Software Quality Assurance Analyst jobs in Middlesex, NJ

Software Quality Assurance Analyst executes testing procedures to ensure that software meets established quality standards. Prepares data sets to test logic, error handling and system workflows. Being a Software Quality Assurance Analyst isolates, reproduces, and tracks defects. Verifies fixes. Additionally, Software Quality Assurance Analyst documents testing according to required procedures. Familiar with software development cycle and quality assurance methodologies. May assist with the creation of new testing scripts and plans. Requires a bachelor's degree or its equivalent. Typically reports to Quality Assurance Manager. The Software Quality Assurance Analyst work is closely managed. Works on projects/matters of limited complexity in a support role. To be a Software Quality Assurance Analyst typically requires 0-2 years of related experience. (Copyright 2024 Salary.com)

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Quality Auditor - Scientific - II
  • Talent Software Services, Inc.
  • Rahway, NJ CONTRACTOR,FULL_TIME
  • Quality Auditor - Scientific - II

    Job Summary: Talent Software Services is in search of a Quality Auditor - Scientific - II for a contract position in Rahway, NJ. Opportunity will be one year with a strong chance for a longterm extension.

    Primary Responsibilities/Accountabilities:

    The GDQ Ops – API organization provides Quality oversight for manufacturing, testing, and release activities associated with clinical-stage API.

    We provide Quality oversight of product development activities integrated with operations and functional partners, while ensuring continuous GMP-compliant clinical supply for internally and externally manufactured API.

    Under the direction of GDQ-Ops Supervision, the Contractor will be responsible for providing quality assurance oversight, performing diverse tasks, and participating in quality related projects.

    Product release, quality system, compliance, document management, and any related activities needed under current Good Manufacturing Practice (cGMP).

    Ensure compliance with applicable GMP regulations, ICH guidelines, Client policies, and procedures.

    The Contractor will support tasks that may include but are not limited to:

    Perform independent quality review and approval of batch records, testing data, and related documents required to release or reject product. Make independent batch release or reject decisions.

    Conduct independent auditing, review, and approval of diverse and complex document types, as required, including deviations, investigations, analytical method validations, method transfers, analytical methods, specifications, certificates of analysis, etc.

    Collect, prepare and analyze data to support quality system metrics and planning.

    Perform document management activities such as cataloging records for long term document storage according to retention policies.

    Support compliance activities such as site readiness, audits, and CAPAs.

    Support quality risk management activities.

    Support projects for continuous quality improvement. Utilize project management skills as needed.

    Provide meeting coordination, facilitation, scribing, and communication.

    Develop, write, technical edit, or review procedures or other standards documents under GMP.

    Other duties as assigned by manager for the flexible functioning of the work group.

    Qualifications:

    Bachelor degree (B.S.) in an appropriate Science or Engineering discipline (engineering, chemistry, biology, biochemistry, microbiology). Minimum of 1 year experience preferred. Recent graduate can be considered.

    Experience should be in the pharmaceutical, biotechnology, chemical, medical device, or closely related industry.

    Knowledge of R&D or clinical supply areas and processes.

    Preferred API knowledge and experience.

    Experience in one or more functional areas such as quality control, quality assurance, laboratory, manufacturing, production, equipment/facilities management, regulatory.

    Good Manufacturing Practice (GMP) or related drug regulation knowledge and expertise.

    Strong leadership, collaboration, teamwork, negotiation, communication, and workload management skills.

    Ability to work in a dynamic R&D environment with rapidly changing needs.

    Demonstrated ability to manage projects, priorities, to meet deliverables and timelines.

    Ability to work across functional and sites, with all levels of staff and management.

    Qualified candidates should have proficiency with Microsoft Suite (Word, Excel, PowerPoint, Teams, etc.) and ability to adapt to learning other electronic systems to support day-to-day work.

    Fully onsite during training period, transitioning to Hybrid role requiring 3 days onsite a week.

    Local candidates preferred

    If this job is a match for your background, we would be honored to receive your application!

    Providing consulting opportunities to TALENTed people since 1987, we offer a host of opportunities including contract, contract to hire and permanent placement. Let's talk!
  • 21 Days Ago

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Quality Specialist - II (Associate)
  • Intelliswift Software, Inc.
  • Rahway, NJ FULL_TIME
  • Qualifications: Education:Bachelor's of Science or Master's degree. Technical emphasis in an appropriate scientific or engineering field preferred; candidates with majors in other fields will be consi...
  • 1 Month Ago

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Financial Analyst
  • Intelliswift Software, Inc.
  • Berkeley Heights, NJ FULL_TIME
  • Pay rate range - $30/hr. to $35/hr. on W2 3 top Skills: Must be bi-lingual (Korean/English) Detail Oriented Advanced Microsoft Office Support overall tasks related to managing and operating developmen...
  • 13 Days Ago

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Quality Auditor - Scientific - II (Associate)
  • Intelliswift Software, Inc.
  • Rahway, NJ FULL_TIME
  • Qualifications: Skills:Bachelor degree (B.S.) in an appropriate Science or Engineering discipline (engineering, chemistry, biology, biochemistry, microbiology). Minimum of 1 year experience preferred....
  • 3 Days Ago

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Manager Quality Assurance
  • Breckenridge Pharmaceutical Inc
  • Berkeley Heights, NJ FULL_TIME
  • Breckenridge Pharmaceutical develops and markets high-quality, added-value and cost-effective generic drugs in the United States. Our products are developed in the group’s own R&D facilities and throu...
  • 17 Days Ago

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Quality Assurance Technician
  • Paragon Staffing, LLC
  • Plainfield, NJ FULL_TIME
  • Paragon Staffing, LLC is a company that specializes in connecting job seekers with employers who are seeking temporary, contract, or permanent positions.Quality Assurance Technician is able to provide...
  • Just Posted

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0 Software Quality Assurance Analyst jobs found in Middlesex, NJ area

Middlesex is a borough in Middlesex County, New Jersey, United States. As of the 2010 United States Census, the borough's population was 13,635 reflecting a decline of 82 (-0.6%) from the 13,717 counted in the 2000 Census, which had in turn increased by 662 (+5.1%) from the 13,055 counted in the 1990 Census. Middlesex was incorporated as a borough by an act of the New Jersey Legislature on April 9, 1913, from portions of Piscataway Township, based on the results of a referendum held on May 6, 1913.[21] The borough's name derives from Middlesex, England.[22][23] According to the United States C...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Software Quality Assurance Analyst jobs
$69,443 to $86,463
Middlesex, New Jersey area prices
were up 1.5% from a year ago

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