GxP IT Quality & Validation Specialist (Hybrid)
TechDigital Group
An established industry player is seeking an IT Quality Compliance Specialist/Analyst to ensure regulatory compliance across the product lifecycle. This hybrid role involves managing the GxP IT Quality Assurance program, reviewing validation deliverables, and supporting inspections. Ideal candidates will have a strong background in the BioTech or Pharmaceutical industry, with expertise in GxP regulations and quality assurance practices. Join a dynamic team where your analytical and interpersonal skills will contribute to maintaining the highest standards of quality and compliance in a fast-paced environment. #J-18808-Ljbffr TechDigital Group
- ...IT Quality Compliance Specialist/Analyst Hybrid role--Local Candidates Only Work Schedule: Mon - Fri, Business Hours... ...assurance mindset for computer system validation for GMP, GDP, GLP space.... ...expertise to read and interpret global GXP regulations, as well as data integrity...SuggestedLocal area
$86k - $121k
...Colgate-Palmolive is seeking a Global Quality System Developer and Validation Analyst to enhance our digital quality systems. This role involves designing... ...human-dependent controls and ensuring compliance with GxP regulations. You will collaborate with cross-functional...Suggested- ...looking for a CSV Consultant in Raritan, NJ to support system validation activities in a regulated environment. The consultant will ensure... ...in Computer System Validation (CSV) and knowledge of GxP standards. Excellent communication skills and ability to handle...Suggested
- ...leading healthcare solutions provider in Edison, NJ is hiring a Quality Specialist to support the compliance program for pharmaceutical storage.... ...ISO or cGMP standards are essential. The position offers a hybrid work model and competitive benefits. #J-18808-Ljbffr...Suggested
- ...change controls, and authoring calibration and maintenance SOPs as well as performing calibrations, maintenance, and qualifications/validations. 2. REQUIRED COMPETENCIES: Knowledge of cGMP and good documentation practices. Knowledge of pharmaceutical, manufacturing and...SuggestedWork at office
- Concordance Healthcare Solutions LLC is looking for a full-time Quality Specialist in Edison, NJ. This role primarily supports the cGMP compliant quality program for pharmaceutical storage and involves managing quality audits, documentation, and vendor evaluations. Ideal...Full timeWork at office
$90.31k - $114.39k
...Veeco Instruments Inc. is seeking a Process Engineer to support process and tool validation for semiconductor manufacturing environments in Franklin Township, NJ. The role involves hands-on work with deposition and etch systems to ensure tools perform reliably and meet...- Sunrise Systems is seeking a Quality Assurance Specialist in Edison, NJ, to support cGMP quality operations. This hybrid role involves reviewing controlled documents, ensuring compliance with manufacturing practices, and supporting both clinical and commercial product releases...
$96.8k - $137k
...Piscataway - Colgate-Palmolive - Travel - up to 10% of time - Hybrid No Relocation Assistance Offered Job Number#173456 - Piscataway... ...primary technical liaison between our Application Security and Quality Assurance teams, creating automated security regression tests targeting...Hourly payLocal areaRelocation$93.46k - $122.67k
Job Overview QA Validation Specialist III role at BioSpace, based in Raritan, NJ. Exempt level position responsible for quality oversight of validation and qualification activities for equipment... ...is a plus. Strong knowledge of GxP compliance. Experience with cGMP regulatory...Work at officeFlexible hours- ...Perform protocol-level verification for DDR memory interfaces and validate compliance Collaborate with architecture, RTL, and system... ...type: Full-time Job function: Engineering and Information Technology Industries: IT Services and IT Consulting #J-18808-LjbffrFull timeContract workWork experience placementRemote work
- ...energy audits and manage projects in New Jersey. This role offers a hybrid work environment, requiring strong technical skills in energy... ...have a Bachelor’s or Master’s degree in engineering and a valid NJ driver’s license. The position comes with comprehensive benefits...
$81.04k
Legend Biotech USA, Inc. is seeking a Risk Assessment Specialist based in Raritan, NJ. The ideal candidate will conduct Quality Risk Assessments and collaborate with teams across QA, QC, Manufacturing, Engineering, and R&D. This position requires a BS degree and experience...- Legend Biotech USA is seeking a Risk Assessment Specialist in Raritan, NJ, responsible for conducting Quality Risk Assessments (QRM) and collaborating with QA, QC, and Engineering teams to enhance compliance with FDA and GMP standards. The ideal candidate holds a BS degree...Full time
- ...Colgate is seeking a Global Quality System Developer and Validation Analyst in Piscataway, New Jersey. In this role, you will lead the design of automated... ...quality systems globally while ensuring compliance with GxP regulations. You will act as a Subject Matter Expert,...
