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Behavior Analyst

Surrey

Upto 26K per annum

Main duties and responsibilities

Provide the support, care and teaching identified in learners' individual learning plans and curriculum

Plan, prepare and deliver sessions and activities to learners supporting the development of knowledge and skills as outlined in their individualised curriculum

Provide behaviourally based support and reduce behaviours that cause barriers to learning and quality of life

Support learners' participation in social, leisure and educational activities within the local community, applying theory-based learning to practice

Facilitate and support learners in decision making, promoting choice and involvement giving full regard to initiatives aimed at promoting individual empowerment

Collect, record and analyse data on learners' progress, ensuring learning support and care is appropriate and effective, making changes where needed

Once trained, administer medication in accordance with company policies and procedures, and ensure that medical emergencies are dealt with appropriately

Participate in relevant training to achieve required qualifications and attend mandatory training days/ courses, on- or off-site, as and when required

PERSON SPECIFICATION

Knowledge, skills and experience

Educated to a degree level

Professional, personal or voluntary experience of working with adults or young people with disabilities

Interest in special educational needs, specifically autism

Passionate about helping others learn and develop skills

A positive, patient, caring and can-do attitude

Ability to work as part of a team and build good working relationships with learners, parents and staff

Ability to keep accurate records and reports to track learner progress

Confidence in maintaining confidentiality and discretion

Personal qualities

Soundly analyses verbal and numerical data

Contributes to improve work methods, outcomes and team performance

Adapts to new ideas and initiatives relevant to own area of work

Manages the workload and completion of tasks by setting timelines and milestones, and involving stakeholders to deliver on time

Invites and builds upon the ideas of others

Building relationships

Follows-up with learners during and after the delivery of services to ensure that their needs have been met

Ensures service is provided to learners during critical periods

Prioritises learners' issues and address them accordingly

Understands the reason behind, or motivation for someone's actions

Recognises what is and is not acceptable/possible at certain times given the Organisational rules, structures, decision-making bodies, power relationships, Code of Conduct and values

Please note: This role is also known as Learning Support Worker

THE POST HOLDER WILL BE SUBJECT TO AN ENHANCED DISCLOSURE AND BARRING SERVICE (DBS) CHECK

REF : G01

About Us

We are dedicated to fostering a diverse and inclusive community. In line with our Diversity and Inclusion policy, we welcome applications from all qualified individuals, regardless of age, gender, ethnicity, sexual orientation, or disability. As a Disability Confident Employer, and part of the Nicholas Associates Group, we are committed to supporting candidates with disabilities, and we're happy to discuss flexible working options.

We are committed to protecting the privacy of all our candidates and clients. If you choose to apply, your information will be processed in accordance with the Nicholas Associates Group of companies Privacy Notice.

Talentmark are recruiting for a Social Value Analyst to join a company in the pharmaceutical industry on a contract basis for 12 months, with potential for extension. This role is hybrid, based in Burgess Hill, with in-office attendance for workshops.

Company:
Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products.

Salary:
220 to 260 per day PAYE, or 291.36 to 344.34 per day Umbrella/Ltd.

Social Value Analyst Role:

• Work with teams across the business so that everyone understands their part in delivering social value.
• Track and coordinate the social value promises made in NHS tenders and contracts.
• Organise volunteering activities and encourage more colleagues to take part.
• Support charity sponsorship agreements, approvals and payments.
• Collect, check and analyse data to produce the annual Social Value Impact Report.
• Track progress against action plans and contract promises using dashboards, and prepare simple impact summaries for customers.

• You have a degree and 3 to 5 years of relevant work experience.
• You have practical experience in social value, sustainability or community impact, and you know how promises turn into real results. Knowledge of UK public sector buying and the National TOMs is a plus.
• You are confident working with data and enjoy checking it and finding insights, not just recording it.
• You can run projects from start to finish and keep actions, people and deadlines on track. You can also manage several tasks at once.
• You communicate clearly, build good working relationships quickly, and are happy using digital and AI tools. Experience with the Social Value Portal is an advantage.

Talentmark are recruiting for a QC Analyst to join a global healthcare provider to hospitals, clinics and homes on a contract basis for 6 months. This role is fully site based in Swindon.

The Company:
Our client is the global leader in enabling pharma, biotech, and consumer health partners to optimise product development, launch, and full life-cycle supply for patients around the world. They have the goal of putting patients first and to help people around the world live better and healthier lives.

