Machinist Experimental Job Description Sample
Machinist Experimental — Prototype Stamping Dies
Machinist Experimental — Prototype Stamping Dies Chrysler Headquarters & Tech Center Auburn Hills, MI 48326, US Job Type:Full Time Date Posted: January 16, 2018 Job ID: 1030793 ApplyRefer A FriendJoin Our Talent Network Share this job
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- Share by Mail Job Overview The Machinist Experimental – Prototype Stamping Dies position requires CNC programing of stamping dies to manufacture prototype, test parts, and low volume production to support product development of prototype vehicle builds. This individual will be required to program soft tooling dies using computer-aided software (NX11) and a 3D model with math data. This machinist must understand how to program, set-up, and operate CNC milling machine to manufacture 3-piece and 5-piece stamping dies for BIW components. In addition, the individual must be comfortable holding tight tolerances, have advance shop mathematic skills to include thorough understanding of metal properties, layout, and manufacturing procedures. This role requires sound knowledge of feeds and speeds for maximum material removal and thorough understanding of GD&T. Qualifications
Eight years of experience in tool and die making or model making
Prototyping/product development background
Ability to use computer aided software to program CNC (Master Cam, Catia, NX, etc…)
Core CNC competencies, with strong knowledge of G&M codes
Ability to read and comprehend complex blueprints
Proficient in Geometric Dimensioning & Tolerance (GD&T) and Datum Referencing
Precision and strong attention to detail
Ability to verify dimensions, alignments and clearances of finished parts for conformance to specifications, using measuring instruments such as calipers, gauge blocks, micrometers and dial indicators
Able to work independently and as part of a team, with limited supervision
Ability to assess speeds and feeds, and make adjustments as necessary to optimize run-time
Ability to track and review tool wear; changing or replacing tools as needed
Working knowledge of computers and Microsoft Office
Ability to frequently bend, reach, and lift objects weighing up to 25 pounds
Ability to follow safety rules, regulations and have good safe shop practices
- Must have own tools
Bachelor of Science degree in Engineering from an ABET accredited or equivalent program
Able to run multiple types of shop equipment (Bridgeport’s, lathes, grinders, etc…)
Efficient use of MS Office suite
Basic understanding of World Class Manufacturing FCA is proud to extend to its employees a compensation and benefits package that is designed to retain their talent and to motivate and reward job performance. Our present compensation program provides for competitive, market based salaries, and annual vacation and holiday time off. We make available a comprehensive health care benefits plan which, depending upon the employee’s role, includes medical, dental, vision and prescription drug coverage. We also offer a disability absence plan, group and optional life insurance program, savings plan, tuition assistance, and vehicle purchase and lease discounts for certain employees, and for their family and friends. Note: Some of the benefits listed above may not apply to summer vacation replacement and temporary employees.
Experimental Machinist - 2Nd Shift
Introduction: The Johns Hopkins Applied Physics Laboratory (APL) is a national leader in scientific research and development. APL is actively seeking an Experimental Machinist to support the Advanced Mechanical Fabrication Group. The Johns Hopkins Applied Physics Laboratory (APL) is located midway between Baltimore and Washington, DC.
Interpret engineering drawings or sketches, fabricate parts, and assemble hardware in support of R&D; programs in accordance with APL quality initiatives. This position is scheduled to work from 330pm to Midnight, Monday through Friday (Second Shift). Overtime may be required.
Duties: 1. Setup, programming, and operation of CNC mills and lathes for end-to-end fabrication with minimal supervision. (80%) 2. Perform in-process inspection using precision measuring instruments (i.e., I.D and O.D. Micrometers, calipers) to ensure hardware will meet customer requirements. (10%) 3. Review work packages for producibility issues. Communicate with the customer as required to achieve end objectives. (5%) 4. Monitor and record duration and completion of work performed in Work Management system in accordance with business and Quality procedures. Achieve and maintain proficiency with all applicable quality processes associated with assigned work. (5%)
Note: This job summary and listing of duties is for the purpose of describing the position and its essential functions at time of hire and may change over time. ## Qualifications
* High school diploma or equivalent.
Minimum 4 years experience in setup, programming, and operating mills and lathes in a precision R&D; environment.
Minimum 2 years of CNC programming experience.
