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24719 jobs

job description: notes:- must have presentation skills & PowerPoint skills- at least 2 years full time work experience- minimum associates degree - skills preferred over Education- former Pharmaceutical experience preferred- bt experience huge plus- .....
under general direction of the potency method development lead, direct and assist in functions supporting potency and impurity methods as appropriate. this role will be focused on work in the bio-analytical development Lab. candidate will perform .....
job description:the claims resolution department is responsible for researching and processing all customer financial claims that are not rebate (commercial or government), return, or chargeback related. this includes invoice-related claims, as well .....
i position summary the reliability Engineer is responsible for providing the maintenance‐related uptime and operating efficiencies of equipment and facility assets. these activities help minimize costs and contribute to the profitability and .....
responsible for execution of the Manufacturing process in a multi-product, multi-line cGMP facility capable of Manufacturing commercial, Clinical and development Drug substance. shift is 6am to 6pm on rotating days (hours/days are non-negotiable), .....
the Scientist filling this position will work within a highly-matrixed team setting on a variety of modalities including Vaccines, viral constructs, therapeutic Proteins, and Monoclonal Antibodies. the contractor will work in a cGMP Testing .....
duration: this is a 12-week engagement bsc/beng plus previous experience in cqv field or equivalent combination of Education and experience. experience in Pharmaceutical/biopharmaceutical industry or related industry/cGMP environment. areas of .....
onsite m-f 8-5:30 pm ideal candidate-industry exp.- bio-tech or Manufacturing, master data experience, SAP, great attention to detail. responsibilities include: process global master data requests for new material creation in accordance with global .....
actual job title = Associate Director or senior manager, Clinical database programming ******important: must to have management experience, Statistical programmers or sdtm programmers for this posting****** typical daily work hours = 8am to 5pm .....
descriptionwhy join us?here at mindera, we are continuously developing a fantastic team, and would love it for you to join us. as a frontend Software developer you will be responsible for building fluid and responsive user interfaces for multiple .....
24719 jobs