QC Manager Jobs in Pennsylvania

Job Title: Seeking Quality Management Representatives Company: Location: Lehigh Valley, PA Description: Growing Company seeks qualified representatives to grow with. Good hours Great pay Bonus Potential Forward your resume to the address listed.

Job Title: Quality Management Specialist - Food Safety Company: Location: Philadelphia, PA Description: Responsibilities Include

Job Title: Quality Supervisor, 2nd Shift, QC, Quality Control, Quality, ISO Company: CyberCoders Location: Harrisburg, PA Description: Minimum Required Skills:Quality Supervisor, 2nd Shift, QC, Quality Control, Quality assurance, Lead,, ISO, Six Sigma, Lean,Quality Supervisor/QC Supervisor - Overnight Shift ( 5pm-5am)Harrisburg, PA areaDirect Hire/PermContact: Register to View is an IMMEDIATE HIRE role, available NOW.PLEASE NOTE: This is an OVERNIGHT SHIFT, with a rotating 12-hour per day schedule.We are currently looking for a quality-minded QC Supervisor for an overnight shift with a local area manufacturer to take on the role of the Quality Supervisor where you will be responsible for performing a wide variety of tasks involving supervision of incoming, in-process and finished product inspection of raw materials and assembled medical devices. This role will be responsible for executing the QC plan set by the QC Manager for his/her shift, including everything from the inspection equipment set-up and change-overs, timely inspection of materials, directing QC technicians, and supervising/conducting quality checks. Some of the additional Job functions performed by this role will include (but not be limited to):• Supervise QC technicians to ensure proper job performance and provide training. • Monitor and report all inspection-related activity. • Coordinate Quality Assurance checks and line clearances with shift Quality Inspector or perform Quality Assurance procedures to ensure consistent product quality and safety. • Supervise or conduct complete inspection equipment change-overs and equipment set-up as required to conduct timely inspections. • Coordinate preventive maintenance with Maintenance Manager to ensure proper operation and calibration of inspection equipment. • Support continuous improvement of all inspection processes by coaching team members to improve performance within the company QMS system, identifying opportunities for improvement, soliciting ideas from team members on how to improve processes, and implementing approved ideas. • Provide feedback on shift results to team members and make recommendations for improvement. The ideally qualified candidate will bring with them the following experience and Qualifications:• High school diploma or GED required. College degree preferred. • 10 years on-the-job training and experience as a supervisor of QC employees required. • Computer skills in MS office products, including Word, EXCEL and database programs are required. • Familiarity with and certification in Six Sigma, LEAN manufacturing or other vigorous quality control programs are highly desirable. • Applicable ISO and FDA experience is highly desirable. • QC Supervisors are responsible for providing leadership on shift to QC employees, handling emergency inspection needs and planned equipment change-overs, performing quality assurance functions, handling emergencies calmly, resolving conflicts among QC employees and enforcing performance standards, as well as working with QC employees in work that involves visual and physical inspection. • QC Supervisors must be able to read and understand all written instructions, communicate well with others, and have excellent vision and manual dexterity. • The ability to work in a clean room environment is an essential job function, as is the ability to communicate effectively orally and in writing with the entire workforce. • The ability to perceive all aspects of the work environment, product and component samples and documentation is essential. • This position requires attention to detail, excellent time, people and document management skills and the drive to complete and follow-through for completeness. • The ability to handle multiple priorities in a fast changing work environment is essential, as is positive interaction with others and reliable attendance.If the shift is something you can handle and you are qualified to perform the maintenance duties, please contact me IMMEDIATELY for consideration at Register to View .Must be authorized to work in the United States on a full-time basis for any employer.Please apply directly to by clicking 'Click Here to Apply' with your Word resume!Looking forward to receiving your resume and going over the position in more detail with you.- Not a fit for this position? Click the link at the bottom of this email to search all of our open positions.Looking forward to receiving your resume!CyberCoders

