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Veterans Stabilization Case Manager II at GOODWILL OF SILICON VALLEY
San Jose, California, United States - Full Time
Skills Needed
Case Management, Participant Support, Trauma Informed Practices, Crisis Intervention, Motivational Interviewing, Data Entry, Documentation, Collaboration, Communication, Problem Solving, Job Readiness Coaching, Career Planning, Housing Navigation, Community Engagement, Organizational Skills, Interpersonal Skills
Specialization
Candidates must have a bachelor's degree in a related field and a minimum of 2 years of experience in workforce development or related services. Proficiency in Microsoft Office and CRM systems is required, along with strong communication and organizational skills.
Experience Required
Minimum 2 year(s)
Regulatory Affairs Specialist at Dexcom
San Diego, California, United States - Full Time
Skills Needed
Regulatory Affairs, Medical Device, Software Development, Technical Documentation, Cross Functional Collaboration, Risk Assessment, Fda Regulations, Iso Standards, Agile Methodologies, Digital Health, Mobile Development, Ai Technologies, Communication Skills, Change Assessment, Validation Activities, Project Management
Specialization
Candidates should have experience in medical device design and development, with knowledge of relevant regulations and standards. Excellent writing and communication skills are essential, along with a passion for the medical device industry.
Experience Required
Minimum 2 year(s)
Regulatory Affairs Specialist at Dr Reddy's Laboratories Limited
Hyderabad, Telangana, India - Full Time
Skills Needed
Regulatory Affairs, Fda Guidelines, Interpersonal Skills, Communication Skills, Attention To Detail, Multi Tasking, English Proficiency, Computer Proficiency, Google Applications, Ms Excel
Specialization
Candidates must have a Bachelor of Science in Pharmacy or Industrial Pharmacy and a minimum of 3 to 5 years of experience in regulatory affairs. Knowledge of FDA guidelines and proficiency in English and computer applications are also required.
Experience Required
Minimum 2 year(s)
Specialist 2, General Affairs at Coherent Corp. Vietnam
Binh Duong, Bình Định Province, Vietnam - Full Time
Skills Needed
Vendor Management, Contract Negotiation, Cost Optimization, Interpersonal Communication, Presentation Skills, Office Management, Ehs Standards, Multitasking, Process Improvement, Event Planning, Administrative Duties, Budget Management, Customer Satisfaction, Team Coordination, Compliance, English Communication
Specialization
Candidates should have a bachelor's degree in relevant fields and at least 3 years of experience in office management or administrative roles. Proficiency in English and strong interpersonal skills are also required.
Experience Required
Minimum 2 year(s)
Specialist 2, General Affairs at Coherent Corp. Vietnam
Thuận An, , Vietnam - Full Time
Skills Needed
Vendor Management, Contract Negotiation, Cost Optimization, Interpersonal Communication, Presentation Skills, Compliance Knowledge, Ehs Standards, Office Management, Administrative Duties, Event Planning, Budget Management, Customer Satisfaction, Process Improvement, Team Coordination, English Communication, Vietnamese Communication
Specialization
Candidates should have a bachelor's degree in relevant fields and at least 3 years of experience in office management or administrative roles. Proficiency in English and Vietnamese communication is also required.
Experience Required
Minimum 2 year(s)
Director, Regulatory Affairs at Prolaio
Chicago, Illinois, United States - Full Time
Skills Needed
Regulatory Strategy, Fda Compliance, 510(k) Submissions, Regulatory Affairs, Medical Device, Qms Environment, Labeling Approval, Marketing Compliance, Regulatory Changes Assessment, Record Keeping, Team Leadership, Consultant Management, Ous Mdr Experience, Samd Knowledge, Digital Health, Cross Functional Collaboration
Specialization
Candidates must possess a Bachelor's degree in a scientific, engineering, or regulatory field, along with over 7 years of leadership experience in medical device regulatory affairs (CDRH), including direct FDA interaction and 510(k) submission experience. A strong command of FDA requirements, global standards, and experience with software-based medical devices are essential.
