Director Of Regulatory Affairs
Current
Dec 2020 - Present
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Daniel Peek Email & Phone Number
Director of Regulatory Affairs at Rayner
at
Rayner
1 work email found
@rayner.com
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✓ Verified July 2026
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Current company
Role
Director of Regulatory Affairs at Rayner
Location
Worthing, England, United Kingdom
Who is Daniel Peek? Overview
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Daniel Peek is listed as Director of Regulatory Affairs at Rayner at Rayner, based in Worthing, England, United Kingdom. AeroLeads shows a work email signal at rayner.com and a matched LinkedIn profile for Daniel Peek.
Daniel Peek previously worked as Director of Regulatory Affairs at Rayner and Head Of Regulatory Affairs at Rayner. Daniel Peek holds Msc, Chemical Research from Ucl.
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Email format at Rayner
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{first}{last}@rayner.com
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Profile bio
About Daniel Peek
As Head of Regulatory Affairs for Rayner Intraocular Lenses, and Rayner Pharmaceuticals, I have had the pleasure to be part of the design, commissioning, validation and approval of our new global HQ and manufacturing site in West Sussex.During the project we have hosted inward audits from ANVISA, BSI, Intertek, SGS, US FDA, Chinese FDA, Korean MFDS, Belarusian Ministry of Health, and Kindom of Saudi Arabia Ministry of Health.During 2018, I successfully led the MDSAP project for Rayner, achieving certification in November.Specialties: International Registration, New Product Development, Quality Systems Management
Listed skills include Quality System, Medical Devices, Gmp, Iso 13485, and 22 others.
Current workplace
Daniel Peek's current company
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12 roles
Daniel Peek work experience
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Head Of Regulatory Affairs
The RA dpeartment consists of three sections; PMS (responsible for Post Market Surveillance and Vigilance), Registrations (responsible for UK and International registration of products), and Pharmaceutical QARA (responsible for the operation of the Rayner Pharmaceuticals Limited Wholesale Dealers Licence).In addition, I am the Deputy Management Representative for the ISO 13485 quality management systems of Rayner IOL and Rayner Pharma, and part of the Project Review Group (the body within Rayner responsible for oversight of all new product development).
Mar 2017 - Dec 2020
Regulatory Affairs Manager
Dec 2013 - Mar 2017
Regulatory Submissions Manager
Responsible for preparing Regulatory Submissions to National Competent Authorities to secure and maintain permissions to place products on the market in over 70 territories. Additionally, in the six month period after the departure of the Documentation Manager, I was responsible for updating and maintaining the Document Control function
Jan 2011 - Dec 2013
Deputy District Commissioner
CurrentSuporting the Adur Valley Scout District for the development of facilities and management of 11 Scout groups, 5 Explorer units, and the District Network, providing learning and fun experiences and #skillsforlife to more than 800 young people aged between 7 1/2 and 25 years old.
Apr 2017 - Present
District Advisor - Development
Providing support to the 10 sccout group executive committes in the district
Oct 2014 - Apr 2017
Group Chairman
Founding Chair of the Group Executive Committee, I helped to establish the group which became the fastest growing in West Sussex within 2 years.
Nov 2015 - Mar 2017
Group Scout Leader
Mar 2013 - Apr 2014
Quality & Regulatory Manager
Pasante Healthcare is a leading supplier of condoms, lubricants and IVDs to the NHS and retail sectors. As QARA Manager I was responsible for the implementation of the ISO 13485 certified QMS, the Kitemarking programme for condoms and the preparation and submission of technical files for CE certification of Medical Devices and In-Vitro Diagnostic Devices under the relevant EU directives and harmonised standards.I was also responsible for export regulation and direct negotiations with customers around the world, with particular focus on the company’s work developing new markets in the Middle East.I was also responsible for export regulation and direct negotiations with customers around the world, with particular focus on the company’s work developing new markets in the Middle East.In addition to this I worked very closely with our Purchasing and Logistics Manager and had responsibility for third party products and the technical aspects of new product development.
Oct 2005 - Jan 2011
Quality Manager
As a member of the senior site management team I was jointly responsible for all aspects of running the business, however my key responsibilities were setting up, running, and maintaining the Quality Management system; accredited to ISO 9002:1994 and the Pharmaceutical Quality Group Code of Practice for Suppliers of Secondary Printed Packaging. I reported directly to the MD and I was directly involved in the company’s strategic planning projects and all staff training.From 2002 to 2005, I was additionally appointed Environmental and Health & Safety Manager, responsible for creating and implementing an integrated management system.
May 2000 - Jul 2005
Principal Qc Analyst
I controlled the daily running of the entire warehouse QC operation. I supervised and took part in all sampling, analysis and evaluation of data relating to any items purchased for use in the factory, which covered raw materials, packaging and bought in finished items to be packed on site. In addition, as the senior QA staff member on site I was involved with GMP issues relating to all on site staff and procedures. I also carried out quality audits of suppliers, and internal functions.In the period 1997-1998, I was seconded to become QA Inventory Controller, responsible for:Monitoring and resolving the stock holding of Raw Materials, Packaging Components, etc.. Co-ordinating the recovery of production batches rejected for various reasons. Issuing and actioning destruction notes for redundant materials. Taking part in the general QA functions of the site. Updating and implementing the AQL system of inspection. Creating and maintaining several business critical QA and QC databases.
Jun 1994 - May 2000
Qc Analyst
Analysis of raw materials and finished products. Environmental monitoring and clerical work.
Jun 1993 - Jun 1994
2 education records
Daniel Peek education
Msc, Chemical Research
Ucl
Bsc, Chemistry
Ucl
FAQ
Frequently asked questions about Daniel Peek
Quick answers generated from the profile data available on this page.
What company does Daniel Peek work for?
Daniel Peek works for Rayner.
What is Daniel Peek's role at Rayner?
Daniel Peek is listed as Director of Regulatory Affairs at Rayner at Rayner.
What is Daniel Peek's email address?
AeroLeads has found 1 work email signal at @rayner.com for Daniel Peek at Rayner.
Where is Daniel Peek based?
Daniel Peek is based in Worthing, England, United Kingdom while working with Rayner.
What companies has Daniel Peek worked for?
Daniel Peek has worked for Rayner, The Scout Association, Pasante Healthcare Ltd, Ccl Label, and Teva Pharmaceuticals.
How can I contact Daniel Peek?
You can use AeroLeads to view verified contact signals for Daniel Peek at Rayner, including work email, phone, and LinkedIn data when available.
What schools did Daniel Peek attend?
Daniel Peek holds Msc, Chemical Research from Ucl.
What skills is Daniel Peek known for?
Daniel Peek is listed with skills including Quality System, Medical Devices, Gmp, Iso 13485, Quality Assurance, Capa, Quality Auditing, and Quality Control.
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