Salary:
13.85 ph PAYE

QC Analyst Role:

• Conduct Finished Product QC release testing as required.
• Support commercial batch release.
• Conduct QC testing using a range of techniques such as Balances, pH meter, UV, Karl Fisher, FT-IR, TLC and Dissolution.
• Perform analytical work with average testing volumes/output whilst generating data.
• Write and review SOPs and technical reports.

• Hold a scientific degree or have equivalent working experience.
• Hands-on experience of working in a cGXP lab environment.
• Working knowledge of HCPL Empower, method development, troubleshooting and validation.
• Any experience in the pharmaceutical industry would be an advantage.

The role is responsible for delivering accurate data, meaningful performance insights, process improvements, and digital solutions that enable informed decision making, optimise operational performance, and support the stable supply of products to customers; to enhance the effectiveness, efficiency, and digital maturity of the supply chain through ownership of supply chain master data, business process management, analytics, and systems support.

Client Details

This role is within the Pharmaceutical industry and is based in Hertfordshire.

Description

• Own and maintain Supply Chain master data governance, ensuring the accuracy and integrity of end to end master and operational data across
• Plan, source, make, deliver and manage finance processes within ERP and supporting systems.
• Develop, maintain and continuously improve digital solutions, dashboards and analytics tools to provide actionable insights on inventory, service, planning, capacity and supply chain performance.
• Leverage digital technologies, automation and AI-enabled tools to improve planning accuracy, increase operational efficiency and support data-driven decision making.
• Act as a key user for supply chain systems, supporting system enhancements, testing, implementation activities and user training where required.
• Lead business process management activities including process mapping, process standardisation, root cause analysis and continuous improvement initiatives across the end-to-end supply chain.
• Identify opportunities to simplify processes, eliminate waste and improve operational performance through Lean, Continuous Improvement and digital transformation methodologies.
• Assist with the review of capacity with Production to smooth the supply flow during periods of constraint.
• Conduct root cause analysis on supply chain issues including shortages, excess inventory, forecast variance and service failures
• Support monthly demand and supply review processes with analysis of planning data.
• Use data-driven insights to support decision-making and recommend actions to improve service, inventory and cost performance.

Profile

A successful Supply Chain Digital Analyst should have:

• Demonstratable experience in supply chain, production planning, procurement, logistics, or manufacturing.
• Experience in pharmaceutical, biotechnology, medical device, healthcare, or FMCG manufacturing preferred.
• Master Data Management and Data Governance.
• Advanced analytical and reporting capability using Excel, Power BI and data visualisation tools.
• Experience of digital supply chain systems and ERP applications (SAP preferred).
• Microsoft Suite focus on Power apps / tools.
• Understanding and practical application of AI-assisted tools to enhance planning, analysis and operational decision making.
• Understanding of MRP (Material Requirements Planning).
• Bachelor's degree in supply chain management, Business Analytics, Business, Operations Management, Engineering, Pharmacy, Life Sciences, or related field.

Job Offer

• Salary ranging from 60,000 to 65,000, dependent on the level of experience.
• 15% performance-based bonus.
• Private health insurance (single coverage).
• Dental insurance (single coverage).
• Life assurance at 4x your annual salary.
• 26 days of annual leave plus bank holidays.
• Hybrid working model with three days per week in the office.

If you're interested in this role, apply now.

People are at the heart of Michael Page. We are committed to creating an inclusive environment. As an inclusive recruiter we welcome applications from people of all backgrounds, identities and experiences. If you require any adjustments or accommodations during the recruitment process, we'll work with you to ensure you can perform at your best.

Accounts Payable Analyst Swindon

Opportunity:

Are you currently working in accounts payable dealing with invoices? Does your experience include managing payment controls and dealing with supplier payments? Want to work for a large pharmaceutical manufacturing company? Yes then this is the role for you!

Your role as an Accounts Payable Analyst based in Swindon will involve processing supplier invoices, completing appropriate checks for business approval and/or PO matches and entering the invoice details onto the ERP system.

Duties and responsibilities include:

• Processing supplier invoices with precision, ensuring correct approvals and purchase order matching.
• Entering invoice data into the companies ERP system accurately and efficiently.
• Upholding compliance with internal controls and company payment policies.
• Managing supplier queries, invoice matching, indexing, and coding.

This is a 6 months contract which will be reviewed for a possible extension or go permanent however this is dependent on the candidate and business performance. The PAYE rate is £13.58 per hour.

