Jobs at HRL Laboratories
HRL Laboratories, a division of Raytheon Technologies, specializes in advanced research for defense, aerospace, and communications systems. With 824 positions open, the lab offers opportunities across electronics, RF technology, software, and materials science.
Candidates typically apply for systems engineering, software development, RF and microwave engineering, data science, cybersecurity, and research scientist roles. The hiring process includes technical assessments, case studies, and interviews that evaluate problem‑solving, coding proficiency, and research acumen. Successful applicants receive competitive compensation, access to cutting‑edge projects, and avenues for publishing their work.
Job Transparency’s listings provide exact salary ranges and employee sentiment scores for HRL positions, enabling you to benchmark offers, negotiate confidently, and assess workplace culture before applying.
Product Manager II -Technical
Company: ARUP Laboratories
Location: Salt Lake City, UT
Posted Sep 13, 2023
Fine Motor Control: Picking, pinching, typing or otherwise working, primarily with fingers rather than with the whole hand as in handling. Sedentary Work: Exerting up to 10 pounds of force occasionally and/or negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects, including the human body. Communicate: Frequently communicate with others. 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. Vision: Having close, far, and peripheral visual acuity to perform a variety of tasks such as make general observations of depth and distance. 41 CFR 60-1.35(c) We are looking for individuals who want to contribute to ARUP's culture of accountability, integrity, service, and excellence. Mobility: The person in this position needs to occasionally move between work sites and inside the office to access file cabinets, office machinery, etc. ARUP Policies and Procedures: To conduct self in compliance with all ARUP Policies and Procedures. Reaching: Extending hand(s) and arm(s) in any direction.
CNC Programmer
Company: Core Laboratories
Location: Other US Location
Posted Sep 12, 2023
The CNC Programmer ensures product quality by collaborating with various functional groups to develop, maintain CNC programs, tooling, and related documentation. They positively impact First Time Yield, On-Time Delivery, and Reduce Set-up and Cycle Times. Key responsibilities include creating and maintaining CNC machining programs, defining and implementing tooling, and continuously improving manufacturing processes. The role requires a Bachelor's degree, 3-5 years of manufacturing experience, and proficiency in CAD/CAM software and G code language.
Project Specialist I
Company: ARUP Laboratories
Location: Salt Lake City, UT
Posted Sep 15, 2023
Fine Motor Control: Picking, pinching, typing or otherwise working, primarily with fingers rather than with the whole hand as in handling. Sedentary Work: Exerting up to 10 pounds of force occasionally and/or negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects, including the human body. Communicate: Frequently communicate with others. 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. We are looking for individuals who want to contribute to ARUP's culture of accountability, integrity, service, and excellence. Mobility: The person in this position needs to occasionally move between work sites and inside the office to access file cabinets, office machinery, etc. 41 CFR 60-1.35(c) Based in Salt Lake City, Utah. ARUP Policies and Procedures: To conduct self in compliance with all ARUP Policies and Procedures. Consider joining our dynamic team.
Quality Assurance Director
Company: Genezen Laboratories
Location: Indianapolis, IN
Posted Oct 04, 2023
Responsible for raw material inspection and release, Quality on the floor, disposition of drug product/drug substance, QA review of quality control data, root cause analysis, risk management, technical writing, deviation, change and CAPA management, document/records management, quality metrics reporting, data integrity, training management, QA review of method qualification/validation, process qualification/validation, and equipment/utilities/ facilities qualification and continuous improvement. Responsible for ensuring internal audits, client audits, supplier quality management, managing regulatory inspections, and quality systems are implemented effectively, efficiently, and compliantly at the site. Help build scalable, phase appropriate Quality systems as the organization continues to grow.ESSENTIAL JOB FUNCTIONS / DUTIESAct as a leader in the Quality organization, helping define and drive the Quality vision, mindset, and culture of the entire company in close collaboration with the Vice President of QA and RegulatoryDevelop overall program, implementation, and continuous improvement of the Quality Systems, which encompass but not limited to: QMS (Deviation, Change Control, CAPA), Documentation, Training, Supplier Management, Internal/Customer Audits and Customer Complaints.Ensure that Quality Systems are designed and operating in a way to provide appropriate support in all GxP areas of the company and are in compliance with current ISO and GMP standards (cGMP) both US FDA and EU applicable to gene therapy as appropriate for early phase clinical trialsDevelop, implement, and maintain corporate policy and procedures for the Quality Management System in accordance with ICH Q10 modelTake lead role in evaluating continuous improvement options for the Quality Systems post initial implementationResponsible for supporting all client projects as the quality lead and attending all meeting for current and prospective clients.Develop user requirements and contribute to the configuration, validation, implementation, and lifecycle management of the electronic Quality Management System (eQMS - Veeva)Develop, implement, and oversee a Quality Supplier Management Program that serves all GxP areas including introduction and qualification of suppliers and materials, supplier material changes, supplier complaintsEnsure that all products manufactured at the site are produced, tested, and released in compliance with