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 experience Education: BS/BA in Biological Sciences or equivalent relevant career experienceQualificationsSkills:0-3 years GMP manufacturing and/or QA related experience Education: 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
- ...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...SuggestedWork experience placementRemote workShift workDay shift
Excelgens
Morris Plains, NJ4 days ago - ...locations from East Hanover, NJ to Denville, NJ in Spring 2026. OVERVIEW We are seeking a proactive and detail-oriented Quality Assurance Associate to support our dynamic manufacturing team. In this vital role, you will ensure that all products meet rigorous quality standards...Suggested
Viscot Medical
Denville, NJ1 day ago $90k - $115k
...vision abilities required by this job include close vision. Education:Bachelor’s degree (BA) from four-year college or university or Associates degree (A.A.) with four to six years related experience and/or training. OR six to eight years related experience and/or training...SuggestedWork at office- Job ID: 25-63915Location: Summit, NJContact: Varun BhardwajContact Email: ****@*****.*** Phone: (***) ***-****Company: MindlanceJob Description: This is a 100% onsite position. This position is scheduled for Sun-Wed (6:30 am -4:30 pm). PURPOSE AND SCOPE OF POSITION...SuggestedHourly payWork experience placementWork at office
- 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...SuggestedWork experience placementWork at office
- ...within a regulated cGMP environment. The primary focus of the QA Specialist role will be to support routine clinical and... ...relevant science or engineering discipline is preferred. Minimum of Associates degree Experience: • 3-5 years of relevant cGMP experience...
Omni Inclusive
Summit, NJ19 hours ago - ...Garonit Pharmaceutical is looking for a detail-oriented QA Associate in Flanders, NJ and Fairfield, NJ. This role supports daily Quality Assurance operations, ensuring product quality and cGMP compliance. Responsibilities include issuing and reviewing batch records, preparing...
Garonit Pharmaceutical
Fairfield, Essex County, NJ2 days ago $105k - $150k
...specification requirements. Knowledge of higher-level quality assurance system requirement documents, with the ability to interpret and apply QA system-level requirements while performing quality assurance duties. Perform accurate mechanical, physical, and visual inspections,...Full timeContract workWork experience placementWork at officeFlexible hoursBastion Technologies
Springfield, NJ19 hours ago- Job Description Job Description Description: Summary of Position Implement and adhere to document control procedures, including version control, document approval, and archiving Create and Edit Documents: Prepare, format, and edit documentation related to product...
electroCore Inc.
Rockaway, NJ12 days ago $60k - $85k
Job Title: Quality Specialist Location: Parsippany, NJ Type: Direct Hire Compensation: $60,000.00 - $85,000.00 Work Model: Remote - offsite Hours: 40.0 Responsibilities Support and administer the Electronic Quality Management System (Veeva), including...Full timeWork at officeLocal areaRemote workSystem One
Parsippany, NJ2 days ago- QA Associate Onsite in Flanders, NJ and Fairfield, NJ Garonit Pharma is seeking a detail-oriented and collaborative QA Associate to support daily Quality Assurance operations and uphold our Quality Management System. This role is essential in ensuring product quality,...
$25 - $34 per hour
...engineering drawings, purchase orders, specifications, and other requirement sources. Adhere to all internal processes, particularly those associated with handling of non‑conforming materials. Act as the central point of communication between quality, engineering, production,...Hourly payFull timeCasual workWork at officeMonday to FridayMarotta Controls
Montville, NJ3 days ago$25 - $35 per hour
...the Material Review Board (MRB) and mandatory corrective action. Job Requirements 0–5 years experience in quality‑related functions Associate of Applied Science (AAS) degree preferred Working knowledge of standard quality concepts, preferred Familiarity with various...Hourly payFull timeFlexible hoursMarotta Controls
Montville, NJ2 days ago$105k - $115k
Job Description The Quality Control Data Senior Specialist supports Quality Control, Operations, and cross‑functional stakeholders by owning the organization, analysis, and usability of QC and customer‑facing laboratory data. This role partners closely with the lab Technical...Work at officeShift workCooperSurgical
Livingston, NJ2 days ago- The Quality Associate will perform independent examination (i.e., audit) of multiple trial‑related activities and documents to determine whether... ...reports, and performs related duties (e.g., issues findings and QA statements) Supports training for site staff, including...Temporary workWork at officeLocal areaFlexible hours
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