Paul Palmer Email and Phone Number
Welcome to a world of pharmaceutical excellence, where quality and compliance meet innovation and precision. I'm your guide, a seasoned Pharmaceutical Consultant dedicated to partnering with Pharmaceutical Heads of Quality and Quality Directors to elevate their industry standards and exceed regulatory expectations.π Your Challenges, My Solutions: Navigating the intricate landscape of pharmaceuticals demands expertise and diligence. Here's how I empower you to overcome your challenges:π Compliance: Staying current with evolving regulations and guidelines from the EMA. Preparing for and responding to regulatory inspections and audits, which can be stressful and time-consuming.π§ͺ Quality Risk Management: Identifying, assessing, and mitigating quality risks is essential for seamless pharmaceutical operations. Together, we'll create robust risk management strategies that safeguard your reputation and your patients' trust.π Data Integrity: In the digital age, data integrity is paramount. I help you implement and maintain systems that ensure data accuracy, security, and reliability, bolstering your decision-making process.π Good Documentation practices: Elevating your documentation practices from standard to exceptional, allowing you to create a quality-centric culture that ensures consistent, accurate, and compliant documentation throughout your organization.π Supply Chain Challenges: Navigating global supply chain complexities is no small feat. I collaborate with you to develop resilient and efficient supply chain strategies, minimising disruptions and maximising effectiveness.With our Core Competence System we enhance the team's expertise by expanding their knowledge and honing their ability to apply acquired insights effectively. Preetham Hiremat - Paul came on board BBUK to support the team in our growth. He has provided complete support to the entire team to enhance their capabilities and in ensuring compliance to various changing regulations. Paul is very quick to adapt and implement new technologies. Very easy to communicate and an extremely social and caring human being.With years of experience and a deep-rooted passion for pharmaceutical excellence, I'm here to guide you toward industry-leading standards and unparalleled quality assurance. Let's work together to create a pharmaceutical landscape where precision and compliance are non-negotiable, and where your organisation thrives.π Ready to transform your pharmaceutical operation? Contact me now to embark on a journey to excellence in compliance, quality, and innovation.
Inceptua Pharmaceuticals
View- Website:
- paulrpalmer.com
- Employees:
- 2
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Pharmaceutical Consultant Responsible Person And Responsible Person ImportInceptua PharmaceuticalsWorthing, Gb
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Director / Pharmaceutical ConsultantPaul R Palmer Limited Jan 2011 - PresentUnited KingdomSpecialising in the Pharmaceutical Industry ; - Training ;- Quality Assurance Mastery, GMP, GDP, Business Process Re-engineering, Data Integrity Computer System Validation and more.- Supplier and Internal auditing, - Regulatory Inspection Preparation and hosting- Rectification of Adverse Regulatory Inspection or Client Audit Observations - Qualified Person /Responsible Person as a consultant in the pharmaceutical industry. - QP audit for declarations- Interim Director / Head of Quality- Quality Management System design, audit and improvement, - licensing support and regulatory advice.If you decide to work with me you will benefit from 35 years in business, a diverse background spanning across many dosage forms with a bespoke service. -
Managing Director / Pharmaceutical ConsultantPharma Quality Services Limited Feb 2019 - PresentUnited KindomPharmaceutical Consultancy guiding manufacturers, distributors and trial sponsors through the ever changing global regulatory requirements.Supporting new licence applications, providing regulatory advice,, offering interim quality management and QP batch release services.Auditing suppliers and performing business improvement audits (self inspection) -
Quality And Compliance DirectorMkb Biopharma Nov 2021 - PresentLondon, England, United KingdomMKB Biopharma Holdings is a team of industry expertsMKB Biopharma is a life science consortium that specialises in investing & acquiring SMEs who doesnβt have an exit plan or that have hit a plateau and need support in their next growth phase. Our approach is centered around fostering synergic collaboration and innovation to accelerate growth, improve patient outcomes, providing strategic support and facilitate mergers and partnerships opportunities to stay ahead of the competition. -
Pharmaceutical Consultant / Qualified Person / Gmp AuditorRational Vaccines Apr 2021 - PresentUnited States & United KingdomPharmaceutical consultant role to support a phase 1 clinical trial to be conducted in England. The suppliers each need a QP audit however this role also includes the provision of strategic advice for accessing the EU / UK market. -
