Pharmaceutical Data Standardization Specialist

We are looking for a Regulatory Affairs Specialist to join our team at Randstad Polska Sp. z o.o.About the Role:Manage multiple CMC variations and source transfers for Finished Products, Intermediates and Active Pharmaceutical Ingredients for pharmaceutical, biopharm and vaccines products (work with the CTD Module 3, Quality part of the dossiers)Lead...

About the CompanyTN Poland is seeking a seasoned Business Analyst to join our team, working on cutting-edge projects in the pharmaceutical industry.With a minimum of 3 years of experience in a similar position, you will leverage your knowledge of Business Analysis techniques and Agile software development principles to drive success.As an expert in...

About the RoleAs a Business Analyst, you will be working on projects for one of the largest pharmaceutical companies in the world, impacting the lives and health of millions of patients.You will collaborate with business units to understand their content management needs, facilitating metrics harmonization and integrating data into a common...

About the Role:The ideal candidate will have a strong background in business analysis and a passion for working with pharmaceutical companies. They will be responsible for collaborating with business units to understand their content management needs, facilitating metrics harmonization, integrating data into a common database, and building solutions to...

Job DescriptionWe are seeking a highly skilled Costing Specialist to join our team at GSK. In this role, you will be responsible for supporting site Costing related activities, control and audit requirements, and driving for excellence in SMAS processes.Key AccountabilitiesSupport site Costing related activities, control and audit requirements.Opportunity to...

Commercial Events SpecialistWe are seeking a skilled Commercial Events Specialist to join our Life Science Services Commercial Excellence team.As a Commercial Events Specialist, you will be responsible for planning and executing various commercial events, including trade shows, conferences, webinars, and internal events.Key responsibilities...

The role of a Pharmaceutical Regulatory Professional is to manage multiple CMC variations and source transfers for Finished Products, Intermediates and Active Pharmaceutical Ingredients for pharmaceutical, biopharm and vaccines products (work with the CTD Module 3, Quality part of the dossiers).About the Position:Lead assigned projects: define and agree...

Senior Python DeveloperWe are looking for a skilled Senior Python Developer to join our team at Sii Polska, where you will work on projects of one of the largest pharmaceutical companies in the world.This is an excellent opportunity to have a real impact on the lives and health of more than 15 million patients by standardizing data and centralizing access to...

Job SummaryWe are seeking a skilled Technical Field Specialist to join our team in Poland. As a Technical Field Specialist, you will be responsible for providing high-quality technical support directly to customers within Poland.You will carry out repairs, on-site commissioning, service, and calibration of customer's inline inspection equipment to stated...

We are looking for a skilled Digital Transformation Specialist to drive the identification of customer needs and broader business objectives, and manage internal activities to ensure that our products and services are competitive, innovative and create great value.About Us: Viseven is a leading global B2B MarTech service provider, empowering Pharma and...

As a Procurement Systems Functional Specialist at TN Poland, you will be responsible for troubleshooting process and workflow related issues to ensure Commercial and other functions using the System can operate effectively.Key responsibilities include ensuring proper quality of data relevant to system and process scope, maintaining connections with...

We are seeking a highly skilled CMC Regulatory Expert to join our team at Randstad Polska Sp. z o.o.Job Description:Manage multiple CMC variations and source transfers for Finished Products, Intermediates and Active Pharmaceutical Ingredients for pharmaceutical, biopharm and vaccines products (work with the CTD Module 3, Quality part of the dossiers)Lead...

Job Overview: User Experience Specialist in Healthcare SectorAbout the CompanyTN Poland is a leading provider of innovative solutions in the pharmaceutical industry, working closely with some of the world's largest companies.We are now seeking a talented User Experience Specialist to join our team, who will be responsible for designing and implementing...

As a Senior Compliance Specialist, you will be responsible for managing multiple CMC variations and source transfers for Finished Products, Intermediates and Active Pharmaceutical Ingredients for pharmaceutical, biopharm and vaccines products (work with the CTD Module 3, Quality part of the dossiers).About the Job:Lead assigned projects: define and agree...

Job OverviewThe EMEA Purchasing Specialist will play a vital role in maintaining, standardizing, and digitalizing purchasing data and processes. This position offers opportunities to develop new standards and more efficient ways of working across the EMEA region.Your Key Responsibilities:Create new vendors and maintain master data on existing vendors in the...

About the RoleWe are looking for professionals with required skills to achieve our goals: GSK is seeking a dedicated Regulatory Project and Data Manager (RPDM) to join our team. The RPDM will work closely with Regulatory Matrix Teams and Early/Medicine Development Teams to provide planning support and resource management for Rx and Vx projects from Commit to...

Company OverviewB. Braun Melsungen AG is a global leader in the medical and pharmaceutical industry, dedicated to protecting and improving people's health.We are committed to innovation, quality, and customer satisfaction.

Job Title: Vendor Master Data Specialist (f/m/x)Mars Global Service is seeking a highly skilled and experienced Vendor Master Data Specialist to join their team.Key Responsibilities:Act as a central point of contact for commercial process queries, including vendor master data management and reporting.Improve the efficiency and effectiveness of existing...

Job Overview:We are seeking a highly skilled Vendor Master Data Specialist to join our team at TN Poland. As a key member of the Commercial Department, you will be responsible for managing commercial processes, including vendor master data management, reporting, and data analysis.About the Role:This is an exciting opportunity to work in a dynamic environment...

Job DescriptionWe are seeking a Senior Regulatory Specialist to join our Polish Hub. This role is responsible for coordinating and developing the CTA/IND lifecycle strategy, ensuring timely content delivery and compliance with GSK policy and procedures.The successful candidate will be accountable for overall work plans and accountable to individual GRLs/TGs...