Regulatory Affairs and Quality Assurance Assistant – Medical Devices - Cambridge
Due to the growth of a medical devices company based in Cambridge, there is need for a new Regulatory Affairs and Quality Assurance Assistant to work with and support the company’s Quality Assurance and Regulatory Affairs Manager. The team provide quality assurance and regulatory affairs advise on the creation of new products and the improvement of existing technologies.
It would be highly advantageous if you have knowledge of design processes, but it’s not essential. This team does not just fill out quality assurance and regulatory documents; this is a team where they will be very involved with the R&D team, providing vital advice on the creation of medical devices, and ensuring the team operates within the FDA 510k, ISO 13485, and FDA 21 CFR Part 820 standards.
It would be ideal if you have both quality assurance and regulatory affairs knowledge. However, people have moved into this role from either regulatory affairs or quality assurance background, but with a general knowledge in the other side.
It is essential that you have medical devices knowledge, especially ISO 13485 and FDA 510k knowledge. Although writing submissions will not be a major part of your role, you will relay information to the teams responsible for this, so ideally you will have done this in the past or at least assisted.
Ideally, you will have QMS experience. If you do have this knowledge, I would advise making it clear on your CV as this is highly desirable in this role.
The products this company has been developing are industry-changing and will improve the lives of people around the world.
It is expected that you would hold a 1st or 2:1 degree within an engineering or sciences discipline along with some experience within regulatory affairs or quality assurance. Although experience working within a medical devices R&D or design team is more important than education.
This is a growing company; due to this, they offer career progression, excellent salary, benefits package, the chance to work on life-improving devices, and share options.
If you have regulatory affairs knowledge in the medical devices sector and are looking for a challenging role, then apply now.
I expect a lot of interest in this role, and the company are looking to recruit quickly. So, if you are interested in this role, I suggest applying immediately or risk missing out.
For more information, please feel free to call Andrew Welsh, Director of Medical Devices recruitment, Science recruitment and Biotech recruitment specialists Newton Colmore Consulting, on +44 121 268 2240 or make an application, and one of our team at Newton Colmore Consulting will contact you.....Read more...
The Regulatory International Operations organization spans over ten Pfizer offices in more than seven time zones. Each year the group supports approximately 40,000 submissions to 175 countries around the world, within both established and emerging markets. The group operates in a dynamic business environment and is a key contributor in ensuring quality dossiers are submitted on time to Health Authorities for the Pfizer portfolio. The Global Registrations & Renewal Support (GRRS) team are a team of operational experts that sit under Regulatory International Operations.
The GRRS team has a strong continuous improvement, project management and change management focus. The team specializes in sourcing Regulatory certificates and samples for the Emerging Market submissions while constantly evaluating and redesigning existing regulatory and operational processes. The team also perform cross-functional critical issue remediation and lead project/change management initiatives at a global scale.
As the Pharmaceutical Industry evolves Regulatory Operations act as a key stakeholders in the innovation, design, and implementation of new technical solutions, process designs and deployment through the global teams and networks.
Job Responsibilities:
This role will support initiatives of varying complexity, for which Regulatory Operations is either an owner or a major stakeholder.
The GRRS apprentice will:
Work in a busy, diverse regulatory environment developing critical business skills and be a valued member of a multidisciplinary team
Day-to-day delivery of regulatory certificates & product samples, working closely with senior leaders of the organisation
Logistics coordination:
Contribute to and manage global projects which aim to drive growth, improve business process and overall consolidate Pfizer’s position as the premier pharmaceutical company. Typical projects can include working on business transformation, building new capabilities, increasing business efficiency, re-designing complex processes or program management efforts in the regulatory operations arena
Partner with internal & external colleagues to support the operation and evaluation of existing processes, driving continuous improvement, learning and applying a variety of continuous improvement tools and methodologies
Main duties and Responsibilities:
Support business analysis and project management efforts to assist in ensuring the success of a broad variety of global initiatives and projects
Issue resolution and escalation for assigned projects
Recognise and analyze potential issues and provide a systematic approach to the solutions of these issues while noting any practical constraints
Contribute business solutions through influential partnerships with internal and external colleagues
Act as a key contributor within the areas of process development, decision making, and change management in the context of regulatory operations
Support cross-functional, global teams as appropriate
Develop and maintain documented procedures and guidelines as necessary
Support in future recruitment of Undergraduates and/or apprentices
Training:
Training for this apprenticeship will be completed online
Training Outcome:
Upon successful completion of the apprenticeship, you will be eligible to apply for other positions within the business
Employer Description:As the specialists in skills for science and technology, our purpose is to make sure your business; your people and our industry are future ready. We are a not-for-profit charitable organisation with a family of commercially focused companies committed to supporting the skills, needs and ambitions across the UK science and technology sector.Working Hours :Monday - Thursday, 9.00am - 5.25pm, Friday, 9.00am - 4.05pmSkills: Communication skills,IT skills,Attention to detail,Organisation skills,Presentation skills,Administrative skills,Analytical skills,Logical,Team working,Creative,Initiative,Patience....Read more...