Excellent verbal communication skills and willingness to interface with customers during the fabrication process.
Positive interpersonal skills and ability to work well in a team-oriented atmosphere.
Ability to read and interpret Geometric Dimensioning and Tolerancing per ANSI Y-14.5.
* Computer skills, e.g., Microsoft Office and Web-based applications.
- Experience with Mastercam CNC programming software.
Special Working Conditions: Working hours are 3:30 PM - Midnight, Monday- Friday. Overtime may be required.
Security: Secret security clearnce is required. Applicants selected may be subject to a Government security investigation and must then meet the eligibility requirements for access to classified information. Eligibility requirements include US citizenship.
Benefits: APL offers a comprehensive benefits package including a liberal vacation plan, a matching retirement program, significant educational assistance, a scholarship tuition program for staff with dependents, and competitive salaries commensurate with skills and experience. For more information about our organization, please visit our web site at www.jhuapl.edu.
Equal Employment Opportunity: Johns Hopkins University Applied Physics Laboratory is an equal opportunity/affirmative action employer that complies with Title IX of the Education Amendments Acts of 1972, as well as other applicable laws, and values diversity in its workforce. Primary Location: *United States-*Maryland-*Laurel
Req ID:* 16016
Nurse Project Manager – Experimental Therapeutics/Interventional Trial
42145BRTitle:Nurse Project Manager – Experimental Therapeutics/Interventional TrialDepartment:Research-Clinical Research Core ProgramsAutoReqId:42145BRStatus:Full Time Standard Hours per Week:40 Job Posting Description:At Boston Children’s Hospital, success is measured in patients treated, parents comforted and teams taught. It’s in discoveries made, processes perfected, and technology advanced. In major medical breakthroughs and small acts of kindness. And in colleagues who have your back and patients who have your heart. As a teaching hospital of Harvard Medical School, our reach is global and our impact is profound. Join our acclaimed Experimental Therapeutics/Interventional Trials team (ET/IT) and discover how your talents can change lives. Yours included. The Nurse Project Manager – Experimental Therapeutics/Interventional Trials (ET/IT) will be responsible for:
Working with investigators and interdisciplinary teams to support the planning, implementation and conduct of research studies in both inpatient and outpatient settings.
Ensures the protection of children as study subjects and maintains ongoing informed consent
Coordinates and provides nursing care and patient education to children enrolled on studies and their families.
Provides study specific education to unit-based nursing staff and responding to their questions. To qualify, you must have:
2 years of nursing experience, (pediatrics or BCH preferred).
Excellent interpersonal and communication skills-both written and verbal. Boston Children’s Hospital offers competitive compensation and unmatched benefits, including affordable health, vision and dental insurance, generous levels of time off, 403(b) Retirement Savings plan, Pension, Tuition Reimbursement, and discounted rates on T-passes (50% off). Discover your best. Boston Children’s Hospital is an Equal Opportunity / Affirmative Action Employer. Qualified applicants will receive consideration for employment without regard to their race, color, religion, national origin, sex, sexual orientation, gender identity, protected veteran status or disability. *LIOffice/Site Location:Boston
Metl Experimental Facility Operator
METL Experimental Facility Operator
8:30 - 5:00
TwitterWe invite you to apply for a METL Experimental Facility Operator position. For this position, we are seeking an entry level or near entry level electrical and/or mechanically inclined equipment operators to join our multi-disciplinary team that includes design engineers, test engineers, fluids and thermal researchers, and experienced technicians. Under supervision, you will design, build, test, operate and trouble-shoot cutting-edge experimental systems and sub-systems with a primary focus on the operations and maintenance of a facility called the Mechanisms Engineering Test Loop (METL).METL is an intermediate-scale liquid metal experimental facility whose purpose is to provide purified R-grade sodium to various experimental test vessels to test components that are required to operating in a prototypic advanced reactor environment. The METL facility will its services to researchers located at Argonne, in the U.S. and internationally.With limited supervision, you will:
Follow written procedures to operate and maintain the METL facility and small and intermediate-scale liquid metal technology facilities.
Provide technical support for experimental and programmatic work in the areas of mechanical, electromechanical, optical, and electrical systems.
Support the research needs of the R&D community who will be installing and testing components in METL.