SOPs, cGMP’s, US FDA, and EU requirements.Establish and continuously improve the Incoming Quality Assurance (IQA), Quality Oversight, and Batch Release programsResponsible for all raw material and final product release from the facilityEstablish department / individual goals and key performance indicators in alignment with company and operational goalsMaintain and report applicable department and delivery metricsEstablish the Quality Management Review Program, including facilitating creation of the presentation materials to include the Key Performance indicators, the meeting agenda, and attendance, and to orchestrate the material presentationManage internal quality improvement initiatives: evaluate internal processes, suggest/design/implement improvements, create/revise relevant SOPs/PoliciesAct as subject matter expert and provide training on all Quality Management Systems, including but not limited to change control, quality events, investigation, and implementation of effective CAPAsOwn and oversee the compilation of the Site Master File (SMF)Coach, train, and develop the Quality teamDevelop budget for department and ensure adherence to the budgetDrive continuous improvement and operational excellence culture through self-detecting and self-correcting processes and systems and instilling strong ownership and accountabilityStay current with regulatory guidance as it applies to the Gene Therapy and early phase clinical trialsAct as a member of the site leadership team and engage in business decision-making from a Quality perspectiveEnsure safe working environment and compliance with OSHA, EHS, Quality, and cGMP procedures and policies within the QA departmentSPECIAL JOB REQUIREMENTSAdaptability required as work schedule may change based on business needsCriminal background check and drug screen requiredOther duties as assignedKNOWLEDGE, SKILLS & EXPERIENCEEDUCATION / CERTIFICATIONS / LICENSESEssential/DesiredBS degree in science or related fieldEssentialIn depth Knowledge in industries regulated in-part by, 21 CFR Part 11, 21 CFR 210, 21 CFR 211, 21 CFR 600, 21 CFR 610, Eudralex Volume 4, ICH Quality Guidelines, and Guidance to Industry dockets, as applicable for early phase clinical trialsEssentialCertified AuditorDesiredON-THE-JOB EXPERIENCE 10+ years of experience Quality Professional in Pharmaceutical and/ or Biological ManufacturingEssential7+ years of experience Quality SystemsEssential5+ years of experience Quality ManagementEssentialExperience conducting Supplier Audits, including for APIDesiredExperience with Phase I/II IND clinical trialsDesiredSKILLS / ABILITIES Manage multiple projects, set priorities, and work in fast-paced environmentEssentialCommunicate confidently and effectively with management, peers, and key stakeholdersEssentialDemonstrate effectiveness in task completion, decision-making, empowerment of others, deviation/nonconformance management, training, and problem solvingEssentialDemonstrated ability to develop quality systems and a quality management planEssentialPHYSICAL DEMANDSWhile performing the duties of this job, the employee is required to meet the following physical demands:Work EnvironmentOccasionally exposed to loud noise levelsPosition can be combination of remote and on-siteRegularly sit for long periods of timeMovementFrequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and armsOccasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawlLiftingFrequently lift and/or move up to 10 poundsOccasionally lift and/or move up to 25 poundsVisionFrequently utilize close vision and the ability to adjust focusCommunicationFrequently required to communicate by talking, hearing, using telephone and e-mailGENEZEN'S VALUE-BASED COMPETENCIESGrowth MindsetBelieve that skill is developed through dedication and hard work.Intelligence & talent are just the starting point.Mistakes are valuable lessons, not shameful indictments.FlexibilityAdapt rapidly to a quickly changing, CDMO environment.Respond by constructively creating & impacting opportunity through active participation.Team FocusWork together; succeed together; fail together.IntegrityDo the right thing, on time, every time.Speak up when needed.Exercise respect.Inclusion Embrace the unique viewpoint of each individual.Join the ongoing journey to a more inclusive workplace and community where we all help each other get better.GENEZEN'S BENEFITSPaid vacation days, amount based on tenurePaid sick time9 observed holidays + 1 floating holiday + 1 volunteer day401(k) plan with company match up to 6% of salary, vested immediatelyShare Appreciation RightsChoice of several healthcare plansFSA and HSA programsDental & vision careEmployer-paid basic term life/personal accident insuranceVoluntary disability, universal life/personal accident insuranceAccidental Death & Dismemberment (AD&D) InsuranceADDITIONAL DETAILSNothing in the job description for this role restricts management’s right to assign or reassign duties and responsibilities to this job at any time.This position is located in Fishers, Indiana.This position requires a criminal background check.Genezen is an Equal Opportunity Employer.Genezen participates in EVerify.Genezen is interested in every qualified candidate who is eligible to work in the United States; however, we are not able to sponsor visas.Genezen is located in Fishers, Indiana, a suburb of Indianapolis. Nearby Indianapolis is home to professional and college sports teams, the Indy 500, a growing art community and the world’s largest children’s museum--to name just a few reasons why this area is a great place to live. Fishers was named the 1 place to live in the US by Money Magazine in 2017 for its livability, safety and entrepreneurship. Every employee contributes to the success of the company and you can be part of that team.PURPOSELeads the Quality Assurance team, including Quality Systems and Quality Operations. Fishers is one of the fastest growing communities in Indiana and is dedicated to supporting a high quality of life for all its residents. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures. WORKING AT GENEZENMany people have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work.