Pharmaceutical ConsultantUniversity College London Feb 2021 - PresentLondon, England, United KingdomI am supporting the QP course delivering one session per module throughout the course duration. Currently on a remote basis since all lectures are taking place online. -
Pharmaceutical ConsultantBrown & Burk Uk Ltd (Bbuk) May 2016 - PresentLondon, England, United KingdomReleasing Qualified Person of commercial products imported from India, supplier audits, self inspections, periodic quality review and compliance advice.Business lead for microbiological investigations -
Qualified Person / Pharmaceutical ConsultantClinigen Group May 2018 - Apr 2024Weybridge, England, United KingdomI switched back to a consulting role with Clingen to focus on the implementation of electronic Quality Management System for the group. I have continued to support them as required on a part time basis performing QP release and support activities such as QTA and client support. -
Group Quality DirectorClinigen Group Jul 2017 - Apr 2018Weybridge, Surrey, United KingdomI joined the Clinigen Pharmaceutical group in 2016 as they had recognised a knowledge gap in their Quality team. Initially I supported them on a part time basis, however when the Quality Director had to leave for personal reasons I stepped in to support them in their preparation for their regulatory inspection.I worked closely with the team directing their activities in preparing for the inspection and communicating myself with the whole company to gain momentum and wider support for the actions required.The result was "the best inspection ever" Shaun Chilton CEO Clinigen Group Plc I will help you achieve your "best regulatory inspection ever" too. Contact me here on LinkedIn with a direct message and I will show you how. -
Qualified Person / Pharmaceutical ConsultantClinigen Group Nov 2016 - Jun 2017Weybridge, England, United KingdomI joined Clinigen first as a consultant Qualified Person to support the team as a releasing QP but also to support the company with increasing the knowledge of current best practices within the Quality Team. -
Pharmaceutical ConsultantPennine Healthcare Feb 2021 - Dec 2022Derby, England, United KingdomI am supporting Pennine with regulatory compliance advice, inspection support, Qualified Person batch release, process improvement and auditing -
Pharmaceutical Consultant / Responsible PersonAccmede Pharmaceuticals Limited Jun 2014 - May 2019London, England, United KingdomPharmaceutical consultant supporting the team in applying for and obtaining a Wholesale Distribution Authorisation then performing the role of Responsible Person while the Quality Manager gained sufficient experience to perform the role with my support. -
Pharmaceutical Consultant / Qualified PersonMediwin Limited Apr 2007 - Jun 2017Littlehampton West SussexThe Managing Director at Mediwin approached me to support them as a Qualified Person carrying out batch release and to help them with advice relating to Good Manufacturing Practices. I helped the company with the implementation of best practices including the Quality Management System. The company grew significantly in volume by adding an additional shift and business automation and introduced a process for Patient Information Leaflet readability analysis the results of which were approved by the MHRA.I advised them on setting up a range of different systems and processes such as implementation of the validation system, cold chain import controls and the process for PIL assessments based on my previous experience.When you need help with your Pharmaceutical Quality Management System and processes please connect with me and contact me with a direct message here on LinkedIn. -
Pharmaceutical ConsultantAlmac Group Oct 2016 - Dec 2016Belfast, Northern Ireland, United KingdomThis was a short term assignment as a Qualified Person for the clinical packaging operation also conducting self inspections. -
Pharmaceutical SpecialistKinapse Limited Nov 2015 - Feb 2016London, England, United KingdomI support a project as Subject Matter Expert for the analysis of the systems and processes in the manufacture and supply of medicinal gases -
Pharmaceutical Consultant / Qualified PersonFisher Clinical Services May 2013 - Jun 2015Horsham, United KingdomSupporting Fisher Clinical as a Qualified Person was an interesting role, I had to carry out clinical batch certification and QP declarations as the primary role. As part of the audit team I identified opportunities for improving the business processes.I worked on a shift basis to support the international clients in particular those in the USA, by working late in the evening 2 or 3 days a week when needed I found it much easier to fulfil the client requirements. The major differentiator for me in support ing our clients was my ability to join calls late in the evening to deliver my expert guidance to colleagues from the USA and their clients in order to facilitate the EU clinical trials they needed to meet their departmental goals and business objectives.Please contact me here on LinkedIn with a direct message to discuss how I can support your needs.
