QA Director Jobs in New Jersey

Job Title: QA Manager for Medical Distributor Company: KSR Location: Piscataway, NJ Description: Kelly Scientific Resources seeks to identify a QA Manager for a medical diagnostic supply distributor who would generate, implement and maintain internal quality procedures and systems to comply with applicable regulatory requirements. This is a temp-to-hire opportunity for an individual with expertise in Quality Assurance, capable of responding to FDA complaints and effectively bringing a company up to compliance. Responsibilities will include establishing a company wide training program in keeping with cGMP requirements; ensuring effective document control and change control processes; implementing effective CAPA Programs; and establishing an effective process for the maintenance of customer complaint records and resolutions. Our client is a relatively small, traditional company with global partners. This position is a new role created out of necessity due to the rate at which this company is growing. They are looking to hire immediately! The contract period will be roughly 3-6 months. Pay: $40-45/hr For immediate consideration, press the APPLY NOW or SUBMIT RESUME button below.

Job Title: Director, Quality Assurance - NJ Company: Dendreon Corporation Location: Morris Plains, NJ Description: Dendreon Job Postings Director, Quality Assurance - NJ Job Type: Regular Full-Time Location: Morris Plains, NJ Job Description: Dendreon is seeking a Director of Quality Assurance who will provide leadership and support for the implementation of Quality Assurance policies and procedures in support of commercial manufacturing at our New Jersey facility. The successful candidate will provide direct support to Product Development, Manufacturing, Supply Operations and Quality Control in order to prepare the site for FDA inspection. The ability to function in a fast-paced environment and communicate effectively is essential to success. General Summary: Directs overall operational leadership in planning and management of quality systems and activities, including resource management and vendor management, which includes the following: Validation program GMP material review and disposition Internal and external quality audits Pre- and post-approval compliance audit preparation Corrective and preventive action program GMP training program Quality engineering Change control Document control Implements corporate Quality policies ensuring finished products conform to company standards and satisfy GMP regulations. Oversees project risk analysis and develop solutions to a variety of complex problems. Collaborates with other departments during planning and process improvement activities to ensure timely completion of all operational areas objectives and milestones. Participates in steering committees that set general business corporate policy and sponsor corporate programs. Interfaces with external customers and FDA during audits and inspections. Mentors and develops department personnel, including supervisory / management staff. Defines framework for department objectives, operation schedule, processes and budgets. Contributes to Quality department strategic management. Job Requirements: Bachelorâ??s degree in a scientific discipline or equivalent. Typically 10 years related experience in cGMP/FDA regulated industry. Typically 5 years experience managing supervisory personnel and contributing toward the development of department strategy. Knowledge of cGMP/QSR and FDA device/drug/biologics regulations. Experience in developing and making formal presentations to executive management. Experience with department budget planning, management and reconciliation. Experience with ERP systems preferred. Working Conditions and Physical Requirements: Ability to gown aseptically for work in Clean Room environments. Some travel may be required. 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. http://www2.recruitingcenter.net/clients/dendreon/publicjobs/controller.cfm?jbaction=JobProfile&Job_Id=10528 http://wrapguy.careercast.com/textjobs/jobs/dendreon_nw/6e5d99bb208fb3516a41d97ff3fe0e7a.html

Job Title: QA Manager Company: The Matlen Silver Group, Inc. Location: Parsippany, NJ Description: This is a Right to hire position, so no 3rd parties of corp to corps please!Manage the QA Leads and QA Analysts ensuring that software development projects are delivered with the highest quality possible. Ensure Quality Assurance processes are followed and executed throughout the QA cycle. Maintain a continuous knowledge of project schedules and their impact to Quality Assurance and GE & ITS as a whole. Partner with the PMO, Delivery Teams, Business Entities and Technical Services to deliver high quality applications to the Business. Responsible for QA strategies with regards to all project entering QA. Responsible for resolving testing scheduling conflicts and providing for coordination of QA activities across releases. . Review and validate QA test estimates based upon project scope, complexity and testability. React quickly to changing priorities and requirements. Responsible for the successful execution of test case planning, development, quality reviews and test case execution. Partners with Quality Compliance to ensure SOX processes are maintained by QA. Reviews and provides QA estimates for Project based upon content, complexity, testability, and thoroughness. Responsibilities Utilize RUP methodology, Manage all QA activities on Projects Create and Implement QA Test execution strategy Partner with the Project Team to derive and provide QA estimates on projects in support of Funding requests. Oversee multiple projects through the QA process in parallel Manage QA Team on Day to Day activities Define test standards, guidelines and best practices aligned with IT goals Evaluate and participate in the selection of