QA Specialist: cGMP Compliance & Batch Release
TechDigital Group
Must have's: Spectrum (Expert/Primary); Paragon (Expert/Primary); Intellimatch (Primary); FHLB (Primary); Bancware; EuroClear; Pershing NetX360; Bloomberg/BMO Capital/JPMorgan Access ICE Data / Remote Plus; Refinitiv DataScope; Vision,SQL Primary escalation for all Treasury incidents during business hours. Key liaison with Treasury business users and external counterparties. Proximity to IDB NYC office.Should be hands-on experience in L2 support .Initial responsibility would be to take transition on existing systems and gradually start providing L2 support for all the Treasury(Spetrum treasury system) and investment systems (other systems mentioned in below skills section) Managing multiple Spectrum hotfix releases/month (UAT + production). Intellimatch app manager responsibilities absorbed after previous manager retired. Spectrum version upgrade. #J-18808-Ljbffr TechDigital Group
- Scorpion Therapeutics is seeking a QA Shop Floor Specialist to provide 24/7 quality oversight across manufacturing... ...site. The role requires applying cGMP standards, reviewing batch records, and acting as Authorized Person for release activities. You will support remediation...SuggestedNight shiftDay shift
$35 - $39 per hour
...of $35-$39 per hour. The ideal candidate holds a science or engineering degree and at least three years in pharma/regulated environments, with strong documentation and QA experience, including batch review and GMP compliance. #J-18808-Ljbffr Johnson Service Group, Inc.SuggestedHourly payContract work3 days per week- Bristol Myers Squibb is seeking a QA Shop Floor Associate on a contract assignment... ...operations in Summit, NJ. You will review batch records, verify procedures, participate... ...continuous improvement while maintaining cGMP compliance. Shift options include Sun-Wed 10pm-8am...SuggestedContract workShift workNight shift
- Bristol Myers Squibb is seeking a Senior Specialist, QA Shop Floor in Summit, NJ to oversee... ...operations. You will ensure adherence to cGMP policies, provide on-the-floor oversight... ...procedural documents while maintaining compliance and continuous improvement. #J-18808-...Suggested
- 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...Suggested
- ...Quality Assurance Specialist position plays a key... ...in supporting the cGMP quality operations... ..., completed batch records, material... ...directly supports release of vector timeline... ...primary focus of the QA Specialist role will... ...ensure consistent compliance with regulatory and...
- 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,...
- ...storage, and trial operations in a fast-paced environment. You will develop workflows, collaborate with R&D, QA, and logistics, and ensure regulatory compliance and meticulous record-keeping. English and Korean business proficiency is preferred. Applicants should have a...
- Kenvue is hiring a Specialist, R&D Quality & Compliance in Summit, New Jersey. Hybrid work location... ...to ensure R&D functions meet cGMP and company procedures.... ...documentation review, audits, study releases support, and regulatory guidance, with QA representation on project...
$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... ...a minimum of 1 year of relevant labeling experience in a cGMP/FDA regulated environment. Candidates should possess strong...Contract work- SGS in Fairfield, NJ is seeking a Specialist I in Quality Assurance to support the maintenance of Quality Systems in a pharmaceutical... ...or Manager. The role focuses on timely testing, ensuring compliance with cGMP, issuing Certificates of Analysis, and participating in SOP...
$25 - $29.13 per hour
...to provide review of production and QC batch records to ensure compliance with Bristol-Myers Squibb policies, standards, procedures, and Global cGMP. Key Responsibilities Perform and document... ...role will report to the Sr. Manager of QA Shop Floor This role will work with...Hourly payContract workWork experience placementLocal area- ...and more exclusive features. Job Title :QA Label Specialist Location : Summit, NJ Hours/Schedule... ...QALC) Labeling Specialist supports the cGMP Label Control operations for the client... ...accurate printed information on labels in compliance with health authority requirements....Contract workAfternoon shift
- ...Assurance and Regulatory Affairs Associate to support day‑to‑day QA activities and global certification efforts. You will help... ...You will work under the Senior QARA Manager to ensure regulatory compliance, contribute to process improvements, and help prepare regulatory...