- ...We are seeking an innovative and highly motivated Senior Quality Validation Specialist, who will contribute significantly to the growth of the Cellares... ...complex scientific issues across multiple projects as it relates to regulatory requirements and strategy ~ Experience...Flexible hours
- Sharpedge Solutions Inc is seeking a candidate based in Raritan to support Business Separation activities for large global and regional GxP Computerized systems. Candidates should have over 10 years of relevant experience in the Pharmaceutical, biotechnology, or medical...Remote work
- ...established industry player is seeking a seasoned professional with over 8 years of experience in Computer System Validation and Quality Management in GxP applications. This role involves guiding project teams through the SDLC, applying FDA guidance, and interacting with...
- ...A leading technology organization in Raritan, New Jersey, seeks a skilled professional to document software and validate specifications for lab instrumentation. Key tasks include gathering requirements, creating infrastructure and data flow diagrams, and performing risk...
- ...We have a job opening for a full‑time Quality Specialist in our Edison, NJ location. The primary... ...documentation. Assist with future validations or revalidations of systems, equipment... ...With the possibility of a work-from-home hybrid model (in‑office part of the week and...Full timeTemporary workWork at officeLocal areaRemote workWork from home
- ...teams. Candidates with skills in project management and technical solution exploration are encouraged to apply. The position offers a hybrid working model, and we are committed to fostering an inclusive workplace where everyone can contribute their unique perspectives. #J...
$70k - $90k
A leading hearing aid company seeks a Quality Assurance Specialist for their Designated Complaint Unit. This hybrid role involves managing and resolving customer complaints, requiring proficiency in complaint handling processes and Microsoft Office tools. Ideal candidates...Work at office- Quality Assurance Specialist, Designated Complaint Unit (Americas) - Hybrid 5 days ago Be among the first 25 applicants WSA is a global leader in the hearing aid industry. Together with our 12,000 colleagues in 130 countries, we invite you to help unlock human potential...Work at officeLocal areaEarly shift
- ...experience. • Animal health GLP auditing experience. Job Title: Quality Specialist- II -Hybrid Job Location: Rahway NJ Duration: 2 years Provide QA... ...management Strong knowledge of FDA bioanalytical method validation guidance required Description SCOPE MEASURES This...
$36 - $43 per hour
...Quality Control Analyst Our client is seeking a detail-oriented Quality Control Analyst to support a portfolio of Energy Efficiency... ...This role is responsible for reviewing project documentation, validating data accuracy, identifying trends and exceptions, and ensuring...Hourly pay- Location: Raritan, New Jersey, 08869 | Work Type: Hybrid | Employment Type: Full-time Industry: Pharmaceuticals... ...Job Summary AAsys Technologies LLC is seeking a Quality/Validation Engineer with hands‑on expertise in GxP‑regulated environments and Computer System Validation...Full time
$106.2k - $167.2k
MSD Malaysia is seeking a qualified individual to join our R&D Quality Assurance Analytics & Tech Systems (AnTS) team in Rahway, New Jersey... ...management, working closely with stakeholders to build the GxP AI Framework. The successful candidate will engage in analytical...$106.2k - $167.2k
Merck & Co. is seeking a qualified individual to join their R&D Quality Assurance team. This role involves supporting AI governance and... ...systems management, collaborating with stakeholders to build a GxP AI Framework. The ideal candidate will possess a Master’s degree...$96.8k - $137k
...Piscataway – Colgate-Palmolive – Travel up to 10% of time – Hybrid No Relocation Assistance Offered. Job Number #173467 –... ...during peak traffic events. Perform backend and data quality testing, including API validation with Swagger/Postman and database verification with SQL...Hourly payLocal areaRelocation- Design, develop, test & implement s/w applications using Loadrunner, Fortify, Spinnaker, Locust, NeoLoad, JMeter, Jenkins, AWS, BlackDuck, Snowflake, Kubernetes, AppDynamics, Java, Informatica, Aurora and DB2. Must be willing to travel & relocate to unanticipated client...Relocation
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