Jack Sinclair

Jack Sinclair Email and Phone Number

QA and RA and Clinical Collaborator @ RRxCo.™
London, GB
Jack Sinclair's Location
London, England, United Kingdom, United Kingdom
About Jack Sinclair

A Business Manager at RRxCo, with a background in the Medical Device and IVD space. A strong expertise in generation of business portfolios within MedTech, and project delivery.Our MedTech services include:- EU MDR & IVDR Technical Documentation Authoring - FDA Regulatory submissions; 510(k), De Novo, PMA- CER, PER & PMCF Authoring- Regulatory Strategy- ISO 13485 QMS development and maintenance- Audits Contact Details:Email: jack@rrxco.comPhone: +447788260835

Jack Sinclair's Current Company Details
RRxCo.™

Rrxco.™

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QA and RA and Clinical Collaborator
London, GB
Employees:
11
Jack Sinclair Work Experience Details
  • Rrxco.™
    Qa And Ra And Clinical Collaborator
    Rrxco.™
    London, Gb
  • Rrxco.™
    Business Manager - Medtech / Pharma / Biotech
    Rrxco.™ Nov 2024 - Present
    London Area, United Kingdom
    Global Partner for Life. Not just your average Consultancy. We are a solution provider that supports the Life Science industry. Joining the best industry experts and recruiters in the industry we can provide the traditional consultancies promise 👉 bespoke, competitive and great value services.+44 (0) 1256 961200www.rrxco.com🔹𝗖𝗢𝗡𝗦𝗨𝗟𝗧𝗔𝗡𝗖𝗬🔹- QMS Implementation & Development, Quality Harmonisation & Training (GxP & ISO), GAP Analysis- Mock & Pre-Approval Inspection, Remediation, Risk Management & Assessment- Submissions & Applications (IND, NDA, ODD, BLA, UCKA, CE, FDA), Regulatory CMC - Authority Meetings (MHRA, EMA, FDA), Pathway Development & Reviews- Clinical Development, Clinical Programme & Project Management- Clinical Operations (Site Management, Feasibility & Study Start-Up)🔹𝗔𝗨𝗗𝗜𝗧𝗜𝗡𝗚🔹- Drug Product/Drug Substance / Medical Device / Dx Devices- Excipients/Raw Materials & Consumables- Contract Research Organisations & Clinical Investigator Sites- Trial Master Files (TMF) & Good Clinical Laboratory Practice (GCLP)- Nonclinical Laboratories and Pre-Clinical Services- Warehouse/Distribution Centres- CSV, Data Integrity & Ancillary Services (Software, Pest Control, etc.)🔹𝗧𝗘𝗖𝗛𝗡𝗜𝗖𝗔𝗟 𝗧𝗥𝗔𝗜𝗡𝗜𝗡𝗚🔹 - Quality (CAPA, Change Control, Investigations & Root-Cause Analysis)- Sterile/Aseptic SME Training- Regulatory (CMC, Strategy, Operations, Clinical)- Good Practices & Efficiencies (GxP & ISO)- Auditing, Risk Management & Assessment🔹𝗦𝗘𝗔𝗥𝗖𝗛 & 𝗦𝗘𝗟𝗘𝗖𝗧𝗜𝗢𝗡🔹 - Quality Assurance (GxP) & Quality Control (Chem, Micro, BioChem)- Process Development (USP, DSP & Analytical) & CMC- Regulatory (Strategy & Operations)- Clinical (Clinical Operations & Product Development)- Operations (Site, Regional & Global Leadership)- Validation & Data Integrity (Process, Equipment, Cleaning & CSV)- Project Management (Technical & PMO)
  • Apotech Consulting
    Business Manager - Medical Devices
    Apotech Consulting May 2023 - Oct 2024
    London, England, United Kingdom
    A Business Manager at Apotech Consulting, a specialist Management Consultancy (CSO) delivering end-to-end managed services to the MedTech, Diagnostic (IVD), Pharmaceutical and Biotech industries.As a trusted global partner and proven life-science specialist, Apotech prides itself on delivering flexible, bespoke solutions tailored to meet the varying needs of its clients.Working out of the London HQ and ParisOur services include:- EU MDR & IVDR Technical Documentation Authoring - UK Responsible Person (UKRP)- FDA Regulatory submissions; 510(k), De Novo, PMA- CER, PER & PMCF Authoring- Regulatory Strategy- ISO 13485 QMS development and maintenance- Clinical Operational support and strategy- Local Agent Support for market expansion
  • Life Science People
    Senior Consultant
    Life Science People Jan 2022 - Mar 2023
    Fitzrovia, London
    Working closely with a number of Medical Device Manufacturers, IVD Organisations and Consultancies throughout the UK, EMA and US (East Coast).Specialities: ISO 13485, Audit, CE Marking, 510(k), Regulatory Affairs, RA, PMA, IDE, FDA, MDD, IVDD, MDR, IVDR, CAPA, ISO14971, Risk Management, Class I, Class IIa, Class IIb, Class III, Medical Devices, Medical Device Directive, Regulatory Affairs, Regulatory Affairs Expert, Regulatory Affairs Specialist, Medical Device Director, ISO 14155, CFR 21, PART 11, FDA, Regulatory Affairs Manager and Regulatory Affairs Associates. Our mission at Life Science People is to make a tangible contribution to global health.We use our expertise to map and secure the highest calibre of talent. Matching them with thought-leading companies which are facilitating global medical advances.We take a collaborative approach when patterning with these organisations across their entire project life cycle, be that drug, device or data platform.We provide a number of bespoke solutions, including scalable embedded recruitment solutions, retained and contingent permanent placements and contractor recruitment and management.
  • Skills Alliance
    Senior Consultant
    Skills Alliance Nov 2021 - Dec 2021
    London Area, United Kingdom
  • Skills Alliance
    Recruitment Consultant
    Skills Alliance Aug 2019 - Nov 2021
    London, United Kingdom
    Skills Alliance is a leading Global Life Sciences executive staffing partner. Providing bespoke solutions for the life sciences and medical technology market for over a decade.• Skills Alliance offer a full portfolio of bespoke solutions tailored to our client’s requirements. These services range from C-suite Executive Search through to Contract/Interim solutions, Benchmarking and an RPO offering.• Skills Alliance has a growing presence in the global Pharmaceutical market having placed candidates across 20+ Countries with skill sets ranging from pre-clinical through to post-approval.• Skills Alliance currently has 100+ pharmaceutical professionals working at sponsor sites or via CROs in the UK and a rapidly growing contract base across mainland Europe.• Office locations across Europe and North America are allowing for rapid growth with a continued focus on our key values that are based around the quality of delivery and client support.BUSINESS UNITS:• R&D - Clinical, Regulatory, Medical, QA, HEOR, Commercial, Biometrics, PVG• Professional Services - IT, A&F, Procurement & Supply Chain, HR & ManufacturingSERVICE LINES:• Executive Search• Database/Advertised Search• Contract recruitment• Interim management• Recruitment Process Outsourcing• Benchmarking ServicesIn my current role, I research, identify and establish new business opportunities through strategic planning and entrepreneurial application, working in a 360 capacity.
  • Antelope
    Business Analyst
    Antelope Jun 2018 - Aug 2018
    Aldgate Tower

Jack Sinclair Education Details

Frequently Asked Questions about Jack Sinclair

What company does Jack Sinclair work for?

Jack Sinclair works for Rrxco.™

What is Jack Sinclair's role at the current company?

Jack Sinclair's current role is QA and RA and Clinical Collaborator.

What schools did Jack Sinclair attend?

Jack Sinclair attended University Of East Anglia.

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