Assistant Director of Development - Philanthropy, Comprehensive Cancer Center Job at Advocate Health Care (Winston Salem)

Assistant director of development - philanthropy, comprehensive cancer center

The Assistant Director of Development - Philanthropy, Comprehensive Cancer Cente...

Location

United States , Winston Salem

Salary:

47.50 - 71.25 USD / Hour

Advocate Health Care

Expiration Date

Until further notice

Requirements

Bachelor’s degree
five years of fundraising experience, including major gifts
experience leading volunteer fundraising boards
ability to work in a complex environment with the personal and technical skills necessary to establish priorities, set objectives, and achieve goals
adeptness in working with high net worth individuals and faculty/physicians
excellent written and oral communication skills
strong leadership and interpersonal skills
ability to relate research and program goals to external audience
capacity to build and maintain long-term relationships
proven presentation abilities

Job Responsibility

Serves as the philanthropic leader for Atrium Health Wake Forest Baptist’s Comprehensive Cancer Center
reports to the Director of Major Gifts
maintains a close working relationship with the Director of the Comprehensive Cancer Center, Director of the Cancer Clinical Service Line and section heads for Hematology/Oncology, Radiation Oncology and Surgical Oncology
supervises at least one Major Gift Officer
leads the cancer fundraising effort on behalf of the Medical Center including raising funds that support education, research, patient aid, and clinical care
develops a philanthropic plan for the Comprehensive Cancer Center and provides strategic oversight of the plan
identify, cultivate, and solicit individuals for major gifts ($50K+) and leadership gifts ($1M+) to the Center
build and maintain a portfolio high-profile prospects
develop strategies for solicitations
work with research, annual funds, events, and special gifts teams to establish and implement strategies for identifying and qualifying major gifts prospects

What we offer

Paid Time Off programs
Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
Flexible Spending Accounts for eligible health care and dependent care expenses
Family benefits such as adoption assistance and paid parental leave
Defined contribution retirement plans with employer match and other financial wellness programs
Educational Assistance Program
Opportunity for annual increases based on performance

Fulltime

New

Sr Principal Engineer - Software Quality

This is where new knowledge is discovered. Baxter’s Research and Development tea...

Location

United Kingdom , Gloucester

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Bachelor of Science or Bachelor of Engineering in Software Engineering, Computer Science, Electrical, Biomedical, or related discipline required
Master’s degree or PhD preferred with 10+ years of progressive experience in software quality engineering, including regulated medical device software and/or digital health platforms
Strong expertise in: ISO 13485 Quality Management Systems
EU MDR (Regulation (EU) 2017/745) and software implications
Software lifecycle standards (e.g., IEC 62304, IEC 82304 where applicable)
FDA software and quality system expectations
Proven ability to integrate Agile development practices with regulatory compliance, including traceability, documentation, and change management
Broad understanding of: Software architecture and system integration
Cloud-based systems, cybersecurity, and data privacy considerations
Software risk management, including hazard analysis and vulnerability management

Job Responsibility

Lead and govern activities that ensure alignment with Baxter’s Product Lifecycle Management (PDLM) and Change Control Management (CCM) processes and compliance with design controls and quality system regulations
Translate Agile software development practices into compliant frameworks that meet Baxter, ISO 13485 and EU MDR expectations, including traceability, documentation, verification, and validation
Ensure effective implementation of software design controls, including: Software requirements and architecture, Risk management (software hazard analysis, cybersecurity risk), Verification and validation strategies (manual, automated, CI/CD pipelines), Configuration and change management
Lead integration of Quality Management System (QMS) processes into software development workflows, including: CAPA and nonconformance handling, Complaint handling and feedback loops into Agile backlogs, Audit readiness and inspection support
Ensure compliance with EU MDR requirements, including: Support for technical documentation and software lifecycle evidence, Alignment of software changes with regulatory impact assessments, Post-market surveillance inputs (e.g., trending, signal detection)
Apply advanced quality and engineering tools including root cause analysis, reliability engineering, and data analytics to improve software quality and system performance
Oversee development of technical documentation supporting: Design history files (DHF) / technical files, Software lifecycle documentation (per IEC 62304 where applicable), Risk management files, Verification and validation reports, Regulatory submissions
Serve as subject matter expert for software quality, cybersecurity, and lifecycle management, providing guidance across teams and influencing enterprise-wide standards
Collaborate closely with Quality, Regulatory Affairs, R&D (software and systems), Product Management, Cybersecurity, Clinical, and Manufacturing teams to ensure software products are safe, effective, secure, and compliant

