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IP Life Science Associate
2 days ago
Top Tier Reps LLC Washington, United StatesJob Description · Job DescriptionYearly Salary: $250,000 to $345,000 · The company is seeking a mid-level patent litigation associate to join their Intellectual Property & Technology Practice Group in our New York, Silicon Valley, or Washington, DC offices. · The Intellectual Pro ...
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Director, Life Sciences
5 days ago
Alvarez and Marsal Washington, United States**Description** · **Director, Life Sciences** · Alvarez & Marsal (A&M) is a premier independent global professional services firm specializing in providing turnaround management, restructuring, performance improvement, and corporate advisory services. · At A&M, our Life Sciences ...
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Life Sciences Corporate – Mid-Level Associate
3 weeks ago
GOODWIN Washington, United StatesJob Details · Goodwin offers a new and exciting opportunity for a mid-level corporate associate to join our award winning Life Sciences team You will join a dynamic practice that concentrates on corporate transactions for cutting-edge high growth, life sciences, healthcare and t ...
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Vanguard-IP Washington, United States Full timeREQUIREMENTS · A strong scientific background and Ph.D. in a relevant life sciences discipline (e.g., molecular biology, biochemistry, genetics, and immunology) are required. For technical professionals, desire to take the patent bar exam or those applying as registered Patent Ag ...
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BGB Group Washington, United StatesJob Description · Job DescriptionKx Advisors is seeking to expand its ranks with an ambitious and motivated Associate Consultant. Kx Advisors provides strategic support to executives at leading Pharmaceutical, Medical Device, and Health IT companies. Our work leverages primary re ...
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BGB Group Washington, United StatesJob Description · Job DescriptionKx Advisors provides strategic support to executives at leading Pharmaceutical and Medical Device companies. Consultants and Senior Consultants at Kx Advisors are a critical part of every project team, and support engagements by managing the resea ...
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Recruiter (Life Science)
2 weeks ago
Intellipro, Inc. Rockville, United StatesThe best suited individuals have a passion and background in life sciences and are capable of working in a less structured, fast-paced environment · Effective IT capabilities including working knowledge of MS Office and Google Apps and openness to learning new systems and cloud S ...
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Analyst – Life Sciences Consulting
3 weeks ago
Sia Partners Elkridge, United StatesSia Partners is a next-generation management consulting firm. We offer a unique blend of AI and design capabilities, augmenting traditional consulting to deliver superior value to our clients. Counting 3,000 consultants in 19 countries, we expect to achieve USD 420 million in tur ...
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Analyst - Life Sciences Consulting
2 weeks ago
Sia Partners Elkridge, United StatesCompany Description · Sia Partners is a next-generation management consulting firm. We offer a unique blend of AI and design capabilities, augmenting traditional consulting to deliver superior value to our clients. Counting 3,000 consultants in 19 countries, we expect to achieve ...
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Analyst Life Sciences Consulting
1 week ago
Sia Partners Elkridge, United StatesSia Partners is a next-generation management consulting firm. We offer a unique blend of AI and design capabilities, augmenting traditional consulting to deliver superior value to our clients. Counting 3,000 consultants in 19 countries, we expect to achieve USD 420 million in tur ...
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Analyst - Life Sciences Consulting
2 weeks ago
Latham BioPharm Group Elkridge, United StatesJob Description · Job DescriptionCompany Description · Sia Partners is a next-generation management consulting firm. We offer a unique blend of AI and design capabilities, augmenting traditional consulting to deliver superior value to our clients. Counting 3,000 consultants in 19 ...
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Deilegal Washington, United States Full timeAM Law 100 Firm's Washington D.C. office is seeking associates to join its Intellectual Property - Life Sciences practice. · Requirements · Experience: Seeking midlevel and senior associate with one to seven years of patent prosecution experience in a biotechnology practice, alon ...
