QC Director Jobs in Pennsylvania

Job Title: Director of Quality - Americas Company: Colorcon Location: West Point, PA Description: Director of Quality - AmericasTracking Code1269Job DescriptionThe Director of Quality - Americas is responsible for oversight of all Quality programs, system, compliance and personnel in the Americas region. Individual will represent Quality as a member of North America’s Regional Leadership Team (RLT) and reports directly to the Americas region President. This position also maintains a dotted line relationship to the Global Director of Quality.  Key responsibilities include: insuring our Quality programs and systems are relevant, effective and meet all applicable regulations for pharmaceutical excipient manufacture and distribution within the Americas, Directs all activities related to product release, oversight of stability program, QA validation, GLP Quality Unit activities, deviations, investigations, MRB, CAPA, and GMP training QA staff. The incumbent will also insure effective implementation of Colorcon’s Quality Mission Statement and manage our various ISO quality certifications.Responsibilities & Duties* Manages regional staff in accordance with organization's policies and applicable regulations. Responsibilities include planning, assigning, and directing work.* Development and execution of local QA systems, policies and procedure to meet Colorcon global standards.* Assures GMP Change Control system tracks all change requests to assure no unauthorized changes are made which result in out of compliance processes, documentation or data associated with regulatory filings or GMP regulations.* Coordination and hosting of customer and regulatory audits.* Management of regional supplier approval including performance of supplier audits.* Oversee process and closure of deviations and investigations within required time frames. Assures an effective CAPA system and Management Review of follow-up actions.* Monitoring and analysis of customer complaints including ensuring satisfactory response to customers.* Supervises the Material Review Board process assuring thorough investigations, reports, and decisions are properly documented.* Leadership and implementation of continuous improvement programs.* Leadership and execution of GMP training and ongoing procedural training.* Member of the Regional Leadership Team and input to the Global Quality TeamRequired Experience* BS 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 for pharmaceutical ingredients.* Experience in managing compliance to ISO-9001 standards.* Understanding and 3 yrs practical experience with Lean / TPC including:FMEA5 SVisual ManagementValue Stream MappingKaizen Events* Understanding of Six Sigma concepts: DMAIC, SPC* Individual must possess strong interpersonal skills, be able to multitask and be self-motivated.* Ability to work in a global, multi-time zone, highly diverse environment.* Ability to manage staff and costs effectively through appropriate resource allocation.* Position requires less then 25% travel with most travel within the US and PR. Some international travel is required.* Physical abilities required in order to tour facilities, observe processes, inspect equipment, and perform other duties include:Standing / walking for extended periods of timeClimbing stairs and laddersWalking on various surfaces (including elevated platforms and catwalks)Lifting and carrying equipment weighing up to 10 lbs.Job LocationWest Point, PA, US.Position TypeFull-Time/Regular

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 and HSE Company: Bombardier Transportation Location: West Mifflin, PA Description: Employer Information About Bombardier Transportation We are Bombardier Get on board, we can drive you further in your career Bombardier Transportation is the number one provider of rail solutions in the world. Our business holds the number one global market position in eight of the ten markets we service. Our product portfolio includes a full range of passenger rail vehicles and we manufacture locomotives, bogies, propulsion and rail control solutions. We design, build and service some of the most intelligent and beautiful rail solutions in t....more info View all our jobs Job We are looking for a Director, Quality and Health and Safety for our site in Pittsburgh, PA. Your role As a member of the PIPPC leadership Team this position is responsible for the lead, execution and overall direction of quality control (QC), quality assurance (QA), and health, safety & environment (HSE) for the Pittsburgh Site of the Propulsion & Controls division. This position is responsible to ensure that the overall Group, Divisional & Site mandates in the quality and HSE areas are implemented and overall performance meets and exceeds expectations. Your challenges Direct, manage, and develop a supplier related quality organization to meet divisional and customer objectives within the PPC Pittsburgh site. Proactively focus on improving performance by measuring and implementing effective corrective/preventive actions and measures. Personally participate in customer quality audits, visit and communication to ensure the best working relationship between suppliers and procurement. Direct the Quality Control efforts through the QC Manager responsible for inspection, test, qualification, etc of operations and supply management performance. Maintain a close working relationship with the Divisional HSE Director to ensure that PPC mandates are implemented and are coordinated with Site HSE initiatives, and are legally applied to US Sites. Is the liaison between Group, Division and Pittsburgh Site HSE staff to ensure full compliance and that all targets related to health, safety and the environment are met. Serve as liaison between group, division and site to coordinate implementation of projects such as ISO 9000, ISO 14000, IRIS, etc. NOTES: Local Residents Preferred (No Relo)

