QA Associate
Artech Information Systems LLC
Company DescriptionArtech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.Job DescriptionThe incumbent will have responsibility to ensure that all aspects of the operational business comply with cGMP legal and regulatory requirements, the Client Pharma Corporate Quality Manual and Policies, and site procedures and business requirements.Coordinates and performs batch record issuance for internally manufactured products Reviews and approves manufacturing and QC related documents for raw material disposition.Reviews and approves manufacturing and QC related documents for manufactured media Performs administrative functions for filing and maintenance of records between QA operations and Document Control Center Support cGMP and associated OJT training to QA and other departments to improve right the first time (RTFT), high quality performance.Control costs within department to meet budget.Complete job-related training in electronic database system along with GMP, safety, and Ethics & Compliance course requirements.Perform or support any other tasks necessary to maintain the product quality and site cGMP compliance, as needed.Skills:0-3 years GMP manufacturing and/or QA related experienceEducation: BS/BA in Biological Sciences or equivalent relevant career experienceQualificationsSkills:0-3 years GMP manufacturing and/or QA related experienceEducation: BS/BA in Biological Sciences or equivalent relevant career experienceAdditional InformationSneha ShrivastavaTechnical Recruiter (Clinical/Scientific)Artech Information Systems LLC360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960Office: View phone number on click.appcast.io | Fax: 973.998.2599Connect with us on - LinkedIn | Facebook | TwitterSummaryType: ContractFunction: Quality AssuranceExperience level: Mid-Senior LevelIndustry: Pharmaceuticals
- ...manufactured media Performs administrative functions for filing and maintenance of records between QA operations and Document Control Center Support cGMP and associated OJT training to QA and other departments to improve right the first time (RTFT), high quality performance...SuggestedImmediate start
Artech
Morris Plains, NJ4 days ago - ...Canfield Imaging Systems in Parsippany-Troy Hills, NJ, seeks a Quality Assurance and Regulatory Affairs Associate to support day-to-day QA activities and regulatory audits. You will assist global device registrations, maintain documentation, and contribute to training...Suggested
Imagingexcellencesymposium
Parsippany Troy Hills, NJ3 days ago - ...Canfield Imaging Systems in Parsippany, NJ is seeking a Quality Assurance: Quality Assurance and Regulatory Affairs Associate to support QA and regulatory activities in a fast-paced medical device environment. The role focuses on audits, regulatory registrations, documentation...Suggested
Canfield Inc
Parsippany Troy Hills, NJ3 days ago - ...verbal communication skills, strong attention to detail, and work well in fast paced environment.Job Description:Support and act as a QA contact for regulatory and certification audits, support and facilitate global medical device registrations with oversight from...SuggestedFull timeImmediate start
Canfield Scientific
Parsippany, NJ3 days ago - ...control of quality check consistency, and analyses the quality audit results. Essential Duties and Responsibilities:Performs SOX and QA audits and supports organization with internal and external audit activities.Supports the organization with initial compliance and ongoing...SuggestedWork experience placement
Excelgens
Morristown, NJ3 hours ago $25 - $45 per hour
...environment. Equivalent combination of education and experience will be considered. Preferred Qualifications Operational Experience: Hands‑on QA experience in an analytical or manufacturing setting, with a strong preference for small molecule manufacturing. Experience with...Contract workWork experience placementINTELLECTT INC
Morris Plains, NJ3 days ago- ...Schuman Cheese in Elgin, IL is seeking a QA Associate - Technical & Regulatory to support QA programs, regulatory compliance, and technical documentation across products and processes. You will help maintain product specifications, manage documentation, and support audits...Full time
Arthur Schuman Master
Fairfield, Essex County, NJ1 day ago $27.85 - $33.5 per hour
Job DetailsJob Location: IL Corporate - Elgin, IL 60124Salary Range: $27.85 - $33.50 Hourly Primary Purpose: The QA Associate - Technical & Regulatory is responsible for supporting quality assurance programs, regulatory compliance, and technical documentation within the...Hourly payFull timeWork at officeRemote workWork visaMonday to Friday- Bristol Myers Squibb is seeking a QA Shop Floor Associate on a contract assignment through ASK Staffing DBA ASK Consulting to support 24x7 quality collaboration across manufacturing, QC labs, and supply chain operations in Summit, NJ. You will review batch records, verify...Contract workShift workNight shift
$25 - $29.13 per hour
...functions. Reporting This role will report to the Sr. Manager of QA Shop Floor This role will work with existing team members to... ...batch record review activities. Education High school diploma/ Associates degree with equivalent combination of education and work...Hourly payContract workWork experience placementLocal area$62k - $141k
Quality Assurance SpecialistThe Opportunity:Participate in the quality assurance process and follow up to ensure that all products and services meet company and client standards and end-user requirements. Apply advanced consulting skills and extensive technical expertise...Full timeContract workPart timeLocal areaRemote workBooz Allen Hamilton
Wharton, NJ3 days ago- Job DescriptionLead Quality Assurance resource needed to provide quality support for global computer validation projects in the ERP area, such as SAP, under the guidance of the Global Quality Computer Compliance team.Job duties will include:Reviewing and providing input...Work experience placementWork at office
LanceSoft
Rockaway, NJ4 days ago - ...perspective within a regulated cGMP environment. The primary focus of the QA Specialist role will be to support routine clinical and... ...in a relevant science or engineering discipline, minimum of an associate's degree, 3-5 years of relevant cGMP experience, experience in FDA...