The Hub Submission Manager Apprentice is accountable for operational management of regional and/or national regulatory dossiers to designated Health Authorities (HAs).
Based within GRS Regulatory & International Operations, this role sits within a team working to tight, business- critical deadlines within a highly regulated environment. Primary focus is on allocated region/countries, with additional responsibility to support other locations through utilization of global tools.
Executing through use of standards and tools, designated regulatory operational tasks e.g. dossier document monitoring receipt, translation management, dossier technical build, dossier dispatch, conforming to regulatory submission milestones and applicable regulatory obligations. Given the global span of the organization, critical features of this role are the ability to successfully interface with multiple cultures and functions from within Pfizer.
Job Responsibilities:
Main Duties:
Drive submission coordination activities for assigned products and/or regulatory procedures as appropriate. Partnering with regional or global CT SMs/or third-party partners, the incumbent will be accountable for supporting submission activities, for the Clinical Trial submission build and delivery.
Provide operational support within the team to execute designated tasks associated with submission.
Accountable for delivering designated tasks with quality and timely as per applicable policy, SOP/Work Instructions, guidelines, or service level agreement.
Adhere to the appropriate use of technical tools, through use of working practices and QC/QA regimes, such that regulatory and internal compliance is preserved.
Commit to completing required on-the-job training courses and Curriculum to ensure compliance is preserved.
Execute regional specific tasks to support on time project delivery.
Partners with other team members on initiatives and non-portfolio projects.
Training:Training for this apprenticeship will be delivered online.Training Outcome:Upon successful completion of the apprenticeship, you will be eligible to apply for other positions within the business.Employer Description:As the specialists in skills for science and technology, our purpose is to make sure your business; your people and our industry are future ready. We are a not-for-profit charitable organisation with a family of commercially focused companies committed to supporting the skills, needs and ambitions across the UK science and technology sector.Working Hours :Monday to Thursday, 9am – 5.25pm. Fridays, 9am – 4.05pmSkills: Communication skills,IT skills,Attention to detail,Organisation skills,Problem solving skills,Administrative skills,Analytical skills,Logical,Team working,Creative,Patience....Read more...
Job Description:
We have a newly created role to join a leading discretionary wealth firm in Glasgow. This is a key hire to join their Risk & Compliance function, supporting the business with a wide variety of tasks from regulatory reporting, conduct risk, prudential requirements and governance. Reporting to the Group Head of Risk & Compliance, the position works closely with senior leadership and carries a high level of autonomy, with end-to-end ownership of core regulatory processes and responsibility for providing expert guidance on FCA requirements impacting investment management activities.
Essential Skills/Experience:
Significant compliance experience within investment management.
Strong working knowledge of the FCA Handbook, including COBS, SYSC, DISP and COLL, as well as AML requirements and Consumer Duty.
Investment Management Certificate or equivalent investment and/or compliance qualification.
Strategic and analytical approach with strong problem-solving capability.
Excellent communication and report-writing skills, with the ability to influence at all levels.
High attention to detail, integrity and resilience in a fast-paced regulatory environment.
Core Responsibilities:
Own and deliver timely, accurate regulatory reporting, including prudential and conduct returns and coordinate regulatory disclosures
Lead the ICARA process
Maintain a forward-looking regulatory horizon scanning programme, assessing regulatory change and overseeing implementation with relevant business stakeholders.
Support the ongoing maintenance and review of regulatory and internal policies, ensuring alignment with regulatory expectations and internal standards.
Deliver a risk-based compliance monitoring plan and coordinate with internal senior stakeholders
Conduct thematic testing across key investment conduct areas, including best execution, market abuse, conflicts of interest and financial promotions.
Operate a proportionate Training & Competence framework
Benefits:
A highly competitive salary
Wider Benefits package
Core-Asset Consulting is an equal opportunities recruiter and we welcome applications from everyone irrespective of age, disability, gender, gender identity or expression, race, colour, ethnic or national origin, sexual orientation, religion or belief, marital/civil partner status or pregnancy.