existing and emerging technologies best fitting test needs. Qualifications * BS in Information Systems or a related area * Minimum of 6 - 8 years experience managing multiple QA project through the QA portions of the SDLC * 3 years with RUP or an equivalent methodology * 3-5 Years using Mercury Quality Center / Test director or other defect/test management tools to produce manager level metrics for process improvement. * 3-5 years experience leading multiple QA process in parallel * Experience with full quality management lifecycle for application development preferred * Proven track record for working effectively with technical and business functions * Excellent communication skills, both written and verbal * Demonstrated ability to analyze existing business functions and recommend alternatives with regard to tools and approaches to their use * Preferred technology experiences in the following areas: * Mainframe system * Web Services Architecture * Application Server Technology * Security Services and Security Access Controls

Job Title: QA Manager - Automation Company: Configuration Management, Inc. Location: Plainfield, NJ Description: MANAGER - QUALITY ENGINEERINGGENERAL RESPONSIBILITIES The ideal candidate will be responsible for designing and developing a cost effective, long-term automation strategy promoting reusable components, low maintenance costs, high efficiency and scalability. The scope of the position is:* Designs, researches and develops strategy and test architecture for a new platform* Designing an infrastructure to validate the requirements, functionality and performance goals for the particular product This is a *hands on* position where the person will be expected to dive into the requirements of the Quality Engineering department, and plans the development of manual and automated regression tests to be implemented for a new platform. It is expected that the candidate in this position will work with Software Development groups, QE Engineers, as well as in-house and over-seas contracted personnel. The candidate will have strong people and lab management skills. Solid communications and project management skills will be required. The person must satisfy required experience and must be passionate about staying current with the latest test automation tools on the market, as well as constantly striving to apply the latest in enhancement techniques into our test automation platforms. Continuously demonstrate ability to propose and develop innovative ideas resolving business or project related issues.RESPONSIBILITIES* Responsible and accountable for the activities and performance of the Quality Engineering discipline* Ensure that the discipline is operationally efficient at all times and its activities stay within the approved budget* Represent the Quality Engineering discipline*s interest at the executive and cross discipline level* Represent the Product Development Organization at internal and external events as required* Participate in the development of the company*s Product Plan. Develop the Quality Engineering portion of the company*s Product Development Plan (resources, schedule, budget)* Responsible for leading large or multiple mid-size geographically spread complex projects requiring increased technical knowledge.* Maintain and coordinate the use of multiple test hardware platforms.* Establishes and communicates common goals and direction for project test team.* Drive the development of overall software test strategy and approach, project schedules and milestones.* Lead staff in the preparation and conduct of testing of new or revised applications/systems and ensure tests are successfully completed and documented. * Develop and lead offshore QE strategies* Provide up-to-date information on project status defects, issues, and project risks.* Lead the development of a consistent testing methodology. Ensure appropriate standards and practices are documented, maintained and applied to all projects and services supplied by the discipline.* Develop overall readiness and risk assessment of new or revised applications/systems and presents to management.* Assigns/Removes Quality Engineering resources to/from a Project Team* Apply appropriate performance metrics, analyze the results and take appropriate actions to ensure the continuous improvement of the discipline (time to market, quality)* Identify, acquire and/or train as necessary, the skill set required to maintain the discipline*s capabilities and competencies to meet the demands of the Product Development Plan* Champion the Product Development Process within the discipline and across the company at all levels* Ensure company policy is enforced in administrative matters (performance reviews, timesheets, vacation time, purchase orders, expense reports, etc.)* Review all commitments made by discipline members to ensure they can be realistically achieved and follow up to make sure they are met (risk management)* Provide an escalation point for Project Management to resolve project issues related to the discipline REQUIRED EXPERIENCE/SKILLS:* Over 12+ years experience in Quality Engineering, business/systems analysis or programming* Previous architectural experience in designing and developing automation test frame works for software based telecom switching solutions * 3 - 5+ years experience managing mid to large-size projects and staff * 3 - 5+ years experience managing offshore projects and teams * Experienced in leading development of automated tests using QTP/Load Runner and/or other tools* 3+ years test experience with real time, PC based, WEB-based, distributed applications deployed on J2EE, Linux, Unix, Windows, and VxWorks.* Programming experience * Experience in telecommunications, IP, Networking protocols, architectures and applications is a must* Experience in security, including security of networks, servers, and VoIP systems.