Omni Inclusive
Summit, NJ5 days ago - ...Bristol Myers Squibb is seeking a Senior Specialist, QA Investigations at the Summit Cell Therapy Facility. You will provide quality oversight, approve deviation investigations and CAPAs, and ensure compliance with regulatory standards across materials, manufacturing,...
Bristol-Myers Squibb
Summit, NJ5 days ago - ...partners.Participates in investigations related to the areas of supervision in order to monitor, measure and optimize or achieve the QA Department and Company goals.Maintain extensive communication with TPMs and other Client groups such as Manufacturing Technology, Supply...Contract workDay shift
Omni Inclusive
Summit, NJ4 days ago - Job-ID33095639Reference26-01781Summary : This Senior Quality Specialist will be responsible for ensuring that NA products manufactured at third party contract sites comply with all the applicable regulations as well as with our corporate quality standards during their whole...Contract work
Katalyst Healthcares & Life Sciences
Parsippany, NJ1 day ago $60k - $80k
...Pharmaceutical is seeking a detail-oriented Senior Quality Assurance Associate to join our growing Quality team, supporting operations at both... ...role in maintaining compliant quality systems, supporting daily QA operations, ensuring accurate GMP documentation, and...Full timeLocal areaGaronit Pharmaceutical Inc.
Fairfield, Essex County, NJ3 days ago$22 - $26 per hour
...Quality Control Associate Pay: $22-$26/hour Location: Parsippany, NJ Schedule: Monday-Friday, 8-hour shift Type: Full-Time How We Understand... ...The candidate would be expected to have actual manufacturing QC/QA experience and be comfortable with precision measurement,...Full timeMonday to FridayShift workSynerfac Technical Staffing
Parsippany, NJ4 days ago$34.97 per hour
A leading staffing firm is seeking a QA CTO Label Specialist to join their team in Summit, NJ. This contract position demands a Bachelor's degree in Science and a minimum of 1 year of relevant labeling experience in a cGMP/FDA regulated environment. Candidates should possess...Contract work$31 - $36 per hour
...minutes. Perform other duties and special projects as assigned. EDUCATION AND EXPERIENCE High School Diploma or GED required Associate Degree in Business Administration, Manufacturing, Quality, or related field preferred. Minimum of two (2) years of experience in...Work at officeShift work- SGS in Fairfield, NJ is seeking a Specialist I in Quality Assurance to support the maintenance of Quality Systems in a pharmaceutical testing laboratory, under supervision of a Team Leader or Manager. The role focuses on timely testing, ensuring compliance with cGMP, issuing...
- ...powered advice on this job and more exclusive features. Job Title :QA Label Specialist Location : Summit, NJ Hours/Schedule :... ...Markets Experience - NYC (Hybrid) Fine Jewelry Quality Assurance Associate New York, NY $50,000.00-$70,000.00 1 week ago New York, NY $90,0...Contract workAfternoon shift
- Bristol Myers Squibb is seeking a Senior Specialist, QA Shop Floor in Summit, NJ to oversee quality across manufacturing, QC, and warehouse operations. You will ensure adherence to cGMP policies, provide on-the-floor oversight, and lead investigations and training initiatives...
- Universal Technical Resource Services, Inc. seeks a Visual Inspector of live ammunition at Picatinny Arsenal to join our Small Caliber Munitions team. You will perform 100% visual inspections of loaded cartridges, whether in loose form or linked belts, and package ammunition...
- Staff Quality SpecialistThe Staff Quality Specialist will evaluate and harmonize existing Quality Management System (QMS) procedures, work instructions, forms, templates, and related documentation across multiple quality subprocesses. The role is responsible for identifying...Work at office
Katalyst HealthCares & Life Sciences
Parsippany, NJ4 days ago - A leading pharmaceutical company is seeking two Senior Quality Specialists on a contract basis to ensure quality assurance and compliance support for clinical products. Responsibilities include detailed batch review, leading quality systems processes, and collaborating ...Contract work
- SGS is a global leader in testing, inspection and certification with a strong focus on quality and compliance. The Specialist I, Quality Assurance supports management in maintaining Quality Systems for a pharmaceutical testing lab, ensuring regulatory compliance and timely...
- Canfield Imaging Systems is seeking a Product Reliability Specialist to bridge customers and engineering, analyzing defective products to prevent future issues. The candidate will organize data, document findings, and drive corrective actions in a fast-paced environment...
$25 - $35 per hour
Position: Quality Specialist - Final Inspection Location: Montville, NJJob Id: 2133-5102-27-R-B # of Openings: 1 Elevate your career at Marotta Controls, a New Jersey Top Workplace three years running! Dedicated...Full timeCasual workLocal areaFlexible hoursMarotta
Montville, NJ3 days ago$165k - $180k
...Objective: NFC is looking to hire an experienced Employment Law Associate for our Chatham, New Jersey office. This position will be filled by a highly motivated, detail-oriented individual who excels in a fast-paced, entrepreneurial environment that values top-quality...Full timeWork at officeFlexible hours2 days per weekNUKK-FREEMAN & CERRA, PC
Chatham, NJ3 days ago
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