Job reference: 16325
To apply for this vacancy applicants must be eligible to work in the UK in accordance with the Immigration, Asylum and Nationality Act 2006.
At Core-Asset, we’re committed to protecting and respecting your privacy. Our privacy statement explains when and why we collect personal information about people who engage with our services, how we use it, the conditions under which we may disclose it to others, and how we keep it secure. We may change this policy from time to time, so please check this policy occasionally to ensure that you’re happy with any changes.
By engaging with us (either by applying for a job we’re advertising, registering through our website, or getting in touch with our business) you’re agreeing to be bound by this policy.
Core-Asset Consulting is committed to protecting the privacy of our candidates, clients and website users. For further information, please refer to our full Privacy Statement available on our website http://www.core-asset.co.uk/about-core-asset/privacy-statement
Core-Asset Consulting offers specialist recruitment services to asset management, accounting & finance, asset servicing, legal and the wider financial services sector in Scotland.
INDPERM....Read more...
Statistical SAS Programmer required to join a team supporting multiple clinical and non clinical studies, particularly focusing on regulatory submissions. The ideal candidate will be an expert in Study Data Tabulation Model, Analysis Data Model, and other CDISC standards.
Skills
BSc or higher in Computer Science, Mathematics or related subject.
SAS programming within the pharmaceutical industry, with a focus on clinical trials.
Familiarity with regulatory submissions, including associated industry guidance and the application of SDTM and ADaM CDISC standards.
CRT or Case Report Tabulation and define.xml standards.
Developing or managing CRT tools.
Role
Program and validate SDTM datasets, including complex efficacy and lab data, and other clinical outputs.
Technical expert in SDTM, ADaM, and other CDISC standards. Provide consultancy, advice, and training to the team.
Program complex non efficacy outputs and figures, perform senior review, and deliver quality control of non statistical outputs.
Comply with regulatory guidelines and requirements, particularly related to CDISC standards, GCP (Good Clinical Practice), and clinical trial documentation.....Read more...
Statistical SAS Programmer required to join a team supporting multiple clinical and non clinical studies, particularly focusing on regulatory submissions. The ideal candidate will be an expert in Study Data Tabulation Model, Analysis Data Model, and other CDISC standards.
Skills
BSc or higher in Computer Science, Mathematics or related subject.
SAS programming within the pharmaceutical industry, with a focus on clinical trials.
Familiarity with regulatory submissions, including associated industry guidance and the application of SDTM and ADaM CDISC standards.
CRT or Case Report Tabulation and define.xml standards.
Developing or managing CRT tools.
Role
Program and validate SDTM datasets, including complex efficacy and lab data, and other clinical outputs.
Technical expert in SDTM, ADaM, and other CDISC standards. Provide consultancy, advice, and training to the team.
Program complex non efficacy outputs and figures, perform senior review, and deliver quality control of non statistical outputs.
Comply with regulatory guidelines and requirements, particularly related to CDISC standards, GCP (Good Clinical Practice), and clinical trial documentation.....Read more...
Product Compliance manager required to drive the certification of product portfolio across international markets.
Requirements
Product compliance experience within a fast paced, technical environment.
Leadership and mentoring skills, with the ability to build and inspire a team.
Detailed understanding of regulatory and compliance frameworks.
Role
Lead product compliance for new and existing products.
Collaborate with internal and external stakeholders to define compliance requirements.
Support product development and ensure alignment with specific market regulations.
Mentor and develop a team.
Stay ahead of industry trends, shaping regulatory requirements to benefit customers and the business.....Read more...
Product Compliance manager required to drive the certification of product portfolio across international markets.
Requirements
Product compliance experience within a fast paced, technical environment.
Leadership and mentoring skills, with the ability to build and inspire a team.
Detailed understanding of regulatory and compliance frameworks.
Role
Lead product compliance for new and existing products.
Collaborate with internal and external stakeholders to define compliance requirements.
Support product development and ensure alignment with specific market regulations.
Mentor and develop a team.
Stay ahead of industry trends, shaping regulatory requirements to benefit customers and the business.....Read more...
A leading aerospace and aviation organisation is seeking an experienced Compliance Investigator to support its Maintenance, Repair and Overhaul (MRO) operations. This is a contract opportunity, based primarily in Oxfordshire, with regular travel required to operational sites across the UK.
The successful contractor will play a key role in ensuring regulatory and operational compliance, conducting in-depth investigations, identifying root causes, and driving corrective and preventive actions. This role sits within a compliance and quality-focused environment and supports the promotion of safety, standardisation, and continuous improvement across multiple locations.
