Documentation Specialist - Change Control Collins Consulting IncDocumentation Specialist - Change ControlBranchburg, NJWork with Change Control, Quality Investigations /CAPA team members, and other cross functional managers/supervisors and development engineers/teams to ensure that controlled documents being revised contain the correct information/parameters per process/product specifications. Participates in project team meetings, working collaboratively with project team members from Manufacturing, Engineering, Process Development, Quality, and other subject-matter experts to develop document content.
Software Controls Engineer ClarapathSoftware Controls EngineerHawthorne, NY$120,000–$160,000 / yearWe are seeking a hands-on engineer who enjoys solving complex automation and motion control challenges, thrives in a collaborative and fast-paced environment, and is passionate about developing innovative medical device and robotics technologies that improve laboratory workflows and patient outcomes. Working closely with mechanical, electrical, software, manufacturing, quality, and customer-facing teams, the Software Controls Engineer will develop reliable, scalable, and maintainable control software that meets performance, safety, and regulatory requirements.
Quality Supervisor Perrigo Company CorporateQuality SupervisorBronx, NYResponsibilities include providing real-time quality support, maintaining quality systems, reviewing and approving quality documentation, supporting investigations, and assisting with audits and inspections to ensure product quality and regulatory compliance. The QA Supervisor is responsible for leading a team of Quality Assurance Inspectors that provides quality oversight for bulk manufacturing, filling, and packaging operations involved in the production of topical and suppository pharmaceutical products.
MTA Quality Manager Sre Engineering DpcMTA Quality ManagerNew York, New YorkEssential Functions Perform QA reviews of submittals in accordance with project procedures and compliance; Work with Project Managers, Resident Engineers, and Quality Managers to assist with performance monitoring and records maintenance of all project reviews and QA/QC reviews; Create and maintain project audit schedule and perform all quality audits; Issue corrective actions and monitor compliance and identify areas of improvement through ongoing QA process; Monitor the effectiveness of the Company, owner, and contractor QA/QC programs and provide training and awareness activities as needed to support continuous quality improvement initiatives; Attend and participate in project meetings, chair project quality meetings, and assist with project management as needed; Implements and follows Company and project safety protocols; All related duties as assigned. BS Degree in Engineering or a related field is strongly preferred; HS Diploma/Equivalent required; Applicable ASQ certification(s) preferred; Ability to understand and interpret written specifications, plans, and construction documents for work orders and build documents; Ability to effectively and tactfully communicate with clients, supervisors, and inspectors; Detail-oriented, with decision making capability to identify non-conformance; A valid, clean driver’s license and personal vehicle to travel to job sites is preferred.
Software Controls Engineer Clarapath, Inc.Software Controls EngineerHawthorne, NY$120,000–$160,000 / yearWe are seeking a hands-on engineer who enjoys solving complex automation and motion control challenges, thrives in a collaborative and fast-paced environment, and is passionate about developing innovative medical device and robotics technologies that improve laboratory workflows and patient outcomes. Role Summary: The Software Controls Engineer will play a key role in the design, development, implementation, and continuous improvement of the control systems and embedded software that power Clarapath's advanced SectionStar and TrimStar Pro platforms.
Global Head, Vaccine Chemistry, Manufacturing and Controls (CMC), Center for Vaccine Innovation and Access (CVIA) PATHGlobal Head, Vaccine Chemistry, Manufacturing and Controls (CMC), Center for Vaccine Innovation and Access (CVIA)New York, NY$320,000–$380,000 / yearProvide strategic and technical guidance to CMC team members on project teams on process development, product analytics, formulation and fill, final manufacturing process and facility design and needs, and quality control thereof, investigational product supply and stability, as well as in vivo and in vitro safety and toxicity testing performed before and during the clinical development to demonstrate non-clinical safety and tolerability of candidate vaccine products. The Global Head of CMC is a member of the CVIA leadership team (CVIA LT) and is responsible for CVIA-wide business plan creation and implementation, change initiative leadership, talent management, and proactive partnership in developing comprehensive cross-disciplinary tactics and enabling exceptional execution through cross-functional collaboration.
AVP Business Risk & Control, Reporting & Governance Madison-DavisAVP Business Risk & Control, Reporting & GovernanceNew York, NY$97,000–$160,000 / yearThis AVP-level opportunity sits within a centralized first-line control function at a leading global financial institution, serving as a key member of a growing Business Risk & Control team responsible for delivering high-quality risk and control reporting, governance coordination, and non-financial risk program execution across the firm. It's an excellent fit for candidates coming out of risk reporting, operational risk, governance, controls, audit, or PMO functions within banking who are ready to take on meaningful ownership in a lean, high-visibility team environment.
Document Control Assistant - 2Nd Shift Amneal Pharmaceuticals, Inc.Document Control Assistant - 2Nd ShiftPiscataway, NJThe Specialist will work in a pharmaceutical production facility and in close collaboration with Quality Assurance, Quality Control and Production with a key-focus on documentation accuracy, quality and integrity. Maintaining lists and postings required for both electronic and hard copy; maintain specific databases in Document Control Department and training records.
Document Control Assistant - 2nd Shift Amneal Pharmaceuticals IncDocument Control Assistant - 2nd ShiftPiscataway, NJ$20–$25 / hourThe Specialist will work in a pharmaceutical production facility and in close collaboration with Quality Assurance, Quality Control and Production with a key-focus on documentation accuracy, quality and integrity. Maintaining lists and postings required for both electronic and hard copy; maintain specific databases in Document Control Department and training records.
