Forums » Regulatory Affairs

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    • June 9, 2017 7:23 AM BST
    • Regulatory Affairs Publishing

    • April 3, 2017 12:07 PM BST
    • Are you eligible to work in the UK (VISA etc)?

      Kind regards,

      Luke Blaney

    • April 2, 2017 9:42 AM BST
    • Regards I G.saikiran (+918499999503) looking for good opportunity in ours company am having good knowledge about Regulatory affairs..

    • March 31, 2017 5:14 PM BST
    • Send me an email to luke.blaney@rbwconsulting.com and I will help you find your next role.

      Kind regards,

      Luke Blaney

    • March 31, 2017 11:44 AM BST
    • 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.

    • March 30, 2017 12:22 PM BST
    • 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

    • March 30, 2017 8:01 AM BST
    • Good Morning Anette, can you email me your CV at all?

      Kind regards,

      Luke Blaney

    • March 29, 2017 10:58 PM BST
    • Find me on LinkedIn, I'm based in Brussels but accept remote working. Good luck, Annette

       

    • March 29, 2017 10:56 AM BST
    • 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

    • March 28, 2017 8:35 AM BST
    • 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!

    • March 28, 2017 7:01 AM BST
    • I am having around 7 years of experience in Regulatory Affairs.Looking for opportunities in Europe

    • March 26, 2017 1:13 PM BST
    • waooo intresting sir

    • March 23, 2017 11:02 AM GMT
    • 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

    • March 22, 2017 7:52 PM GMT
    • 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

    • March 24, 2017 1:01 PM GMT
    • 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.

    • March 23, 2017 10:40 AM GMT
    • 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.

    • March 21, 2017 4:41 PM GMT
    • Click the title of this post for the requirements :)

    • March 21, 2017 4:39 PM GMT
    • 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!

    • March 23, 2017 10:41 AM GMT
    • 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

    • March 21, 2017 4:12 PM GMT
    • 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

    • March 22, 2017 10:08 AM GMT
    • 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

    • March 18, 2017 3:42 AM GMT
    • 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 

       

    • March 21, 2017 4:29 PM GMT
    • 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!

    • March 18, 2017 3:52 AM GMT
    • 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,

       

    • March 17, 2017 10:41 PM GMT
    • 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?