Key ResponsibilitiesCompliance Investigations & Root Cause Analysis
Conduct thorough investigations into compliance-related incidents, discrepancies, and safety concerns
Perform MEDA investigations where required
Apply Root Cause Analysis methodologies such as 5 Whys, Fishbone Diagrams, and Fault Tree Analysis
Identify Human Factors and Human Performance contributors
Analyse trends and systemic issues, ensuring sustainable corrective actions are implemented
Regulatory & Quality Assurance
Ensure adherence to applicable aviation regulatory frameworks, including Part 145 and associated UK/EASA requirements
Support compliance with CAMO, Part 21 G, and military aviation regulations where applicable
Work closely with Quality and Assurance teams to support audits and inspections
Support regulatory audits and coordinate responses to findings, ensuring timely closure of non-conformances
Process Improvement & Risk Mitigation
Collaborate with cross-functional teams to improve maintenance procedures and operational effectiveness
Recommend and support implementation of risk mitigation strategies
Promote best practice in safety, human factors, and compliance monitoring
Stakeholder Engagement & Reporting
Produce clear, structured investigation reports with recommendations for senior stakeholders and regulators
Engage with engineering, maintenance, production, and safety teams to improve compliance awareness
Maintain accurate investigation records and track corrective and preventive actions (CAPA)
Essential Experience & Skills
Proven experience conducting compliance investigations within an aviation maintenance or aerospace environment
Strong expertise in Root Cause Analysis and structured problem-solving techniques
In-depth knowledge of UK CAA and EASA regulatory frameworks, particularly Part 145
Solid understanding of Human Factors, Human Performance, and limitations
Experience reviewing technical documentation, maintenance records, and regulatory requirements
Background in audits and inspections within a maintenance or regulated environment
Strong analytical, report-writing, and stakeholder communication skills
Proficiency with Quality Management Systems (QMS) and compliance monitoring tools
Desirable Experience
Experience with MEDA investigations
Knowledge of CAMO, Part 21 G, and/or military aviation regulations (MRP 145, MIL CAMO)
Familiarity with ISO 9001, AS9100, or equivalent aviation quality standards
Experience using Lean, Six Sigma, or continuous improvement methodologies
Ability to engage confidently with stakeholders at all levels
Qualifications & Experience Essential
Formal training in Root Cause Analysis and investigative techniques
Security Clearance (SC) or the ability to obtain clearance
Desirable
Aviation Safety Management Systems (SMS) certification
Aviation Auditor or Lead Auditor certification
Lean Six Sigma Green or Black Belt
Extensive background in compliance, investigation, or audit roles within an aviation MRO setting
This contract role would suit a compliance-focused aviation professional who thrives in regulated environments and is comfortable working across multiple sites.
Applications are welcomed from all suitably qualified contractors regardless of gender, background, or personal characteristics.
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Job Description:
Our client, a leading financial services firm, is looking for a Compliance Officer to join their team in Newcastle. This is a fantastic opportunity for a compliance professional to play a pivotal role in supporting the business in meeting its regulatory obligations while fostering a strong, client-first compliance culture. The role requires strong pensions knowledge.
Skills/Experience:
Excellent communication skills, with the ability to explain complex regulatory requirements to both technical and non-technical audiences.
Strong attention to detail and the ability to identify risks, inconsistencies, or breaches.
Proven analytical skills, with experience applying FCA regulations across a variety of business contexts.
Ability to manage competing priorities and regulatory deadlines while maintaining high standards.
Commercial awareness and business acumen, balancing compliance requirements with organisational objectives.
Strong written skills, with the ability to draft clear, accurate, and compliant documentation.
Core Responsibilities:
Translate FCA regulations, guidance, and publications into clear, actionable advice for the business.
Provide timely responses to queries, identify potential risks, and escalate issues appropriately.
Review and approve financial promotions and materials to ensure adherence to FCA requirements.
Act as a compliance stakeholder in new initiatives, offering guidance on governance and regulatory considerations.
Promote compliance awareness across the organisation, embedding values of integrity and customer-focus at all levels.
Core-Asset Consulting is an equal opportunities recruiter and we welcome applications from everyone irrespective of age, disability, gender, gender identity or expression, race, colour, ethnic or national origin, sexual orientation, religion or belief, marital/civil partner status or pregnancy.
Job reference: 16244
To apply for this vacancy applicants must be eligible to work in the UK in accordance with the Immigration, Asylum and Nationality Act 2006.
At Core-Asset, we’re committed to protecting and respecting your privacy. Our privacy statement explains when and why we collect personal information about people who engage with our services, how we use it, the conditions under which we may disclose it to others, and how we keep it secure. We may change this policy from time to time, so please check this policy occasionally to ensure that you’re happy with any changes.