* Experience with telecom Gateways, Media servers, and Application Servers, and PBXs from vendors like Cisco, Avaya, Nortel, Lucent/Alcatel.* Experience with scripting languages including Python, Perl, and Shell. * Excellent communication skills including written and spoken English as well as the ability to present complex technical and behavioral topics to diverse groups during conference calls and large meetings. * Demonstrate a proven ability to manage multiple high priority tasks with competing priorities. Must be highly organized and detail-oriented. Proactively address issues, be a self starter.* Knowledge of general Software Engineering life cycle development methodologies.* Excellent written and verbal communication skills.* Ability to analyze and balance facts, priorities, and alternatives to make sound decisions and recommendations.* Ability to evaluate past decisions to improve effectiveness of future decisions and development efforts.* Ability to understand and communicate complex technical concepts to all levels of the organization.* Outstanding problem solving skills, including the ability to look for non-standard problem solutions, this is key to this position.* Ability to learn and apply new technologies and learn and understand details of third party applications and technologies.* Firm knowledge of Software Development Lifecycle and Test methodologies (Rational Unified Process, Agile development). * Proven ability to manage multiple projects, geographically spread teams under tight deadlines, often with competing priorities and complexities * Ability to prioritize along critical path and meet project milestones and deliverable dates* Proven working knowledge of testing methods, tools, and software testing best practices ( such as Mercury QTP, Load Runner, Rational ClearQuest) * Ability to understand and translate business requirements and Use Cases into testable requirementsREQUIRED EDUCATION:* Must have a Bachelor or Masters Degree of Engineering, Computer Sciences or equivalent field.CONTACT:Oliver EatonRecruiting Manager CM Register to View ext. 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Job Title: QA Manager - NJ Company: Dendreon Corporation Location: New Brunswick, NJ Description: QA Manager - NJJob Type: Regular Full-TimeLocation: Morris Plains, NJJob Description:Dendreon seeking a highly motivated QA Manager to help build our New Jersey QA team and participate in the preparation of the site for FDA inspection. This is an excellent opportunity for someone to provide leadership in a fast-paced, high-volume production environment with high quality and regulatory standards. Efficiency, accuracy and excellent communication skills are essential to success in this position.General Summary:The QA Manager will provide leadership and support for the development and implementation of Quality Assurance Policies and Procedures. In addition, the Quality Assurance Manager will provide direct support to the NJ Immunotherapy Manufacturing Facility as described below.* Hiring and supervision of Quality Assurance staff that covers multiple work shifts..* Review and approval of GMP controlled documents including SOPs.* Manages the NJ site Material Review Board.* Issues batch records and labeling in support of immunotherapy manufacturing.* Provides for batch record review and disposition of immunotherapy products.* Performs lot packet review and disposition of raw materials.* Ensures initiation, investigation, and closure of lot related deviations, non-conformances, and CAPAs.* Provides support for the recall of non-conforming materials, investigations associated with product complaints, and biological product deviation reports.Job Requirements:* Bachelor's degree in a scientific discipline or equivalent.* Typically 7 years related experience in cGMP/FDA regulated industry.* Typically 3 years leadership experience.* Knowledge of cGMP/QSR and FDA device/drug/biologics regulations is required.* Proficient in MS Office applications.* Experience with ERP and/or MRP systems preferred.Working Conditions and Physical Requirements:* May be required to work alternate shifts.* Ability to gown aseptically for work in Clean Room environments.* Some travel may be required.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: QA Manager/JAS Company: Shain Associates Location: Berkeley Heights, NJ Description: Seeking a full time QE Manager to work in either our Fairfield, CT office or NJ facility. This is an exciting opportunity for creative individuals who want to combine the environment of a startup with the resources and stability of an established company. The ideal candidate will be responsible for designing and developing a cost effective, long-term automation strategy promoting reusable components, low maintenance costs, high efficiency and scalability. The scope of the position is:•      Designs, researches and develops strategy and test architecture for a new platform•      Designing an infrastructure to validate the requirements, functionality and performance goals for the particular product This is a “hands on” position where the person will be expected to dive into the requirements of the Quality Engineering department, and plans the development of manual and automated regression tests to be implemented for a new platform.  It is expected that the candidate in this position will work with Software Development groups, QE Engineers, as well as in-house and over-seas contracted personnel.  The candidate will have strong people and lab management skills.  Solid communications and project management skills will be required. The person must satisfy required experience and must be passionate about staying current with the latest test automation tools on the market, as well as constantly striving to apply the latest in enhancement techniques into the IPC test automation platforms. Continuously demonstrate ability to propose and develop innovative ideas resolving business or project related issues.