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BA/BS Degree, BA/BS Degree or LPN 4 or more years of experience in clinical research, with minimum of 2 years of that experience at a pharmaceutical company or CRO, including participation in ...
Description: BSc/BEng plus previous experience in CQV field or equivalent combination of education and experience. Experience in pharmaceutical/biopharmaceutical industry or related ...
Description: SCHEDULE: Sunday 7am-11am Monday 7am-2:30 pm Tuesday 7am-4:30 pm Wednesday 7am-2:30pm Thursday 7am-1:30pm. Off Friday-Saturday. Must be flexable with working over some ...
Description:Must have experience with chromatographic techniques (HPLC highly preferred).For a chemist II it would be expected that the individual has been performing HPLC routinely for at least one ...
Transforming into digital technology for data management to bring our regulatory compliance into a higher standard of data use and protection, Global Regulatory Affairs CMC & Devices is being ...
Coordinate test samples for evaluation at internal and external contract laboratories, including calculation of sample numbers required for testing, ensuring proper labelling of samples, and clear ...
This role, DM Lead, will be responsible for overseeing both in-house and outsourced clinical trials. The DM Lead will collaborate heavily with the CRO DM and the study teams to ensure DM activities ...
Position Responsibilities Review clinical data from ongoing studies to ensure scientific quality Develop Protocol and ICF documents / amendments Conduct literature review Submit clinical ...
The role is to provide process development lab support to process development operations for support and lifecycle development of a viral product. The successful candidate will apply fundamental ...
Seeking a highly motivated individual with direct experience in next generation sequencing (NGS) to the Inflammation CV and Fibrosis Sequencing Research Group (ICF SRG) at company’s ...
Associate Scientist will be responsible for supporting analytical activities within Biologics Process Development (PD). The role will involve supporting in-process analytical testing, delivering ...
Qualifications: • Bachelor’s Degree in Microbiology, Biology or related scientific discipline. Minimum of 1 - 2 years of experience in biopharmaceutical industry, preferably working in a ...
Bring Your Own Device (BYOD)/LaptopThe Chemist 1 will provide testing and technical support in the Analytical QC Laboratory.ResponsibilitiesThese functions may include:• Processing and testing ...
Manager, Medical Device Epidemiology and Real-World Data Sciences. In this role, you will execute RWE surveillance and safety studies to meet EU-MDR requirements. In addition, you will take part ...
Shift Time : Mon-Fri 8am-5pmDefault Job Description: Chemistry lab technicians assist chemists in their lab work. As time progresses, lab technicians are completing a greater number of tasks ...
Client is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will ...
Bachelor's Degree or OUR equivalent is required, typically in nursing or scientific field; or R. N. by Associate's Degree with relevant experience is acceptable.Note: These could be LC based ...
The selected candidate will work in laboratory and perform dissolution testing using biorelevant media, devices and procedures for APIs and drug formulations to facilitate biopharmaceutics risk ...
• Shift start and end time may be staggered across a shift team to provide wider coverage across the operational day, and also may vary from those times listed below.• 1st shift 8am – ...
Job Description Summary: We are seeking a Biocompatibility Specialist who will make an important contribution to patient safety by supporting projects/programs in terms of biocompatibility of ...
