NewBAS Systems Specialist JobotBAS Systems SpecialistWorcester, MA$35–$50 / hourInformation collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. This role will work closely with project managers, engineers, and customers to deliver high-quality HVAC controls and systems integration solutions across a variety of commercial and institutional facilities.
Accounting Specialist Kforce Inc.Accounting SpecialistAttleboro, MA$60,000–$65,000Kforce's client, a growing organization located in the Attleboro, MA area, is seeking a detail-oriented Accounting Specialist to support invoicing, reporting, and account maintenance functions. Employee pay is based on factors like relevant education, qualifications, certifications, experience, skills, seniority, location, performance, union contract and business needs.
NewContracts and Compliance Specialist GCR Professional ServicesContracts and Compliance SpecialistAyer, Massachusetts$98,000–$100,000 / yearThe Contracts & Compliance Specialist will manage the full lifecycle of government and commercial contracts while ensuring compliance with FAR, DFARS, ITAR, and other applicable regulations. This role is critical to minimizing risk, maintaining contractual integrity, and supporting operations within a highly regulated environment.
Equipment Specialist, Senior - Secret DCS CorporationEquipment Specialist, Senior - SecretBedford, MA$90,220–$130,000 / yearSupport configuration control by processing, tracking, and recommending dispositions for change notices, ecps, deviation/waiver requests, service bulletins, deficiency reports, Airworthiness Directive Notes, and qcps. Provide integrated logistics support, including provisioning, source coding, maintenance data collection, configuration management data, QDR analysis, and identifying alternate sources of supply for DMS/MS issues.
Electronic Documentations Specialist BC ForwardElectronic Documentations SpecialistDevens, MA$30.82–$33.82 / hourFull timeThe ideal candidate will have strong experience in GxP/GMP documentation systems, electronic document control, and Microsoft Office and a proven ability to administer controlled documents, ensure compliance, and drive clear, concise documentation . TSR is a trusted staffing and workforce solutions partner with more than 50 years of experience delivery highly qualified talent to support clients' most critical business and technology initiatives.
NewElectronic Documentations Specialist Sunrise Systems IncElectronic Documentations SpecialistMADescription: Summary: This opportunity will support the documentation control and management of the CSO functional areas by coordinating activities related to GxP/GMP documentation system and administrating associated controlled documents and their processes to ensure compliance. Demonstrate excellence in writing clear, good grammar and punctuation practices as well as attention to detail with concise business-related documents.
Credit Quality Analyst (Loan Documentation Specialist) - Waltham, MA Canon Recruiting GroupCredit Quality Analyst (Loan Documentation Specialist) - Waltham, MAWaltham, MAThe Document Administrator works with various business partners (clients, sales, credit underwriting, legal, and operations) to collect, review, and complete due diligence such as Insurance, UCC, Good Standing, Title, Collateral, etc. to ensure the loan documentation package is prepared correctly and ready to close on time for the client. Works closely with Client Managers, Credit and Portfolio Officers, Agency Management, internal and external legal counsel, and many internal operational support units to ensure seamless execution of transactions.
NewClinical Documentation Specialist Integrated Resources, IncClinical Documentation SpecialistLexington, MassachusettsContractorJob DescriptionPosition Details:Client Direct ClientLocation Lexington, MAJob Title Clinical Documentation SpecialistDuration 10+ MonthsMust have skill-set Clinical Documentation Specialist is responsible for QC Review of pre-study and study documents, coding of administrative and regulatory documents, verification of documentation, maintenance of document tracking system, collaborating with CTM to determine to issues in regulatory documentation, and creates study specific document checklists in collaboration with the CTM and medical research. Clinical Documentation SpecialistA Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms.
RN Clinical Documentation Specialist - Ensemble Health Partners Day Kimball Healthcare IncRN Clinical Documentation Specialist - Ensemble Health PartnersCTExperience We Love: Minimum of five years acute care nursing experience with specific medical/surgical, Intensive Care, or Emergency Department experience Excellent interpersonal skills including excellent verbal and written communication skills; proficient in and demonstrate excellent physician relations Ability to organize and present information clearly and concisely; excellent computer and keyboarding skills; high degree of prioritization skills. Job Responsibilities: Completes initial patient medical record review within 24-48 hours of patient's admission; completes subsequent reviews of patient's medical record reviews every 24-48 hours and enters review findings in CDE software system Assigns Principal diagnosis, CC/MCC (complication and comorbidity/major complication and comorbidity), evaluate for Severity of Illness (SOI) and Risk of Mortality (ROM) on all patients while in-house.