•        Responsible and accountable for the activities and performance of the Quality Engineering discipline•        Ensure that the discipline is operationally efficient at all times and its activities stay within the approved budget•        Represent the Quality Engineering discipline’s interest at the executive and cross discipline level•        Represent the Product Development Organization at internal and external events as required•        Participate in the development of the company’s Product Plan. Develop the Quality Engineering portion of the company’s Product  Development Plan (resources, schedule, budget)•        Responsible for leading large or multiple mid-size geographically spread complex projects requiring increased technical knowledge.•        Maintain and coordinate the use of multiple test hardware platforms.•        Establishes and communicates common goals and direction for project test team.•        Drive the development of overall software test strategy and approach, project schedules and milestones.•        Lead staff in the preparation and conduct of testing of new or revised applications/systems and ensure tests are successfully completed and documented. •        Develop and lead offshore QE strategies•        Provide up-to-date information on project status defects, issues, and project risks.•        Lead the development of a consistent testing methodology. Ensure appropriate standards and practices are documented, maintained and applied to all projects and services supplied by the discipline.•        Develop overall readiness and risk assessment of new or revised applications/systems and presents to management.•        Assigns/Removes Quality Engineering resources to/from a Project Team•        Apply appropriate performance metrics, analyze the results and take appropriate actions to ensure the continuous improvement of the discipline (time to market, quality)•        Identify, acquire and/or train as necessary, the skill set required to maintain the discipline’s capabilities and competencies to meet the demands of the Product Development Plan•        Champion the Product Development Process within the discipline and across the company at all levels•        Ensure company policy is enforced in administrative matters (performance reviews, timesheets, vacation time, purchase orders, expense reports, etc.)•        Review all commitments made by discipline members to ensure they can be realistically achieved and follow up to make sure they are met (risk management)•        Provide an escalation point for Project Management to resolve project issues related to the discipline •        Over 12+ years experience in Quality Engineering, business/systems analysis or programming•        Previous architectural experience in designing and developing automation test frame works for software based telecom switching solutions •        5+ years experience managing mid to large-size projects and staff •        5+ years experience managing offshore projects and teams •        Experienced in leading development of automated tests using QTP/Load Runner and/or other tools•        3+ years test experience with real time, PC based, WEB-based, distributed applications deployed on J2EE, Linux, Unix, Windows, and VxWorks.•        Programming experience  •        Experience in telecommunications, IP, Networking protocols, architectures and applications is a must•        Experience in security, including security of networks, servers, and VoIP systems.•        Experience with telecom Gateways, Media servers, and Application Servers, and PBXs from vendors like Cisco, Avaya, Nortel,  Lucent/Alcatel.•        Experience with scripting languages including Python, Perl, and Shell. •        Excellent communication skills including written and spoken English as well as the ability to present complex technical and behavioral topics to diverse groups during conference calls and large meetings. •        Demonstrate a proven ability to manage multiple high priority tasks with competing priorities. Must be highly organized and detail-oriented. Proactively address issues, be a self starter.•        Knowledge of general Software Engineering life cycle development methodologies.•        Excellent written and verbal communication skills.•        Ability to analyze and balance facts, priorities, and alternatives to make sound decisions and recommendations.•        Ability to evaluate past decisions to improve effectiveness of future decisions and development efforts.•        Ability to understand and communicate complex technical concepts to all levels of the organization.•        Outstanding problem solving skills, including the ability to look for non-standard problem solutions, this is key to this position.•        Ability to learn and apply new technologies and learn and understand details of third party applications and technologies.•        Firm knowledge of Software Development Lifecycle and Test methodologies (Rational Unified Process, Agile development). •        Proven ability to manage multiple projects, geographically spread teams under tight deadlines, often with competing priorities and complexities •        Ability to prioritize along critical path and meet project milestones and deliverable dates •        Proven working knowledge of testing methods, tools, and software testing best practices ( such as Mercury QTP, Load Runner, Rational ClearQuest) •        Ability to understand and translate business requirements and Use Cases into testable requirementsREQUIRED EDUCATION•        Bachelors Degree in Computer Science or Electrical Engineering is required.•        Masters Degree in Computer Science or Electrical Engineering is preferred.Please refer to job code JAS when responding to this ad.

