Current jobs related to Regulatory Specialist and Senior Specialist - United Kingdom - IQ Endoscopes Limited

  • Biocide Regulatory Lead

    3 weeks ago

    United Kingdom VRS Regulatory Full time

    About the Role - An excellent opportunity for a biocide regulatory specialist who is looking for a career step into managing a small team. You will become this company’s go-to biocide person. You will provide strategic advice, expertise, and manage the workload and development of more junior biocide colleagues. This role will be a combination of hands-on...

  • Fully Remote

    3 weeks ago

    United Kingdom VRS Regulatory Full time

    About the Role - An excellent opportunity for a biocide regulatory specialist who is looking for a career step into managing a small team. You will provide strategic advice, expertise, and manage the workload and development of more junior biocide colleagues. This role will be a combination of hands-on technical registration work, project management and...

  • Regulatory Compliance Specialist

    4 weeks ago

    United Kingdom 1485 Ltd Full time €33,000 - €40,000

    Location: Cheshire Salary: £33,000 - £40,000 + Bonus This is a newly created role with a rapidly expanding supplements business. With state of the art offices (including an in-house gym!), the business has brought production in-house in recent times, which has created a lot of new challenges from a technical perspective. We're looking for a...

  • Regulatory Affairs Data Specialist

    2 weeks ago

    greater manchester, england, United Kingdom LANXESS Deutschland GmbH Full time

    Business Unit / Group Function: Production, Techn., Safety & EnvironmentWork Arrangement: Fully RemoteLevel of Experience: IntermediateContract Type: Regular PermanentLANXESS UK is a specialty chemical company with several production sites working on a broad range of activities. From the blending of inorganic pigments to the production of urethane...

  • Senior Medical Information Writer

    3 weeks ago

    United Kingdom SRG Full time €400

    Pharma Client based in Dublin looking to hire a Senior Medical Information Writer/ Manager Or Medical Information Specialist. 6 month initial contract with high likelihood of extension. Day rate = Approx €400+ per day if based in Ireland or c£350+pd if working remotely from UK. Flexibility dependent on level of expertise / relevant experience. ...

  • Senior Clinical Field Specialist

    4 weeks ago

    United Kingdom The Mullings Group Full time

    In recent decades treatment of heart attacks by minimally invasive percutaneous coronary intervention (PCI) has significantly improved the outcomes for patients. However, successful re-opening of the narrow or blocked coronary arteries does not always restore blood flow to the entire heart muscle. Our client is developing a first in class medical device...

  • Senior HR Compensation Specialist

    4 weeks ago

    United Kingdom OpSec Security Full time

    Senior HR Specialist, Compensation and Reward OpSec Security the world leader in brand protection and an integral part of Crane NXT, a $1.5 billion dollar business with over 4,750 associates worldwide ;safeguards the revenues and reputations of more than half of the Fortune 100. We effectively address Brand, Piracy, and Fraud risks that brands face due to...

  • Senior Regulatory Writer

    3 weeks ago

    United Kingdom Complete Regulatory | An IPG Health Company Full time

    Complete Regulatory is part of IPG Health Medical Communications, who is home to the world’s most celebrated and awarded Med Comms agencies. We are 800 experts obsessed with combining science, creativity, and technology to create exceptional medical communications solutions for our clients. We provide class-leading writing support and consultancy...

  • Senior HR Compensation Specialist

    4 weeks ago

    United Kingdom OpSec Security Full time

    Senior HR Specialist, Compensation and RewardOpSec Security the world leader in brand protection and an integral part of Crane NXT, a $1.5 billion dollar business with over 4,750 associates worldwide ;safeguards the revenues and reputations of more than half of the Fortune 100. We effectively address Brand, Piracy, and Fraud risks that brands face due to to...

