regulatory affairs lead and chief pharmaceutical officer

Angus Cheung

Chief Executive Officer Aerovision Technology Limited Jun 2020 – Present 1 month Hong Kong Hong Kong SAR CEO China Aircraft Services Limited Jul 1997 – Jun 2020 23 years Education The Chinese University of Hong Kong The Chinese University of Hong Kong Master of Business Administration - MBA The Hong Kong Polytechnic University The Hong Kong Polytechnic University The University

Role of regulatory affairs in the pharmaceutical industry

Regulatory Affairs plays a crucial role in the pharmaceutical industry and is involved in all stages of drug development and also after drug approval and marketing The drug development process is a lengthy complex and extremely costly albeit necessary process Pharmaceutical companies use all the data accumulated during discovery and development stages in order to register the drug and thus


Leadership We are led by a seasoned management team an experienced board of directors and accomplished scientific founders with extensive experience across the biotechnology and pharmaceutical industries Management Team Board of Directors Founders Scientific Advisors Dr Samarth Kulkarni Chief Executive Officer Read bio Dr Samarth Kulkarni Chief Executive Officer

Our Leadership Team

Johnson Johnson is a company of enduring strength We've been privileged to play a role in helping millions of people the world over be well and stay well through more than a century of change As the science of human health and well-being has grown we've been able to grow along with it Even more important we've helped shape and define what health and well-being means in everyday lives

Regulatory Affairs jobs

Business Lead (Chemicals) - Regulatory Affairs Ashton-Under-Lyne Tameside Greater Manchester North West England England United Kingdom Covance Job Overview:Do you have significant experience in the Chemicals regulatory business?Are you looking to raise your profile and work for a

Position: Head of Regulatory Affairs Location: Cambridge

Position: Head of Regulatory Affairs Location: Cambridge MA Reporting to: Chief Medical Officer Our client is a well-funded clinical-stage biopharmaceutical company advancing novel peptide technology to develop a new class of therapeutics for cancers and other diseases Their goal is to use their proprietary drug platform to create first-in-class therapeutics that may be able to address


CHIEF OPERATIONS OFFICER Location: Johannesburg South Africa : Employment Type: Full Time: Seniority Level: Senior (such as regulatory market access public policy etc) as well as at least 2 of these years in 'people influencing' roles At least 10 years experience in an Operational Management role of which at least 5 years needs to be in the Pharmaceutical Industry in engaging with

Director Clinical Research / Chief Medical Officer

Director Clinical Research / Chief Medical Officer We are looking for a dedicated and structured candidate to lead our clinical team at AlgiPharma Depending on the candidate profile this could be either a Director of Clinical Research or Chief Medical Officer The candidate will be responsible for the overall clinical development and participate in the regulatory strategy from pre-clinical

Dicerna™ Hires Industry Veterans to Lead Regulatory

Dicerna™ Hires Industry Veterans to Lead Regulatory Affairs and Patient Advocacy Jun 13 2019 PDF Version — Steven Kates Ph D Joins Company as Vice President Regulatory Affairs — — David Caponera Appointed Head of Patient Advocacy and Patient Services — CAMBRIDGE Mass --(BUSINESS WIRE)--Jun 13 2019-- Dicerna™ Pharmaceuticals Inc (Nasdaq: DRNA) (the


Biocompatibility for Medical Devices Clinical Evaluations and Investigations Drug Device Combination Products EU IVD Regulation and Strategy EU Medical Device Law EU Medical Device Regulation Medical Device Regulatory Affairs in Global Markets Post Market Surveillance and Vigilance Software and AI Sterilisation and Reprocessing of Medical Devices TRAINING COURSE: Medical Device Regulatory

Scientific Affairs

Until June 2017 he served as Chief Operating Officer Global Generic Medicines Europe As part of that role he also led all activities integrating Actavis Generics into Teva in Europe as Chief Integration Officer Europe In addition he was responsible for the negotiations to get the approval of the European Commission and all associated divestment activities Christoph has been a member of the