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Life Science Teacher
2 weeks ago
Prince William County Public Schools Manassas, United StatesLIFE SCIENCE TEACHER - 195 DAY- JOB STATUS: · - OPEN- EFFECTIVE: · POSTING DATE: · - 05/10/2024- CLOSING DATE: · - 06/01/2025 04:30 PM- POSTING NUMBER: · SCHOOL/DEPARTMENT: · - Saunders MS- LOCATION: · - Manassas,VA- POSITION TITLE: · - LIFE SCIENCE TEACHER - 195 DAY- ADDITIONAL- ...
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Marketing Communications Manager- Life Sciences
2 weeks ago
Mettler-Toledo International, Inc Columbia, United StatesOur Opening and Your Responsibilities · As our Marketing Communications Manager, you will be responsible for Marketing Communications strategy and execution with a goal to drive target market awareness and customer engagement, demand generation, and ultimately sales growth. You ...
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Phase I Oncology Clinical Research Associate
6 days ago
Randstad Life Sciences US Bethesda, United StatesCompetitive Pay: $90+/HR commensurate with experience · Title: Clinical Research Associate-This will be a home based role when not traveling. · Position type: This is a 1 year contract position that is eligible for renewal. · Location: Bethesda, MD or Washington D.C. or Northern ...
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Analyst Life Sciences Consulting
3 weeks ago
Sia Partners Elkridge, United StatesIn this role you will support the organization in providing program management and general services to life sciences companies and institutions to advance novel life science products (therapeutics, vaccines, diagnostics, and devices), primarily in th Science, Analyst, Support, Cl ...
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Analyst – Life Sciences Consulting
3 weeks ago
Latham BioPharm Group Elkridge, Maryland, United States PermanentJob Description · In this role you will support the organization in providing program management and general services to life sciences companies and institutions to advance novel life science products (therapeutics, vaccines, diagnostics, and devices), primarily in the areas of c ...
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Life Sciences Inventory Specialist
2 weeks ago
Kolon TissueGene Rockville, United States**Essential Job Functions and Duties** · **Inventory Management**: · - Stockroom services (material handling, purchasing/order entry/inventory management, material shipment and receipt). · - Routinely register, update, and monitor inventory levels at vendor locations. · - Manage ...
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Analyst - Life Sciences Consulting
3 weeks ago
Latham BioPharm Group Elkridge, United States**Company Description** · Sia Partners is a next-generation management consulting firm. We offer a unique blend of AI and design capabilities, augmenting traditional consulting to deliver superior value to our clients. Counting 3,000 consultants in 19 countries, we expect to achi ...
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Learning And Development Specialist
6 days ago
GForce Life Sciences Gaithersburg, United StatesLearning and Development Partner · Duration: 12-month contract · 3 days/week onsite in Gaithersburg, MD · Responsibilities: · Work closely with project leads to gather technical content from R&D subject matter experts. Using a solid understanding of R&D you will assimilate and ...
Supplier Quality Engineer, Life Sciences - Washington DC, United States - Spacelabs Healthcare LLC
Description
Job DescriptionResponsibilities:
Supporting the development teams of all business areas, working within the project teams on new or sustaining product development projects.
Support the remediation and maintenance of all Technical Documentation Files.
Support the maintenance of the Essential Requirements Checklists / General Safety and Performance Requirements checklist.
Assist with the compliance to changes to standards such as EN , ROHS3, REACH, and Global regulatory requirements applicable to Spacelabs' products
supporting the manufacturing teams of all business areas, working within the teams on new or sustaining product improvements.
Perform Manufacturing floor walkthroughs.
Executes Corrective and Preventive Action (CAPA), including root cause identification, action planning, reporting, and completion of remedial action plans.
Trains other team members on the CAPA process.Facilitates an effective Internal Quality Audit program: Plan, perform, and document internal audits.
Drive compliance activities and improvements, covering, but not limited to, risk management, design and development, safety, manufacturing, purchasing, process control, labeling, usability, and service.
Supports and/or facilitates quality system tool updates (Computer System Validation plan, protocol, report).Drive product continuous improvement efforts for legacy products and processes: Utilizes measurement system analysis (MSA) to track product quality, to include Statistical Process Control (SPC), I-charts, or other methodologies, as well as identifying quality opportunities associate with Product Failure Methods and Effects Analysis (PFMEA) and Control Plans.