Job Title: Director, Care & Quality Management Company: UPMC Location: Seneca, PA Description: UPMC Northwest, located approximately 90 miles north of Pittsburgh, is hiring a full-time director, care and quality management to help support the day to day operations of the Care and Quality Management Department at its Seneca location. The nursing director, care and quality management designs, implements and maintains effective processes to ensure the provision of quality care management services which fulfill the expectations and needs of the hospital. This position requires a bachelor’s degree, previous care management experience as well as understanding of clinical and care management processes. Now is a great time to join the team of the premiere health care provider in Venango County, UPMC Northwest. We  also offers a variety of benefit options designed to provide personal security, convenience, and assistance to you and your family. With this flexibility and choice, you can decide which options best meet your needs. View complete job requirements and apply at www.upmc.com, Click Careers at UPMC, and Quick Search UPMC Jobs. Select Advanced Search and enter 1058469 in the Job Opening ID field. EOE

Job Title: Director, Quality Management Systems Company: Company Confidential Location: Philadelphia, PA Description: Please refer to this CODE # EC 0309 when inquiringPosition: Director, Quality Management SystemsLocation: Blue Bell, PA Duration:Permanent Compensation: to $130,000Education: 4 year degreeExperience: 5+ yearsPrimary Outcomes: To develop, implement and maintain the Quality Management System that achieves strategic and operational Quality goals as established in the strategic planning process. To establish the Quality Management System as a customer and industry recognized value add To support the regional field operations in the delivery of superior Quality work for the company and customer. Responsibilities:•Manage the development, implementation, and maintenance of Quality Management System in compliance with applicable industry standards (i.e. ISO).•Work with senior management to strategically develop and align Quality Management System priorities and activities.•Communicate Quality principles and practices throughout the organization and ensure alignment with strategic objectives and work with regional operations and corporate departments to ensure effective implementation of Quality Management System.•Interface with large clients and work closely with project teams to develop and deploy project specific quality plans that comply with contractual quality requirements and deliver customer satisfaction.•Work closely with Continuous Improvement Managers to integrate quality processes and continuous improvement methodology based on Lean principles and practices focused on customer value, employee engagement, process standardization, built-in-quality, waste elimination, and continuous improvement.Contact: Ruth Keller Phone: Register to View (weekdays - 8 AM to 8 PM ET) E-Mail: ruth- Register to View Page: http://www.rakeller.com/

Job Title: SAP Quality Management Functional Analyst, Monroeville,... Company: Computer Sciences Corporation Location: Monroeville, PA Description: Essential Job Functions* Codes, tests, debugs, implements, and documents highly complex programs. Develops complex test plans to verify logic of new or modified programs.* Designs systems and programs to meet highly complex business needs. Prepares detailed specifications from which programs are developed and coded. Creates appropriate documentation in work assignments such as program code, and technical documentation.* Gathers information from existing systems, analyzes program and time requirements. Assists project manager in preparing time estimates and justification for assigned tasks.* Supports project personnel in resolving fairly complex program problems. Works with client and management to resolve issues and validate programming requirements within their areas of responsibility. Provides technical advice on complex programming.* May serve as technical project lead; provides leadership and work guidance to less experienced personnel. Conducts quality assurance activities such as peer reviews.* Provides consulting services in a technical and/or managerial capacity to management and technical staff. May represent company in presentations or conferences involving customers, co-contractors, suppliers, competitors, academia or the public.QualificationsBasic Qualifications* Bachelors degree or equivalent combination of education and experience* Bachelors degree in computer science, mathematics or related field preferred* Seven or more years of programming or testing experience* Experience working with appropriate programming languages, operating systems and software* Experience working with relational databases to facilitate programming softwareOther Qualifications* 5 years SAP Quality Management. * 3 years SAP configuration, writing functional specifications, gathering customer requirements and SAP problem solving and trouble shooting. * Must be a U.S. Citizen or Green Card Holder. * Position  is on-site in Monroeville, PA with some travel.* Strong skills in programming* Strong personal computer and business solutions software skills* Strong analytical and problem solving skills for design, creation and testing of programs* Good interpersonal skills to interact with customers and team members* Good communication skills to work effectively with team members, support personnel, and clients* Good leadership skills to guide and mentor the work of less experienced personnel* Ability to work as part of team and independentlyPlease refer to job code 526514 when responding to this ad.