By engaging with us (either by applying for a job we’re advertising, registering through our website, or getting in touch with our business) you’re agreeing to be bound by this policy.
Core-Asset Consulting is committed to protecting the privacy of our candidates, clients and website users. For further information, please refer to our full Privacy Statement available on our website http://www.core-asset.co.uk/about-core-asset/privacy-statement
Core-Asset Consulting offers specialist recruitment services to asset management, accounting & finance, asset servicing, legal and the wider financial services sector in Scotland.
INDPERM....Read more...
Learning about the insurance industry, how it is regulated, how firms are governed and the importance of compliance to corporate success.
Helping organise the team through the team planner, diaries, annual leave and compliance trackers.
Ensuring that response timeframes are met for any complaints.
Support with the production of presentations and papers by gathering the necessary data and formatting using Word, Excel, PowerPoint as required.
Helping construct various important, business wide reports e.g. regulatory queries including licencing referrals, upcoming Regulatory Developments and Compliance metrics.
Assisting the team with Broker TOBA requests – preparing agreements, answering queries and maintaining the TOBA database.
Completion of Exception reporting and liaising with business on findings. Escalating responses to management when required.
Aiding the business in meeting regulatory deadlines.
Dealing with correspondence and general departmental queries.
Assist team members in the completion of key and ad hoc projects.
Organising Compliance away/focus days alongside senior management. Training Outcome:Compliance Officer / Manager.Employer Description:Welcome to Markel where we take great pride in what we do. To us, insurance isn’t just a policy - it’s a vital promise that gives people and businesses the confidence to move forward, each and every day. Here, you’ll find exceptional people, without the ego. People who’ll bring out your best, and support you at every step, because it’s who we are and the secret to our success.
We are a leading global speciality insurer with a truly people first-approach. With over 5,000 employees across the globe, finding creative solutions for complex risks is our passion. And our broad array of tools and knowledge allows us to create tailored coverage solutions for even the most complex needs. Working Hours :Monday - Friday, times to be confirmed.Skills: Communication skills,IT skills,Attention to detail,Organisation skills,Analytical skills....Read more...
Assist in issues relating to, quality incidents, non-conformances
Support in the production of KPIs on Quality assurance processes including Quality incidents , non-conformances, and customer complaints and monitoring these in the electronic log
Help maintain the QC departments documentation system and records in accordance with all appropriate regulatory requirements
Develop towards being the first point of contact in relation to requests from the regulatory affairs department
Provide quality support to the plant operations, as necessary
Support the plant trials procedure in relation to quality assurance
Assist in the process for third party analysis samples as per individual markets and regulatory requirements
Support to produce appropriate certification in relation to the registration and importation purposes for YaraVita and YaraAmplix tested product where required
Ensuring all associated paperwork is completed properly, accurately and on time
Training:
Training is run online with our training provider, the training and coaching sessions will be delivered 1 day per fortnight throughout the training course
You will access the training at work on your work laptop
Training Outcome:
On completion we would look to the successful candiate progressing to become the QA Lead Technician
Employer Description:We are part of the global company Yara International ASA and are a leader in the product development, manufacture and marketing of speciality nutrients & biostimulant products for use in regenerative agriculture worldwide.
At Yara, we will do everything in our power to lead a food system transformation through Climate neutrality, Regenerative agriculture and Prosperity
www.yara.com/this-is-yara/yara-at-a-glance/
Working Hours :Monday to Friday
Shifts to be confirmedSkills: Communication skills,IT skills,Attention to detail,Organisation skills,Problem solving skills,Analytical skills,Logical,Team working,Initiative,Work to deadlines....Read more...
The Company:
This organisation is a market leader in the supply of LPG across the UK, with a well-established presence supporting a wide range of industrial and commercial clients. They provide tailored energy solutions to help customers reduce costs and carbon emissions through innovative products and services.
Benefits of the LPG Project Engineer
£45k-£55k Basic Salary
£12% Bonus
Company car
Pension
25 Days holiday
Bupa private Dental and Healthcare
The Role of the LPG project Engineer
This role is to take ownership of end-to-end LPG infrastructure projects from concept through to commissioning
As Project Engineer, you will combine technical excellence with commercial acumen, managing LPG installations in different sectors from aggregates to distilleries, supporting businesses to transition to greener fuel.