Experience Required
Minimum 5 year(s)
Business Affairs Legal Intern at Create Music Group
, , United States - Full Time
Skills Needed
Agreement Drafting, Contract Review, Document Creation, Salesforce, Project Management, Communication, Detail Oriented, Self Learning, Microsoft Office, Adobe, Music Industry Knowledge
Specialization
Candidates must be currently enrolled in law school and possess strong organizational and communication skills. An interest in the legal field and some music industry experience is preferred.
Regulatory Affairs Specialist at Dexcom
Vilnius, Vilnius County, Lithuania - Full Time
Skills Needed
Regulatory Affairs, Medical Device Industry, Technical Skills, Research Skills, Problem Solving Skills, Communication Skills, Advertising Review, Promotional Materials, Project Management, Compliance, Team Collaboration, Veeva Promo Mats, Documentation Management, Regulatory Strategy, Market Authorization, Post Approval Changes
Specialization
Typically requires a minimum of 2-4 years of related experience in the medical device industry and a high school diploma or equivalent. Strong technical, research, and problem-solving skills are essential, along with the ability to articulate complex ideas clearly.
Experience Required
Minimum 2 year(s)
Academic Affairs Coordinator at Webster University
Webster Groves, Missouri, United States - Full Time
Skills Needed
Attention To Detail, Verbal Communication, Written Communication, Microsoft Office, Excel, Data Organization, Data Tracking, Data Reporting, Problem Solving, Customer Service, Confidentiality, Organizational Skills, Planning, Prioritization, Multi Tasking, Software Aptitude
Specialization
A Bachelor's Degree is required, with a Master's Degree preferred. Candidates should have strong communication skills, attention to detail, and experience working with data.
Experience Required
Minimum 2 year(s)
Regulatory Affairs Associate at RIVERPOINT MEDICAL LLC
Portland, Oregon, United States - Full Time
Skills Needed
Regulatory Submissions, Fda 510(k), Eu Mdr, Technical Documentation, Risk Analysis, Customer Service, Quality System, Clinical Evaluation, Post Market Surveillance, Product Labeling, Scientific Rationale, Regulatory Requirements, Medical Devices, Iso13485, Mdsap
Specialization
Candidates should have 1-5 years of experience in Regulatory Affairs related to medical devices and a solid understanding of relevant regulations. The ability to create technical dossiers and assess project risks is essential.
Experience Required
Minimum 2 year(s)
Regulatory Affairs Specialist at GSK
Seoul, , South Korea - Full Time
Skills Needed
Regulatory Affairs, Product Registration, Life Cycle Management, New Chemical Entity, Line Extension, Labeling Update, Regulatory Submissions, Stakeholder Communication, Regulatory Agency Guidelines, Safety Issues Handling, Impact Analysis, English Communication, Collaboration, Registration Planning, Regulatory Update, Strategic Planning
Specialization
Candidates should have at least 3 years of regulatory experience and a bachelor's degree in a relevant field such as Pharmacy or Life Sciences. Knowledge of regulatory agency guidelines and proficiency in English communication are also required.
Experience Required
Minimum 2 year(s)
Specialist Corporate Affairs at PMCL-JAZZ
Islamabad, Islamabad Capital Territory, Pakistan - Full Time
Skills Needed
Stakeholder Management, Government Relations, Policy Analysis, Regulatory Compliance, Communication, Ms Office
Specialization
A Bachelor’s degree in business administration, public administration, or economics is required. Proficiency in MS Office and strong communication skills are also necessary.
Regulatory Affairs Specialist at 3M
São Paulo, São Paulo, Brazil - Full Time
Skills Needed
Regulatory Affairs, Medical Devices, English Proficiency, Communication Skills, Organizational Skills, Attention To Detail, Cross Functional Collaboration, Audit Participation, Global Strategy, Market Access, Cosmetic Regulatory Experience, Microsoft Office Proficiency, Curiosity, Creativity, Compliance, Product Licensing
Specialization
A Bachelor’s degree or higher from an accredited institution and experience in Regulatory Affairs in Medical Devices are required. Advanced English speaking and writing competency is also necessary, along with additional qualifications that could enhance success in the role.