Job Title: Quality Supervisor - Construction Company: Location: Philadelphia, PA Description: Philadelphia-based Design-Builder seeks on-site Qualtiy Supervisors for jobs throughout Pennsylvania, Maryland, West Virginia and Virginia. Must be willing to travel. Job Description: On-Site supervision of delivery of Construction Projects with regard to Quality Control and Quality Assurance procedures. Complete frequent reports and logs of QA/QC. May require travel to sites throughout Pennsylvania, Maryland, Virginia and West Virginia with stays ranging from 1 week to 1 months. Requirements: Thorough understanding of issues related to construction quality control and assurance. 5+ Years of experience in Construction Industry 2+ Years of experience in Quality Control / Quality Assurance Preferences: Bachelor or Associate Degree in Construction Management, Engineering, or Architecture Prior experience in working within and around operating railroad activities, particularly Amtrak. Please send resume to Register to View We are only accepting resumes via email. Please do not phone our office regarding this posting. CVM Construction 400 Cresson Blvd PO Box 398 Oaks, PA 19456 www.cvmconstruction.com Search For: quality supervisor, road construction, maintenance, surface treatments, excavation & grading, concrete & asphalt paving, concrete structures & rehab, storm and Sanitary sewers, waterlines, management, railroad.

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

Job Title: Director, Quality Engineering Company: Altria Location: Berwyn, PA Description: Job details Req ID 41306BR Business Title Director, Quality Engineering Business Global Quality Sub-Business Renal Support Country United States State/Province Illinois Location of Position McGaw Park - Gr, IL Shift_ 1st Job Description The Director of Quality Engineering will be responsible for globally managing the overall product quality for Baxter Renal Division??s currently marketed Peritoneal Dialysis (PD) systems and disposables. This position is primarily responsible for product sustaining quality activities and will also initiate, evaluate and maintain programs necessary to ensure a level of quality consistent with company standards and regulations. The position provides leadership for the identification and resolution of critical quality issues that may impact the Division. Work with cross-functional departments on Life Cycle Management (LCM) teams, CAPA investigations, complaint investigations and providing quality engineering support to design and process modifications at Baxter manufacturing plants around the world. Direct and lead a team of Quality Engineers to perform these duties and continuously improve their professional development and job performance. Mentor others in the areas of Quality Engineering and Quality System regulations. Implement and enforce Baxter quality policies and procedures related to area of responsibility Provide leadership for product and process change control including generating Design Plans, reviewing design inputs, outputs, verification, validation and design transfer strategies. Lead Risk Management activities for sustaining engineering projects. Demonstrate quality assertiveness and be able to independently represent the Quality function in various roles such as product support and lifecycle management. Assist in decision making for process improvement efforts Support and/or lead post market activities such as complaint investigation, complaint trending, CAPA, and Field Corrective Action processes Support global Renal manufacturing facilities and associated manufacturing and supplier changes Provide Quality input to DHF/risk remediation activities Support internal and external quality audits and FDA inspections Implement continuous improvement in products and processes in area of responsibility Recruit, retain, train, develop, manage and lead QEs assigned to PD systems and disposables Provide inputs to department budgets and assist in controlling expenses Provide information used to maintain regulatory filings including technical files Collect, monitor and act on key quality metrics Job Requirements Minimum of 10 years experience in Quality, Engineering or Manufacturing of complex Medical Devices Minimum of 7 years management experience Bachelor??s degree in Engineering or Science required, advanced Engineering degree desired ASQ certification (CQE, CMQ/OE, CQA, etc.) and/or Six Sigma certification desired. Certification is expected within 2 years of employment Demonstrated success in supervising and directing a team of quality engineers; able to coach, train and develop quality engineers within the company Ability to mentor and develop quality engineers to the highest professional and performance standards through appropriate training and certifications Knowledge of the global Regulatory and Quality requirements for the manufacture and marketing of medical devices ; knowledge of ISO 13485, FDA Part 820 QSR, ISO 14971, MDD 93/42/EEC and other related regulations and standards Direct experience in electromechanical, software-driven, systems is desired; experience in drug or solution products is a plus Strong technical, analytical and problem solving skills, including strong project management skills Strong interpersonal and leadership skills, including influencing skills and ability to work in a highly matrixed, consensus-driven cross-functional organization Excellent verbal and written communication skills as well as presentation skills Experience working with multifunctional, global teams within Baxter desired Ability to make quick, sound decisions with limited data Ability to solicit feedback and information from others in an open environment Ability to build relationships across functional boundaries at multiple levels Ability to implement tactical plans with little or no supervision Eliminates or minimizes barriers to progress. Anticipate potential conflict situations for proactive solutions Manage conflict situations to result in win-win outcomes Percent Travel Required 30% Index Monitor

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: Area Manager Quality Company: United States Steel Location: Fairless Hills, PA Description: United States Steel Corporation Fairless Hills location is seeking an Area Manager Quality. Duties include, but are not limited to: Oversees the quality assurance function of the galvanizing sheet metal product line Ensures customer specification for product is met Responds to customer issues Analyzes and solves quality problems Responsible for managing metallurgical testing laboratory Knowledge of ISO and TS quality management systems Administer company safety policy

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.