You'll work directly with clients, contractors, and regulatory authorities, serving as the technical expert throughout project lifecycles while ensuring absolute compliance with safety standards
Lead end-to-end project delivery with full ownership of planning, scheduling, and budget management
Design technical solutions including functional specifications, engineering drawings, and calculations (pressure drops, storage sizing, venting)
Ensure regulatory compliance with IGEM/UP Codes of Practice, GSIUR, BS EN standards, and building regulations
Provide on-site engineering authority during construction, installation, and commissioning phases
Manage stakeholder relationships with clients, contractors, suppliers, and regulatory bodies
Lead safety reviews including HAZOP, HAZID, and risk assessments throughout project development
Support business growth by providing technical expertise for proposals, tenders, and feasibility studies
The Ideal Person for the LPG Engineer
3+ years project engineering experience in LPG, Industrial Gases, Oil & Gas, or related energy sectors
Strong knowledge of LPG system design, storage, and distribution infrastructure
In-depth understanding of IGEM/UP Codes of Practice (UP/1, UP/2, UP/10, UP/16) and UK LPG regulations
Proficiency in 2D AutoCAD and ability to interpret/create P&IDs and technical schematics
Project management qualification (Prince2, APM, PMI, or equivalent)
Excellent communication skills with ability to translate technical information for diverse audiences
Full UK driving licence
If you think the role of LPG Engineer is for you, apply now!
Consultant: David Gray
Email: davidg@otrsales.co.uk
Tel no.: 0208 397 4114
Candidates must be eligible to work and live in the UK.
About On Target
At On Target, we specialise in sales, technical and commercial jobs in the Engineering, Construction, Building Services, Medical & Scientific, and Commercial & Industrial Solutions sectors, enabling our consultants to become experts in their market sector. We place all levels of personnel, up to Director across the UK and internationally.....Read more...
We are seeking a passionate and experienced Registered Service Manager to lead a supported living service in Liverpool.
As the Registered Service Manager, you will:
Inspire and develop your team to deliver exceptional, person-centred care.
Oversee recruitment, supervision, and performance management.
Manage budgets and ensure financial processes are followed.
Maintain compliance with all regulatory and safeguarding standards.
Act as the CQC Registered Manager, ensuring quality assurance and reporting.
Build strong relationships with internal teams, external agencies, and the local community.
What We're Looking For:
Proven leadership experience in social care.
NVQ Level 5 in Social Care Management (or equivalent) or RMA qualification.
Knowledge of CQC Key Lines of Enquiry (KLOE) and regulatory frameworks.
Budget management experience.
Excellent communication and IT skills.
Flexibility for evenings, weekends, and on-call duties.
Benefits Include:
Enhanced sick and maternity/paternity pay.
Two wellbeing days per year.
Blue Light Discount Card and Costco membership*.
Free occupational health, counselling, and wellbeing services.
Fully funded training and nationally recognised qualifications.
Generous annual leave and workplace pension scheme.
Recognition programs and long service awards.
Travel-to-work schemes and retail discounts.
Important Information:This role requires a DBS check (cost covered). We may close this vacancy early if we receive sufficient applications.
....Read more...
JOB DESCRIPTION
The International Regulatory Specialist is responsible for providing regulatory support to Rust-Oleum's international business. The international business encompasses the entire range of our company's products, including paints, coatings, and cleaners.
This position involves reviewing chemicals, product formulations, and labels to ensure global compliance. In addition, this position serves as Rust-Oleum's lead for chemical registrations for import into various countries. Responsibilities include communicating with sales teams, suppliers, and consultants, completion and maintenance of chemical registrations, and proactively staying informed about and implementing emerging regulations.
RESPONSIBILITIES:
Provide global compliance support to sales teams in multiple regions such as Asia, Australia, New Zealand, Latin/Central America, Middle East, and Africa
Support new product launches by reviewing chemical/supplier information for global compliance and authoring compliant Safety Data Sheets using Product Vision software and provide label requirements
Review existing product lines for global compliance
Work with suppliers to register chemicals to allow company's products to enter new marketplaces
Renew/maintain and complete periodic reporting for existing registrations
Track global regulations that will impact Rust-Oleum's products
Classify products for transportation according to DOT, IMDG, and IATA regulation
REQUIRED SKILLS AND EXPERIENCE
B.S. in science or engineering
Experience with international regulations
At least 3 years related experience
Able to work with minimal supervision
Ability to multi-task and handle several projects simultaneously
Works well under pressure
Works well in a team environmentHere's what you can expect every day:
Be part of a regulatory team that supports a >$1B company
Competitive compensation package commensurate with experience.
Medical, dental, life and vision insurance, disability coverage, a pension plan and a company-matched 401(k).