NewSr Quality Assurance Documentation Specialist Candel Therapeutics IncSr Quality Assurance Documentation SpecialistNeedham, MA$88,000–$100,000 / yearEssential Areas of Responsibility: Administers Document Management Program and provides support to end users for the creation, revision, and retirement of documents including: Reviews GxP documents and records for completeness and compliance with internal procedures and applicable regulations and ensures ALCOA++ principles are followed to ensure data robustness. Administers the Training Management Program and provides support to end users for the maintenance of training activities including: Maintains user roles, training curricula, and training assignments.
RN Clinical Documentation Specialist - Referrals Ensemble Health PartnersRN Clinical Documentation Specialist - ReferralsCTEducates key healthcare providers such as physicians, nurse practitioners, allied health professionals, nursing and care coordination regarding clinical documentation improvement, documentation guidelines and the need for accurate and complete documentation in the health record. Works collaboratively with co-works and management to effectively resolve root cause issues that impact payor contracts, hospital operations, or departmental to maintain reimbursement and minimize appeal requests and/or denials.
Oasis, Coding and Quality Documentation Specialist Emerson HospitalOasis, Coding and Quality Documentation SpecialistConcord, MA$36.75–$47.82 / hourThis role focuses on data integrity, workflow efficiency, and the precise application of coding guidelines to support the agency"s financial and regulatory health. Home Care Clinical Specialist-OASIS (HCS-O), or Certification of OASIS Specialist-Clinical (COS-C) required.
Sr Quality Assurance Documentation Specialist Candel TherapeuticsSr Quality Assurance Documentation SpecialistNeedham, MAFull timeAdministers Document Management Program and provides support to end users for the creation, revision, and retirement of documents including: Reviews GxP documents and records for completeness and compliance with internal procedures and applicable regulations and ensures ALCOA++ principles are followed to ensure data robustness. Administers the Training Management Program and provides support to end users for the maintenance of training activities including: Maintains user roles, training curricula, and training assignments.
Document Control, Senior Specialist Lantheus Holdings IncDocument Control, Senior SpecialistBedford, MA$111,000–$185,000 / yearThe position serves as a key business partner to corporate and site functions in maintaining document lifecycle controls within the electronic document management system (eDMS), TrackWise Digital, supporting inspection readiness, driving document management process improvements, and ensuring the integrity, accessibility, and compliance of controlled quality documentation. Support internal audits, external audits, customer audits, and regulatory inspections by providing requested controlled documents, document history, and evidence of document control compliance.
Document Control Specialist Spirax Group plcDocument Control SpecialistMAYou will work closely with internal stakeholders across Quality, Manufacturing, Engineering, Supply Chain, and Operations, partnering regularly with subject‑matter experts and document owners to ensure documentation and training accurately reflect site processes and quality expectations. Watson-Marlow Fluid Technology Solutions is part of Spirax Group, a FTSE100 and FTSE4Good multi-national industrial engineering Group with expertise in the control and management of steam, electric thermal solutions, peristaltic pumping and associated fluid technologies.
Document Control Specialist, Quality The Steely GroupDocument Control Specialist, QualityBedford, MAThis role will work closely with members of the Document Control team and support routine daily operations for Document Management. This position will primarily be responsible for the processing and maintaining of GxP documents throughout their lifecycle with a focus on issuance and reconciliation.
Electronic Document Control Specialist - GMP SOKOL GxP ServicesElectronic Document Control Specialist - GMPDevens, MA$64,064–$70,304The Electronic Document Control Specialist will support Manufacturing Engineering by formatting, editing, uploading, routing, and tracking controlled documents through the Veeva document-management system. Experience supporting GMP, GxP, medical device, clinical-trial, or other regulated-product documentation.
NewQuality Assurance (QA) Document Control Specialist II Collins Consulting, IncQuality Assurance (QA) Document Control Specialist IIWorcester, MassachusettsFull timeUnder direct supervision, perform day-to-day Document Control activities: Process DCR packages and review for correctness and completeness; monitor and update in-process documents; create, assign and archive QA controlled lab notebooks and logbooks; assist in managing the electronic document management system; assist in managing access to Master Documents in the Document Control Vault; and create reports. Proficient with computers and word processing software (i.e. Microsoft Office products).High school diploma with 2 + years of general document control experience.