Job Title: Associate Director, Quality Systems Company: MedImmune Location: Philadelphia, PA Description: Associate Director, Quality Systems 1864197 My company shares my passion for helping to improve human health around the world.' 'This is My MedImmune.' Those who join MedImmune feel a sense of ownership about their future. They thrive with a recognized leader in the biotechnology industry and the wholly-owned subsidiary of AstraZeneca plc. Here, you will join passionate professionals who advance science, technology and medicine to develop products designed to help people live better lives. You will excel in an environment characterized by respect, integrity and growth opportunities... that encourages both individual contribution and collaborative entrepreneurial thinking. Our products and/or product candidates are designed to address areas of need in infection, oncology, respiratory disease and inflammation, cardiovascular/gastrointestinal disease and neuroscience. Explore a MedImmune career as we strive to better more lives, more often, around the world. Title: Associate Director, Quality Systems Location: PA, Philadelphia - NON SALES Req: 02276 Manages the Quality Systems program of the PA site to support the manufacturing, testing and release of licensed and clinical Finished Product under the FDA, European regulations and MedImmune standards and procedures. Manages the staff of the Quality Systems group by giving leadership in the areas of compliance and document management. Performs management duties such as hiring, performance reviews, and employee development plans where required, and recommendations for salary adjustment * Ensures site compliance is maintained for all operations (manufacturing, QC, Facility/engineering, logistics) at PA site * Ensures that PA Quality Systems are in compliance with corporate policies and procedures. * Manages the Quality Systems for Change Management, Documentation and Deviation handling * Acts as the primary QA and compliance expert for PA projects (site specific or Technology Transfer) and provides technical expertise to resolve issues related to non-compliance and CAPA's * Reviews and approves regulatory submissions for completeness and accuracy of any change made to the PA facility procedures that would affect regulatory compliance * Acts as one of the Quality Leads during Regulatory Inspections * Organizes the Technical training for the Quality Systems staff Mimimum 10 years experience in pharmaceutical industry of which minimum 5 years in the manufacturing, QC or QA/Validation of biologics (rec. proteins, antibodies (MCA) or vacccines) Established Leadership in (bio) pharmaceutical Industry for a minimum of 5 years. Minimum Bachelors Degree at a minimum in the sciences (ie. Biology, Microbiology, Chemistry). Membership of a professional body e.g. ISPE, PDA. If you are interested in this position please - Apply online at www.medimmune.com/careers and search for Req #. 02276 MedImmune is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, gende

Job Title: SAP Quality Management Functional Analyst, Monroeville, PA with some travel Company: Computer Sciences Corporation Location: Monroeville, PA Description: Codes, tests, debugs, implements, and documents highly complex programs. Develops complex test plans to verify logic of new or modified programs.Designs systems and programs to meet highly complex business needs. Prepares detailed specifications from which programs are developed and coded. Creates appropriate documentation in work assignments such as program code, and technical documentation.Gathers information from existing systems, analyzes program and time requirements. Assists project manager in preparing time estimates and justification for assigned tasks.Supports project personnel in resolving fairly complex program problems. Works with client and management to resolve issues and validate programming requirements within their areas of responsibility. Provides technical advice on complex programming.May serve as technical project lead; provides leadership and work guidance to less experienced personnel. Conducts quality assurance activities such as peer reviews.Provides consulting services in a technical and/or managerial capacity to management and technical staff. May represent company in presentations or conferences involving customers, co-contractors, suppliers, competitors, academia or the public.

Job Title: Director of Quality Company: MRINetwork Location: Philadelphia, PA Description: At Management Recruiters International —The Merwin Group, we specialize in the placement of outstanding talent in scientific industries. Job Overview Our global pharmaceutical client in suburban Philadelphia is looking for a Director of Quality. Key responsibilities include: insuring all Quality programs and systems are relevant, effective and meet all applicable regulations; directing all activities related to product release, oversight of stability program, QA validation, GLP Quality Unit activities, deviations, investigations, MRB, CAPA, and GMP training of QA staff. RequirementsBS and 10 years experience of Quality Assurance in a pharmaceutical environment including GMP/GLP experience. A minimum of 3 years of management experience working for a multinational organization. Experience in managing compliance to FDA regulations. Experience in managing compliance to ISO-9001 standards. Understanding and 3 years practical experience with Lean / TPC.This position is eligible for relocation benefits.