Job Title: QC/QA Manager Company: Smith Hanley Consulting - Pharmaceuticals Location: Kinnelon, NJ Description: If you are interested in growing professionally within an innovative, highly respected organization, we invite you to explore this excellent growth opportunity!!!  Smith Hanley Consulting Group is looking for a QC/QA Manager needed for a Biotech Manufacturing Company near Marietta, Georgia.  This is a 6 - 12 month consulting position so the candidates must be within a commutable distance from the facilities.  This is for candidates with GLP and GMP experience. Job description: o In charge of overall Quality Control/Assurance program including ISO and CLIA. o Create and maintain Quality Control/Assurance program. o Establish and maintain documented system for QC/QA, ISO and CLIA compliance. o Monitor and review product quality. o Assure compliance to specifications on raw materials and manufactured goods. o Oversee QC/QA, ISO and CLIA program and activities. o Provide training in QA, GMP and CLIA. o Other duties as assigned. Minimal requirements: o Must have a Bachelor's or Master's degree in Biological/Medical Sciences or equivalent. o At least 4 years experience in management of QC/QA, ISO, FDA Regulatory and/or CLIA compliance. o Excellent management, interpersonal, communication and computer literacy skills. o Highly self-motivated with leadership ability. Fluency in both English and Mandarin a huge plus, but not a requirement., Not Specified PLEASE APPLY USING THIS BUTTON ONLY

Job Title: Quality Assurance Manager Company: Company Confidential Location: Paterson, NJ Description: About the JobHigh-Graphics Corrugated Box Manufacturer located in Northern New Jersey is seeking a Quality Assurance/Quality Control Manager for its manufacturing facility.  Basic Functions:       This position is responsible for quality control to ensure that all products and materials meet customer requirements and/or specifications.  The Quality Control Manager will inspect and test products at various stages in the production process. He/she will establish testing procedures to determine compliance with customer specifications.  The Manager will also perform testing on incoming raw materials to measure product performance under a variety of conditions. The Quality Control Manager is responsible for the documentation of test results.  The manager will also oversee the company ISO-9001 compliance.Accountabilities and Responsibilities:·         Actively supervise the quality control function and staff.·         Establish, refine, and ensure compliance with quality control procedures to ensure that the product made meets the customer's specifications.·         Ensure that quality requirements and quality policy are adequately defined and distributed and that procedures are in place to support them.·         Maintain appropriate lab testing equipment to perform appropriate testing of produced boxes as well as applicable incoming raw materials.·         Ensure that staff is trained and versed in the use of lab testing equipment.·         Apprise management of internal and external customer quality problems and provide recommendations for improvement with follow-up for results.·         Establish and maintain procedures for timely collection, appropriate analysis of data, and distribution of quality and job performance information.·         Collaborate in the diagnosis and evaluation of manufacturing quality problems with other staff member to determine cause, assign responsibility for corrective action, and report results.·         Develop and implement training programs for quality control staff to ensure understanding of quality objectives and programs.·         Establish an incoming materials inspection process in collaboration with internal customers and inspect incoming material for compliance with pre-determined specifications.·          Establish a relationship with external customers to understand their box requirements and the nuances of their line filling equipment.  Develop and maintain a file of customer requirements.·         Ensure safe working conditions for staff.·         Lead the problem-solving team initiatives to reduce waste and solve quality problems.·         Maintain the company’s quality management system compliant to ISO-9001 requirements.  This function includes control of quality system documents and data control, training, auditing, control of non-conformance and corrective-preventative action.·         Organize and conduct internal quality audits in all departments affected by the ISO-9001 standard.  Provide formal training in the functions of quality systems auditing to key personnel in all departments.·         Ensure that our ISO 9001 standards continuously reflect best business practices. Nature and Scope:    This position covers all operations of the company.  ·         Extensive knowledge of packaging and/or manufacturing industry. ·         Undergraduate degree in related field (preferred). ·         Training in statistical process control and quality techniques.·         Knowledge of MSWord, PowerPoint  and Excel Reporting Relationships:     Other positions reporting to the same superior position: V.P. Sales/COO, CFO and Plant ManagerSubordinates reporting to this position: Quality StaffWork Environment:  Normal office as well as plant environment.Intensive vendor and customer contact.  Frequent customer visits.