Develop, fabricate, troubleshoot, repair, calibrate, purchase, and maintain a variety of complex electronic and mechanical apparatus, plant/process equipment, and subsystems that support the METL facility and the experiments conducted in that facility.
Assist in the design and test electronic systems which typically consist of power supplies and controllers, data logging hardware, and equipment for temperature and valve control. Note: This description describes the general nature of work but is not intended to be a comprehensive list of all duties and responsibilities. We expect you to have:
Some experience with experimental design and operation including instrumentation (thermocouples, pressure transmitters, flow meters, level, etc.) specification, installation and operation.
Some LabVIEW/Eurotherm/industrial control experience is desirable + Liquid metal technology expertise is desirable.
Some familiarity with industry standards and practices for electrical and/or mechanical systems.
Knowledge of mechanical equipment (motors, pulleys, gears, pumps, valves, etc.), thermal effects on materials and components (expansion, evaporation, etc.), and operation of a personal computer.
Knowledge of metallurgy, heat transfer and fluid mechanics is desirable.
Maintain knowledge and awareness of Laboratory policies and procedures.
Skilled in oral and written communication.
The position may include shift work because METL will be operated 24 hours per day once operational. The requirements for the desired levels are as follows:
ST1 Level: Technical institute or AA degree and 1-3\
years of related work experience, Bachelor’s Degree in Engineering and 1\
years of related work experience, or equivalent.
ST2 Level: Technical institute or AA degree and 5\
years of related work experience, Bachelor’s Degree in Engineering and 2\
years of related work experience, or equivalent. You will be placed at the appropriate level (ST1 or ST2) depending upon depth and breadth of relevant knowledge, skills, and experience brought to the position. As an equal employment opportunity and affirmative action employer, Argonne National Laboratory is committed to a diverse and inclusive workplace that fosters collaborative scientific discovery and innovation. In support of this commitment, Argonne encourages minorities, women, veterans and individuals with disabilities to apply for employment. Argonne considers all qualified applicants for employment without regard to age, ancestry, citizenship status, color, disability, gender, gender identity, genetic information, marital status, national origin, pregnancy, race, religion, sexual orientation, veteran status or any other characteristic protected by law.
Senior Director, Clinical Development, Translational & Experimental Medicine, CVM
Janssen Research and Development, L.L.C., a member of Johnson and Johnson's Family of Companies, is recruiting for an Senior Director, Clinical Development, Translational & Experimental Medicine, Cardiovascular/Metabolism (CVM) located in Raritan, NJ. At the Janssen Pharmaceutical Companies of Johnson & Johnson, what matters most is helping people live full and healthy lives. We focus on treating, curing and preventing some of the most devastating and complex diseases of our time. And we pursue the most promising science, wherever it might be found. Janssen Research & Development, LLC discovers and develops innovative medical solutions to address important unmet medical needs in oncology, immunology, neuroscience, infectious diseases and vaccines, and cardiovascular and metabolic diseases. Please visit http://www.JanssenRnD.com for more information. We are Janssen. Our mission drives us. Our patients inspire us. We collaborate with the world for the health of everyone in it. Thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to inclusion. Proud to be an equal opportunity employer. The Sr. Director will serve as a Clinical Leader in the Cardiovascular/Metabolism (CVM) Translational & Experimental Medicine Group, with a focus on drug development for metabolic and cardiovascular projects. The Sr. Director will have broad responsibilities including:
Providing strategic leadership on managing/addressing specific project/program-related issues and presenting to and negotiating with the CVM and Janssen leadership teams on development plans or program-related issues.
Accountable for the design the Translational Early Development Plan and the clinical development strategy for early stage compound(s), in collaboration with CVM Discovery, Biomarkers, Development, and other functional partners.
Accountable for the medical oversight, conduct, and analysis of the appropriate first in human (FIH), proof of pharmacology (POP), proof of mechanism (POM), and proof of concept (POC) studies for NME early development programs and mechanistic trials and clinical pharmacology studies supporting all phases of development for the Metabolism and Cardiovascular portfolio.
Leading the Clinical Team, responsible for the timely completion, content, and quality of key deliverables including protocols, clinical study reports and submissions to health agencies
Presenting and/or responding to questions at meetings with Health Authorities.