Risk Assessment / Technical Document Specialist LancesoftRisk Assessment / Technical Document SpecialistLexington, MA$92This contractor role is responsible for modernizing technical system documentation across Quality Control Lab Systems and performing structured data integrity risk assessments to enable risk-based optimization of procedural controls. Apply the client global Quality Risk Management (QRM) / ICH Q9 principles to evaluate data integrity controls such as audit trail review, backup/restore verification, and user access management.
Senior Document Control Specialist Actalent IncSenior Document Control SpecialistMilford, MA$20–$24 / hourStrong attention to detail and self-checking skills The job requires a minimum of a associate degree in the sciences or equivalent and at least 1-3 years' experience in documentation systems preferable in an FDA regulated industry. This includes the retrieving of quality documents/records/trend data and any other documentation requested during these inspections • Assist in continuous improvement initiatives.
Risk Assessment /Technical Document Specialist US Data Management LLCRisk Assessment /Technical Document SpecialistLexington, MAThe Risk Assessment/Technical Document Specialist serves as a subject matter expert across both IT systems and data integrity for a Takeda quality control lab systems engagement, ensuring solutions are compliant, inspection ready, and operationally efficient. Unless reasonable accommodations can be made, while performing this job the consultant shall: Work onsite at the Lexington, MA facility a minimum of 3 days per week, with 4 to 5 days during onboarding and as needed for workshops, risk assessments, and stakeholder engagement.
NewClinical Document Management Specialist IV Integrated Resources, IncClinical Document Management Specialist IVLexington, MassachusettsContractorJob DescriptionNOTE:TMF BackgroundPharma Industry experience (couple of years) Clinical Trial Experience (few years) GCP Experience (few years) Not senior level experience (doesn't need a decade worth of experience) Bachelor's degree requiredDay to day Mtg of TMF-early planning and setup all the way to study closeout and performing of consolations and archival activitiesFocusing on TMF lifecycle as a whole TMF assigned specific trials to work on Day to day activities include:QC of documents (paper and electronic)Team meetings (communicating issues to CTA/CRA) FilingJOB DESCRIPTION:Reporting to the Clinical Documentation Team Lead, and working in collaboration with the clinical study teams, the Clinical Document Management Specialist (CDMS) is responsible for the management and oversight of Trial Master File (TMF) records from set-up through to final archival of the clinical trial, ensuring compliance with company SOPs and processes, and all applicable regulations. Current awareness of regulatory requirements for clinical trials (ICH/GCP).Associates/Bachelor's degree or equivalent preferredKey Skills, Abilities, and CompetenciesSufficient knowledge of regulatory requirements and ICH-GCP guidelines to support records managementDemonstrated ability to work independently, take initiative, complete tasks to deadlinesRequires strong attention to detail, document organization skills, establishing priorities, scheduling and meeting deadlinesSolid communication skills and strong customer focus with ability to interact in a global, cross functional organizationAbility to communicate effectively with external vendors, including issue escalation, and responding to enquiries and concernsMust be able to work in a fast paced environment with demonstrated ability to prioritize multiple competing tasks and demands.
Quality Specialist The Panther GroupQuality SpecialistWest Boylston, MATrainingAssists in the development and maintains associate training curriculum, which consists of documentation, training records, training matrix and materials. Documents any non-conformances and ensures all product non-conformance paperwork is complete and is included in the work order package.
NewClinical Document Specialist (RN) UMass Memorial Health Care IncClinical Document Specialist (RN)Worcester, MA$91,644.80–$164,944 / yearDrawing upon clinical knowledge and experience, closely collaborates with physicians and other team members to ensure that patient records accurately document the status, complexity and intensity of patient conditions and care. Major Responsibilities: Works collaboratively with physicians, nurses, and other staff to ensure accurate and complete medical record documentation to appropriately reflect severity of illness and risk of mortality.
Final Release Specialist - 1st shift VulcanFormsFinal Release Specialist - 1st shiftDevensThe Final Release Specialist II supports the batch final release processes and performs functions necessary to ensure that all relevant manufacturing records and documentation are assembled, reviewed, and completed in a compliant efficient manner. Attend weekly planning meeting as the Quality Assurance representative and work with Operations, Customer Service, Distribution, Engineering and all other cross functional departments to ensure commitments and customer needs are met.
