Submission Operations Manager for Pharmaceutical Industry

Company Overview:Randstad is a global leader in recruitment and HR services, providing top talent to clients across various industries. Job Description:As a Submission Archiving Specialist in the Pharmaceutical Industry, you will play a crucial role in maintaining regulatory information for one of the world's largest pharmaceutical companies. Key...

**Overview**Square One Resources Sp. z o.o., a renowned provider of innovative solutions, is seeking an exceptional Senior Technical Program Manager for Pharmaceutical Solutions to join our team.This is a part-time engagement that involves leading the development of cutting-edge software solutions for the pharmaceutical industry.As a Senior Technical Program...

Company OverviewManpower Group Sp. z o.o. is a global leader in the employment services industry, operating in 82 countries and boasting over 70 years of experience.Job DescriptionAs a Regulatory Scientist, you will be responsible for providing crucial support to RSIL and RRL in navigating complex regulatory landscapes and optimizing product strategies.Key...

Company OverviewOur client, a leading pharmaceutical company, is seeking a highly skilled Regulatory Affairs Manager to oversee the submission operational management and execution of electronic publishing of regulatory submissions. This role involves working closely with cross-functional teams to ensure timely and accurate submission of regulatory documents...

Overview of the RoleThe Pharmaceutical Regulatory Specialist will be responsible for ensuring compliance with regulatory requirements and guidelines throughout the product development and registration process.This involves managing operational submission processes, delivering high-quality regulatory submissions, and collaborating with cross-functional teams...

As a Compliance and Strategy Manager, you will be responsible for developing and implementing regulatory strategies to optimize product development and commercialization. You will work closely with regional and global teams to drive alignment between regional and global strategies. Our goal is to provide job seekers with new opportunities, helping them find...

Required Skills and Qualifications">The following skills and qualifications are required:">Relevant experience in regulatory affairs and submission publishing;Excellent communication and project management skills;Ability to work independently and as part of a team;Strong attention to detail and ability to meet deadlines.">Benefits">We offer a range of...

Job Overview: The Document Management Lead - Pharma Industry will be responsible for managing the operational delivery of regulatory documents for product registration and compliance. This role will involve managing a team and coordinating plans for packages of documents sent. The ideal candidate will have a strong background in regulatory affairs and...

Required Skills and QualificationsTo excel in this position, you will need to possess a unique blend of technical knowledge and soft skills. Some key qualifications include:- A university degree in Life Sciences, Pharmacy, or a related field- Professional experience in the pharmaceutical/medical industry- Strong understanding of the product development...

About the RoleThis is an exciting opportunity to join our team as a Regulatory Affairs Manager. In this role, you will play a critical part in the submission operations group, overseeing the execution of regulatory submissions to national and regional regulatory agencies and operating companies. You will be responsible for managing the submission process...

We are looking for an experienced Global Clinical Operations Specialist to collaborate with our client – a leading company in the pharmaceutical and clinical research industry.If you are passionate about working with data and want to join a team delivering international projects in the field of global clinical operations, this opportunity is for you.Our...

Job OverviewWe are seeking a skilled Technical Project Manager to join our team at Michael Page. As a Technical Project Manager, you will play a critical role in driving project excellence and ensuring the successful delivery of projects. You will work closely with the team to facilitate meetings, document minutes, and prepare reports, while also creating...

A Pharmaceutical Data Insights Expert is needed to support our client’s global clinical operations. As a key member of the team, you will be responsible for analyzing and interpreting complex data sets, identifying trends, and providing actionable insights to inform business decisions.The role involves:Analyzing large datasets using statistical...

ManpowerGroup Sp. z o.o., a global leader in the employment services industry, is seeking an experienced Regulatory Affairs Expert to join our team. Our company has over 70 years of experience, operating in 82 countries, with a presence in Poland since 2001. We strive to provide job seekers with new opportunities, helping them find employment that matches...

Company OverviewAt ManpowerGroup, we understand the importance of regulatory compliance in the pharmaceutical industry. As a global leader in workforce solutions, we provide cutting-edge recruitment and talent management services to help our clients succeed. Our commitment to excellence drives us to deliver top-notch professionals who can navigate complex...

Job DescriptionAs a Regulatory Affairs Specialist in Electronic Document Management, you will be responsible for maintaining regulatory information in a structured and secure environment to enable appropriate access, retrieval, and integrity. This involves archiving electronic submission documents and related communications in the official repository,...

Job DescriptionWe are looking for an HR Advisor to work with our healthcare clients on various projects. The ideal candidate will have experience in the pharmaceutical/medical branch and international organizations. They should be able to provide guidance and support to our clients on HR-related matters.As an HR Advisor, you will work closely with our...

**Company Profile**At Booksy, we're on a mission to help people around the world feel great about themselves every day. Our team is passionate about empowering entrepreneurs and supporting customers in arranging 'me time' moments.**Job Summary**As a Business Development Manager, you'll be responsible for seeking clients from enterprise beauty and non-beauty...

Job Summary: We are seeking a highly skilled Regulatory Affairs Specialist in Submission Archiving to join our team. As a key member of our regulatory affairs team, you will be responsible for maintaining and managing regulatory information in a secure and structured environment. Key Responsibilities:Develop and implement processes to ensure accurate and...

We are looking for a skilled professional to join our team as a Logistics Operations Manager. In this role, you will be responsible for overseeing the daily operations of our logistics department, ensuring that all tasks are completed efficiently and effectively.Key Responsibilities:Provide analysis with logistics tools and metrics.Analyze, interpret, and...