Associate Director of Clinical Operations Management

Are you ready to take on a leadership role in driving change and building a strong and newly established, global Clinical Operations Management function?

Your role will be critical in optimizing the end-to-end execution of clinical trials and implementing a simplified new operational model set up to accelerate the trial startup phase, drive operational effectiveness, provide scalability, and ensure consistency in execution. You will be part of a workstream defining and ensuring roll out of the newly established COM function within GCO.

Clinical Operations Manager

Do you want key operational responsibility in phase 1-4 clinical trials as part of a high performing team?

As Clinical Operations Manager you are indispensable in the trial, leading and executing all the operational aspects throughout the different trial stages. You work closely with the Clinical Project Manager who is responsible for the clinical and strategic deliverables.

QA Assistant, GS-5, QAC

This position is embedded in the Quality Assurance Centre (QAC), where teams have coreresponsibilities around quality assurance and quality control of supply processes and the productswe procure and deliver.

The incumbent will beresponsible for assisting the Quality Assurance Specialist (non-pharma) in the management of all aspects of Pre-Delivery Inspection (PDI) arrangements for non-pharma items from initial request tofinal invoice certification.

Formulation Scientist

Are you looking to use and grow your experience in formulation development in a broad role with independent responsibilities? Do you want to drive formulation projects and contribute to the strategic development of future products?

In this role, your overall focus will be formulation development of drug products. Your responsibilities will cover formulations used for toxicology and clinical studies through the development phases and all the way to the commercial drug product.

Laborant til meget velfungerende peptidkemi laboratorie

Som laborant i vores peptid laboratorie er dit og kollegernes fokus at skabe grundlaget for udvikling af nye lægemidler. Du giver dit vigtige bidrag ved at bruge størstedelen af din tid med at arbejde hands-on i vores state-of-the-art laboratorie.

Du får et meget alsidigt job med ekstraordinært gode muligheder for at lære nyt og udvikle dig. Du kommer til at udføre alle typer af opgaver fra betjening af robotter og forskellige instrumenter til vedligehold og procesoptimering. Du kommer også til at arbejde med databehandling og dokumentation.

Senior Research Technician

Do you want to work with data and HPLC analysis?

You will spend most of your time on HPLC analysis in our modern laboratory, which is designed to provide the best technologies and optimal working conditions.

Collaborating cross-functionally with our research scientists on both daily operations and projects, you will:

• Perform analytical method development in close collaboration with the responsible scientists
• Support formulation development studies with analyses

Senior Research Technician

Do you want to use your experience and problem-solving skills to work with pharmaceutical product development and early-stage development with a focus on characterization (MFI, DSC, HPLC)?

As a senior research technician, you will spend most of your time in the lab, where your primary role will be to prepare, plan, and perform pharmaceutical development work, including stability studies.

Clinical Project Manager

Do you want impact, freedom to perform, global perspective and super colleagues?

As experienced Clinical Project Manager, you naturally know that your success is built on your ability to generate high quality data at high pace and within agreed budgets – without jeopardizing the good relationship to the people and partners involved. Another vital part of your road to success is your ability to think outside the box and handle (unforeseen) challenges on the way.

(Senior) Drug Substance Specialist

We are currently seeking a (Senior) Drug Substance Specialist who is energized by collaborative and fun teamwork, excels in handling complex tasks, and enjoys continuous learning.

Your responsibilities will include late-stage drug substance development, up-scaling and process validation as well as support in the commercial phase. Effective coordination with external partners is a significant aspect of this role.

Ambitious Project Manager to lead key strategic projects

Are you an experienced Project Manager motivated by making a difference? Then look no further – Pharmacosmos is looking for a Project Manager who can solve complex problems across our value chain and deliver impact to the organisation.

As Project Manager, you will become a key member of a small project management team in Pharmacosmos. You will be allocated to important strategic projects that you will lead and drive to completion to the satisfaction of all involved stakeholders using your existing toolbox and competencies for managing projects.

Senior Scientist, Infectious Disease Vaccine Discovery and Research

You will conduct various laboratory activities with the primary goal of producing reliable test results and optimizing lab procedures while adhering to correct procedures as well as health and safety guidelines. The role also includes documentation and reporting of results both in writing and in different forums.

You will work with dedicated colleagues in an inspiring and fast-moving environment with a collaborative and innovative spirit.

Kemiker til QC med GMP-erfaring

Syntese A/S søger en erfaren kemiker med kompetencer og interesse for analytisk kemi og GMP. Stillingen er en udvidelse af nuværende team.

Dine primære opgaver er at indgå i afdelingens daglige drift, hvor du supporterer og godkender analyser i et tæt samarbejde med dine kollegaer i teamet. Du udarbejder afvigelser, opdaterer SOP´er og vedligeholder kvalitetssystemerne.

Regulatory Affairs Clinical Specialist

Due to many activities in our exciting clinical development projects, we are seeking two new colleagues to our Regulatory Affairs function.

Your key responsibilities will be to contribute with regulatory expertise to global strategies and execution within your assigned project(s). You will be the regulatory responsible in the clinical trial teams and provide regulatory guidance and support for the planning, execution, and reporting of clinical trials worldwide.