Final Release Specialist - 2nd Shift VulcanFormsFinal Release Specialist - 2nd ShiftDevensThe Final Release Specialist II supports the batch final release processes and performs functions necessary to ensure that all relevant manufacturing records and documentation are assembled, reviewed, and completed in a compliant efficient manner. Attend weekly planning meeting as the Quality Assurance representative and work with Operations, Customer Service, Distribution, Engineering and all other cross functional departments to ensure commitments and customer needs are met.
NewQuality Systems Specialist - Manufacturing - Shirley, MA Michael Page InternationalQuality Systems Specialist - Manufacturing - Shirley, MAAyer, Massachusetts$80,000–$83,000 / yearFull timeLead Iso Audits & Shape Qms Strategy At A Global ManufacturerLead ISO audits & shape QMS strategy at a global manufacturer. They operate across multiple critical industries and are known for investing in employee growth, inclusion, and long-term career development.
NewSenior Clinical Document Management Specialist Integrated Resources, IncSenior Clinical Document Management SpecialistLexington, MassachusettsContractorPharmaceutical experience- doesn't necessarily need to be exclusive to TMF/ CDM experience- must haveDirect experience (in-depth) with TMF related roles- must haveClinical Document Management experienceExperience with clinical trial can be consideredCan consider candidates with lots of years of experience in a clinical setting as long as they have in-depth TMF experienceExperience working with electronic TMF- nice to haveMinimum 5 years of pharmaceutical industry experience related to clinical document managementFamiliarity with various aspects of clinical trials and regulatory submissions, as well as strong knowledge of document management best practices. DUTIES/RESPONSIBILITIES:Managing studies from start-up to close outWorking with CRO's for a large number of studiesEntire lifecycle management of TMFResolving findings and communicating it to the right peopleSenior staffs mentor the regular CDM staff and oversees day-to-day processesInvolved in internal audits and external inspectionsMake sure that they know the location of all the documentsArchive Corporation of documentsQUALIFICATIONS:Someone with management/mentoring responsibility in the past- a very strong nice to haveMin.
NewClinical Document Management Specialist Integrated Resources, IncClinical Document Management SpecialistLexington, MassachusettsContractorResponsibilities70% Responsible for high quality clinical document deliverables across multiple, global assigned studies in support of GCDO ensuring effective lifecycle management of the clinical section of the TMF.• Key contributor and member of the clinical study team• Monitors completeness and quality of the Clinical TMF, including elements outsourced to CRO• Ensures effective communication and issue escalation internally and with external vendors• Oversees consolidation and archive preparation of clinical TMF, liaising with CRO partners to ensure compliance with company SOPs and timelines throughout the process.• Ensures compilation of CSR appendices in accordance with Shire's process20% Supports inspection readiness for GCDO through periodic quality assessment of clinical records.• Associates/Bachelor's degree or equivalent preferredKey Skills, Abilities, and Competencies• Sufficient knowledge of regulatory requirements and ICH-GCP guidelines to support records management• Demonstrated ability to work independently, take initiative, complete tasks to deadlines• Requires strong attention to detail, document organization skills, establishing priorities, scheduling and meeting deadlines• Solid communication skills and strong customer focus with ability to interact in a global, cross functional organization• Ability to communicate effectively with external vendors, including issue escalation, and responding to enquiries and concerns• Must be able to work in a fast paced environment with demonstrated ability to prioritize multiple competing tasks and demands.•
Program Support Specialist-Pumps Surface IPT CIRCOR International IncProgram Support Specialist-Pumps Surface IPTMAThe specialist assists in coordinating schedules, tracking program deliverables, maintaining records, supporting customer requirements, and facilitating communication across engineering, operations, supply chain, quality, contracts, and sales teams. Assist Program Managers in tracking schedules, milestones, deliverables, and production status to ensure program execution within scope, budget, and timeline requirements.
Final Release Specialist II - 2nd Shift VulcanForms IncFinal Release Specialist II - 2nd ShiftMA$22.60–$31 / hourThe Final Release Specialist II supports the batch final release processes and performs functions necessary to ensure that all relevant manufacturing records and documentation are assembled, reviewed, and completed in a compliant efficient manner. Attend weekly planning meeting as the Quality Assurance representative and work with Operations, Customer Service, Distribution, Engineering and all other cross functional departments to ensure commitments and customer needs are met.