Skills:

To apply for the Accounts Payable Analyst role you will have the following skills:

• Accounts Payable process experience.
• Working with suppliers.
• Excellent verbal, analytical, inter-personal skills.
• A team player who thrives in a fast-paced, collaborative environment.

How to Apply:

To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website.

If this sounds like the role for you or a colleague then please do not hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information.

For a list of our current vacancies, please visit the Quality Start website.

If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role.

Quality Start are acting as a specialist recruitment consultancy for this role.

Accounts Payable Analyst Swindon

Opportunity:

Are you currently working in accounts payable dealing with invoices? Does your experience include managing payment controls and dealing with supplier payments? Want to work for a large pharmaceutical manufacturing company? Yes then this is the role for you!

Your role as an Accounts Payable Analyst based in Swindon will involve processing supplier invoices, completing appropriate checks for business approval and/or PO matches and entering the invoice details onto the ERP system.

Duties and responsibilities include:

• Processing supplier invoices with precision, ensuring correct approvals and purchase order matching.
• Entering invoice data into the companies ERP system accurately and efficiently.
• Upholding compliance with internal controls and company payment policies.
• Managing supplier queries, invoice matching, indexing, and coding.

This is a 6 months contract which will be reviewed for a possible extension or go permanent however this is dependent on the candidate and business performance. The PAYE rate is £13.58 per hour.

Skills:

To apply for the Accounts Payable Analyst role you will have the following skills:

• Accounts Payable process experience.
• Working with suppliers.
• Excellent verbal, analytical, inter-personal skills.
• A team player who thrives in a fast-paced, collaborative environment.

How to Apply:

To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website.

If this sounds like the role for you or a colleague then please do not hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information.

For a list of our current vacancies, please visit the Quality Start website.

If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role.

Quality Start are acting as a specialist recruitment consultancy for this role.

About The Role
Team - Risk Intelligence & Ops MI
Working Pattern - Hybrid - 2 days per week in the Vitality London or Bournemouth Office. Full time hours per week.
We are happy to discuss flexible working!

Top 3 skills needed for this role:

• Extensive Healthcare Analytics Expertise
• Advanced Claims Data Insight
• Proven Strategic Stakeholder Influence

Regulatory Affairs Specialist

Location: West London
Hours: 40 hours per week

Are you an experienced Regulatory Affairs professional with a strong background in food, beverage or FMCG labelling?

I'm recruiting on behalf of a globally recognised drinks business looking to add a Regulatory Affairs Specialist to its EMEA team in London. This is a fantastic opportunity to join a fast-paced, highly innovative organisation, supporting a substantial pipeline of new product launches, flavour extensions and packaging changes across European markets.

The Role

Working as part of the EMEA Regulatory team, you'll take ownership of labelling development and regulatory compliance, ensuring products meet relevant EU food and beverage legislation.

Key responsibilities will include:

• Leading label development and compliance reviews for new products, flavour extensions and packaging changes.
• Reviewing product labels and artwork for accuracy and compliance with EU food and beverage regulations.
• Coordinating artwork approvals with internal creative, graphics, marketing and regulatory teams, as well as external partners.
• Monitoring and interpreting regulatory developments across EU markets, assessing their potential impact on existing and future products.
• Supporting product and raw material registrations, testing requirements and associated regulatory documentation.
• Working closely with international colleagues to ensure consistency across corporate labelling and compliance standards.
• Supporting technical product queries relating to areas such as allergens, added sugars and vegan/vegetarian suitability.
• Maintaining accurate regulatory documentation and identifying opportunities to improve and streamline existing processes.

About You

We're looking for someone who ideally has:

• 3-5+ years' Regulatory Affairs experience within food, beverages or dietary supplements.
• A degree in a scientific or related discipline.
• Strong working knowledge of EU food and beverage legislation and labelling requirements.
• Hands-on experience with label development, artwork approval and compliance reviews.
• Exposure to product or raw material registration would be highly advantageous.
• Excellent attention to detail with the ability to manage multiple projects and priorities simultaneously.
• Strong communication skills and confidence working with stakeholders across different functions and international markets.
• Beverage industry experience would be particularly advantageous.

Why Apply?

This is an excellent opportunity to join an internationally recognised, market-leading beverage business with a significant European presence and an exciting innovation pipeline.

You'll work in a highly collaborative international environment, gain exposure to a wide range of European markets and play an important role in bringing new products and innovations to market.

Interested? Apply today or get in touch with me directly for a confidential conversation and further information.

All candidates must have full UK working rights. Unfortunately, my client cannot facilitate those on a PSW Visa or requiring sponsorship

Regulatory Affairs Specialist - Dundee - Office Based.