  • Senior HR Compensation Specialist

    4 weeks ago

    United Kingdom OpSec Security Full time

    Senior HR Specialist, Compensation and RewardOpSec Security the world leader in brand protection and an integral part of Crane NXT, a $1.5 billion dollar business with over 4,750 associates worldwide ;safeguards the revenues and reputations of more than half of the Fortune 100. We effectively address Brand, Piracy, and Fraud risks that brands face due to to...

  • Compliance Specialist

    3 weeks ago

    United Kingdom MERJE Full time

    Compliance Specialist – Payments & Crypto Part-Time Contract Role Competitive day rate We are seeking an experienced Compliance Specialist with a demonstrable track record of operating at Head of Compliance / Chief Compliance Officer level with expertise in payments and cryptocurrency for a part-time contract role . This is an exciting...

  • Senior Portfolio Management Specialist

    4 weeks ago

    United Kingdom Tandem Interim Full time

    Job Title: Senior Portfolio Management Specialist (Remote) Contract Duration: 3-Month Rolling Contract Location: Remote (CEMEA Region) Role Overview: Our client, a prominent financial services organization is seeking a highly skilled Senior Portfolio Management Specialist to join their team on a remote basis. This role will involve providing...

  • Senior Portfolio Management Specialist

    4 weeks ago

    United Kingdom Tandem Interim Full time

    Job Title: Senior Portfolio Management Specialist (Remote)Contract Duration: 3-Month Rolling ContractLocation: Remote (CEMEA Region)Role Overview:Our client, a prominent financial services organization is seeking a highly skilled Senior Portfolio Management Specialist to join their team on a remote basis. This role will involve providing strategic support...

  • Conduct Risk Specialist

    3 weeks ago

    United Kingdom MERJE Full time

    Contract Opportunity: Conduct Risk & Customer Outcomes Specialist – Home & Motor Claims Remote | 3-Month Contract | £500-£700 per day (Outside IR35) Are you an experienced risk and compliance professional with expertise in home and motor insurance claims? We’re looking for a Conduct Risk & Customer Outcomes Specialist to join our client a leading ...

  • Contract Management

    3 weeks ago

    United Kingdom Career Moves Group I B Corp™ Full time

    This client are a global leader in Market Research, the role offers the possibility of being fully remote, the clients offices are in central London so there may be occasional (once monthly) travel to London. The client are looking to implement significant savings on their external contract spends, and this role will play a major part in delivering those...

  • Senior Director Regulatory Affairs

    4 weeks ago

    United Kingdom Planet Pharma Full time

    We're partnered with a growing innovative biotech who are leaders in creating cutting-edge therapies with the potential to treat cancer. Their leading development programs utilize a unique antibody format that can target tumours through multiple mechanisms. With their continued growth, they are now looking for a Senior Director of CMC Regulatory Affairs...

  • Senior Director Regulatory Affairs

    4 weeks ago

    United Kingdom Planet Pharma Full time

    We're partnered with a growing innovative biotech who are leaders in creating cutting-edge therapies with the potential to treat cancer. Their leading development programs utilize a unique antibody format that can target tumours through multiple mechanisms. With their continued growth, they are now looking for a Senior Director of CMC Regulatory Affairs to...

  • Senior Director Regulatory Affairs

    4 weeks ago

    United Kingdom Planet Pharma Full time

    We're partnered with a growing innovative biotech who are leaders in creating cutting-edge therapies with the potential to treat cancer. Their leading development programs utilize a unique antibody format that can target tumours through multiple mechanisms. With their continued growth, they are now looking for a Senior Director of CMC Regulatory Affairs to...

  • Senior UK Immigration Specialist

    4 weeks ago

    United Kingdom Alchemy Global Talent Solutions Full time

    Are you an experienced UK corporate immigration professional looking for an exciting opportunity with a global law firm? This modern, forward-thinking firm is seeking a Senior UK Immigration Specialist to join their dynamic team. With fully remote working and a high-volume caseload, this role is perfect for someone looking to make an impact in a fast-paced...