Providing key input into diligence activities.
Previous Supervisory experience overseeing various position levels would be a strong asset. #JNJPhysicians Qualifications Qualifications for the Senior Director Clinical Leader include:
MD (or equivalent), MD/PhD, PhD or PharmD all with a basic science research background will be required.
Board certification in Internal Medicine (or Pediatrics), Endocrinology is preferred, but backgrounds in Cardiology, Nephrology, and GI/Hepatology will be considered.
Detailed and thorough understanding of metabolic disorders, including diabetes, obesity, and related comorbidity disease (e.g., cardiovascular, renal or liver disease), in drug development is required.
Demonstrated successful post-doctoral research and publications in metabolic disorders is required
Requires at least 7 years of experience in industry and/or academia in early development clinical research and development (including Phase 0-2a studies).
Strong leadership skills with the ability to influence is required.
Up to 10% annual travel (domestic and international) may be required. Primary Location United States-New Jersey-Raritan Organization Janssen Research & Development, LLC. (6084) Job Function Clinical Research non-MD Requisition ID 0089180118
Des Moines Skilled: Experimental Mechanic
Experimental Mechanic position Primary Function: Performs one or more of the following in a team environment on experimental tractors, machines and/or implements in a laboratory and/or field: (1) Lays out and fabricates experimental parts and production templates working from ordinary formed views, dimensioned work planes and work axis and/or straight views. (2) Assembles and operates units to check function. (3) Builds complicated mechanical, hydraulic and/or electronic tests for mechanical and structural failure. (4) Sets up and completes performance tests of units in field operation. (5) Diagnoses trouble, overhauls and adjusts major mechanical, electrical, and hydraulic work in field tests. Types of Machines, Tools and Equipment Used or Operated: Machines such as: punch presses, arc welders, brazing equipment, brake, shear, nibbler, rolls, drill press, grinder, saw, arbor press, spot welder, mechanic’s tools, measuring instruments, meters, gages, test vehicles, instrumentation equipment, tractors, implements, transport vehicles, trucks, various hand tools, etc. Job Details: Work is not closely supervised. Maintains a safe work environment. Details are dependent on duties assigned but in general consists of one or more parts of the primary function plus one or more of the following:
Follows written or verbal instructions.
Coordinates work as directed with product engineering and/or sales personnel.
Assists with details and plans for field testing of equipment.
Work is performed on bench, floor, machine or test equipment in laboratory or field.
Plans procedures and determines methods of performing operation.
Diagnoses trouble and makes all repairs and adjustments as required to complete test.
Builds required holding devices needed for performance of job.
Disassembles units after tests and checks for misalignment and wear.
Fabricates parts by cutting, bending, machining, etc. and/or welding and performs assembly work.
May instruct and direct other team members.
Records findings, analyzes function and makes recommendations.
Makes complete written reports including details of crop and field conditions, performance, quality and amount of work performed.
Lubricates, adds coolant and cleans equipment.
Cleans work area and performs other miscellaneous duties inherent to the job. May also perform duties such as:
Prepares and loads equipment for movement to test site.
Makes personal contacts with dealer and branch personnel to finalize arrangements for tests.
Performs setup on machine for test, including assembly, adjusting, fueling and lubrication.
Operates equipment under field test conditions.
Install and/or operate instrumentation for tests. John Deere is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to, among other things, race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, or status as a qualified individual with disability.
Research Associate III Pediatric- Clinical Experimental Immunology & Infectious Diseases (Ceiid)
Min Qualifications Bachelor's degree in basic science or equivalent and 5 years of related experience or Master's degree in basic science or equivalent and 3 years of related experience required. JOB DESCRIPTION: Conducts a variety of non-routine research assignments and experiments.
Salary RangeCommensurate with experience. This position is in the pay band code: SC22.
