Manager, Workforce Planning & Controlling Amer Sports CorpManager, Workforce Planning & ControllingNew York, NY$125,000–$145,000 / yearCoordinate and align workforce planning communities by translating planning targets and assumptions into clear direction for planners, influencing local finance controllers and stakeholders without direct authority, and proactively identifying risks and misalignments before they impact delivery. Manage each cycle as a structured project with clearly defined milestones, owners, dependencies, and deliverables, while ensuring HR and Finance planners stay aligned with timelines across all Brands, Regions, and Group Functions.
Senior Mechanical Controls Engineer - Mission Critical DLR GroupSenior Mechanical Controls Engineer - Mission CriticalNew York, NY$84,700–$144,430 / yearLead multiple projects and staff over multiple regions to assure local teams of engineers know the specific design criteria of projects and train engineering teams on design of control systems. As part of the engineering team at DLR Group you will be responsible for the design of control systems from schematics through construction administration for buildings across a variety of sectors including Higher Education, Culture & Performing Arts, Healthcare, K-12, Justice/Civic, Mission Critical, and Energy.
NewSenior Sales Associate, HVAC Controls Carrier CorporationSenior Sales Associate, HVAC ControlsClifton, NJ$79,000–$158,000 / yearAt Automated Logic, we've been developing and supporting intelligent building solutions that have helped customers, including small businesses to Fortune 500 corporations, operate their buildings more efficiently for over 40 years. Through cutting-edge advancements in climate solutions such as temperature control, air quality and transportation, we improve lives, empower critical industries and ensure safe transport of food, lifesaving medicines and more.
Project Controls Specialist - Document - 90414045 - New York (New York, NY, US, 10119) AmtrakProject Controls Specialist - Document - 90414045 - New York (New York, NY, US, 10119)New York, NY$78,600–$101,844 / hourOur values of ‘Do the Right Thing, Excel Together and Put Customers First’ are at the heart of what matters most to us, and our Core Capabilities, ‘Building Trust, Accountability, Effective Communication, Customer Focus, and Proactive Safety & Security’ are what every employee needs to know and do to be most impactful at Amtrak. In accordance with DOT regulations (49 CFR § 40.25), Amtrak is required to obtain prior drug and alcohol testing records for applicants/employees intending to perform safety-sensitive duties for covered Department of Transportation positions.
NewSenior Sales Associate, Hvac Controls Carrier CorporationSenior Sales Associate, Hvac ControlsNew York, NY$79,000–$158,000 / yearAt Automated Logic, we've been developing and supporting intelligent building solutions that have helped customers, including small businesses to Fortune 500 corporations, operate their buildings more efficiently for over 40 years. Through cutting-edge advancements in climate solutions such as temperature control, air quality and transportation, we improve lives, empower critical industries and ensure safe transport of food, lifesaving medicines and more.
Associate Director - Project Controls (Life Sciences) Turner & Townsend LtdAssociate Director - Project Controls (Life Sciences)NYAny unsolicited resumes/CVs submitted through our website or to Turner & Townsend personal e-mail accounts, are considered property of Turner & Townsend and are not subject to payment of agency fees. Turner & Townsend are seeking an experienced Associate Director- Project Controls to join our team and lead the delivery of a multi-billion dollar pharmaceutical project.
Project Controls Specialist Cushman & WakefieldProject Controls SpecialistChatham, New JerseyIn addition to a comprehensive benefits package, Cushman and Wakefield provide eligible employees with competitive pay, which may vary depending on eligibility factors such as geographic location, date of hire, total hours worked, job type, business line, and applicability of collective bargaining agreements. The Project Controls & Data Governance Specialist is responsible for establishing and maintaining centralized project controls and robust data governance frameworks across client’s global real estate and workplace portfolio in accordance with either C&W’ delivery process, the client’s delivery process, or both.
Senior Quality Engineer QUANTUM COMPUTING, INC.Senior Quality EngineerHoboken, NJThe Company’s portfolio of core technology and products offer unique capabilities in the areas of high-performance computing, artificial intelligence, cyber security as well as remote sensing applications. The Senior Quality Engineer (SQE) develops and maintains quality control plans to ensure the products meet required internal or external specifications.
