Regulatory Affairs Jobs in Life Sciences’ Post

Is 2024 the year with a huge hiring budget? If not, we have brilliant experts to support you! 🔹 Regulatory Project Manager 🔹 Global Regulatory Lead 🔹 Clinical Regulatory Expert 🔹 Regulatory CMC Expert 🔹 Labelling Specialist We offer flexible service models based on your needs: ✔ FTE/partial FTE insourcing ✔ Project support ✔ Specialist consulting Does your regulatory team need support? Let's connect! [email protected] #regulatoryaffairs #drugdevelopment #qualityassurance  #pharmacovigilance #pharma #pharmaceuticals #biotech #marketaccess #pharmabusiness

Is 2024 the year with a huge hiring budget? If not, we have brilliant experts to support you! 🔹 Regulatory Project Manager 🔹 Global Regulatory Lead 🔹 Clinical Regulatory Expert 🔹 Regulatory CMC Expert 🔹 Labelling Specialist We offer flexible service models based on your needs: ✔ FTE/partial FTE insourcing ✔ Project support ✔ Specialist consulting   Does your regulatory team need support? Let's connect! [email protected] #regulatoryaffairs #drugdevelopment #qualityassurance #pharmacovigilance #pharma #pharmaceuticals #biotech #marketaccess #pharmabusiness

We regard the 300 % increase in members of our professional networks in about a year as proof of the growing interest in our life science park. Currently, 193 individuals from 121 companies and organizations are members of one or more of our five networks, dedicated to Regulatory Affairs (divided into the subgroups MedTech and Pharmaceuticals), Quality Assurance, Pharmacovigilance, and Medical Writing, up from 60 individuals in March 2023. If you are interested in becoming a member, please visit the link in comment below!   #network #regulatoryaffairs #ra #medtech #pharmaceuticals #qualityassurance #qa #pharmacovigilance #medicalwriting #lifescience #sciencepark

Does this sound familiar? A complex and demanding regulatory project just crash landed on your desk. Decisions must be made. Specialists need to be aligned. Deadlines must be met. For situations like this, we have brilliant experts to support you immediately. ·      Regulatory Project Manager ·      Global Regulatory Lead ·      Clinical Regulatory Expert ·      Regulatory CMC Expert ·      Labelling Specialist We offer flexible service models based on your needs: ·      FTE/partial FTE insourcing ·      Project support ·      Specialist consulting Does your regulatory team need support? Let's connect! [email protected] #regulatoryaffairs #drugdevelopment #qualityaffairs #pharmacovigilance #pharma #pharmaceuticals #biotech #marketaccess #pharmabusiness

For today's #EmployeeSpotlight, Senior Regulatory Affairs Manager, Kelly Reich, was asked, "What do you enjoy most about working at Biologics Consulting?" She said, "I have been at Biologics Consulting since 2001 and have thoroughly enjoyed the continuing opportunities to grow and learn. In my role providing regulatory strategy and advice, I work on application support and maintenance across a broad range of product types and therapeutic areas which keeps me on the leading edge of scientific developments in pharmaceuticals. By maintaining expertise in both innovative product types and changing regulations, I help sponsors unravel new challenges with both existing and new product classes. It excites me to engage in continuous learning in my career and to have the opportunities to share the insights I have gained with my clients. Each time I have the opportunity to develop a regulatory strategy, I re-review the regulations and re-read FDA guidances as well as build on my previous experience to provide relevant and timely advice. These days it’s unusual for people to stick with a job for 20 years, but the job is always changing and challenging to me so there is always something to pique my interest and professional growth. The Regulatory Affairs Team at Biologics Consulting is highly collaborative so when a colleague works on a unique project type, we all have the opportunity to learn from that experience and offer our collective knowledge and expertise to the sponsors we serve." #regulatoryaffairs

Careers in Drug Regulatory Affairs - Explore the intricacies of a regulatory affairs working and career options that it can provide #regulatoryaffairs #career #reglatory #licensing #productdevelopment #marketing #pharma #pharmaceuticals https://lnkd.in/dxGZEY4G

have lost my job few months back in Pharma. Any leads would be highly appreciated. I would really appreciate any assistance, even if it's as simple as liking, sharing, reposting, or commenting on this post to help increase it's visibility. Total Exp: 0.8 years Skills: Clinical Trials , Clinical Data Management , Pharmacovigilance ,B.pharma and MySQL. Notice Period: Immediate joiner #pharma #Immediatejoiner #pharmaceutical #pharmaceutical #pharmacovigilance #clinicaltrials #clinicaldatamanagement #linkedinconnection #linkedin #jobseeker #jobhunting

👉🏼 MedAssessment is a game-changer in pharmacovigilance for Early Drug Development. ✅ The combination of MedAssessment's expertise together with practical, efficient operations offers a level of quality that you won't find anywhere else in the market. 💬 Here's what a VP Clinical Operations had to say: "Because of their quality impact, MedAssessment allowed us to delay increasing headcount for pharmacovigilance activities. The combination of MedAssessment's ability to hold the bigger safety story together with practical, efficient operations means quality you don't get from other providers." 🌐 Are you looking for pharmacovigilance support? Look no further! MedAssessment has got you covered! Learn more: medassessment.com #DrugDevelopment #QualityDeliverables #Expertise #CustomerTestimonial #datascience #clinicaltrials #clinicalresearch #pharmaceuticalindustry #pharmacovigilance #medassessment

Happy Wednesday! #hiring for a regulatory affairs Sr Manager/Director/VP for an up and coming pharmaceutical company with exciting pipeline! If you are experienced in handling end-to-end RA matters, get excited talking about RA strategy and passionate about bringing more innovative medication options to patients, this may be a great fit for you. Feel free to get in touch for a confidential chat. *p/s: For non-RA people. RA is NOT just about dossiers submission. These folks are capable of magic! The more I connect and understand, the more I am left in awe with the work they do to bring new medication/ device into market. #supercool #regulatoryaffairs