Experience Required
Minimum 2 year(s)
Decedent Affairs Coordinator at Emory Healthcare
Atlanta, Georgia, United States - Full Time
Skills Needed
Communication Skills, Listening Skills, Windows Based Pc Skills, Microsoft Office, Decedent Care, Funeral Home Experience
Specialization
A high school diploma or GED is required, with a preference for a baccalaureate degree in a health-related field or mortuary sciences. Previous experience in Decedent Care or a Funeral Home is strongly preferred.
Experience Required
Minimum 2 year(s)
Director of External Affairs at Plymouth Housing Group
Seattle, Washington, United States - Full Time
Skills Needed
Public Policy, Advocacy, Community Engagement, Data Analysis, Project Management, Budget Management, Relationship Building, Public Speaking, Collaboration, Organizational Leadership, Human Services, Policy Making, Problem Solving, Inclusivity, Networking, Communication
Specialization
Candidates must have a bachelor's degree in public policy or a related field, along with a minimum of five years of relevant experience in human services or government affairs. Experience in advocacy and community leadership is also essential.
Experience Required
Minimum 5 year(s)
Regulatory Affairs Specialist at Nature's Bakery
Chicago, Illinois, United States - Full Time
Skills Needed
Regulatory Affairs, Ingredient Compliance, Project Management, Attention To Detail, Us Food Regulations, Label Review, Certification Management, Documentation Creation, Supplier Coordination, Audit Management, Non Gmo Certification, Fast Paced Environment, Independent Execution, Quality Assurance, Legal Text Creation, Product Specification
Specialization
Candidates should have 3-5 years of experience in food sector regulatory affairs and expertise in US food regulations. Experience with non-GMO certification is preferable, along with strong organizational skills.
Experience Required
Minimum 2 year(s)
Regulatory Affairs Principal at Danaher - Canada
Sunnyvale, California, United States - Full Time
Skills Needed
Regulatory Affairs, New Product Development, Regulatory Submissions, Cross Functional Collaboration, Regulatory Strategy, Project Management, Continuous Improvement, Regulatory Intelligence, Assay Development, Software Projects, Quality Assessment, Presentation Skills, Communication Skills, Problem Solving, Team Collaboration, Health Authorities Interaction
Specialization
Candidates must have a Bachelor's degree with 8+ years of experience, a Master's degree with 6+ years, or a Doctoral degree with 3+ years in applicable fields. Experience in regulatory submissions and project management is essential.
Experience Required
Minimum 10 year(s)
Regulatory Affairs Specialist at Merck Serono SA
Warszawa, Pomeranian Voivodeship, Poland - Full Time
Skills Needed
Regulatory Affairs, Project Management, Stakeholder Management, Communication Skills, Regulatory Compliance, Dossier Review, Submission Management, Quality Control, Attention To Detail, Proactive Communication, Product Registration, Artwork Approval, Health Authorities Interaction, Cross Functional Alignment, Time Management, Strategic Activities Execution
Specialization
Candidates should have a university degree in pharmacy or medicine and 2-4 years of experience in regulatory affairs. Strong project management skills, attention to detail, and proficiency in English and Polish are essential.
Experience Required
Minimum 2 year(s)
Public Affairs Manager India at Air Liquide
, , India - Full Time
Skills Needed
Public Affairs, Government Relations, Public Relations, Strategic Thinking, Communication Skills, Media Relations, Crisis Management, Networking, Brand Management, Legislative Affairs, Regulatory Affairs, Content Management, Social Media, Stakeholder Engagement, Training, Team Management
Specialization
Candidates should have a Bachelor's or Master's degree in a relevant field and at least 7 years of experience in public affairs or related areas. Strong strategic thinking and communication skills are essential, along with knowledge of public policy processes.
Experience Required
Minimum 5 year(s)
Regulatory Affairs Specialist at Nox Medical
Reykjavik, , Iceland - Full Time
Skills Needed
Regulatory Affairs, Medical Devices, Technical Documentation, Quality Management System, Compliance, Audits, Analytical Skills, Communication Skills, Attention To Detail, Organizational Skills, Problem Solving Skills, Research Skills, Design Reviews, Market Surveillance, English Proficiency, Technological Skills
Specialization
Candidates must have a B.Sc degree in Biomedicine, Engineering, or a related field, along with experience in regulatory affairs within the medical devices or pharmaceutical industry. Strong analytical, communication, and organizational skills are essential for this role.