The Regulatory Specialist is a key member of the Compliance Team, responsible for supporting and maintaining regulatory compliance across the business. The role focuses on ensuring that products, processes and quality systems meet applicable UK, Swiss, EU and international regulatory requirements.

Working closely with internal stakeholders and regulatory authorities, the Regulatory Specialist provides regulatory expertise across product registrations, vigilance, regulatory intelligence, change assessments and technical documentation.

Key Responsibilities

• Manage regulatory activities
• Oversee regulatory compliance activities including vigilance, regulatory intelligence, change assessments and regulatory submissions.
• Act as a key point of contact with regulatory authorities, including the MHRA and Swissmedic.
• Manage product inclusion activities for the UK and Swiss markets, ensuring products meet relevant regulatory requirements.
• Assess changes to regulatory requirements, legislation and quality standards and determine their impact on the Quality Management System.
• Support the implementation of regulatory and quality requirements across the organisation.
• Manage and maintain technical documentation
• Provide clear regulatory advice and communicate effectively with internal stakeholders, including executive-level leadership.
• Support the ongoing development and maintenance of quality and compliance systems.
• Identify opportunities to improve regulatory processes, communication and productivity.
• Maintain awareness of relevant company policies, regulatory requirements and industry best practice.
• Support other compliance and regulatory activities as required by the Compliance Manager.

Experience & Qualifications

• Degree or equivalent qualification, preferably within a life sciences discipline.
• Relevant experience within the life sciences, medical device or similarly regulated industry.
• Experience within the In-Vitro Diagnostics (IVD) sector would be advantageous.
• Strong knowledge of Quality Systems, Quality Assurance and regulatory compliance.
• Knowledge of relevant standards and regulations, including ISO 13485, 21 CFR, MDSAP, EU IVDD/IVDR and ISO 14971.
• Experience working with Electronic Document Management Systems (EDMS).
• Proficiency in Microsoft Word, Excel and PowerPoint.

Skills & Competencies

• Strong attention to detail with a high level of accuracy.
• Excellent organisational and time-management skills.
• Strong written and verbal communication skills.
• Confident communicating with senior and executive-level stakeholders.
• Ability to interpret regulatory requirements and assess their impact on business and quality systems.
• Self-motivated, proactive and committed to continuous professional development.
• Able to work effectively both independently and as part of a small, collaborative team.

We are looking for an experienced Compliance Engineer to join a exciting medical device organisation and support regulatory compliance across the full product lifecycle.

This medical device Compliance Engineer opportunity would suit someone with strong technical documentation experience who enjoys working across Quality, Engineering, NPD and Manufacturing within a highly regulated environment.

The Role

As Compliance Engineer, you will be responsible for creating, reviewing and maintaining regulatory and technical documentation to ensure products remain compliant and audit-ready.

Key Compliance Engineer responsibilities will include:

• Authoring and maintaining Technical Files, Design Dossiers and regulatory documentation.

• Supporting EU MDR and UK regulatory compliance activities.

• Preparing technical reports, declarations and compliance records.

• Supporting regulatory submissions, registrations and market access activities.

• Reviewing documentation for accuracy, completeness and regulatory compliance.

• Managing documentation updates following design, process or regulatory changes.

• Supporting risk management and design control documentation.

• Assisting with Notified Body, Competent Authority and external audit requirements.

• Monitoring changes to regulations, standards and guidance.

• Supporting post-market compliance and regulatory change assessments.

• Contributing to continuous improvement of Quality and Regulatory processes.

About You

The successful Compliance Engineer will ideally have:

• Experience within medical devices (ISO13485), pharmaceuticals or another regulated life sciences environment.

• Strong experience creating and maintaining controlled technical documentation.

• Knowledge of EU MDR 2017/745, ISO 13485 and ISO14971

• Understanding of design control, risk management and technical documentation requirements.

• Experience supporting regulatory submissions or Technical File activities.

• Excellent technical writing and attention to detail.

• Strong organisational and cross-functional communication skills.

The Compliance Engineer will work closely with Quality, Engineering, Product Development and Manufacturing teams, providing compliance input into both existing products and new product development.

This Compliance Engineer position offers the opportunity to take ownership of meaningful compliance activities while developing broader exposure across regulatory submissions, product lifecycle management and international medical device requirements.

If you are a medical device Compliance Engineer looking for a technically varied role within a regulated medical device environment, apply to discuss the opportunity in more detail.