Specific Job Related DutiesPerform Flow Cytometry on a FACScanto II (high level skills) Bioplex Assays Luminex assays Isolation of RNA/DNA from human cells Upkeep and Maintenance of Luminex 100, Magpix (both BioRad and Luminex), FACScanto II Upkeep and Maintenance for all Equipment in Pediatric Immunology Upkeep and Maintenance of Pediatric Immunology Laboratories Maintain Equipment Inventory for Pediatric Immunology Assist CEIID Laboratory Manager in maintenance of CO2 and LN2 upkeep Assist CEIID Laboratory Manager in general upkeep of all Laboratory Equipment, especially
80C freezers (including de-icing all
80C freezers weekly) Assist CEIID Laboratory Manager in Contract Management for all equipment Assist CEIID Laboratory Manager in Laboratory Hurricane Preparedness (including After-Storm E1 lab restoration) Assist CEIID Laboratory Manager in Equipment Inventory Maintenance
Equal Employment OpportunityUTMB Health strives to provide equal opportunity employment without regard to race, color, national origin, sex, age, religion, disability, sexual orientation, gender identity or expression, genetic information or veteran status. As a VEVRAA Federal Contractor, UTMB Health takes affirmative action to hire and advance women, minorities, protected veterans and individuals with disabilities. Full/Part Time: Full-Time
Job Type:* Regular
Job Title:* Research Associate III Pediatric- Clinical Experimental Immunology & Infectious Diseases (CEIID)
Job ID:* 58418 Location: Galveston
Business Unit:* SOMED
Postdoctoral Research Fellow - Computational And Experimental Neuroplasticity Laboratory
Web Announcement Postdoctoral Research Fellow – Computational and Experimental Neuroplasticity Laboratory The George Mason University Computational and Experimental Neuroplasticity Laboratory (http://krasnow1.gmu.edu/CENlab/avrama.html) of Kim “Avrama” Blackwell invites applications for a Postdoctoral Research Fellow/software engineer position to begin immediately. George Mason University has a strong institutional commitment to the achievement of excellence and diversity among its faculty and staff, and strongly encourages candidates to apply who will enrich Mason’s academic and culturally inclusive environment.
The successful candidate will contribute to ongoing cutting-edge research in computational systems biology and neuroscience by further development of our stochastic reaction-diffusion software, NeuroRD, and further development of parameter optimization software. The position involves design and implementation of new features for both software products, providing technical support to lab members developing NeuroRD models and investigating the role of calcium dynamics and cell signaling pathways in learning and plasticity; and writing journal articles and giving presentations on the new software features. CENlab is an interdisciplinary, dynamic, and creative research group at Mason’s Krasnow Institute for Advanced Study, located in northern Virginia (15 miles west of Washington, D.C.).
* Ph.D. in a relevant field (e.g., computer science, physics, bioinformatics, engineering) and at least one publication in reputable journal;
Experience in software development (scientific software, Python, and C++ or JAVA is preferred); * Expertise with Unix operating systems; and
Knowledge of stochastic processes. The incumbent will have office space, a Unix computer workstation, and a post-doctoral level salary supplemented by excellent state employee benefits. More information may be found at:
NeuroRD website: https://github.com/neurord;
Krasnow Institute for Advanced Study: http://krasnow.gmu.edu; and
George Mason University: http://www.gmu.edu/. George Mason University is an innovative, entrepreneurial institution with national distinction in a range of academic fields. # Special Instructions to Applicants For full consideration, applicants must apply for position number F8816z at http://jobs.gmu.edu/; complete and submit the online application; and upload a cover letter, CV, and a list of three professional references with contact information. # Mason Ad Statement Great Careers Begin at Mason! George Mason University is an innovative, entrepreneurial institution with national distinction in both academics and research. Mason holds a top U.S. News and World Report “Up and Coming” spot for national universities and is recognized for its global appeal and excellence in higher education. Mason is currently the largest and most diverse university in Virginia with students and faculty from all 50 states and over 135 countries studying in over 200 degree programs at campuses in Arlington, Fairfax and Prince William, as well as at learning locations across the commonwealth. Rooted in Mason’s diversity is a campus culture that is both rewarding and exciting, work that is meaningful, and opportunities to both collaborate and create. If you are interested in joining the Mason family take a look at our current opportunities and catch some Mason spirit at jobs.gmu.edu/! George Mason University, Where Innovation is Tradition. Department: Office of Research
Criminal Background Check:* Standard Background Check
Motor Vehicle Background Check:* No
Restricted Position?:* Yes, is not eligible for layoff or severance benefits. Job Category: Research Faculty
Role (State) Job Title:* Postdoctoral Research Fellow
- Computational and Experimental Neuroplasticity Laboratory
- Working Title:* Postdoctoral Research Fellow
- Computational and Experimental Neuroplasticity Laboratory
Job Type:* Full-Time
Position Number:* F8816z
Recruit Number:* Faculty
- 7158 Location: Fairfax, VA
Salary:* Commensurate with education and experience. For Full Consideration, Apply by: October 10, 2017 Posting Date: 09/13/2017 Open Until Filled?: Yes
Telework Friendly?:* No
Equity Statement:* George Mason University is an equal opportunity/affirmative action employer, committed to promoting inclusion and equity in its community. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Campus Safety Information: Mason’s Annual Security and Fire Safety Report is available at http://police.gmu.edu/annual-security-report/
Research Scientist, Experimental Design And Causal Inference
Research Scientist, Experimental Design and Causal Inference (Menlo Park, CA) Facebook's mission is to give people the power to build community and bring the world closer together. Through our family of apps and services, we're building a different kind of company that connects billions of people around the world, gives them ways to share what matters most to them, and helps bring people closer together.
