|
The New Jersey Quality Assurance Association
|
|
Job Opportunities
NJQAA Members can submit job listings for posting on this page. Listings will generally be removed after 30 days unless an extension of the listing is requested. Please send job descriptions to eagold@optonline.net.
This listing page is provided as service to our members. The NJQAA takes no responsibility for any of the listing information.
Posted 04/28/09
QA/QC Manager
ACTEGA Radcure, Inc. is a small specialty chemical manufacturer selling coating and adhesives to the labeling industry. We are searching for a roll-up-your-sleeves, get-out-on-the-floor individual who thrives wearing many hats. The person should be a focused performer with demonstrated strengths in quality, chemistry, safety, team building, time management and organizing/facilitating progress. This position reports to the Vice President of Operations.
Requirements:
- BS with 5+ yrs compliance/QA.
- The successful candidate is a strong communicator with excellent interpersonal skill. This position requires a Bachelors Degree in Chemistry combined with 5+ years of progressing experience in Quality Control and Assurance and should have expertise of ISO 9000.
- Quality Systems Management is very strongly preferred.
Compliance/QA/Quality Systems Management experience from research, quality, operations, labs, or manufacturing
- Provides QA guidance and mentors other colleagues
- May be involved in metrics tracking and presentation
- Good knowledge of Microsoft Office Suite and Microsoft Project is essential.
Responsibilities:
- Manage the day-to-day Quality Control function
- Develop and maintain SOPs.
- Manage our quality systems as our ISO 9000 Coordinator and lead our efforts for continuous improvement.
- Develop and maintain systems and procedures to ensure products meet the established quality standards and our customers' specific quality assurance requirements. This may include:
- Define and document the accepted quality standards for all products.
- Develop and maintain the documentation of production process SOP's (Standard Operating Procedures), bill of materials and specification data sheets.
- Perform analysis of production rework. Determine the root cause and create action plans to eliminate future recurrences.
- Administration of Vendor & Component Qualification process.
- Tracking of quality objectives.
- Perform other duties as required.
- Develop, evaluate and maintain effective health/safety policy and procedures to comply with corporate and regulatory requirements, these activities include but are not limited to Safe Operating Procedures, Hazard Communication, and Lockout/Tagout.
- Perform safety related administrative tasks, to include compliant program recordkeeping, equipment procurement, Workers' Compensation case management, and responding to inquiries.
Anyone interested in this position is asked to contact Greg Parker at 973 808 1002, Greg.Parker@altana.com or Paul Mayer 203 303 3163, paul.mayer@altana.com
Posted 03/16/09
Manager Software Quality Assurance (Princeton, NJ)
Come join an industry leader where you will have the opportunity to manage, supervise, and mentor a team of software quality assurance (SQA) test engineers. Work directly with our development teams to recommend and determine appropriate test environment requirements (hardware, software, networking, etc.). Continually provide software quality assurance (SQA) expertise to the Senior Director of Development Operations. Research new test products and technology to determine which tools and utilities are most applicable. Proactively suggest product and service offering enhancements and resolutions based on understanding of impact, risks, performance, and usability. Manage the preparation, development, maintenance and execution of test reports and release documentation.
Must have a thorough knowledge of SDLC methodologies, quality assurance methodologies, including automated testing, manual testing, and performance testing, and experience executing comprehensive test suites for web applications. Must exhibit a sense of responsibility with a focus on quality deliverables.
Knowledge of network architecture, .NET Framework, databases, (SQL Server preferred), web applications and web services in reference to testing and test results is required.
Prior work experience in a clinical operations and/or regulated biopharmaceutical environment is strongly desired., and an understanding of the clinical trial process is preferred.
Education/Experience: A bachelor's degree in Computer Science or equivalent is desired and at least 5 years experience in testing and delivering web solutions in a business environment is required. Experience working at a software development company directly with software development teams is required. Must have prior experience managing software quality assurance teams. Experience using SQL Server and .NET technologies is also desired.
For more information and to apply, please visit us at: www.parexel.com
JWilks@clinphone.com
Last Modified: Tue, Apr 28, 2009