Wallboard Quality Sample Temp Veterans Sourcing GroupWallboard Quality Sample TempBuchanan, NYMust be willing to wear required PPE, including hard hat, hearing protection, safety glasses, high-visibility vest, safety boots, and cut-resistant gloves when required. Following training, the employee may remain on the day shift or transition to an evening schedule beginning around 3:00 PM or later depending on production coverage requirements.
Quality Engineer GpacQuality EngineerNew York, NY90000–130000You will work closely with the Launch Engineer and interface with site customer quality engineering, product engineering, and manufacturing staff to develop and execute the quality control system. GPAC (Growing People and Companies) is an award-winning search firm specializing in placing quality professionals within multiple industries across the United States since 1990.
NewQuality Analyst Macpower Digital Assets Edge Private LimitedQuality AnalystNew York, NY$112,000 / yearThe ideal candidates should have at least 4+ years of experience in QA methodologies and validations to ensure quality control, 4+ years of expertise with Selenium WebDriver using the TestNG Java framework, and 4+ years of experience testing Middleware technologies' web services (SOAP, REST) with SOAPUI. Job Summary: We are seeking Quality Analyst for Onsite Assignments in New York, NY to support the State of New York's Department of Social Services (DSS) in various critical IT initiatives.
NewSenior Quality Specialist Katalyst Healthcares & Life SciencesSenior Quality SpecialistParsippany, NJTrack audit findings for suppliers to completion and ensure timely closure of audit reports and ensure adequate CAPAs are developed by external manufacturers, suppliers and monitor their closures. Lead the scheduling, execution, reporting and tracking of onsite audits of external manufacturers and suppliers to confirm that these operations are performed in compliance with EH's Global QMS and meet all relevant regulatory requirements.
Supplier Quality Engineer II The Cooper Companies IncSupplier Quality Engineer IILivingston, NJ$80,000–$100,000 / yearAll resumes submitted by search firms/employment agencies to any employee at CooperSurgical via-email, the internet or in any form and/or method will be deemed the sole property of CooperSurgical, unless such search firms/employment agencies were engaged by CooperSurgical for this position and a valid agreement with CooperSurgical is in place. Act as a quality assurance consultant in the development and implementation of quality systems in compliance with FDA QSR, ISO 13485, MDD and CMDCAS and other relevant requirements at partner suppliers/vendors in order to support operations and development engineering.
Quality Engineer Smiths Group PlcQuality EngineerElmwood Park, NJThe ideal candidate is hands-on, technically strong, and comfortable working directly with machinists, inspectors, manufacturing engineering, programming, production, purchasing, and quality leadership to identify process risks, investigate nonconformances, develop corrective actions, and implement practical solutions on the shop floor. In addition to strong computer skills, the candidate should have practical knowledge of CNC machining processes, inspection methods, GD&T, blueprint interpretation, gage usage, material traceability, root cause analysis, corrective action, and quality system requirements in a regulated manufacturing environment.
Senior Engineer - Protection & Control AtkinsRealisSenior Engineer - Protection & ControlEdison, NJ$110,000–$150,000 / yearNote to staffing and direct hire agencies: In the event a recruiter or agency who is not on our preferred supplier list submits a resume/candidate to anyone in the company, AtkinsRéalis family of companies, we explicitly reserve the right to recruit and hire the candidate(s) at our discretion and without any financial obligation to the recruiter or agency. The Protection & Controls Engineer reports to our Protection & Controls Technical Manager and requires working independently on fast paced technically complex design projects.
Senior Quality Specialist External Manufacturing and Supplier Management Sunrise Systems IncSenior Quality Specialist External Manufacturing and Supplier ManagementParsippany, NJ$35–$45 / hourTrack audit findings for suppliers to completion and ensure timely closure of audit reports and ensure adequate CAPAs are developed by external manufacturers, suppliers and monitor their closures. Lead the scheduling, execution, reporting and tracking of onsite audits of external manufacturers and suppliers to confirm that these operations are performed in compliance with EH's Global QMS and meet all relevant regulatory requirements.
Senior Engineer - Protection & Control AtkinsRealis Group IncSenior Engineer - Protection & ControlNew York, NY$110,000–$150,000 / yearNote to staffing and direct hire agencies: In the event a recruiter or agency who is not on our preferred supplier list submits a resume/candidate to anyone in the company, AtkinsRéalis family of companies, we explicitly reserve the right to recruit and hire the candidate(s) at our discretion and without any financial obligation to the recruiter or agency. The Protection & Controls Engineer reports to our Protection & Controls Technical Manager and requires working independently on fast paced technically complex design projects.
Vice President, Project Controls WSP Global IncVice President, Project ControlsNY$180,000–$240,000 / yearAny unsolicited resumes, including those submitted to hiring managers or other business leaders, will become the property of WSP and WSP will have the right to hire that candidate without reservation - no fee or other compensation will be owed or paid to the recruiter, employment agency, or other staffing service. WSP USA is providing the compensation range that the company in good faith believes it might pay and/or offer for this position within the state of Colorado, based on the successful applicant's education, experience, knowledge, skills, and abilities in addition to internal equity and specific geographic location.
Data Center Portfolio Controls Strategy Lead Oracle CorpData Center Portfolio Controls Strategy LeadNY$102,300–$209,500 / yearWorking cross-functionally with PMO Integration, E2E Program, Finance, Site Project Controls, Construction, Design, Commissioning, Operations, and Reporting Automation teams, this position drives consistency in how portfolio performance is measured, communicated, and acted upon. Reporting within the Chief of Staff (CoS) Portfolio Governance organization, this role provides leadership visibility into portfolio health by connecting cost performance, schedule execution, delivery risk, milestone attainment, and business outcomes.