Project Coordinator
Company: Core Laboratories
Location: Other US Location
Posted Sep 12, 2023
The Project Coordinator assists the Project Management team in generating laboratory reports, tracking progress, and preparing preliminary data for clients. They ensure quality control and compliance with ISO procedures, review PVT data, and perform assigned functions. The role involves preparing final PVT reports, issuing scope of work, and addressing maintenance issues. The job requires an Associate's degree or equivalent experience, strong language and mathematical skills, computer proficiency, and the ability to apply common sense understanding. The employee must possess a valid driver's license and meet MVR criteria. The work environment involves exposure to moving mechanical parts, fumes, toxic chemicals, and moderate noise levels.
Staff Software Configuration Manager - Git Admin
Company: Dolby Laboratories
Location: San Francisco, CA
Posted Sep 29, 2023
Dolby is seeking a Software Configuration Management (SCM) specialist to join their team. The ideal candidate will have extensive experience in Git administration, large file systems management, and AWS services. They will be responsible for designing, deploying, and maintaining enterprise-level source code management systems, configuring GitLab Multi Services and Multi Regions Deployment, and managing permissions and nomenclature. The role involves working across functional teams to ensure continuous operation of the Git environment, automating processes, and implementing improvements. The candidate should have a strong understanding of Git architecture, experience with CI/Automation tools, and proficiency in Python and Shell. A BS degree in Computer Science or a related field is required, along with experience with monitoring tools, SQL, and relational databases administration.
PharmaDx Senior Project Manager
Company: ARUP Laboratories
Location: Salt Lake City, UT
Posted Sep 24, 2023
Communicate: Frequently communicate with others. Fine Motor Control: Picking, pinching, typing or otherwise working, primarily with fingers rather than with the whole hand as in handling. Creates new processes and procedures, as applicable. Sedentary Work: Exerting up to 10 pounds of force occasionally and/or negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects, including the human body. Other duties as assigned. Vision: Having close, far, and peripheral visual acuity to perform a variety of tasks such as make general observations of depth and distance. 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. ARUP Policies and Procedures: To conduct self in compliance with all ARUP Policies and Procedures. Essential Functions: Provides project leadership, management, and oversight throughout projects, including the planning for ongoing support, compliance and quality post-deployment. Mobility: The person in this position needs to occasionally move between work sites and inside the office to access file cabinets, office machinery, etc.