Experience Required
Minimum 2 year(s)
Veterans Stabilization Case Manager II at GOODWILL OF SILICON VALLEY
San Jose, California, United States -
Full Time

Start Date

Immediate

Expiry Date

03 Apr, 26

Salary

34.0

Posted On

03 Jan, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Case Management, Participant Support, Trauma-Informed Practices, Crisis Intervention, Motivational Interviewing, Data Entry, Documentation, Collaboration, Communication, Problem-Solving, Job Readiness Coaching, Career Planning, Housing Navigation, Community Engagement, Organizational Skills, Interpersonal Skills

Industry

Retail

Description
Job Details Job Location: Main Plant - San Jose, CA 95112 Position Type: Full Time Education Level: 4 Year Degree Salary Range: $30.00 - $34.00 Hourly Travel Percentage: Up to 50% Job Shift: Day This is a full-time, in-person position for the Veterans Services Program, located at 1600 Technology Dr, San Jose, CA. Summary At Mission Services of Silicon Valley, our purpose is simple and powerful: to help people build skills, find meaningful work, and thrive in our community. For nearly 100 years, we’ve been a trusted partner in connecting opportunity with people’s potential. By working hand in hand with local experts, employers, and community members, we create pathways to education, employment, and lasting economic mobility. As a team, we are committed to: Empowering one another to do our best work and grow together. Building strong partnerships and serving as a driving force for economic opportunity in Silicon Valley. Modeling teamwork, integrity, and cultural intelligence in everything we do. Acting with mutual respect for each other, our community, and the nvironment we share. The Stabilization Case Manager II (CM II) provides intermediate-level case management and participant support within Mission Services programs. CM IIs operate with greater autonomy, manage more complex cases, and ensure participants move from crisis to stability through coordinated housing, employment, and supportive services. The CM II uses trauma-informed practices, maintains high-quality documentation, and collaborates closely with internal and external partners to support long-term participant success. CM IIs may be assigned to: – Employment-Based programs (STRIVE, AB109, HVRP, NOW, CTE, Expandability) – Housing-Based programs (SSVF, BSCC) – Integrated service teams as needed Job Responsibilities Case Management & Participant Support (40%) Conduct comprehensive intakes, eligibility determinations, and barrier assessments within required program timelines. Develop individualized stabilization, housing, or employment plans with participants, ensuring goals are measurable and updated monthly. Provide trauma-informed coaching, motivational interviewing, crisis intervention, and problem-solving support. Maintain a consistent meeting cadence with participants (weekly, bi-weekly, or per program standards). Support participants in resolving barriers such as transportation, food insecurity, legal issues, documentation needs, behavioral health access, childcare, and technology. Coordinate warm handoffs to internal teams (Career Navigators, Housing Navigators, Healthcare Navigators) and external partners. Track progress toward stabilization, housing, or employment goals, adjusting interventions based on participant needs. Perform fieldwork as required, including home visits, employer visits, drop-ins at interim housing sites, site verifications, and partner meetings. Respond to crises promptly and develop short-term stabilization plans within 72 hours. Conduct safety assessments as needed and follow escalation protocols for risk, mandated reporting, or critical incidents. Employment or Housing Stabilization Services (35%) Depending on assignment: Employment-Based: • Deliver job readiness coaching, career planning, and employment navigation. • Provide job leads, employer introductions, and placement support. • Monitor 30/60/90-day retention and address workplace barriers. • Support participants in accessing training, credentials, or transitional work programs. Housing-Based: • Assist participants in identifying, securing, and maintaining safe, affordable housing. • Conduct unit habitability reviews and coordinate with landlords. • Support housing retention through ongoing case monitoring. • Navigate participants through benefits, rental assistance, and subsidy programs. Documentation, Compliance & Data Quality (15%) Maintain 98% timely and accurate data entry (within 48 hours). Ensure all required documents, case notes, plans, and assessments meet audit standards (CARF, VA, DOL, City/County). Participate in file audits and correct issues promptly. Use CRM systems (CaseWorthy, HMIS, or program-specific systems) with reliability and consistency. Intake forms Assessments (VI-SPDAT, employment assessments, needs assessments) IHP/IEP plans Income verification, housing verification, habitability forms Supportive service requests HMIS ROI and consent forms • Participate in internal audits, CARF reviews, VA compliance checks, and