Makes quality decisions on products of questionable quality, safety, or efficacy based on drawings, specifications, fit, functionality, testing, risk assessment, customer requirements, and postmarket surveillance data.
Gathers and presents product quality performance statistics on a regular basis.Initiates and leads the development of test methods, tooling, techniques, and procedures for parts analysis and investigation. Advises management on quality-related continuous process improvement opportunities for Design and Change Control and manufacturing.
Perform investigations to identify and eliminate the cause of product and process nonconformances.
Drive programs and projects to reduces product Field Failure Rate, address Hot Topics, and resolve Top Issues from the field.
Assess trending metrics, establish standardized reporting mechanisms, analyze results to identify emerging trends and improvement opportunities, and effectively communicate results through appropriate venues.
Analysis of customer complaints related to manufacturing and product design, to include coordinating investigation and reporting of findings and recommendations.
Collaborate with Operations staff to initiate, perform evaluations, and implement action plans to eliminate root causes of non-conformances.Collaborate with Supplier Quality and Supply Chain to drive projects and programs at Supplier sites.
Participate in continuous improvement activities.
Support the Master Validation Plan (MVPs) for Spacelabs products
Support Validation and Verification activities across the organization.
Act as the primary reviewer for Quality Engineering for Engineering Change Orders that support legacy products and processes.
Develop and maintain Service MVPs
Perform other related duties as required.
Makes risk-based decisions as required to support corporate policies.
Upholds the Company's core values of Integrity, Innovation, Accountability, and Teamwork.
Demonstrates behavior consistent with the Company's Code of Ethics and Conduct.
Ensure that direct report(s) are trained and evaluated on their knowledge and adherence to the Company's values, Code of Ethics and Conduct, and applicable compliance policies.
It is the responsibility of every Spacelabs Healthcare employee to report to their manager or a member of senior management any quality problems or defects in order for corrective action to be implemented and to avoid recurrence of the problem.
Duties may be modified or assigned at any time to meet the needs of the business.Qualifications:
~ Bachelor's degree in an engineering or related discipline, (Computer/Software, Biomedical, Mechanical, Electrical).
~7+ years related Engineering / quality engineering experience.
~5+ years of experience with medical device regulatory and quality systems.
~ Experience supporting the implementation of Software as a Medical Device (SaMD) or Software within a device required.
~ Experience reading, interpreting, and correcting CAD drawings/ schematics.
~ Experience maintaining Technical Files, GSRPCs, Risk Management Files, Usability Engineering Files, Design History Files, MVP's, and Change Control documentation.
~ Experience with statistical analysis and data mining.
~ Experience working with teams under design controls and during new product development to follow the QMS and comply with current regulations and standards.
#LI-Hybrid
Please review our benefits here: Life at OSI
The specific programs and options available to any given employee may vary depending on eligibility factors such as geographic location and date of hire.
Please note that the salary information shown above is a general guideline only. Salaries are based upon candidate experience and qualifications, as well as market and business considerations.NOTICE TO THIRD PARTY AGENCIES
OSI Systems, Inc. and its subsidiaries (collectively "OSI") does not accept unsolicited resumes from recruiters or employment agencies.
If any person or entity, including a recruiter or agency, submits any information, including any resume or information regarding any potential candidate, without a signed agreement in place with OSI, OSI explicitly reserves the right to use such information, and pursue and/or hire such candidates, without any financial obligation to the person, recruiter or agency.
Any unsolicited information or resumes, including those submitted directly to hiring managers, are considered and deemed to be the property of OSI.
Equal Opportunity Employer - Disability and Veterans
EEO is the Law
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OSI Systems, Inc
has three operating divisions:
(a) Security, providing security and inspection systems, turnkey security screening solutions and related services; (b) Healthcare, providing patient monitoring, diagnostic cardiology and anesthesia systems; and (c) Optoelectronics and Manufacturing, providing specialized electronic components and electronic manufacturing services for original equipment manufacturers with applications in the defense, aerospace, medical and industrial markets, among others.
