QA Validation Specialist — GMP, IQ/OQ/PQ, On-site
Cibo Vita
Cibo Vita is seeking a QA Validation Associate to support validation protocols for equipment, processes, and cleaning cycles at our Totowa, NJ site. You will contribute to on-floor IQ/OQ/PQ trials, collect data, and ensure documentation integrity for regulatory audits. Ideal candidates have 1–3 years in quality/manufacturing in regulated environments, with GMP/HACCP understanding and strong technical writing abilities to communicate findings across cross-functional teams. #J-18808-Ljbffr Cibo Vita
- Job Description The QA Validation Associate supports the development... ...Practices (GMP) and ensuring our Totowa... ...Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ). Record raw data, observations... ...Lead. Maintain the site validation master file...WebsiteWork at officeShift workWeekend workDay shift
- ...pharmaceutical manufacturer. The role focuses on authoring and revising QA documentation and Master Batch Records to support sterile... ...on documentation standards, and ensuring compliance with FDA and GMP regulations using MS Office tools. #J-18808-Ljbffr Piper CompaniesWebsite
- ...Purpose." Job Summary : The QA Validation Supervisor oversees the development... ..., ensures compliance with GMP and industry regulations, and... ...validation trials, including IQ, OQ, and PQ activities. Ensure all... ...platforms. Working Conditions On‑site role in a food manufacturing...WebsiteShift work
$90k - $115k
...client in Fairfield, NJ is looking for a Validation Engineer for a Full time position.Pay is... ...bodies and standards (ISO13485, 21 CFR 820, GMP).Requirements:Requires a 4-yr engineering... .../ (GxP) industry is required.Validation (IQ,OQ,PQ) or PPAP (Production Part Approval...SuggestedFull time- ...Validation Consultant Client is seeking validation consultants to support... ...and identified gaps in the site's validation program. The primary... ...to assess whether existing IOQ/OQ documentation is robust enough, identify gaps between OQ and PQ, and determine whether current...Website
- ...QA SpecialistReporting to the AAA Site Remediation Lead, the AAA Remediation QA Specialist is responsible for GMP quality assurance oversight of remediation activities and the on-time execution... ...will be a strong focus on equipment validation, compliance, record backlog...WebsiteLocal area
- ...Job Description Job Description Validation Specialist Lynkx Staffing LLC specializes in placing talented professionals in the Biotechnology... ...and CSV protocols and preparing final reports for IQ, OQ and/or PQ of basic cell processing and QC lab equipment. The ideal...Work at officeFlexible hours
- Evermark is seeking a Quality Specialist focused on OTC validation at contract manufacturing sites. You will oversee validation programs to ensure products meet 21 CFR 210/211, OTC monographs, and MoCRA, maintaining a state of control. This full-time contract (1099) role...WebsiteRemote jobFull timeContract work
- ...Nature’s Garden snacks, seeks a Food Processing Machinery Specialist at our Madison, NJ site. This on-site, full-time role focuses on running and... ...Ideal candidates have 3+ years with manufacturing machinery, GMP/SOP proficiency, and knowledge of pasteurization processes...WebsiteFull timeShift work
$125k - $140k
...functional initiatives, drive strategic improvements, oversee process validations, implement continuous improvement strategies, and support... ...sterilization workflows.Lead large scale process validations (IQ/OQ/PQ), process characterization efforts, and statistical...WorldwideFlexible hours$86k - $120k
Quality Assurance Compliance Specialist, Qunol Location: Pine Brook, NJ You’ve built experience... ...experts ready to shape what’s next. As a QA Compliance Specialist, you’ll bring your... ...team, our 13 best-in-class manufacturing sites and 4 specialized science and innovation...WebsiteWork at officeWorldwide$116k - $159.5k
...Newark, CA, and will be an on-site role. In this role, you will have... ...requirements, verification/validation planning and execution, first... ...management plan, quality control plan, IQ/OQ/PQ/PV protocols and reports to... ...of ISO 13485, 21 CFR 820, and GMP requirements.Proven experience...WebsiteFull timeImmediate startFlexible hours$90k - $115k
...and proficiency in the Quality Assurance Specialist II role Candidate should demonstrate knowledge... ...CooperSurgical for this position and a valid agreement with CooperSurgical is in place... ...to maintain cross functional, and cross site processes and procedural consistency for...WebsiteWork at office$115k - $135k
...leadership in development, optimization, validation, and design transfer of medical device... ...large scale process validations strategies (IQ/OQ/PQ), process characterization efforts, and... ...with others in and across departments/sites and external contacts (suppliers, test laboratories...WebsiteInternshipWork at officeWorldwideHome officeFlexible hours$120k - $145k