Claudette Meye

Chief Executive Officer CMs interior Design Aug 2018 – Present 1 year 11 months Akwa Douala Cameroon Personal Assistant Nareser S L 2016 – Jan 2017 1 year Douala Planning and Organisation Education CAE Oxford Aviation Academy Certificate de securism et sauvetage Airline Flight Attendant 2017 – 2018 siantou university complex Telecommunication and Media Studies Languages

Regulatory Affairs Manager Jobs

A leading pharmaceutical company based in Johannesburg North is searching for an experienced Medical Affairs Manager to be responsible for managing the medical aspects of a defined therapeutic areas (TA) including the MSLs * Interact with regulatory affairs market access/pricing reimbursement and pharmacovigilance departments * Minimum 2 years of medical affairs experience

Urgent! Pharmaceutical regulatory affairs jobs in

Search and apply for the latest Pharmaceutical regulatory affairs jobs in Pakistan Verified employers Full-time temporary and part-time jobs Competitive salary Job email alerts Free fast and easy way find a job of 3 700+ postings in Pakistan and other big cities in Pakistan Start your new career right now!

Angus Cheung

Chief Executive Officer Aerovision Technology Limited Jun 2020 – Present 1 month Hong Kong Hong Kong SAR CEO China Aircraft Services Limited Jul 1997 – Jun 2020 23 years Education The Chinese University of Hong Kong The Chinese University of Hong Kong Master of Business Administration - MBA The Hong Kong Polytechnic University The Hong Kong Polytechnic University The University

Job Search

Atellas Pharma Madrid have an exciting opportunity for a physician with previous experience in Pharmaceutical Medical Affairs to become an integral part of the team and assume responsibility of a pipeline product within Nephrology This role would be a great development opportunity for an MSL or Regulatory Affairs Manager Job ID: 1220 Division: Regulatory Affairs Employment Class:

Regulatory Affairs Jobs Kildare

Quality Regulatory Affairs Officer Send me Job Alert emails with jobs matching: regulatory affairs Jobs in kildare Please enter your email address Please enter a valid email address Director Regulatory Affairs RFT Group - Pharmaceutical Division 100000 - or more Updated 13/06/2020 Dublin This role will have dual reporting lines to the US Regulatory functional head and to the

VP/SVP Global Regulatory Affairs

Reporting to the Head of RD and Chief Medical Officer the VP/SVP of Global Regulatory Affairs oversees all regulatory affairs for Voyager Therapeutics This executive will lead cross-functional teams to develop and implement regulatory strategy and summarize scientific data and submission packages to US and international regulatory agencies This individual will be responsible for the

Anna Jlia Bencsik

As a Global Regulatory Affairs Associate I had the opportunity to work with Anna on large and important project During the time Anna and I worked together I found her to be very efficient proactive well-organized and responsible Anna managed her time perfectly meeting all deadlines and keeping an excellent quality of work She has always showed good communication skills and she is highly

Ayat Yousri

Regulatory Affairs Senior Officer at Julphar Gulf Pharmaceutical Industries نبذة عني Regulatory Affairs Senior Officer with more than 5 years experience and expertise in Regulatory documentation review and submissions of Drug product dossiers to different Health authorities in the Gulf and MENA region النشاط Ali Tawfiq thank you for making my life easy during the trainings

Andreas Panayi

I am a Pharmacovigilance and Regulatory Affairs Officer with a passion for development and the consistent growth as an individual and also as part of a team I have always been keen on being part of the pharmaceutical industry and subsequently the healthcare system which given my current role has been my main objective I am ways looking forward and working towards offering as much as I can

Alexandre Cruz

Experienced Regulatory Affairs Pharmacist with a demonstrated history of working in the pharmaceuticals medical device and cosmetic industry Strong legal professional skilled in Pharmaceutics Quality Management Pharmacovigilance Biotechnology Medical Devices Cosmetic Products and Healthcare Atividades A QUICK GLANCE OF REQUIREMENTS OF PMS PMCF

Verity Pharma

Taniya has 20 years of experience in Canadian and Global pharmaceutical regulatory affairs Taniya obtained her Hons BSc in Molecular Genetics and Molecular Biology from the University of Toronto followed by a PhD in Neuropharmacology from the University of Nottingham and an MBA from Boston College Taniya then began pursuing her career in regulatory affairs Her corporate background

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