Job Title: Director, Quality Assurance - NJ Company: Dendreon Corporation Location: New Brunswick, NJ Description: Director, Quality Assurance - NJJob Type: Regular Full-TimeLocation: Morris Plains, NJJob Description:Dendreon is seeking a Director of Quality Assurance who will provide leadership and support for the implementation of Quality Assurance policies and procedures in support of commercial manufacturing at our New Jersey facility. The successful candidate will provide direct support to Product Development, Manufacturing, Supply Operations and Quality Control in order to prepare the site for FDA inspection. The ability to function in a fast-paced environment and communicate effectively is essential to success.General Summary:* Directs overall operational leadership in planning and management of quality systems and activities, including resource management and vendor management, which includes the following:* Validation program* GMP material review and disposition* Internal and external quality audits* Pre- and post-approval compliance audit preparation* Corrective and preventive action program* GMP training program* Quality engineering* Change control* Document control* Implements corporate Quality policies ensuring finished products conform to company standards and satisfy GMP regulations.* Oversees project risk analysis and develop solutions to a variety of complex problems.* Collaborates with other departments during planning and process improvement activities to ensure timely completion of all operational areas objectives and milestones.* Participates in steering committees that set general business corporate policy and sponsor corporate programs.* Interfaces with external customers and FDA during audits and inspections.* Mentors and develops department personnel, including supervisory / management staff.* Defines framework for department objectives, operation schedule, processes and budgets.* Contributes to Quality department strategic management.Job Requirements:* Bachelor's degree in a scientific discipline or equivalent.* Typically 10 years related experience in cGMP/FDA regulated industry.* Typically 5 years experience managing supervisory personnel and contributing toward the development of department strategy.* Knowledge of cGMP/QSR and FDA device/drug/biologics regulations.* Experience in developing and making formal presentations to executive management.* Experience with department budget planning, management and reconciliation.* Experience with ERP systems preferred.Working Conditions and Physical Requirements:* Ability to gown aseptically for work in Clean Room environments.* Some travel may be required.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: Contract QA MANAGER Company: Berman Larson Kane Location: Paramus, NJ Description: SALARY: $40-$45/hr-- Long Term contract DESCRIPTION: Implement and maintain quality initiatives through audits and investigations of processes and programs to assess SOP and GMP compliance. Ensure daily quality functions are performed. Oversee and preview and audit batch records; may release incoming and outgoing supplies. Manage quality oversight of assigned projects through interaction and consultation with clients, project and study teams, and associated development groups. Ensures timelines are met. Assists management with deviation management, cross-functional investigations, follow-up to audits, and corrective actions. Review and approve change control of systems and equipment. Act as a resource to the department by providing training and key input regarding QA processes. Ensures consistent auditing and reporting by direct reports. Manage internal and external audit schedules. May coordinate and conduct internal and external audits Management responsibilities may include professional development, performance appraisals, and employee counseling for junior staff. Assigns work and reviews workload for all direct reports. Supervises staff by establishing goals that will increase knowledge and skill levels, and by delegating tasks commensurate with skill level. May participate in customer audits and performs supplier audits. Communicates audit schedules and timelines. Responds to client inquiries. REQUIREMENTS: Bachelor's Degree in business, science or related field 5 years of Quality Assurance including management experience. Experience in pharmaceutical industry. Per 21 CFR and international regulatory agency requirements Experience of GMP, SOPs and auditing techniques. Possess good verbal and written communication skills. Possess good problem solving, risk analysis and negotiation skills. Must be able to work within a team environment. Possess good computer skills. Please submit your resume in MS Word format (.doc), Rich Text Format (.rtf) or Text (.txt). No Third Parties please. Must be authorized to work full-time in the United States for any employer. Berman Larson Kane regrets that we are unable to provide relocation assistance. Watch our FREE Career Transition Coaching Webinars A list of current and past webinars is available here. Search a list of current BLK Employment Opportunities View this month's BLK Career Report Visit the BLK Employment Blog Apply Here Our Jobs rotate on a regular basis. Please see our website for a complete listing. Berman Larson Kane regrets that we are unable to provide relocation assistance Please do not use the HotJobs Apply Now Button, Use the one above and Apply through our https://searchlight.cluen.com/candidateLogin.asp?GUID=&layout=&compid=&searchid=&sfilter=0&position=&department=&state=&city=®ion=&advanced=&TextString=&StartNum=1&att1=&att2=&att3=