Final Release Specialist - 1st shift VulcanForms IncFinal Release Specialist - 1st shiftMA$22–$31 / hourThe Final Release Specialist II supports the batch final release processes and performs functions necessary to ensure that all relevant manufacturing records and documentation are assembled, reviewed, and completed in a compliant efficient manner. Attend weekly planning meeting as the Quality Assurance representative and work with Operations, Customer Service, Distribution, Engineering and all other cross functional departments to ensure commitments and customer needs are met.
NewQuality Control Specialist Doyon Technical ServicesQuality Control SpecialistHanscom AFB, Massachusetts$55,000–$78,000 / yearFull timeThe employee is required to have close visual acuity to perform an activity such as: preparing and analyzing data and figures; viewing a computer terminal; reading; visual inspection involving small defects, small parts and/or operation of machines (including inspection); using measurement devices. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.
NewQA/QC Specialist I Integrated Resources, IncQA/QC Specialist ILexington, MassachusettsContractorJob DescriptionPosition Details:Location Lexington, MAJob Title QA/QC Specialist 1Duration 6+ MonthsJob Function and Description:To provide QA support for the manufacture, packaging and control of clinical trial materials to ensure compliance with GMP and perform GMP release of IMP and to ensure compliance with market regulations. QA/QC Specialist IA Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms.
Computer Systems Validation (CSV) Engineer / Specialist Alpha Business SolutionsComputer Systems Validation (CSV) Engineer / SpecialistLexington, MA$35–$45 / hourThis role is responsible for developing and executing validation documentation, ensuring regulatory compliance, validating system interfaces and data integrity, and collaborating with cross-functional teams to deliver compliant computerized system implementations. The ideal candidate will have hands-on experience with Computer Systems Validation (CSV) , preferably involving MODA and/or LabWare systems, and a strong understanding of GxP , GAMP 5 , 21 CFR Part 11 , and validation lifecycle management.
Accounts Payable Specialist The Steely GroupAccounts Payable SpecialistHybrid, Waltham, MAThis role researches and clears invoice issues such as PO/receipt mismatches, price/quantity variances, missing approvals, tax concerns, and vendor master discrepancies by partnering with Procurement, Receiving, and business stakeholders. Exception Management & Issue Resolution - 30% Investigate and resolve invoice holds and discrepancies (e.g., PO/receipt mismatches, price/quantity variances, duplicate invoices, missing approvals, vendor master issues).
NewQuality Control Specialist Doyon Properties IncQuality Control SpecialistMA$55,000–$78,000 / yearThe employee is required to have close visual acuity to perform an activity such as: preparing and analyzing data and figures; viewing a computer terminal; reading; visual inspection involving small defects, small parts and/or operation of machines (including inspection); using measurement devices. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information.
Continuous Improvement Specialist Avient CorporationContinuous Improvement SpecialistHolden, MAFull timeBy playing to win, acting customer centric, driving innovation and profitable growth, collaborating seamlessly across Avient, and motivating and inspiring and developing others and yourself you will accelerate your ability to achieve Avient's strategic goals, to meet our customer needs, and to accomplish your career goals. ResponsibilitiesThe Continuous Improvement Specialist is responsible for leading site-wide training governance, supporting continuous improvement initiatives, and coordinating onboarding and capability-building activities across all functions.
NewFinancial Management Specialist- Active DoD-Issued Secret Security Clearance Macpower Digital Assets Edge Private LimitedFinancial Management Specialist- Active DoD-Issued Secret Security ClearanceHanscom AFB, MA$100,000–$120,000 / yearThe ideal candidate is local to Bedford, MA or nearby areas, a highly skilled financial management professional with experience supporting DoD acquisition and sustainment programs, particularly within the Air Force, and possess a strong understanding of DoD budgeting, funds control, and compliance regulations, and holds an Active DoD-issued Secret Security Clearance. This role requires expertise in DoD acquisition phases (DoD 5000.2) and proficiency with DoD financial management regulations (DoD 7000.14) to ensure proper budgeting and financing of acquisition and sustainment programs.
Logistics and Production Control Specialist RTXLogistics and Production Control SpecialistMassachusettsAs part of our commitment to maintaining a secure hiring process, candidates may be asked to attend select steps of the interview process in-person at one of our office locations, regardless of whether the role is designated as on-site, hybrid or remote. RTX considers several factors when extending an offer, including but not limited to, the role, function and associated responsibilities, a candidate’s work experience, location, education/training, and key skills.
