Regulatory Documents Jobs in Aberdeen Sct

Business Development Executive LE GBSGartner for Legal Risk & Compliance provides General Counsel and legal executives with actionable objective business and technology insights that drive smarter decisions and stronger performance on an organizations mission-critical priorities. At Gartner we guide...

Please note that this role is based in the United order to enable us to meet the statutory and regulatory obligations of the United Kingdom immigration system you must have the appropriate immigration permission needed to work and reside in the United Kingdom.This role will be a full-time 12-month...

Job DescriptionOverviewAre you excited to make a difference in how major nuclear programmes are delivered Do you excel in identifying embracing and adopting new technology and approaches to deliver safer faster better Do you enjoy establishing systems of work that are repeatable scalable automated e...

Senior/Principal Medical Writer Remote/Hybrid/In Office - UKTrilogy Writing & Consulting AnIndegeneCompanyis currently looking to hire Senior/PrincipalMedical Writers (f/w/d) to support our growing company in producing high-quality regulatory documentation for the international pharmaceutical indus...

Career CategoryRegulatoryJob DescriptionHOW MIGHT YOU DEFY IMAGINATIONIf you feel like youre part of something bigger its because you are. At Amgen our shared missionto serve patientsdrives all that we do. It is key to our becoming one of the worlds leading biotechnology companies. We are global col...

Regulatory Affair Specialist Join our team!At Baker Hughes we are transforming the future of energy. With operations in over 120 countries we are developing and deploying industry-leading technologies and services to take energy forward. For more than a century our inventions have revolutionized ene...

Job Description:Scientific & Regulatory Affairs (SRA) Specialist EuropeLocation: Slough United KingdomSalary: 36000 - 45000 (based on the level of experience) annual bonus benefitsAs an associate of the Scientific & Regulatory Affairs in the Mars Snacking team you will support several iconic brands...

ROLE SUMMARYThe clinician medical monitor may contribute towards providing medical and scientific expertise and oversight for Clinical Trials.The clinician medical monitor may be required to design a development strategy for multiple protocols designed to obtain worldwide approval for a compound or...

Work Flexibility: HybridJoin our Belfast team as a Quality Systems Specialist - Document ControlPosition Summary:The Document Control Specialist is responsible for managing organizing and maintaining controlled documents to ensure compliance with FDA regulations ISO 13485 and company quality managem...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

Hours: Part Time 20-25 hours per week (preferred days Monday-Thursday hours can be discussed)Location:Hybrid (40% from our office in Leeds)Salary: 24000 - 28500 (Pro-Rata)Contract:Fixed Term (12 month maternity cover)DBS: A basic check will be required (For more information please read our Policy...

POSITION SUMMARYYou will be responsible for scientific oversight data integrity and quality of clinical trial(s) in support of the development strategy for programs within the Late-Stage Oncology portfolio.KEY RESPONSIBILITIESClinical development expert for assigned studies maintaining current scien...

At GSK we have bold ambitions for patients aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines combining our understanding of the immune system with cutting-edge technology to transform peoples li...

Including but not limited to the following:Shape and develop the clinical development plans while adhering to the highest scientific and ethical standardsDesign conduct and report Sobi-sponsored studies in close collaboration with the rest of the clinical development team the clinical study teams re...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

At Gilead were creating a healthier world for all people. For more than 35 years weve tackled diseases such as HIV viral hepatitis COVID-19 and cancer working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight aga...

Air Export AOG Agent will serve in an operations capacity responsible for processing export shipments including accompanying export documentation. Major duties and responsibilities to include but not limited to:Track and Trace shipments.Prepare handle and process shipment documentation- including ho...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAt Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier cleaner and...

Job Description SummaryThe Global Program Clinical Head (GPCH) in CVM is the global clinical leader responsible for one or more clinical programs across indications involving one or multiple compounds. The GPCH owns the risk benefit assessment for the program(s) and as the leader of Global Clinical...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...