Quality Specialist
Real Staffing
We are seeking an experienced Quality Specialist to join a growing Regulatory Affairs & Quality Assurance team supporting medical device, pharmaceutical, and combination product sterilization operations. This role is ideal for a quality professional who thrives in a GMP-regulated environment and is passionate about driving compliance, process improvements, and quality excellence. Key Responsibilities Manage the Change Control process, including ECO documentation, SOP creation, revisions, and approvals Maintain and administer the company-wide training program Certify and recertify employees on quality policies and procedures Manage the Approved Supplier List and supplier qualification activities Oversee incoming inspection processes Ensure compliance with FDA regulations and industry standards, including QMSR, 21 CFR Parts 210/211, ISO 13485, and ISO 14971 Collaborate with Operations, Engineering, Validation, R&D, and Quality teams to support project execution and regulatory compliance Support operational excellence initiatives while maintaining quality and performance objectives Qualifications Required: Bachelor's degree in Engineering, Science, or a related field (or equivalent experience) 3-7 years of Quality experience in a GMP-regulated industry Certified Quality Engineer (CQE) or equivalent qualification Strong knowledge of cGMP, QMSR, ISO 13485, and ISO 14971 Excellent communication, organizational, and project management skills Ability to manage multiple priorities in a fast-paced environment Strong analytical, problem-solving, and decision-making abilities Authorized to work in the United States Preferred: Experience in contract sterilization, medical device, pharmaceutical, or combination product environments What Success Looks Like The ideal candidate is a proactive quality professional who takes ownership, drives projects to completion, and builds strong cross-functional relationships while ensuring the highest standards of compliance and quality. If you're looking for an opportunity to make a meaningful impact in a highly regulated and growing industry, we'd love to hear from you. EOE Statement: Specialist Staffing Group is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. In addition to base pay, direct-hire employees may be eligible for client offered benefits such as medical, dental, and vision coverage, and paid leave where required by applicable law. Eligibility may vary based on factors such as location and hire date and is subject to change. #J-18808-Ljbffr
- ...limited to Work with suppliers to complete required supplier surveys and maintain supplier survey files. Maintain and archive supplier quality paper records. Monitor supplier quality TW records to ensure timely closure Support supplier quality associates as needed....SuggestedPermanent employmentTemporary workWork at officeWorldwide
- ...Review. Developing PowerPoint presentation with input from global business owners. Collaborating to complete deliverables with global Quality Teams. Reviewing Quality System reports in Veeva QMS and associated dashboards to support data presentation to executives. Provide...Suggested
$40 - $48 per hour
...Piper Companies is currently looking for an experienced Quality Control Specialist in Branchburg, New Jersey (NJ) to work for a pharmaceutical cell therapy company. Must have experience with Flow Cytometry experience. Responsibilities for the Quality Control...Suggested$32 per hour
...Quality Specialist Guardian of Quality and Compliance by Design following the quality requirements and deliverables for Food Safety initiatives in raw material specifications (mainly RMPS and testing specifications) to full compliance to Quality, Food Safety and Regulatory...SuggestedHourly pay- The Quality Specialist is responsible for supporting and maintaining the Quality Management System (QMS) for medical device, pharma and combination device sterilization operations. This role is responsible for managing the change control process, creating and updating...SuggestedContract work
- ...Johnson & Johnson Innovative Medicine is seeking a Sr. Specialist, External Quality (Synthetics) to provide end-to-end quality support for external manufacturers and strategic partners, ensuring consistent delivery of pharmaceutical products that meet safety and regulatory...
- ...Amneal is seeking a QA Stability Specialist in New Jersey to implement, lead, and manage the iStability/LIMS software for all ANDA batches, entering data and performing statistical evaluation as needed. You will create studies, review stability protocols and reports,...
$30 - $32 per hour
...Job Description Job Description Job Title: Quality Specialist Job Description As a Quality Specialist, you will be the guardian of quality and compliance by design, ensuring that quality requirements and deliverables are met from idea to launch. You will represent...Full timeContract workTemporary workMonday to Friday- ...A biotechnology company in New Jersey seeks a QA Change Control Specialist II responsible for quality oversight in a cell therapy manufacturing facility. Applicants should possess a Bachelor's degree in Science and a minimum of two years' experience within a cGMP environment...