Program Support Specialist-Pumps Surface IPT Circor CareersProgram Support Specialist-Pumps Surface IPTWarren, MassachusettsThe specialist assists in coordinating schedules, tracking program deliverables, maintaining records, supporting customer requirements, and facilitating communication across engineering, operations, supply chain, quality, contracts, and sales teams. Assist Program Managers in tracking schedules, milestones, deliverables, and production status to ensure program execution within scope, budget, and timeline requirements.
PAYROLL AND TIME TRACKING SPECIALIST City of Worcester MAPAYROLL AND TIME TRACKING SPECIALISTWorcester, MA$27.23–$33.23 / hourESSENTIAL ELEMENTS: Serve as a primary customer service point of contact for employees and personnel surrounding all Workday, HCM, payroll, time tracking, absence benefits and Human Resources-related inquiries in person, by phone or via email. Monitor and respond to general human resource inquiries and appropriately, triage and route issues to Payroll, Benefits, Human Resources, Time Tracking, or Workday technical staff or third parties as appropriate.
Clinical Sample Analysis Specialist Integrated Resources, IncClinical Sample Analysis SpecialistWaltham, MAWork independently within the Clinical Sample Analysis team and collaborate effectively with other teams to ensure alignment of global Olink processes. Install, operate, maintain and repair laboratory equipment, systems and supplies in close communication internally within PSX and instrument vendors.
Senior Production Control Specialist CogmedixSenior Production Control SpecialistWest Boylston, MassachusettsCogmedix is a FDA-registered, ISO 13485–certified design, manufacturing, and services provider to medical device innovators, specializing in complex electromechanical, laser-based, and electro-optical systems through its Medical Technology Brought to Life mission. Ensure that all tasks and resources are methodically arranged prior to the initiation of production or ECO changes to avert discrepancies and ensure unimpeded operations.
GMP QC Compliance Specialist (Remote) LNN Pace Analytical Life SciencesGMP QC Compliance Specialist (Remote)MassachusettsRemoteThe role is critical in bridging day-to-day laboratory operations with the broader site quality framework, ensuring inspection readiness at all times and supporting the integrity of data generated in support of product release, stability, and method lifecycle activities. The incumbent provides expert guidance on regulatory requirements, leads audit readiness initiatives, oversees quality management system activities, and serves as a mentor and subject matter expert (SME) for QC laboratory staff.
Senior Media Tech Specialist Brandeis UniversitySenior Media Tech SpecialistWaltham, MASpecialist will: Lead the execution of media and A/V projects to implement new, and refresh existing tech-enabled spaces on campus, including conducting physical and software installations for related tasks and projects, ensuring timely communications, developing full project documentation, conducting ongoing program reporting, metrics and predictive analytics, and leading training and instructional programs for constituents on user operation of installed technology. Research, design and recommend current and emerging technology solutions in both hyflex and traditional technology enabled spaces on campus, to include media & A/V related computing, presentation, video services, sound systems and audio reinforcement.
Media Production Specialist Aquila TechnologyMedia Production SpecialistLexington, MARemoteTuition & Training Reimbursement- 5K annually for pre-approved, Eligible full-time team members who have completed a minimum ofsix (6) months of employment may apply for tuition reimbursement for approved, job-related courses taken through an accredited college or university. Candidates that possess a love for technical challenges, a desire to constantly learn, and the desire to establish themselves as critical players within a team will enjoy calling Aquila Technology home.
Manufacturing Specialist - Weekday Night Shift VulcanFormsManufacturing Specialist - Weekday Night ShiftDevensTypes of machinery include LPBF additive printers, vacuum furnaces, ultrasonic cleaning systems, media blast systems, EDM, and CNC mills. VulcanForms Inc. is a manufacturer of complex, high value engineered components in serial production at the world's most powerful additive foundry.
Manufacturing Specialist - Weekend Nights VulcanFormsManufacturing Specialist - Weekend NightsDevensTypes of machinery include LPBF additive printers, vacuum furnaces, ultrasonic cleaning systems, media blast systems, EDM, and CNC mills. Some knowledge of Import/Export Compliance, Customs documentation, ITAR, Incoterms (Commercial Invoices, Shipper Export Declaration).
Manufacturing Specialist, Weekday Day Shift VulcanFormsManufacturing Specialist, Weekday Day ShiftDevensTypes of machinery include LPBF additive printers, vacuum furnaces, ultrasonic cleaning systems, media blast systems, EDM, and CNC mills. VulcanForms Inc. is a manufacturer of complex, high value engineered components in serial production at the world's most powerful additive foundry.