- ...Our long-tenured client, a well-established distribution company that is growing its product lines, is searching for a QA/QC and Compliance Specialist to support their purchasing, quality control and regulatory compliance work. This is an onsite role in Essex County, NJ...Second jobWork at officeOverseasMonday to FridayFlexible hours
- ...QA Specialist Reporting to the AAA Site Remediation Lead, the AAA Remediation QA Specialist... ...a strong focus on equipment validation, compliance, record backlog elimination, and sterility... ...of AAA RLT objectives by ensuring cGMP-Compliance with focus on Successful Health...Local area
- ...business hours) The primary responsibility of the Global QA Patients Operations Specialist is to support the Onboarding and Maintenance of... ...including deviation management, change management, CAPA, compliance guidance. • Contribute to the Key Performance Indicating...Flexible hours
- 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
- ...Assurance and Regulatory Affairs Associate to support audits, registrations, and documentation for medical devices. You will help maintain QA processes, ensure training documentation is complete, and assist with global regulatory submissions. The role requires a Bachelor’s...
- Canfield Imaging Systems, Parsippany, NJ, seeks a Quality Assurance and Regulatory Affairs Associate to support QA activities, audits, and regulatory submissions for medical devices. The role emphasizes documentation control, training administration, and collaboration...
- ...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 cross...Contract work
- ...NJ seeks a Quality Assurance and Regulatory Affairs Associate to support QA activities, audits, and documentation in a fast-paced medical device setting. You will help maintain ISO 13485 compliance, assist with regulatory filings for global markets, and develop QA...
- ...plasma center processes to ensure overall compliance with CSL Operating Procedures as well... ...The Role Perform final QA review and release for all shipment and associated documents... ...compliance with CSL procedures and policies cGMP OHSA FDA and other regulations as applicable...Full timeLocal areaImmediate startShift work
- ...University Alumni Regulatory Site Quality Specialist JOB DESCRIPTION A large CPG client of... ...Certificates of Analysis, as well as GMP batch records, packaging protocols, clinical labeling... ..., and serving as a backup for the QA Manager. REQUIRED SKILLS AND EXPERIENCE...
- Valcor Engineering Corporation in Springfield, NJ is seeking a Quality Specialist to compile, review, and maintain quality documentation and customer data packages to ensure compliance with customer and regulatory requirements. You will collaborate with Quality, Manufacturing...
- Solventum is seeking an Advanced Supplier Quality Support Specialist to maintain supplier quality control systems and documentation. You will ensure accuracy, compliance, and readiness for audits while collaborating with quality, engineering, manufacturing, and operations...Remote job
$27.85 - $33.5 per hour
....85 - $33.50 Hourly Primary Purpose: The QA Associate - Technical & Regulatory is responsible... ...quality assurance programs, regulatory compliance, and technical documentation within the... ...with established standards Review batch records, production documentation, and quality...Hourly payFull timeWork at officeRemote workWork visaMonday to Friday- ...Quality Specialist The Quality Specialist is responsible for compiling, reviewing, and... ...documentation and customer data packages to ensure compliance with customer and regulatory... ...initiating the package at top-level kit release and organizing all documentation for final...Work at officeLocal area
$25 - $45 per hour
Senior Quality Specialist (Contract) Position Type: Contract Duration... ...quality assurance and compliance support for our developmental... ...You will play a key role in batch disposition, quality system execution... ...Experience: Hands‑on QA experience in an analytical or...Contract workWork experience placement- ...experienced Inspector to conduct airworthiness inspections and support quality assurance activities. The role involves ensuring compliance with regulatory standards, creating accurate work orders, and collaborating with team members to meet production schedules. A trade...
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