contract monitoring. • Resolve data corrections and discrepancies within 5 business days. • Maintain file organization and documentation standards meeting 90% audit accuracy. Cross-Functional Collaboration & Partnerships (10%) Coordinate services with internal teams (Career Navigators, Housing Navigators, Employment Specialists). Participate in case conferencing, huddles, and interdisciplinary meetings. Build and maintain relationships with referral partners, community organizations, and employer partners. Represent MSSV with professionalism at outreach or partner events Maintain accurate and timely documentation in program databases aligned with funders, CARF, and internal compliance standards. Qualifications Required Qualifications/Experience The ideal candidate possesses the following qualifications, skills, and abilities: Bachelor's degree in Business, Human Services, Education, or related field (or equivalent combination of education and experience). Minimum 2 years of experience in workforce development, career coaching, job placement, or related services. Equivalent experience may include teaching, academic advising, recruiting, training facilitation, case management, or other roles requiring individualized coaching, employer engagement, and measurable outcome achievement. Proficiency in Microsoft Office, Google Workspace, and CRM/case management systems and workforce development management platforms Preferred Qualifications/Experience Experience working with diverse and underserved populations (veterans, unhoused, individuals with disabilities, or trainees). Familiarity with ADA requirements and reasonable accommodations, and ability to support participants and employers in applying inclusive workplace practices. Proven track record of building and maintaining professional networks that generate tangible business results, Experience using data to inform program requirements and decision-making Familiarity with OKR (Objectives and Key Results) or similar goal-setting frameworks Knowledge of labor market trends, hiring incentives, and workforce development best practices. Strong communication, presentation, and employer relationship-building skills. Aptitudes/skills/temperament Data analysis and interpretation skills to identify trends and inform strategy Comfort with ambiguity and ability to balance competing priorities in dynamic environments Strategic thinking with ability to connect daily activities to broader organizational mission Continuous improvement or Growth mindset with willingness to experiment and learn from both successes and failures Attention to detail and strong organizational skills. Ability to manage multiple priorities in a fast-paced environment. Strong interpersonal skills and ability to build trust with diverse populations, accountability, empathy, and cultural awareness. Excellent written and oral communication skills. Ability to collaborate across teams and community partners. Key Performance Indicators Success in this role will be measured by the ability to: Stabilize Participants Through Rapid, High-Quality Case Management Improve Housing & Income Outcomes Through Coordinated Navigation Deliver Integrated Navigation Across Housing, Employment, Benefits & Stability Services Strengthen Compliance, Quality, and Professional Excellence (Cross-Functional) Job Requirements: Reliable transportation Possess a valid California Driver’s License. Must be computer literate. Knowledge of MS Office required. Working and Physical conditions Location: Goodwill of Silicon Valley's headquarters in San Jose. There is regular contact with the public, business, and community agencies. The position requires minimal supervision. The job involves sedentary work, frequently sitting for an extended period in front of a computer monitor. This position may occasionally require lifting objects up to 20 lbs. Responsibilities may be added, deleted or changed at any time at the discretion of management, formally or informally either orally or in writing Mission Services of Silicon Valley is an Equal Opportunity and Affirmative Action Employer encouraging diversity in the workplace. All qualified applicants will receive consideration for employment without regard to their race, color, creed, religion, national origin, citizenship status, ancestry, sex, age, physical or mental disability unrelated to ability, marital status, family responsibilities, pregnancy, genetic information, sexual orientation, gender expression, gender identity, transgender, sex stereotyping, order of protection status, protected veteran or military status, or an unfavorable discharge from military service, and other categories protected by federal, state or local law
Responsibilities
The Stabilization Case Manager II provides intermediate-level case management and participant support, ensuring participants move from crisis to stability through coordinated housing, employment, and supportive services. Responsibilities include conducting intakes, developing individualized plans, and providing ongoing support to resolve barriers.
