Chromatography Specialist for Pharmaceutical Analysis

At Novo Nordisk A/S, we are seeking a highly skilled Chromatography Specialist to join our team. As a key member of our Quality Control department, you will play a vital role in ensuring the quality of raw materials and excipients for pharmaceutical production.About the PositionIn this challenging and dynamic role, you will be responsible for supporting a...

OverviewFUJIFILM Diosynth Biotechnologies is a leading Contract Development Manufacturing Organization (CDMO) in the pharmaceutical industry. Our mission is to 'Advance Tomorrow's Medicines' by providing high-quality services from pre-clinical investigations to commercial GMP production.

FUJIFILM Diosynth Biotechnologies, a leading biologics contract development and manufacturing organization, is seeking a skilled System Automation Specialist to join its team in Hillerød, Denmark.As a System Automation Specialist, you will play a key role in the Utility Automation team, providing technical support for plant utilities and manufacturing...

Job DescriptionWe are seeking a skilled Pharmaceutical Process Engineer - Regulatory Compliance Specialist to join our team at Novo Nordisk A/S. As a key player in the Validation Support team within the Project Quality Management (PQM) department, you will be responsible for ensuring that validation structures and processes are robust and effective.In this...

Job DescriptionAs a Senior Chemistry Scientist, you will be part of a dynamic team that supports the development and implementation of analytical methods for the biologics Drug Substance (DS) production and global release of commercial products (DS/Drug Product).Key Responsibilities:Implementing and supporting multiple chemistry methods for technology...

Job OverviewAseptic quality assurance is a critical component of pharmaceutical production. As an Aseptic Quality Assurance Specialist at Novo Nordisk, you will play a vital role in ensuring the quality and safety of our products. This position requires a strong understanding of pharmaceutical manufacturing processes and regulations.Key Responsibilities-...

Hamlyn Williams is seeking a seasoned DeltaV Systems Specialist to bridge pharmaceutical manufacturing and automation engineering, ensuring reliable and compliant DeltaV systems critical for high-quality production.About the RoleThis role involves configuring and maintaining DeltaV infrastructure, validating systems to meet pharma GxP standards, and...

About the JobWe are seeking a highly skilled Quality Specialist to join our team of professionals dedicated to ensuring the highest quality standards of our products. As a key member of our team, you will play a pivotal role in driving improvement and standardisation across the organisation.Key ResponsibilitiesDefine, monitor, and improve activities,...

About the RoleWe are seeking a highly skilled Metrology Specialist to join our team. As a key member of our device metrology and quality control department, you will be responsible for planning calibration tasks, managing measuring equipment in SAP, and handling internal calibration documentation.Your primary tasks will include:Planning calibration tasks,...

About the RoleWe are looking for an experienced Quality Assurance Specialist to join our team in Hillerød. The successful candidate will be responsible for ensuring the quality strategy is implemented and adhered to, both internally and externally.Key ResponsibilitiesDevelop and implement quality strategies to ensure compliance with regulatory...

We are seeking a highly skilled Senior Quality Improvement Specialist to join our team in API Manufacturing 4, 25K Multi-Product Facilities. This is an exciting opportunity for a seasoned professional with expertise in Good Manufacturing Practice (GMP) to drive quality-related improvements and lead audit and inspection setup within the four departments.Key...

We are seeking an Analytical Expert for Pharmaceutical Production to join our Quality Control team at Novo Nordisk A/S. As a key member of our team, you will play a crucial role in ensuring the quality of raw materials and excipients for pharmaceutical production.About the DepartmentSourcing QC is part of Sourcing Operations, responsible for the incoming...

About Novo Nordisk A/S">Novo Nordisk is a leading global healthcare company with a legacy of driving change to defeat serious chronic diseases.">We recognize the importance of diverse perspectives and collaboration in achieving our goals. Our employees are key to our success, and we strive to create an inclusive culture that celebrates diversity.">The...

About the RoleAs a Lead Process Improvement Specialist in our Primary Packaging Development department, you will play a pivotal role in driving process excellence and strategic direction for container closure development. Your primary focus will be on understanding user needs, addressing process gaps, and collaborating with cross-functional teams to ensure...

Company OverviewNovo Nordisk A/S is a leading biotech company specializing in the production of Active Pharmaceutical Ingredients (APIs). Our mission is to improve patient care by delivering innovative solutions.

At Novo Nordisk A/S, we are seeking a highly skilled Senior GMP Expert to join our Device Manufacturing Development (DMD), Product Control and Global Support department.The successful candidate will have a strong understanding of Good Manufacturing Practices (GMP) regulations and requirements, with practical experience in the pharmaceutical industry. They...

Job RequirementsTo excel in this role, you'll need:Master's degree in mechanical engineering or a similar technical field.At least 5 years of metrology experience in a GMP-controlled environment, preferably in the medical device or pharmaceutical industry, with ISO standard expertise.Excellent communication skills to explain complex issues to...

Job DescriptionIn this role, you will contribute to ensuring the quality of raw materials for pharmaceutical production through high-level chromatographic analysis work. You will review chromatographic analyses, problem-solve, and update methods to maintain quality standards.You will work closely with chemists, laboratory technicians, and colleagues in...

About the TeamYou will become part of a highly skilled and engaged team that appreciates a good, social working environment with lots of fun while delivering results of high quality. Our colleagues offer expert knowledge and sparring in GMP, automation, project management, validation, mechanics, and compliance.Main ResponsibilitiesEnsure GMP compliance as...

About the RoleWe are seeking a highly motivated and organized professional to support our department in maintaining compliance with current Good Manufacturing Practice (cGMP) regulations.Key ResponsibilitiesCollaborate with the team to identify continuous improvement opportunities and implement process enhancements.Drive transparency initiatives for key...