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

New

Eng II, Electrical

This is where new knowledge is discovered. Baxter’s Research and Development tea...

Location

India , Bengaluru

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Bachelor's Degree in Electrical/ Electronic engineering with 4-7 yrs. of work experience in design and development, testing of complex electrical/ Electronic components/ subsystems/ products
Experience in electromechanical hardware development, preferably medical devices or other highly regulated products such as military hardware
Ability to generate alternative solutions to problems or processes
Strong interpersonal skills with the ability to work collaboratively with others in a team environment
Excellent background in fundamentals of circuit design and analysis
Experience with industry leading software tools for schematic entry and PCB layout design
Experience with established development tools and processes. Especially PSpice, OrCAD, Mentor's DxDesigner and Expedition
Hands-on experience with analog/digital circuit and embedded systems designs is required
Hands-on experience with embedded platforms, 8-, 16- and 32-bit microcontrollers, Arm Cortex-M series processors
Experience in CAN, SPI, I2C and UART

Job Responsibility

Identifies technical problems, provides innovative, creative solutions
shares technical knowledge with team
Understanding of business, market, industry and competitive knowledge & integrating into technical solutions that can be readily adapted to changes in technology and/or clinical use
Generates alternatives and takes reasonable risks while solving technical problems
Work and collaborate closely with Project Manager & Team leads to define and solve engineering changes/problems to make products that meet all performance and functional criteria within required project schedule, with minimum guidance
Participate in design/change reviews with the Sustaining Team and Engineering Change Board – justify design detail and collaborate with other team members
Completes detailed, high quality technical documentation of product designs through the generation and maintenance of design requirement specifications, engineering prints, material specifications and bills-of-materials
Uses existing engineering tools and best practices to report and track product and process metrics
Challenges project teams and established work processes and proactively finds creative methods to reach desired performance levels
Informs others proactively about developments or issues that affect their work, and their ability to meet commitments

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

New

Associate Marketing Manager

This is where your work makes a difference. At Baxter, we believe every person—r...

Location

Malta , Marsa

Salary:

36000.00 EUR / Year

Baxter

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Marketing, Business, Life Sciences, Engineering, or a related field
advanced degree (MBA or similar) is a plus
Minimum 5–7 years of experience in product marketing, product management or commercial roles within medical devices, healthcare, or other regulated industries

Job Responsibility

Drive global marketing strategy and execution across the full product lifecycle for the Access portfolio
Serve as the primary commercial representative for new product development (NPD), sustaining project organization (SPO) initiatives, and in-market optimization
Work cross-functionally with R&D, Regulatory Affairs, Medical, Quality, Supply Chain, Finance, and regional marketing teams
Own and execute global marketing strategy for the Access/Sets portfolio
Develop and maintain portfolio roadmaps, prioritization recommendations, and resource needs
Identify unmet customer needs and growth opportunities through market analysis, competitive benchmarking, and customer engagement
Serve as the global marketing member on project core teams for NPD and SPO initiatives
Define and communicate market and customer requirements
Lead or support market research activities
Conduct market impact assessments for product changes and own assigned marketing deliverables

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Health & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
Competitive benefits
Discretionary bonuses
Long-term incentive

Fulltime

New

Pharmacy Technician

We’re building a world of health around every individual — shaping a more connec...