Veterans Stabilization Case Manager II at GOODWILL OF SILICON VALLEY
San Jose, California, United States - Full Time
Skills Needed
Case Management, Participant Support, Trauma Informed Practices, Crisis Intervention, Motivational Interviewing, Data Entry, Documentation, Collaboration, Communication, Problem Solving, Job Readiness Coaching, Career Planning, Housing Navigation, Community Engagement, Organizational Skills, Interpersonal Skills
Specialization
Candidates must have a bachelor's degree in a related field and a minimum of 2 years of experience in workforce development or related services. Proficiency in Microsoft Office and CRM systems is required, along with strong communication and organizational skills.
Experience Required
Minimum 2 year(s)
Regulatory Affairs Specialist at Dexcom
San Diego, California, United States - Full Time
Skills Needed
Regulatory Affairs, Medical Device, Software Development, Technical Documentation, Cross Functional Collaboration, Risk Assessment, Fda Regulations, Iso Standards, Agile Methodologies, Digital Health, Mobile Development, Ai Technologies, Communication Skills, Change Assessment, Validation Activities, Project Management
Specialization
Candidates should have experience in medical device design and development, with knowledge of relevant regulations and standards. Excellent writing and communication skills are essential, along with a passion for the medical device industry.
Experience Required
Minimum 2 year(s)
Regulatory Affairs Specialist at Dr Reddy's Laboratories Limited
Hyderabad, Telangana, India - Full Time
Skills Needed
Regulatory Affairs, Fda Guidelines, Interpersonal Skills, Communication Skills, Attention To Detail, Multi Tasking, English Proficiency, Computer Proficiency, Google Applications, Ms Excel
Specialization
Candidates must have a Bachelor of Science in Pharmacy or Industrial Pharmacy and a minimum of 3 to 5 years of experience in regulatory affairs. Knowledge of FDA guidelines and proficiency in English and computer applications are also required.
Experience Required
Minimum 2 year(s)
Specialist 2, General Affairs at Coherent Corp. Vietnam
Binh Duong, Bình Định Province, Vietnam - Full Time
Skills Needed
Vendor Management, Contract Negotiation, Cost Optimization, Interpersonal Communication, Presentation Skills, Office Management, Ehs Standards, Multitasking, Process Improvement, Event Planning, Administrative Duties, Budget Management, Customer Satisfaction, Team Coordination, Compliance, English Communication
Specialization
Candidates should have a bachelor's degree in relevant fields and at least 3 years of experience in office management or administrative roles. Proficiency in English and strong interpersonal skills are also required.
Experience Required
Minimum 2 year(s)
Specialist 2, General Affairs at Coherent Corp. Vietnam
Thuận An, , Vietnam - Full Time
Skills Needed
Vendor Management, Contract Negotiation, Cost Optimization, Interpersonal Communication, Presentation Skills, Compliance Knowledge, Ehs Standards, Office Management, Administrative Duties, Event Planning, Budget Management, Customer Satisfaction, Process Improvement, Team Coordination, English Communication, Vietnamese Communication
Specialization
Candidates should have a bachelor's degree in relevant fields and at least 3 years of experience in office management or administrative roles. Proficiency in English and Vietnamese communication is also required.
Experience Required
Minimum 2 year(s)
Director, Regulatory Affairs at Prolaio
Chicago, Illinois, United States - Full Time
Skills Needed
Regulatory Strategy, Fda Compliance, 510(k) Submissions, Regulatory Affairs, Medical Device, Qms Environment, Labeling Approval, Marketing Compliance, Regulatory Changes Assessment, Record Keeping, Team Leadership, Consultant Management, Ous Mdr Experience, Samd Knowledge, Digital Health, Cross Functional Collaboration
Specialization
Candidates must possess a Bachelor's degree in a scientific, engineering, or regulatory field, along with over 7 years of leadership experience in medical device regulatory affairs (CDRH), including direct FDA interaction and 510(k) submission experience. A strong command of FDA requirements, global standards, and experience with software-based medical devices are essential.
Experience Required
Minimum 5 year(s)
Business Affairs Legal Intern at Create Music Group
, , United States - Full Time
Skills Needed
Agreement Drafting, Contract Review, Document Creation, Salesforce, Project Management, Communication, Detail Oriented, Self Learning, Microsoft Office, Adobe, Music Industry Knowledge
Specialization
Candidates must be currently enrolled in law school and possess strong organizational and communication skills. An interest in the legal field and some music industry experience is preferred.