Whether we're creating new products or helping a small business expand its reach, people at Facebook are builders at heart. Our global teams are constantly iterating, solving problems, and working together to empower people around the world to build community and connect in meaningful w
Ad-Director, Early Clinical Development And Experimental Sciences - IO
Summary: Qualified physician or scientist with experience in the pharmaceutical/biotechnoloigy sector, or academic clinical setting. Works with supervisor and other members of the cross-functional study team to author/contribute to early clinical development protocols and facilitate execution of study activities and data summarization.
Contributes to/leads the cross-functional study team on the following activities, including but not limited to:
Collaborates on/designs POC-enabling human studies, First-In-Human (FIH) studies, POC (clinical and/or pharmacologic) studies as per clinical strategy. Responsible for the relevance and accuracy of medical science underpinning of clinical study based on thorough scientific review and consultation with internal and external experts. o Reviews, edits and finalizes clinical trial plans o Organizes and conducts consultations with global opinion leaders • Reviews and finalizes the medical and scientific portions of clinical study concepts (CSCs) and clinical study protocols (CSPs) and amendments. Reviews and edits documents related to trials, such as monitoring plans, SAPs, amendments, IRB/IEC submissions and regulatory submissions.
Accountable, with input from Clinical Trial Management and Biostatistics and Data Management for timely clinical trial execution and quality of deliverables: o Leads and supervises the Clinical Team to produce high quality program deliverables on schedule o Identifies program, trial or data risks, creates and implements mitigation strategies o Maintains and develops relationship with key study investigators o Organizes clinical expert consultations, steering committees and data safety monitoring boards as required o Reports to supervisor and management on clinical trial findings and milestones o Responsible for the medical content of clinical study reports o Reviews all medical/scientific publications related to clinical trial • Analyzes the benefits and risk aspects of an assigned therapeutic candidate: o Responsible for the analysis of clinical data, including safety monitoring o Responsible for activities and procedures that ensure patient safety • Ensures Clinical Team compliance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety. Authors/contributes to clinical sections of communications/documentation for regulatory agencies and may participate in meetings as needed. Conducts detailed literature reviews and analysis of development opportunities from mechanistic, pharmacological and clinical development perspectives.
Working with the ECD&ES Disease Area Lead, takes lead on various collaborations with TFA Research and Regeneron Genetic Center (RGC) colleagues to understand current and emerging targets/molecule program, provide clinical input on potential disease areas/indications, and design clinical experiments that corroborate or inform the biology for decision-making purposes.
Education: M.D. degree. Board Certification/eligibility in a relevant therapeutic area preferred, along with relevant industry experience, or Ph.D. degree.
Post-doctoral experience preferred, or Bachelors degree in biomedical subject, masters degree preferred, along with relevant industry experience. Experience 2-4 years prior industry experience or practice experience, preferably in a research/academic setting Experience in analysis of clinical and basic research information from a wide range of topics. Effective communications (verbal & written) and presentation skills are essential.
Must be able to work productively in a fast-paced collaborative environment. Demonstrated critical thinking skills and sound decision-making This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regenerons unwavering commitment to combining good science & good business.
To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place.
In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.
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