Hybrid work week (3 days in office/2 days remote).Salary Target Range: $80,000 - 90,000, bonus eligible
From big benefits to small, we take care of our associates! After 30 days of employment, you will be eligible for a benefits package that includes medical, dental, life, disability and business travel insurance, flexible spending accounts, EAP, stock purchases and vacation/sick days/parental leave.
We also offer a 401(k) plan after three months of employment. Associates are vested in the RPM Pension plan after completing five years of service. Rust-Oleum offers 9 paid holidays and one floating holiday per year. You are also eligible to earn three weeks of vacation on an annualized basis.
Rust-Oleum is an equal opportunity employer. Employment selection and related decisions are made without regard to sex, race, age, disability, religion, national origin, color, or any other protected class.Apply for this ad Online!....Read more...
Avionic System Design Engineer required to work as part of a team across aircraft, aviation and satellite connectivity.
Requirements
Avionics systems and SATCOM technology experience of Iridium, Inmarsat, Viasat, Starlink or similar.
DOORS, JAMA or similar systems engineering tool knowledge.
BEng in Electronics Engineering or related ideally with postgrad qualifications.
UAV regulations, safety standards ARP4754, ARP4761, DO178 or DO254 desirable.
Role
Avionic system design, development, and implementation.
SATCOM system integration of Iridium, Inmarsat, Viasat, Starlink.
Design review including testing, validation and regulatory compliance.....Read more...
Avionic System Design Engineer required to work as part of a team across aircraft, aviation and satellite connectivity.
Requirements
Avionics systems and SATCOM technology experience of Iridium, Inmarsat, Viasat, Starlink or similar.
DOORS, JAMA or similar systems engineering tool knowledge.
BEng in Electronics Engineering or related ideally with postgrad qualifications.
UAV regulations, safety standards ARP4754, ARP4761, DO178 or DO254 desirable.
Role
Avionic system design, development, and implementation.
SATCOM system integration of Iridium, Inmarsat, Viasat, Starlink.
Design review including testing, validation and regulatory compliance.....Read more...
Dental Nurse role in Sheffield (South East Sheffield) As a Dental Nurse for this well established practice , you’ll play a key role looking after every patient and supporting your dentist. With your understanding of Private, NHS and UDA treatments, together with your knowledge of GDC and other regulatory responsibilities, you’ll set the highest standards for your team and your patients.
What does the role look like?
Passionate about delivering excellent patient care at all times. Working with clinical freedom, to allows us to choose the right solution with each patient.
Understand the importance of teamwork within the surgery and how you can work effectively to support the dentists
Possess excellent organisational and influencing skills, using these to ensure that the practice delivers effective care
Understand Private and NHS dentistry – supporting offering treatment options to patients and how you can best drive surgery efficiency and help the practice performance goals
Sharing your knowledge and being a role model to any Trainee/Apprentice Nurses within your practice, buddying them through their initial induction and acting as an extra support as they learn
Demonstrating your full understanding of GDC and other regulatory responsibilities
Embrace the importance of your own CPD and ongoing professional development
To be considered for this role, you must have a relevant live or pending GDC registration and have exprience as a Dental Nurse. In return you will get;
yearly equivalent of £27,000
Your GDC registration and medical indemnity fees covered
Extra day of annual leave for your Birthday!
Annual leave package which increases with your length of service
Comprehensive training and verifiable CPD (free online and in person courses)
Access to Advanced Qualifications
Uniform provided
....Read more...
Are you an experienced Product Manager with strong knowledge of CCTV, access control, and surveillance technologies? This is an exciting opportunity to join an organisation specialising in innovative CCTV solutions for public service vehicles, including buses, trains, HGVs and emergency services.
Responsibilities of the Product Manager – CCTV job based in Hampshire:
Define and communicate the product vision, strategy, and roadmap for CCTV systems used in public service vehicles.
Analyse market trends, customer requirements, and competitor activity to shape ongoing product innovation.
Ensure all CCTV products comply with relevant UK, EU, and international standards, including public service vehicle regulations, data privacy requirements, and surveillance technology standards.
Project manage new CCTV business opportunities and lead product development activities.
Monitor industry regulations to maintain compliance with public safety, data protection, GDPR, and broader CCTV legislation.
Engage with key stakeholders such as fleet operators, transport authorities, and regulatory bodies to refine product requirements.
Skills & experience required of the Product Manager – CCTV job based in Hampshire:
Provable product management experience, ideally within video surveillance, transportation technology, or public safety sectors.
Strong hands-on knowledge of CCTV hardware, video streaming protocols, surveillance systems, and integration with vehicle technologies.
