Regulatory Affairs Publishing
Regulatory Affairs Publishing
Are you eligible to work in the UK (VISA etc)?
Kind regards,
Luke Blaney
Regards I G.saikiran (+918499999503) looking for good opportunity in ours company am having good knowledge about Regulatory affairs..
Send me an email to luke.blaney@rbwconsulting.com and I will help you find your next role.
Kind regards,
Luke Blaney
I have aprox. 17 years experience in Pharmaceutical industry (Quality control, R&D, Validation, Regulatory Affairs CIS region) and I am looking for new opportunity in Europe in Regional office of Pharmaceutical company.
Please find me on LinkedIn and look into my profile...I am interested in regulatory affairs vacancy for medical device industry. I have also sent my resume to given email id.
Regards
Hemali
Good Morning Anette, can you email me your CV at all?
Kind regards,
Luke Blaney
Find me on LinkedIn, I'm based in Brussels but accept remote working. Good luck, Annette
I am looking to connect with UK Regulatory Affairs and Quality Assurance Professionals that are looking for new opportunities. I have had some very interesting roles come in this March and am keen to speak with anybody who would be interested in these. Drop me an email to Luke.Blaney@RBWConsulting.com or call me on +44 (0) 1293 584 300. Kind regards,Luke Blaney
Would love to talk with you. Please email me and we can speak more. My email is luke.blaney@rbwconsulting.com - I look forward to hearing from you!
I am having around 7 years of experience in Regulatory Affairs.Looking for opportunities in Europe
waooo intresting sir
Hi Roushan,
Would be more than happy to have a conversation with you. If you want to email me, my details are ross.apted@rbwconsulting.com.
All the best,
Ross
Hello! I am a Ph.D. Medicinal
Chemist and R&D professional with drug discovery experience in
biotech/pharmaceutical industries. As a researcher, I realized I had a passion
to understand the processes involved in the development of a
therapeutic/biotech product relative to the preclinical research phase. I attended
a training course on the submission process for Investigational New Drug (IND),
New Drug Application (NDA) and Post Marketing. After successful completion, I
discovered that my interest lay in CMC regulatory affairs. I am seeking a
career transition from research to regulatory affairs, preferably CMC in the
greater Boston area. I am keen to share my resume to any leads or contacts. –
Best regards, Roushan
Hi Nagesh, thanks for your reply. Drop me an email to Luke.Blaney@RBWConsulting.com with a copy of your CV and I will take a look.
Thank you again for replying and apologies for the delay in my response. I unfortunately don't receive notifications from Pharmemed.
I have work experience about 10 years of pharmaceutical industries in QC-Microbiology.I Would like to know if I am eligible for this vacancy. Thank You.
Click the title of this post for the requirements :)
Please call +44 (0) 1293 584 300 or email Luke.Blaney@RBWConsulting.com if you would like to learn more - I look forward to hearing from you soon!
I have work experience about 10 years of pharmaceutical industries in QC-Microbiology.I Would like to know if I am eligible for this vacancy. Thank You
POSITION REQUIREMENTS: · BA/BS or MS degree in Life Sciences, Engineering, or health care-related discipline · 5+ years of experience in the medical device industry · preferably in a small manufacturing/R&D environment · experience with medical writing, clinical studies, regulatory submissions, and regulatory reviews · Must have experience developing, writing, and organizing all aspects of the IDE/PMA/510(k)'s and CE Submissions · Ability to independently analyze and interpret novel clinical, medical and scientific data · Current knowledge of current U.S. FDA and global (Canada, Australia, European Union, Latin America, India, China, etc.) regulatory requirements within the medical device industry. · Excellent organizational skills and attention to detail · Strong analytical, management, communication and interpersonal skills. Good knowledge of MS Office, Internet, databases, etc. · Ability to work with minimal supervision in a busy environment · Excellent writing skills and the ability to write scientific summaries · Must be able to handle multiple assignments and perform in a diverse cross-functional team environmentContact me for details!Rachel Carey - rcarey@clintelservices.com
Hi Hafsa,
Apologies, I never received the notification from this.
I know we have spoken previously regarding my colleague Ross who works in the US and hopefully you have had a chance to speak with him?
Let me know if I can be of more help.
Kind regards,
Luke Blaney
Hi!
Hope you are doing well.
As someone who is in the regulatory affairs industry, do you have any recommendations of regulatory recruiters in the US? I understand you are based in the UK but if you have any connections or recommendation of any recruiters here, it would really be helpful.
Regards,
Hafsa
Hello!
I am currently seeking Regulatory Affairs Professionals for a relatively junior
position based in Richmond, VA. Key prerequisites of the role are an understanding of prescription drug
products, FDA regulations and guidances on Advertising and Promotion, 1-3
years’ experience in the pharmaceutical industry focused on Ad/Promo as a
Regulatory Reviewer and also a Bachelor’s degree in a bio-medical science or
related field.
Get in touch today
on +1 646 586 9087, or via email on ross.apted@rbwconsulting.com for a chat!
Luke Blaney said:
Hi Hafsa, I would love to have a chat with you. Please drop me an email with your CV to luke.blaney@rbwconsulting.com and we can see what we have on the books for you. Are you available on Monday for a quick telephone conversation?
Hi Luke, I just saw your message on here, I've sort of ended up texting you on your original post too.
I'll e-mail you my resume and Monday is definitely good for a conversation. I'll leave all the details in the e-mail.
Regards,
Hi Hafsa, I would love to have a chat with you. Please drop me an email with your CV to luke.blaney@rbwconsulting.com and we can see what we have on the books for you.
Are you available on Monday for a quick telephone conversation?