Location

United States , Gastonia

Salary:

16.50 - 25.00 USD / Hour

CVS Health

Expiration Date

August 29, 2026

Requirements

Must comply with any state board of pharmacy requirements or laws governing the practice of pharmacy, which includes but is not limited to, age, education, and licensure/certification
If the state board of pharmacy does not address or mandate a minimum age requirement, must be at least 16 years of age
If the state board of pharmacy does not address or mandate a minimum educational requirement, must have a high school diploma or equivalent, or be actively enrolled in high school or high school equivalency program
State-level licensure and national certification requirements vary by state
Regular and predictable attendance, including nights and weekends
Ability to complete required training within designated timeframe
Attention and Focus: Ability to concentrate on a task over a period of time
Ability to pivot quickly from one task to another to meet patient and business needs
Ability to confirm prescription information and label accuracy, ensuring patient safety
Customer Service and Team Orientation: Actively look for ways to help people, and do so in a friendly manner

Job Responsibility

Living our purpose by following all company SOPs at each workstation to help our Pharmacists manage and improve patient health
Following pharmacy workflow procedures at each pharmacy workstation (i.e., production, pick-up, drive-thru, and drop-off) for safe and accurate prescription fulfillment
Contributing to positive patient experiences by showing empathy and genuine care: creating heartfelt and personalized moments while serving patients at pick-up, drive-thru, and over the phone
keeping patients healthy by offering immunizations and other services at the register and over the phone
and demonstrating compassionate care by solving or escalating patient problems
Completing basic inventory activities, as permitted by law, and as directed by the pharmacy leadership team, such as accurately putting away medication deliveries and completing cycle counts, returns-to-stocks, waiting bin inventories, etc.
Contributing to a high-performing team, embracing a growth mindset, and being receptive to feedback
actively seeking opportunities to expand clinical and technical knowledge needed to better assist patients
Remaining flexible for both scheduling and business needs, while contributing to a safe, inclusive, and engaging team dynamic
voluntarily traveling to stores in the market to work shifts as needed by the business

What we offer

medical coverage
dental coverage
vision coverage
paid time off
retirement savings options
wellness programs

Fulltime

New

Senior Manager, FLC

This is where new knowledge is discovered. Baxter's Research and Development tea...

Location

India , Bengaluru

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Bachelor's or Master's degree in Electrical/Electronics OR Mechanical OR Biomedical Engineering or related field
15+ years of experience in medical device or complex electro-mechanical product development
5+ years in functional leadership roles managing multi-disciplinary teams
Proven experience in global, matrixed R&D environments
Strong knowledge of: Electrical systems (electronics, embedded, control systems). Mechanical systems (materials, fluids, structures, plastics). System integration and verification methodologies
Deep expertise in electro-mechanical system design and integration
Strong people leadership, coaching, and organizational development skills
Ability to define and execute R&D strategies and influence senior stakeholders
Expertise in decision-making under ambiguity and complex problem-solving
Strong communication and stakeholder management skills

Job Responsibility

Define and execute the strategy for Hardware and Systems Verification functions, aligned with business and product roadmaps
Build, scale, and lead high-performing teams across Electrical, Mechanical, and V&V engineering disciplines
Drive organizational capability development, including talent pipeline, succession planning, and competency building
Influence global R&D strategies, technology roadmaps, and engineering best practices
Act as a technical and functional leader recognized across business units for programs of significant impact
Lead and oversee end-to-end product development lifecycle: Concept development, Architecture definition, Detailed design, Verification & validation, Transfer to manufacturing, Post-market sustainment
Ensure successful delivery of complex electro-mechanical systems integrating hardware, embedded software, and controls
Drive sustenance engineering, including root cause investigations, field issue resolution, and product enhancements
Partner with Program Management to ensure delivery within quality, cost, and schedule targets
Provide technical oversight across Electrical systems (mixed-signal, power electronics, sensors, control systems) and Mechanical systems (structural design, fluid management, plastics, disposables, simulation)

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

New

Core Team Lead - Sr Manager

This is where new knowledge is discovered. Baxter’s Research and Development tea...