...portfolios. This role drives the development, validation, commercialization, lifecycle management... ...product platforms and manufacturing sites.Lead packaging component specifications,... ...strategies and protocols including: IQ, OQ, PQ, Process validation, Packaging validation...WebsiteWork at officeWorldwideFlexible hours- ...Manager Quality Assurance Validation Computerization Systems... ...in the review and QA approval of system validation... ...Part 11, GAMP5, and EU GMP Annex 11 requirements... ...Design Specifications, IQ, OQ, PQ, Traceability Matrix,... ...Participate in supplier site Validation Assessments/...WebsiteFor contractorsWork at office
- ...tubing length that is greater than 1 meter.Alarm Criticality (Process Engineer) – Identify response and criticality of equipment across site and potential impact to the product. The frequency at which alarms are assessed should be based on their criticality. Equipment to...Website
- ...We are excited to announce our Quality Assurance Specialist opening! The Quality Assurance Specialist will provide... ...and continuity of standards of operation. The QA Specialist will conduct internal audits at all sites and generate audit reports with the findings, collaborate...WebsiteWork at officeLocal areaMonday to FridayFlexible hours
- Piper Companies is seeking an experienced GMP Manufacturing Documentation Specialist to support sterile injectable technology transfer programs in Ridgefield, New Jersey. The role focuses on authoring, revising, coordinating, and driving approval of GMP manufacturing documentation...Website
- 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...
- ...jobs directly through our career's website (Careers - Smiths Group plc)By clicking the link above or any third-party link within this posting, you are leaving this site and going to a third-party website where the third-party website's terms and privacy policy apply...Website
- Piper Companies is seeking two GMP Manufacturing Documentation Consultants to join a 12-month, on-site engagement in Ridgefield, NJ. The role centers on authoring and maintaining Master Batch Records (MBRs) and other GMP documentation for a sterile injectable program. Ideal...WebsiteMonday to Friday
- Quality Assurance Associate III - 244917 Responsibilities On-site role providing QA oversight for manufacturing operations. Review and approve... .... Audit and approve pre-/post-executed batch records, validation reports, and product/label specifications in compliance with...WebsiteFull timeWork at officeFlexible hours
$118.1k - $200.76k
...execution. The ideal candidate possesses the analytical skills to identify data trends and the manufacturing engineering expertise to go on-site at suppliers and implement solutions such as process automation, tooling/fixturing improvements, and control plans.Responsibilities:...WebsiteFull timeLocal areaFlexible hours$18 - $22 per hour
...compliance with company quality standards, GMP, HACCP, SQF (or equivalent), and all regulatory... ...quality-related KPIs and report trends to site leadership and HQ Quality. Drive... ...At least 2+ years in a lead or supervisory QA role. ~ Strong ability to communicate in...WebsiteHourly payWork at officeMonday to Friday- Cibo Vita in Totowa, NJ, is seeking a QA Validation Supervisor to oversee the validation activities ensuring compliance with quality standards. This role involves leading cross-functional teams, managing timelines, and ensuring documentation is audit-ready. The ideal candidate...
- ...Quality Assurance Compliance Specialist Allendale, NJ Lynkx... ..., qualification and validation reports, QC data. Supports... ...years’ + experience in QA in a life sciences... ...Manufacturing Practices (GMP), Good Documentation Practices... ...available. No on-site cafeteria available....WebsiteNight shift
- ...experienced Facility Manager to lead multi-site facility, utility, and maintenance... ...predictive maintenance, support audits and validations, manage vendors and capital projects, and... ..., ISO 13485, ISO 9001, OSHA, CMMS, and IQ/OQ/PQ processes Proven leadership, vendor management...Website
- ...requirements. The candidate should have a Bachelor's degree in a scientific discipline or relevant experience, strong understanding of GMP and GLP, and at least one year of experience in the beauty or CPG industry. The role involves routine analytical testing and...Website
- Job-ID32818011Reference26-01397 Job Description: We are seeking an experienced Process Validation Engineer to support new pharmaceutical manufacturing projects within a sterile GMP environment. This role will focus on process validation, technology transfer, and qualification...
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