Accounting Specialist
Company: POLARIS Laboratories
Location: Indianapolis, IN
Posted Sep 22, 2023
It is your responsibility to report defective, damaged or lost PPE, or equipment that does not fit properly, to your Manager.The following safety training for POLARIS Laboratories employees to complete includes: Hazmat, OSHA, RCRA, Methylene Chloride, Contingency Plan, POLARIS Quality System, Internal Auditor The knowledge, skills, and abilities of a successful candidate: The individual must possess the following knowledge, skills and abilities and be able to perform the essential functions of the job, with or without reasonable accommodation. POLARIS Laboratories, LLC provides the required PPE. PREFERRED QUALIFICATIONS Knowledge of Sage fixed asset software Self motivated and directed learner Able to work independently with little supervision Basic knowledge of accounting Able to identify and resolve issues Able to analyze processes for improved efficiencies or errors Detail oriented Organized Highly developed time management skills Advanced written and verbal communication skills Important qualifications: Advanced knowledge of excel and Netsuite or other accounting software A minimum of 4 years working in a busy accounting department doing the same type of work. What you will do: Below is the estimated percent of time you will spend on duty or task be successful: 50% Daily, weekly and monthly invoice processing 5% Accounting projects as assigned by Accounting leadership 5% Assigning a general ledger account to a transaction 5% Process Accounts receivables and Accounts Payables 2% Be backup for the vendor bill process 5% Collect on past due accounts 1% Post and reconcile credit card transactions 5% Prepare bank deposits 10% Serve as the accounting contact person 5% Organize and maintain accounting filing system 1% Assist in preparing financial reports 5% Ensure invoicing procedure is being followed in accordance with Quality System 1% Work closely with accounting consultants to process year end In addition to performance of the essential functions, you may be required to Collaborate with departments throughout the organization to address account payable needs and issues Additionally, while you perform your tasks you must also: Adhere to and support of the POLARIS Employee Handbook inclusive of the Standards of Conduct Learn and support of the quality management system Other duties as assigned Safety Requirements when entering the lab: OSHA laws require the use of the following Personal Protective Equipment (PPE) when performing work duties that have the potential of risk to your health or safety: Protective eye wear Team members will be trained in the proper use and care of assigned PPE. As a member of a dynamic group, you will also frequently provides assistance or ownership of special projects that may cross into other areas of accounting. As an Accounting Specialist at POLARIS Laboratories you will provide financial, clerical and administrative assistance to maintain accurate and on-time invoices to customers.
Salesforce Administrator II
Company: ARUP Laboratories
Location: Salt Lake City, UT
Posted Sep 24, 2023
Recommends, tests, deploys, and maintains Visual Force pages. Recommends, tests, deploys, and maintains Apex classes and triggers. Fine Motor Control: Picking, pinching, typing or otherwise working, primarily with fingers rather than with the whole hand as in handling. Sedentary Work: Exerting up to 10 pounds of force occasionally and/or negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects, including the human body. Audits, uncovers, and resolves data integrity issues. Performs bulk imports, updates, and exports of data. Communicate: Frequently communicate with others. 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. Creates and manages custom objects, fields, formulas, analytic reports and dashboards. Mobility: The person in this position needs to occasionally move between work sites and inside the office to access file cabinets, office machinery, etc.
Project Manager II
Company: Core Laboratories
Location: Houston, TX
Posted Sep 12, 2023
The Environmental Project Manager is responsible for overseeing environmental projects, including quoting, sample coordination, data calculation, and report delivery. The role requires expertise in environmental soil testing, ASTM standards, lab analysis, and customer service. The position involves working flexible hours, including evenings, weekends, and holidays. Key duties include serving as the primary point of contact, collaborating with clients, preparing and submitting quotations, lab work instructions, and project reports, monitoring project progress, and adhering to HSE policies. The ideal candidate should have a Bachelor's degree in environmental science or a related field, 5 years of project management experience, and expertise in environmental soil testing methods and ASTM standards.
C&GESS Support Engineer-Americas
Company: Dolby Laboratories
Location: Greater LA Area
Posted Sep 29, 2023
Dolby is seeking a seasoned professional with extensive experience in cinema design and construction to oversee the implementation of Dolby Cinema offerings globally. The role involves managing project tasks, schedules, and on-site duties to ensure successful completion within specifications, timelines, and budget constraints. The ideal candidate should have a Bachelor's degree, solid knowledge of Digital Cinema equipment, and experience in managing complex projects with multiple stakeholders. They must be comfortable working independently, managing multiple tasks simultaneously, and traveling domestically and internationally as needed. Dolby offers a collegial culture, challenging projects, excellent compensation, and a flexible work approach.
Senior Design Engineer
Company: Core Laboratories
Location: Other US Location
Posted Sep 12, 2023
The Senior Design Engineer works independently and collaboratively across departments to design oilfield perforating guns, setting equipment, and other mechanical products. They apply creativity and innovation to research and develop new products, perform engineering calculations, and guide interdepartmental support. The role requires a Bachelor's or Graduate degree in Engineering, relevant experience, and proficiency in engineering software. The employee will have daily involvement in tool assembly and testing, requiring physical strength and aptitude. The work environment is mainly in an office with exposure to manufacturing and testing facilities, and occasional exposure to explosive materials and various weather conditions.