Regulatory Affairs Specialist at Dexcom
Vilnius, Vilnius County, Lithuania - Full Time
Skills Needed
Regulatory Affairs, Medical Device Industry, Technical Skills, Research Skills, Problem Solving Skills, Communication Skills, Advertising Review, Promotional Materials, Project Management, Compliance, Team Collaboration, Veeva Promo Mats, Documentation Management, Regulatory Strategy, Market Authorization, Post Approval Changes
Specialization
Typically requires a minimum of 2-4 years of related experience in the medical device industry and a high school diploma or equivalent. Strong technical, research, and problem-solving skills are essential, along with the ability to articulate complex ideas clearly.
Experience Required
Minimum 2 year(s)
Academic Affairs Coordinator at Webster University
Webster Groves, Missouri, United States - Full Time
Skills Needed
Attention To Detail, Verbal Communication, Written Communication, Microsoft Office, Excel, Data Organization, Data Tracking, Data Reporting, Problem Solving, Customer Service, Confidentiality, Organizational Skills, Planning, Prioritization, Multi Tasking, Software Aptitude
Specialization
A Bachelor's Degree is required, with a Master's Degree preferred. Candidates should have strong communication skills, attention to detail, and experience working with data.
Experience Required
Minimum 2 year(s)
Regulatory Affairs Associate at RIVERPOINT MEDICAL LLC
Portland, Oregon, United States - Full Time
Skills Needed
Regulatory Submissions, Fda 510(k), Eu Mdr, Technical Documentation, Risk Analysis, Customer Service, Quality System, Clinical Evaluation, Post Market Surveillance, Product Labeling, Scientific Rationale, Regulatory Requirements, Medical Devices, Iso13485, Mdsap
Specialization
Candidates should have 1-5 years of experience in Regulatory Affairs related to medical devices and a solid understanding of relevant regulations. The ability to create technical dossiers and assess project risks is essential.
Experience Required
Minimum 2 year(s)
Regulatory Affairs Specialist at GSK
Seoul, , South Korea - Full Time
Skills Needed
Regulatory Affairs, Product Registration, Life Cycle Management, New Chemical Entity, Line Extension, Labeling Update, Regulatory Submissions, Stakeholder Communication, Regulatory Agency Guidelines, Safety Issues Handling, Impact Analysis, English Communication, Collaboration, Registration Planning, Regulatory Update, Strategic Planning
Specialization
Candidates should have at least 3 years of regulatory experience and a bachelor's degree in a relevant field such as Pharmacy or Life Sciences. Knowledge of regulatory agency guidelines and proficiency in English communication are also required.
Experience Required
Minimum 2 year(s)
Specialist Corporate Affairs at PMCL-JAZZ
Islamabad, Islamabad Capital Territory, Pakistan - Full Time
Skills Needed
Stakeholder Management, Government Relations, Policy Analysis, Regulatory Compliance, Communication, Ms Office
Specialization
A Bachelor’s degree in business administration, public administration, or economics is required. Proficiency in MS Office and strong communication skills are also necessary.
Regulatory Affairs Specialist at 3M
São Paulo, São Paulo, Brazil - Full Time
Skills Needed
Regulatory Affairs, Medical Devices, English Proficiency, Communication Skills, Organizational Skills, Attention To Detail, Cross Functional Collaboration, Audit Participation, Global Strategy, Market Access, Cosmetic Regulatory Experience, Microsoft Office Proficiency, Curiosity, Creativity, Compliance, Product Licensing
Specialization
A Bachelor’s degree or higher from an accredited institution and experience in Regulatory Affairs in Medical Devices are required. Advanced English speaking and writing competency is also necessary, along with additional qualifications that could enhance success in the role.
Experience Required
Minimum 2 year(s)
Decedent Affairs Coordinator at Emory Healthcare
Atlanta, Georgia, United States - Full Time
Skills Needed
Communication Skills, Listening Skills, Windows Based Pc Skills, Microsoft Office, Decedent Care, Funeral Home Experience
Specialization
A high school diploma or GED is required, with a preference for a baccalaureate degree in a health-related field or mortuary sciences. Previous experience in Decedent Care or a Funeral Home is strongly preferred.
