Medication Lead Job at 360 Resourcing Solutions (Stroud)

Medication Lead

The Nelson Trust is a leading charity supporting people to achieve long-term rec...

Location

United Kingdom , Stroud

Salary:

29000.00 - 30500.00 GBP / Year

360 Resourcing Solutions

Expiration Date

Until further notice

Requirements

NVQ Level 3 in Health & Social Care (or working towards) is desirable
Willingness to complete, or currently undertaking, an Advanced Medication Management qualification
Proven experience of medication administration and audit processes in a care or residential setting
Strong organisational skills with excellent attention to detail
Confidence liaising with healthcare professionals and managing clinical information
Knowledge of medication governance and safe medicines management (desirable)
Previous management or supervisory experience (desirable)
A professional, empathetic and non-judgemental approach aligned with The Nelson Trust values

Job Responsibility

Lead on the safe receipt, storage, administration, stock control and disposal/return of medication across four residential houses
Oversee and maintain the electronic MAR (eMAR) system, ensuring accuracy and timely recording
Administer medication when required, in line with competency and safety standards
Liaise with GP surgeries, pharmacies and healthcare professionals to ensure timely prescribing and supply of medication
Conduct regular medication audits, identifying risks, trends and areas for improvement
Monitor, report and investigate medication errors and near misses, embedding learning into practice
Coordinate all service user healthcare appointments, including follow-up and transport arrangements
Line manage the Medication Assistant and drivers, providing oversight and support

What we offer

25 days annual leave plus bank holidays
Employer pension contribution of 6%
Access to ongoing training, professional development and supervision
A supportive, values-led organisation committed to staff wellbeing and development

Fulltime

New

Team Leader Children's Home

We are recruiting on behalf of our client, a highly reputable residential childr...

Location

United Kingdom , Hatfield

Salary:

31200.00 GBP / Year ▼

Brook-St Hiredonline

Expiration Date

Until further notice

Requirements

NVQ Level 3 in Children and Young People, Residential Care
Previous experience in a residential care setting, preferably in a Team Leader role
Strong leadership, organisational, and communication skills
A full driving licence is essential

Job Responsibility

Oversee the completion of documentation, including chronologies, placement plans, and weekly reports
Lead shifts, ensuring activities, wellbeing walks, and residents' sessions are effectively carried out
Address residents' complaints in the absence of the Registered Manager
Monitor residents' wellbeing, including feeding and bathing charts, and provide mental health check-ins
Facilitate engaging activities for children within or outside the center
Conduct medication audits, fire drills, and ensure health and safety compliance across the center
Liaise with social workers, attend meetings, and manage weekly family schedules and reports
Supervise and support night staff to meet service needs
Notify OFSTED of serious events when necessary and coordinate with accounts on invoicing and spreadsheets
Participate in the on-call rota system and complete incident reports within 24 hours

What we offer

Competitive hourly rate of £15 per hour
The chance to make a real impact on the lives of children
Opportunities for professional development and growth within a supportive team environment
Annual Leave
Pension

Fulltime

New

Clinical Director Laboratory - Divisional

The Clinical Director of the Laboratory for Midlands Division directs one or mor...

Location

United States , Columbia

Salary:

Not provided

MUSC Health

Expiration Date

Until further notice

Requirements

Bachelor's degree in medical technology or Allied Sciences
Certification as a MT (ASCP registered)
5 years of management experience in a hospital setting
Knowledge of state, federal (CLIA), and Joint Commission regulations
Certification as a MT (ASCP registered)

Job Responsibility

Directs one or more major functional areas of a department, a department, or a business unit
Manages two or more professional and support staff including subordinate managers
Directs the analysis, planning, implementation, and expenditures and budget tracking of major operational projects or initiatives
Provides recommendations to the leaders throughout the organization
Leads in developing strategies and implementation plans to improve and standardize all aspects of operations
Ensures that reports of test results include all pertinent information required for interpretation and that meet regulatory compliance
Ensure that consultation is available to the laboratory's clients on matters relating to the quality of the test results reported and their interpretation concerning specific patient conditions
Directs the strategic initiatives of the laboratory addressing communication with internal and external customers for a timely response to new clinical service trends and program planning
Maintaining effective reimbursement processes through coding reviews and support to Charge Services with current best practice billing definitions
Advise, negotiate, manage and administer all contracts into which the lab may enter

Fulltime

New

Foreign Pharmacy Grad - International Pharmacy Intern

You’ve invested a lot of time and energy in your education. Now you want the cha...

Location

United States , Gloucester City

Salary:

30.00 - 42.00 USD / Hour

CVS Health

Expiration Date

August 28, 2026

Requirements

High School Diploma or General Equivalent Development (GED)
Doctorate (PharmD) or equivalent Pharmacist degree from a Non-US accredited school of pharmacy
active Pharmacy Intern license in state where district is located
0 to 3 years of prior relevant work experience
Foreign Graduate from a Non-US Accredited college or school of pharmacy prior to beginning Non-US Accredited Foreign Graduate Training Program at CVS
Strong communication and presentation skills
Have regular and predictable attendance including nights and weekends
Complete any additional tasks as directed by supervisor or manager
Complete all required training and obtain required licensure (if applicable) within guidelines
Lift and exert up to 20 lbs. of force occasionally, up to 10 lbs. of force frequently, and a negligible amount of force regularly to move objects to and from, including overhead lifting

Job Responsibility

Lead with Heart – display empathy and compassion for your patients, customers, caregivers, and colleagues on your team
Support your Pharmacy manager in motivating, inspiring, and developing their Pharmacy Support Staff by balancing assignments that maximize colleagues’ strengths, address development opportunities, and decrease knowledge gaps
Identify critical business opportunities and meaningful solutions to drive growth and improve performance in your pharmacy and work toward successfully implementing those solutions by leading your team to achieve specified goals
Adapt to change and adjust plans to thrive in a dynamic community healthcare setting
Seek new ways to grow, collaborate with others, and deliver better outcomes
Align others around our purpose to bring your heart to every moment of your health and gain support and commitment
Facilitate a ‘team’ culture that promotes caring, energy, enthusiasm, and pride
Apply acquired knowledge to help drive healthy outcomes and differentiate CVS from competitors
Greet each customer in a courteous and professional manner both in-store and at the drive thru window
Assist all pharmacy and front store customers with their questions and concerns

What we offer

Medical, dental, and vision coverage
Paid time off
Retirement savings options
Wellness programs

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

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

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Medication Lead

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Medication Lead

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