QA R&D Chemist I Tris Pharma IncQA R&D Chemist IMonmouth Junction, NJ$85,000–$95,000 / yearPerforms testing of raw materials, packaging components, IP, FP and/or ST samples including dissolution, assay, related compounds analysis, content/blend uniformity, particle size distribution by Malvern/Sieve, bulk and Tap density, cleaning validation and other tests according to the analytical methods, United States Pharmacopeia (USP) procedures in a regulated laboratory environment. Operates general analytical instruments during raw material, IP and FP testing such as High Pressure Liquid Chromatography (HPLC), UltraPerformance Liquid Chromatography (UPLC), Gas Chromatography (GC), Ultra Violet visible spectroscopy (UV/Vis), automatic titration, Infra-Red Spectroscopy (IR), Malvern Mastersizer, Thin Layer Chromatography (TLC) and dissolution apparatus (Distek).
Quality Assurance Documentation Lead Tris PharmaQuality Assurance Documentation LeadMonmouth Junction, NJ$77,522–$101,750 / yearAlso req's skills (3 yrs) in: current working knowledge of cGMPs in the pharmaceutical industry; maintaining Quality documentation, compliant w/ quality policies, practices, SOPs and cGMPs; quality documentation systems and control tools (MasterControl packet process and Management of Change process), incl supporting MasterControl systems on doc change requests - DCR Packet (PKT), Specifications, Test Methods, Stability Protocol, and Master Batch Records (SPTM); day-to-day operation incl issuance, archival and reconciliation of GxP physical records; MS Office; working in fast paced, matrixed, team env of internal and external team members, and (2 yrs) in: collecting and compiling relevant data for APR presentation and report summary for resin-based extended-release tablets/powder/oral suspension products and collaborating with various depts and SMEs to ensure APR sub-reports are submitted and (1 yr) in: stability chambers chart recorders, calibration and preventive maintenance (PM) stickers; notifying QA Stability Mgmt of errors or discrepancies; SLIM database to perform various research and routine tasks and assisting in daily pulling samples from stability database and stability chambers; transferring stability samples to appropriate dept; daily filing of stability change of custody records; issuing stability request forms and labels; assisting with loading new stability samples into chambers; ensuring APR schedule and timeline are followed. Utilize SLIM DB for research and routine tasks; perform daily stability sample pulls (controlled & non-controlled), transfers to appropriate depts, filing of chain-of-custody records, issuance of stability requests and labels, loading of new samples into chambers, and documentation of activities.
Sr. Specialist, Quality Assurance RevanceSr. Specialist, Quality AssuranceNewark, New JerseyProvide quality oversight for Facilities/Utility System/Equipment (FUSE) Qualification, Analytical Instrument Qualification (AIQ) and Computerized Systems Validation/Assurance(CSV/CSA) and applies risk-based methodology to validation/qualification efforts in accordance with current regulatory requirements and industry guidance. Provides quality oversight of steady state activities (System Audit Trail Reviews, User Account Maintenance, Periodic Reviews) and quality records (deviations, CAPAs, and changes controls) for GxP Facilities, Utilities, Equipment, Analytical.
Quality Assurance Technician III TiltEdge Solutions LLCQuality Assurance Technician IIIParsippany, NJ$35Position: Quality Assurance Technician III Work Location: Parsippany, NJ 07054 Pay rate: $35.00/hr Duration: 3+ Months role with high chances of extension/conversion Shift: 7:00 am - 4:00 pm Job Description: Responsible for claim evaluations and conducts various testing activities and analysis on sample material. Experience navigating quality control, analytical testing, or product development within the roofing or construction materials sector is highly desirable.
Sr. Quality Manager DC Enterprises (iLABS Inc. and Affiliated Companies:)Sr. Quality ManagerMahwah, NJQuality Manager leads Quality Assurance, Quality Control, and Microbiology for cosmetics, OTC drugs, dietary supplements, partnering with internal teams, external stakeholders and other third-party partners to ensure product quality, compliance, and continuous improvement. Experience with FDA inspections, ISO audits, and third-party audits, demonstrated success in investigations, CAPA Management, change control, validation, supplier quality, laboratory controls, product disposition, risk-based quality systems, and continuous improvement initiatives.