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Pharmaceutical Consultant / Quality Assurance Manager / Qualified PersonPatheon Inc. Jul 2011 - May 2013Swindon, United KingdomWorking as QA manager and QP for Patheon Development Services respoonsible for the QA team in the area of Investigational Medicinal Products.We manufacture Sterile IMP's in vials, and prefilled syringes and several specialised dosage forms. We also help companies design new formuation and manufacture solid dosage forms particularly tablets and capsules but also have the capability to commercialise new products after registration.We cover all development phases and can also assist with compilation of documents for registration.
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Quality Assurance ManagerBiogen Idec Feb 2010 - Mar 2011I'm in Maidenhead traveling to Denmark and Ireland regularly and absolutely loving it. I'm always in a rush but hey thats life -
Qualified Person / Quality ControllerErigal Ltd Apr 2009 - Oct 2009Radio pharmaceutical manufacturing FDG for Positron Emmission Tomography -
Head Of Quality / Qa Manager / Qualified PersonCordia Healthcare Limited Dec 2004 - Mar 2009Parallel Import business head of quality, QP and QA Manager for up to 11 staff including contract and F/T Qualified Persons.
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Quality SpecialistGenerics Uk Apr 2003 - Dec 2004Employed on a contract basis while finishing my training to become a Qualified Person to allow me to carry out batch release for medicinal products.
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Quality Systems ManagerNovartis Jul 2001 - Mar 2003Responsible for managing the Quality System at Novartis Pharmaceuticals Based in Horsham West Sussex UK -
Quality Assurance ManagerGiesecke And Devrient Jan 2001 - Jun 2001Alperton, LondonI was recruited to develop and implement a Quality Management System to satisfy the requirements of ISO 9001.I created the system and trained the team then recruited and trained a new department to run the management system.http://www.gi-de.com
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Gmp ConsultantBms Laboratories Aug 2000 - Nov 2000Beverley, HumbersideThis was a small pharmaceutical manufacturing company which I joined to help them improve GMP compliance.
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Qc Microbiologist / QaSmith And Nephew Medical Limited Jul 1986 - Jul 2000I started at Smith and Nephew Hull from school and worked through a number of roles in Microbiology, QC and QA while studying for my Degree in Applied Biology and MSc in Quality Management part time.
Paul Palmer Education Details
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Brighton UniversityPharmaceutical Studies -
Business Administration And Management, General -
David BeggPharmaceutical Law -
Brighton UniversityPharmaceutical Sciences -
Humberside UniversityQuality Management -
Huberside UniversityApplied Biology
Frequently Asked Questions about Paul Palmer
What company does Paul Palmer work for?
Paul Palmer works for Inceptua Pharmaceuticals
What is Paul Palmer's role at the current company?
Paul Palmer's current role is Pharmaceutical Consultant Responsible Person and Responsible Person Import.
What schools did Paul Palmer attend?
Paul Palmer attended Brighton University, Quantic School Of Business And Technology, Quantic School Of Business And Technology, David Begg, Brighton University, Humberside University, Huberside University.
Who are Paul Palmer's colleagues?
Paul Palmer's colleagues are Farah Nadeem.
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Paul Palmer
Head Of Football @ St Dunstan'S College. Lewisham Secondary Schools District Football Coordinator. Lewisham Borough Community Fc Committee Member.London -
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