Location

United States , Raleigh

Salary:

152000.00 - 209000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Bachelor's degree in a relevant field, such as engineering, science, or business
Minimum 5 years of experience in product development, with at least 3 years in a leadership role
Proven experience in leading complex engineering projects with cross-functional teams
Strong ability to convert business and customer needs into clear project objectives
Outstanding skills in project management, risk assessment, and issue resolution
Comprehensive understanding of technical, quality, regulatory, and compliance requirements
Demonstrated ability to manage budgets and resources efficiently
Excellent communication skills to convey project status and key decisions to collaborators effectively
A collaborative approach, driving alignment and successful implementation of project initiatives
Applicants must be authorized to work for any employer in the U.S.

Job Responsibility

Lead cross-functional project teams, aligning engineering, marketing, supply chain, quality, regulatory, and other collaborators to achieve project objectives
Translate business and customer needs into project goals, strategies, and implementation plans that support company objectives
Drive alignment across multiple business units to deliver connected platform requirements and product development initiatives
Develop, maintain, and adapt project plans, ensuring ongoing alignment of team priorities, achievements, and deliverables
Identify, assess, and mitigate project risks
manage issues, resolve conflicts, and implement contingency plans as needed
Ensure projects satisfy technical, quality, regulatory, and compliance standards while following corporate product development procedures
Manage project budgets, prioritization, and cost controls to ensure efficient execution and delivery
Communicate project status, progress, and key decisions to senior leadership and collaborators, building positive relationships to ensure successful outcomes and the happiness of interested parties

What we offer

Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
Flexible Spending Accounts
Educational assistance programs
Paid holidays
Paid time off ranging from 20 to 35 days based on length of service
Family and medical leaves of absence
Paid parental leave

Fulltime

New

Eng II, Systems

This is where new knowledge is discovered. Baxter’s Research and Development tea...

Location

India , Bengaluru

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Bachelor's Degree in Mechanical engineering, Electrical Engineering, Electronics Engineering, Software Engineering, Computer Science, Bio-Medical, Industrial Engineering or related field
3 to 6 yrs of experience, mainly in System engineering function of Electro-Mechanical System Design
Experience in Medical Device development, FDA Regulations and MDR
Exposure to Usability Engineering Process
Experience in QFD, Pugh Matrix, CTQ, DFR, DFX
Strong interpersonal skills with the ability to collaborate with others in a team environment
Understanding of and adherence to FDA, ISO and IEC design control procedures, regulations and standards
Demonstrated experience in accomplishing objectives
Able to deliver on multiple projects simultaneously
Self-motivated with good interpersonal skills

Job Responsibility

Identify and define internal and external customer needs, functions, performance, usability and safety requirement for product or solution with thorough knowledge and understanding constraints - Business and Regulatory, Design trade-offs and Risk assessment early in the development cycle working independently or under the guidance of senior staff
Provide your technical expertise to ensure that the project successfully meets cost, quality and schedule targets throughout the product life cycle
Excels in the development of Use Case for product or solution based on intimate knowledge of customers and their environments
Use tools such as DOORS, POLARION or equivalent and excels in the management of requirements and decomposition of system level requirements to modules
Carry out risk management process in accordance with the EN ISO 14971 throughout product life cycle to ensure compliance and product safety
Identify development issues and facilitates in the resolution using optimal technology solutions
Supports in the Usability Engineering activities to ensure the application of human factor in the development of products or solutions to demonstrate compliance to IEC 62366 and FDA guidance
Knowledge in the application of principles of Reliability and Robustness in the development of products or solutions
Completes detailed, high quality technical documentation to capture and communicate designs
Support integration issues during development tests and ensure module / system development is successful

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

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Assistant Director of Development - Philanthropy, Comprehensive Cancer Center

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