Sr. Director Of Quality Operations Harrow, Inc.Sr. Director Of Quality OperationsLedgewood, NJStrong computer skills in Microsoft Office Suite, database management, and documentation preparation (Word, PowerPoint, Excel, and others must be able to learn additional software and programs, as required). Provide leadership over investigations into out-of-specification analytical results and deviations during compounding activities to determine root cause and identify CAPAs to prevent recurrences.
Document Control Analyst Exp Global IncDocument Control AnalystNew York, NY$50,000–$80,000 / yearHere, you join a team that leverages differences, harnesses their entrepreneurial spirit in an employee-owned company, that believes diversity is what gives us strength, seeks sustainable results and shares ambitions for each other, our clients and the communities we are part of and serve. We are an entrepreneurial, multidisciplinary firm of approximately 5,000 professionals across North America with a history of successfully delivering some of the most complex infrastructure projects across North America.
Quality Assurance Officer Operations Novartis AGQuality Assurance Officer OperationsEast Hanover, NJ$30,200–$56,000 / yearContribute in maintaining the local quality system as per GMPs and corporate guidelines and in assuring the respect of the GMPs and Health Authorities requirements at local levelSupport the QP in the preparation of batches release documentsCollaborate in redaction of site GMP documentation and preparation and printing of batch documentationCollaboration in data compilation of Product Reviews, oversight on investigations and monitoring of resulting actions are checked and approved. Major accountabilities: Supervise the general conditions of hygiene of the premises subject to its managementContribute in assuring the validation/qualification status of the production site, equipment, training of personnel and management of quality documentationResponsible for the provisional release for the shipment of batchesWork in shift with other QA officers to oversight the production and quality control activities.
Director, GTS Quality Systems BeOne Medicines AGDirector, GTS Quality SystemsHopewell, NJ$172,500–$232,500 / yearThis role will be primarily GTS-facing, with accountability for translating Quality business needs and QMS process requirements into technology execution plans, managing application operations, coordinating project delivery, overseeing vendors and managed service partners, and ensuring reliable, compliant, and scalable Quality technology solutions. Director, Quality Systems and Validation and serve as a Global Technology Solutions leader responsible for the technology operations, deployment, and lifecycle support of enterprise Quality Management System (QMS) platforms, Veeva Quality applications, other Quality Assurance systems, and related GxP applications.
Senior Manager, Quality Systems Supergoop!Senior Manager, Quality SystemsNew York, NY$125,000–$150,000 / yearThis role will partner cross-functionally with Innovation (Product Development and Packaging), Regulatory, Operations, Supply Chain, and external manufacturing partners to embed quality at every stage from formula development to finished goods release. Supergoop! is seeking a strategic and hands-on Senior Manager, Quality Systems to build, implement, and lead a robust, scalable Quality Management System (QMS) across our product lifecycle.
NewPrincipal Supplier Quality Engineer The Cooper Companies IncPrincipal Supplier Quality EngineerLivingston, NJ$120,000–$160,000 / yearThe Principal Supplier Quality Engineer drives quality excellence across the product lifecycle and partners with Engineering, Operations, Procurement, Regulatory Affairs, R&D, Manufacturing, and business leadership to ensure supplier processes and product quality meet regulatory, customer, and business requirements. Scope: The Principal Supplier Quality Engineer serves as the highest-level technical authority within Supplier Quality Engineering and provides enterprise-wide leadership for supplier quality strategy, technical risk management, product realization, and supplier compliance activities.
Deputy Director Of DS Manufacturing Quality Systems SanofiDeputy Director Of DS Manufacturing Quality SystemsPearl River, NY$113.25–$163.58 / hourAs Deputy Director, Drug Substance (DS) Manufacturing Quality Systems at our Pearl River site, you'll lead and develop a broad Quality Systems organization - spanning Principal Investigators, Technical Writers, and Quality Systems Support Associates - responsible for the full lifecycle of manufacturing quality records: deviation investigations, CAPAs, effectiveness checks, periodic reviews, and QMS document updates. Lead and develop an agile Quality Systems team - including Principal Investigators, Technical Writers, and Quality Systems Support Associates - coordinating work assignments to meet fluctuating business needs while sustaining a strong learning and development culture.