  • Senior UK Immigration Specialist

    4 weeks ago

    United Kingdom Alchemy Global Talent Solutions Full time

    Are you an experienced UK corporate immigration professional looking for an exciting opportunity with a global law firm? This modern, forward-thinking firm is seeking a Senior UK Immigration Specialist to join their dynamic team. With fully remote working and a high-volume caseload, this role is perfect for someone looking to make an impact in a fast-paced...

Regulatory Specialist and Senior Specialist

4 weeks ago

United Kingdom IQ Endoscopes Limited Full time

This role is a hybrid opportunity working from our Chepstow office 2 days a week fixed as Tuesday and Wednesday and 3 days from home.
Our culture at IQ Endoscopes
VALUES : We work together to achieve shared goals through our values…
PASSIONATE: We show our pride and enthusiasm
INNOVATIVE: We challenge, question and push past the status quo
EMPOWERED: We support our people to explore their own potential
INCLUSIVE: We understand the value of an alternative perspective
TRANSPARENT: We are open to our people, sharing information and knowledge

Equity, Diversity and Inclusion at IQ Endoscopes
At IQ Endoscopes we work hard, but we give ourselves a break. We support each other, but we question and challenge each other’s thinking. We recruit highly skilled professionals and specialists, but we collaborate and listen to each other’s opinions and ideas. It doesn’t matter where you come from, what your background or beliefs are, who you love or how you express yourself. What matters is that you are you, and you can be you within our team. Our inclusive culture has grown organically as a result of focusing on recruiting the right person with the right skills. Nothing else. Plain and simple.
We welcome applications from the neuro enlightened community. Talk to us if you have any ideas about how we can improve our recruitment process. We want to know hr@iqendoscopes.co.uk.

Your opportunity
IQ Endoscopes is seeking a motivated individual to fulfil the Regulatory Affairs Specialist role which will play a key part in IQ Endoscope’s Regulatory and Quality department. This position will support various regulatory and quality-related processes and will assist in obtaining, maintaining, and supporting regulatory submissions to ensure compliance with industry standards and regulatory requirements.
 
What we will give you
Hybrid working fixed and 2 days on site Tuesday and Wednesday
25 days annual leave plus bank holidays
2 additional paid ‘Disconnect Days’ per year following probation
2 additional days paid dependents leave & paid compassionate leave per year: entitlement from day 1
Enhanced pension 5% paid by employer & 3% employee
Refer a friend bonus
£100 equipment allowance
Health Shield: Employee health & wellbeing platform encompassing:
o 24/7 EAP service
o A cashback service for both essential and non-essential health and well-being treatments
o GP Anytime: 24/7 access to a phone or chat based GP
o Face to face counselling: referral where required through EAP service
o Access to online health screening, physiotherapy & skin detection
o Employee PERKS & gym discount scheme
 
Your main responsibilities
Compile and update Technical Documentation for UK and EU submissions for existing and new products.
Review and approve product and process change requests as needed to ensure regulatory compliance.
Support the development and maintenance of clinical evaluation documents in compliance with EU MDR and UK MDR.
Update and maintain Post-Market Surveillance (PMS) and Post-Market Clinical Follow-up (PMCF) activities.
Review and approve product labelling to ensure regulatory compliance.
Ensure ongoing compliance by keeping regulatory processes, including SOPs and WIs, updated and aligned with current legislations.
Assist in the preparation and submission of 510(k) for the US market.
Support quality function in handling complaints, change control, deviation, and CAPA.
Assist in global registration activities.
Provide regulatory support to internal stakeholders across the business as needed.
 
What you must have
A degree level qualification or equivalent in a relevant scientific discipline.
Minimum of 2 years of experience in similar role within medical device regulatory affairs.
Working knowledge of MDR 2017/745, UK MDR and US FDA 21 CFR 820.
Strong knowledge of Quality Management Systems (e.g. ISO 13485).
Experience in compiling and submitting Technical Documentation.