Proven experience setting up and demonstrating CCTV solutions in both analogue and IP formats.
Familiarity with video surveillance systems, IoT devices, and vehicle-specific technologies.
Understanding of regulatory requirements and standards in surveillance, fleet operations, and transportation safety.
Benefits for the Product Manager – CCTV job based in Hampshire:
Bonus scheme
Company car
Hybrid/Remote working
Private healthcare
If this job opportunity as a Product Manager– CCTV based in Hampshire could be of interest, send your CV to bwiles@redlinegroup.Com or call Ben on 01582 878816 / 07471 181784.....Read more...
Quality Compliance Engineer required to ensure the quality and compliance of manufactured electronic products with input across the full product life cycle and processes.
Skills
Quality tool experience of PFC, PFMEA, CP, MSA and statistical tools ideally SPC.
8D reporting.
ISO9001 and IATF16949 quality standards
REACH and RoHS regulations.
Role
Product regulation compliance including REACH, RoHS, Conflict Minerals, etc. reports.
Liaise with customers on quality and participate in customer audits.
Monitor and improve customer quality indicators, handling complaints through 8D reports.
Perform internal audits and contribute to continuous improvement of the Quality Management System.
Coordinate communication between customers and suppliers for regulatory compliance.....Read more...
We are seeking a qualified B1 Licensed Engineer, with A320 experience, to join our team. The role focuses on maintaining aircraft airworthiness, safety, and performance in compliance with legal and company standards. You will be responsible for performing and overseeing inspections, managing equipment, and maintaining regulatory documentation.
Responsibilities
Ensure compliance with EASA and UK CAA regulations for airworthiness and safety.
Perform and supervise maintenance tasks, ensuring adherence to safety procedures.
Keep licenses, qualifications, and training up to date.
Provide team support through briefings, safety checks, and technical updates.
Essential Criteria
Valid UKCAA B1 License.
A320 experience with all engine types, including PW1100G.....Read more...
We are looking for a qualified B1 Licensed Engineer to join our team. The role involves ensuring the airworthiness, safety, and performance of aircraft, with a focus on compliance with all legal and company standards. You will be responsible for maintaining tooling, equipment, and documentation, as well as overseeing aircraft and component inspections.
Key Responsibilities:
Ensure airworthiness and safety in line with regulatory standards (EASA, CAA).
Oversee maintenance tasks efficiently and ensure compliance with procedures.
Maintain valid licenses, qualifications, and training.
Support the team through briefings, safety compliance, and technical updates.
Essential Criteria:
Valid UKCAA License
A320 (all engines) experience....Read more...
Quality Compliance Engineer required to ensure the quality and compliance of manufactured electronic products with input across the full product life cycle and processes.
Skills
Quality tool experience of PFC, PFMEA, CP, MSA and statistical tools ideally SPC.
8D reporting.
ISO9001 and IATF16949 quality standards
REACH and RoHS regulations.
Role
Product regulation compliance including REACH, RoHS, Conflict Minerals, etc. reports.
Liaise with customers on quality and participate in customer audits.
Monitor and improve customer quality indicators, handling complaints through 8D reports.
Perform internal audits and contribute to continuous improvement of the Quality Management System.
Coordinate communication between customers and suppliers for regulatory compliance.....Read more...
We are seeking a qualified B1 Licensed Engineer, with A320 experience, to join our team. The role focuses on maintaining aircraft airworthiness, safety, and performance in compliance with legal and company standards. You will be responsible for performing and overseeing inspections, managing equipment, and maintaining regulatory documentation.
Responsibilities
Ensure compliance with EASA and UK CAA regulations for airworthiness and safety.
Perform and supervise maintenance tasks, ensuring adherence to safety procedures.
Keep licenses, qualifications, and training up to date.
Provide team support through briefings, safety checks, and technical updates.
Essential Criteria
Valid UKCAA B1 License.
A320 experience with all engine types, including PW1100G.....Read more...
We are looking for a qualified B1 Licensed Engineer to join our team. The role involves ensuring the airworthiness, safety, and performance of aircraft, with a focus on compliance with all legal and company standards. You will be responsible for maintaining tooling, equipment, and documentation, as well as overseeing aircraft and component inspections.
Key Responsibilities:
Ensure airworthiness and safety in line with regulatory standards (EASA, CAA).
Oversee maintenance tasks efficiently and ensure compliance with procedures.
Maintain valid licenses, qualifications, and training.
Support the team through briefings, safety compliance, and technical updates.
Essential Criteria:
Valid UKCAA License
A320 (all engines) experience....Read more...