Experience Required
Minimum 2 year(s)
Director of External Affairs at Plymouth Housing Group
Seattle, Washington, United States - Full Time
Skills Needed
Public Policy, Advocacy, Community Engagement, Data Analysis, Project Management, Budget Management, Relationship Building, Public Speaking, Collaboration, Organizational Leadership, Human Services, Policy Making, Problem Solving, Inclusivity, Networking, Communication
Specialization
Candidates must have a bachelor's degree in public policy or a related field, along with a minimum of five years of relevant experience in human services or government affairs. Experience in advocacy and community leadership is also essential.
Experience Required
Minimum 5 year(s)
Regulatory Affairs Specialist at Nature's Bakery
Chicago, Illinois, United States - Full Time
Skills Needed
Regulatory Affairs, Ingredient Compliance, Project Management, Attention To Detail, Us Food Regulations, Label Review, Certification Management, Documentation Creation, Supplier Coordination, Audit Management, Non Gmo Certification, Fast Paced Environment, Independent Execution, Quality Assurance, Legal Text Creation, Product Specification
Specialization
Candidates should have 3-5 years of experience in food sector regulatory affairs and expertise in US food regulations. Experience with non-GMO certification is preferable, along with strong organizational skills.
Experience Required
Minimum 2 year(s)
Regulatory Affairs Principal at Danaher - Canada
Sunnyvale, California, United States - Full Time
Skills Needed
Regulatory Affairs, New Product Development, Regulatory Submissions, Cross Functional Collaboration, Regulatory Strategy, Project Management, Continuous Improvement, Regulatory Intelligence, Assay Development, Software Projects, Quality Assessment, Presentation Skills, Communication Skills, Problem Solving, Team Collaboration, Health Authorities Interaction
Specialization
Candidates must have a Bachelor's degree with 8+ years of experience, a Master's degree with 6+ years, or a Doctoral degree with 3+ years in applicable fields. Experience in regulatory submissions and project management is essential.
Experience Required
Minimum 10 year(s)
Regulatory Affairs Specialist at Merck Serono SA
Warszawa, Pomeranian Voivodeship, Poland - Full Time
Skills Needed
Regulatory Affairs, Project Management, Stakeholder Management, Communication Skills, Regulatory Compliance, Dossier Review, Submission Management, Quality Control, Attention To Detail, Proactive Communication, Product Registration, Artwork Approval, Health Authorities Interaction, Cross Functional Alignment, Time Management, Strategic Activities Execution
Specialization
Candidates should have a university degree in pharmacy or medicine and 2-4 years of experience in regulatory affairs. Strong project management skills, attention to detail, and proficiency in English and Polish are essential.
Experience Required
Minimum 2 year(s)
Public Affairs Manager India at Air Liquide
, , India - Full Time
Skills Needed
Public Affairs, Government Relations, Public Relations, Strategic Thinking, Communication Skills, Media Relations, Crisis Management, Networking, Brand Management, Legislative Affairs, Regulatory Affairs, Content Management, Social Media, Stakeholder Engagement, Training, Team Management
Specialization
Candidates should have a Bachelor's or Master's degree in a relevant field and at least 7 years of experience in public affairs or related areas. Strong strategic thinking and communication skills are essential, along with knowledge of public policy processes.
Experience Required
Minimum 5 year(s)
Regulatory Affairs Specialist at Nox Medical
Reykjavik, , Iceland - Full Time
Skills Needed
Regulatory Affairs, Medical Devices, Technical Documentation, Quality Management System, Compliance, Audits, Analytical Skills, Communication Skills, Attention To Detail, Organizational Skills, Problem Solving Skills, Research Skills, Design Reviews, Market Surveillance, English Proficiency, Technological Skills
Specialization
Candidates must have a B.Sc degree in Biomedicine, Engineering, or a related field, along with experience in regulatory affairs within the medical devices or pharmaceutical industry. Strong analytical, communication, and organizational skills are essential for this role.
Experience Required
Minimum 2 year(s)