Job Title: Quality Supervisor - Med Device Company: Location: Harrisburg, PA Description: Job Summary: The QC Supervisor Level 2 is responsible for performing a wide variety of tasks involving supervision of incoming, in-process and finished product inspection of raw materials and assembled medical devices. He/she is responsible for executing the QC plan set by the QC Manager for his/her shift. This includes inspection equipment set-up and change-overs, timely inspection of materials, directing QC technicians, and supervising/conducting quality checks. As required, he/she will work along-side inspection technicians in work that requires manual dexterity, visual acuity and speed to perform the task at the required rate. He/she is also responsible for ensuring that all QC technicians follow specific written work instructions and providing training and corrective feedback, when required. He/she will record quality-related data and information. Duties will also include assuring QC areas are properly maintained, inspection equipment is within calibration and that areas are cleared for inspection to avoid mix-ups Essential Job Functions: · Supervisory Role: Supervise QC technicians to ensure proper job performance and provide training. Provide positive and corrective feedback to QC technicians on meeting expectations for inspection, quality, safety, on-time delivery, waste and attendance. Monitor and report all inspection-related activity. Ensure that material inspections are completed on time and according to specifications and all applicable SOPs and work descriptions. Maintain order and cleanup of assigned work area.· Quality Assurance: Coordinate Quality Assurance checks and lin clearances with shift Quality Inspector or perform Quality Assurance procedures to ensure consistent product quality and safety. Document according to SOPs.· Maintenance: Supervise or conduct complete inspection equipment change overs and equipment set-up as required to conduct timely inspections. Coordinate preventive maintenance with Maintenance Manager to ensure proper operation and calibration of inspection equipment. Continually monitor environmental systems to ensure clean rooms are operating within environmental specifications.· Continuous Improvement: Support continuous improvement of all inspection processes by coaching team members to improve performance within the company QMS system, identifying opportunities for improvement, soliciting ideas from team members on how to improve processes, and implementing approved ideas. Report progress on quality, safety, delivery, waste and attendance and other key measures in accordance with report schedule set by operations management. Provide feedback on shift results to team members and make recommendations for improvement. Report and address any conditions or actions that are inconsistent with safe and effective operations.· Support QC Manager: Support QC Manager by reacting to change productively, accepting additional assignments positively and controlling rumors or negative comments or behaviors. Act as a positive example to workforce. Education/Experience Required: High school diploma or GED required. 10 years on-the-job training and experience as a supervisor of QC employees required. College degree preferred. Computer skills in MS office products, including Word, EXCEL and database programs are required. Familiarity with and certification in Six Sigma, LEAN manufacturing or other vigorous quality control programs are highly desirable. Applicable ISO and FDA experience is highly desirable. QC Supervisors are responsible for providing leadership on shift to QC employees, handling emergency inspection needs and planned equipment change-overs, performing quality assurance functions, handling emergencies calmly, resolving conflicts among QC employees and enforcing performance standards, as well as working with QC employees in work that involves visual and physical inspection. QC Supervisors must be able to read and understand all written instructions, communicate well with others, and have excellent vision and manual dexterity. The ability to work in a clean room environment is an essential job function, as is the ability to communicate effectively orally and in writing with the entire workforce. The ability to perceive all aspects of the work environment, product and component samples and documentation is essential. This position requires attention to detail, excellent time, people and document management skills and the drive to complete and follow-through for completeness. The ability to handle multiple priorities in a fast changing work environment is essential, as is positive interaction with others and reliable attendance. Physical/Mental Demands of Job: Posture Standing 20 % of time Standing to operate equipment and perform quality test functions. Walking 15 % of time Walking throughout facility to monitor activity. Sitting 65 % of time Sitting to operate equipment, prepare reports and perform inspection Strength Lifting 50 Lbs for Material handling functions. Carrying 50 Lbs for Material handling functions. Pushing 100 Lbs for Material Carts Pulling 100 Lbs for Material Carts Stooping Performing area cleanup, maintenance, and equipment changes. Reaching Performing inspection operations and equipment change-overs. Dexterity Performing quality testing. Oral Must be able to communicate orally with coworkers. Auditory Must be able to understand oral instructions and perceive working environment and emergencies. Vision Perform inspection operations, observe QC employees, perform quality tests, perform equipment maintenance and change-overs. Color Must be capable of distinguishing product types and defects. Depth Perception Performing inspection operations, equipment maintenance and change-overs. Conduct and attendance X Must be able to maintain self-control in challenging circumstances and be very reliable in attendance and punctuality.