Are you seeking an exciting and fulfilling new opportunity? Join our dynamic team at WEP Clinical, where your contributions will play a key role in driving impactful solutions and improving outcomes for clients and patients. We
Company Description Eurofins BioPharma Product Testing Leiden B.V., part of the globally operating Eurofins Scientific network, is a leading GMP-certified contract laboratory serving the (bio)pharmaceutical industry. Based at the Leiden Bio Science Park, we provide a
Job Description EHS compliance engineer (Quality Control department) Purpose of the role As a SHE Compliance Engineer, you support the CoE Quality department by driving safety, health, and environmental compliance. You develop and implement the annual
Cryoport Systems is a comprehensive supply chain partner for the life sciences industry, delivering specialized solutions to meet the challenges of the biopharmaceutical, cell and gene therapy, reproductive medicine, and animal health markets. Our offerings span logistics,
We’re here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We’ve made incredible scientific breakthroughs
Tijdelijke CRA positie in Nederland Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our
Mavericks Wanted When was the last time you achieved the impossible? If that thought feels overwhelming, you might want to pause here, but if it sparks excitement.read on In 2015, we pioneered a “moneyball for biotech”
Company Description Statistics show that women and underrepresented groups tend to apply to jobs only if they meet 100% of the qualifications. Sobi encourages you to change that statistic and apply. Rarely do candidates meet 100%
Job Description This is a highly visible leadership role at the forefront of Oncology Regulatory Affairs, offering the opportunity to shape regional regulatory strategy, develop talent, and drive impact for patients across Europe. If you are
Mavericks Wanted When was the last time you achieved the impossible? If that thought feels overwhelming, you might want to pause here, but if it sparks excitement.read on In 2015, we pioneered a “moneyball for biotech”
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
Work ScheduleStandard Office Hours (40/wk) Environmental ConditionsAble to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Loud Noises (Equipment/Machinery), Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning,
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
As our Qualified Person (QP)/ Responsible Person (RP) you are certifying the finished product and are responsible for ensuring that each finished medicinal product batch has been manufactured in accordance with GMP, the terms of the
A leading global biopharmaceutical organization is seeking an experienced Senior Associate QA to provide hands‑on quality support within a GMP manufacturing and packaging environment. This role is based on site in Breda and operates within a 24/7
Job Description Job Title: Operations Manager Department: Operations Location: Hoofddorp - Netherlands Reporting Line: Sr Director of Operations – Europe CSafe is seeking an Operations Manager to lead the growth of our passive manufacturing capability at
GMP Manufacturing Specialist Start: ASAP Duration: Long-term Contract Opportunity Location: South Limburg, Netherlands Hours: Full-time (5-Shift Rotation) Sector: Advanced Therapies / Biopharmaceutical Manufacturing Role Overview Were supporting a globally recognized organization within the advanced therapies sector in
Compensation: €3,000 - €4,000 gross per month, plus a 27% shift allowance. Are you looking for a role where you can contribute to life-changing therapies while working in a highly regulated manufacturing environment? Then this opportunity
Our client is an international biopharmaceutical organization focused on developing and bringing to market novel treatments for rare and ultra-rare genetic and immunological conditions. The company is patient-driven at its core, pairing strong scientific capability with genuine
As a Validation Engineer, you help pharmaceutical, biotech and medtech organisations ensure that manufacturing processes are robust, compliant and scientifically justified. In this role, your focus is on mixing processes and hold-time studies: two critical areas