- ...Legend Biotech US is seeking a QA Shop Floor Specialist in Raritan, New Jersey, to provide quality oversight in the production of CAR-T products. This exempt-level position involves maintaining compliance in a cGMP cleanroom and supporting manufacturing activities. You...
- ...Legend Biotech is seeking a QA Shop Floor Specialist in Raritan, NJ to provide on-site quality oversight of autologous CAR‑T production in a cGMP cleanroom. You will ensure GDP-compliant documentation, support aseptic manufacturing, and drive quality improvements across...Weekend work
- ...Posted Thursday, July 23, 2026 at 4:00 AM Quality Analyst Location: Multiple Locations (Daily Travel Required) – Middlesex, Somerset, Warren Counties, etc. Join Beacon Specialized Living Services Beacon is a nationally recognized behavioral health organization providing...
- ...Legend Biotech in Raritan, NJ seeks a QA Shop Floor Specialist to oversee quality during autologous CAR-T production in a cGMP cleanroom. You will ensure compliance with GDP, review SOPs, and support batch release in SAP for in-house reagents. The role requires 0-2+ years...Weekend work
- ...A leading healthcare company is looking for a Quality Assurance Incoming Specialist II based in Raritan, NJ. The role involves overseeing the quality and compliance of materials for CAR-T production in a regulated environment. Candidates should have a Bachelor's degree...
$83.71k - $109.87k
...of an immunotherapy in the treatment of multiple myeloma. QA Laboratory Compliance Specialist III Legend Biotech is seeking a QA Laboratory Compliance Specialist III as part of the Quality team based in Raritan, NJ . Role Overview The QA Lab Compliance (QALC) specialist...Permanent employmentFull timeTemporary workFor contractorsWork experience placementWork at officeLocal areaImmediate startWorldwideFlexible hours- Legend Biotech in Raritan, NJ is seeking a QC Analyst I (IPL) to perform QC testing related to manufacturing of cell therapy products for clinical trials and commercial operations in a controlled GMP environment. The role requires a Bachelor's degree in science or engineering...Weekend workAfternoon shift
$90k - $210k
...Quality Control Analyst We are seeking an innovative, creative, and detail-oriented Quality Control Analyst to join our team in Bridgewater, New Jersey. This position will be responsible for routine and non-routine QC testing according to Standard Operating Procedures...Flexible hours$69.5k - $102.35k
Johnson & Johnson, QA Specialist II (1 of 2) - Application via WayUp Join to apply for the Johnson & Johnson, QA Specialist II (1 of 2)... ...profoundly impact health for humanity. Learn more at Job Function: Quality Job Sub Function: Quality Assurance Job Category: Professional...Contract workTemporary workPart timeLocal areaImmediate startAfternoon shift$83.71k - $109.87k
...immunotherapy for multiple myeloma. QA Laboratory Compliance Specialist III - Location: Raritan, NJ Role Overview The QA Lab Compliance... ...) Specialist III is an exempt level position responsible for quality and compliance oversight over all functions of the Quality...Temporary workWork experience placementWork at officeWorldwideFlexible hours$70.67k - $92.76k
QA Document Control Specialist I/II/III Legend Biotech is a global biotechnology company dedicated to treating life‑threatening diseases... .... Perform tasks in a manner consistent with safety policies, quality systems and cGMP requirements. Review and approve SOPs and...Work experience placementFlexible hours- ...Job Description Job Description We are seeking an innovative and highly motivated Senior Quality Validation Specialist, who will contribute significantly to the growth of the Cellares team. The Quality Validation team at our IDMO Bridgewater facility will be responsible...Flexible hours
- ...Job Title: Quality Assurance Specialist-Junior Work Location: Bridgewater, NJ Contract: 8-9+ Months Job Description/Summary: The primary responsibility of this position involves the daily management of commercial Product Quality Complaints. The...Contract workWork at office
- ...Job Description Job Description We are seeking a detail-oriented and operationally rigorous Quality Control Raw Material Analyst to join our Quality Control (QC) team in Bridgewater, New Jersey. The primary focus of this position is to support raw material incoming...Contract workFlexible hours
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