Aurora, IL, is seeking a 2 nd Shift QC Supervisor. This position is responsible for the direct reporting of quality technicians with a dotted line to the sanitarians. In addition the 2 nd Shift QC Supervisor will: Schedule technicians to line assignments. Audit all line/HACCP paperwork completed by technicians. Coordinate microbiological analysis of products submitted for outside testing and follow-up on positive results. Report findings of monthly internal GMP audits. Write procedures for quality manual. Instrumental in the implementation and training of new and existing procedures. Participate in customer/consumer complaints. Provide direction in raw material rejection with the assistance of the purchasing department in documenting rejected/on hold material. Requirements: Bachelor’s Degree in science related field. 3 - 5 years experience in food manufacturing environment. 3 - 5 years experience supervisory experience. Advanced knowledge of GMP/HACCP Strong analytical ability Attention to detail Proficient in Word, Excel and MS Office Programs. |
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