BMY Data Entry Remote jobs ? Work From Home, No Experience, No Degree

BMY Data Entry Remote jobs - Work From Home, No Experience, No Degree

Job Responsibilities: Associate, Quality Control Data Review...

Hiring Organization: BMY

Educational Requirements: Bachelor Degree

Industry: Private

Salary: $35-40$/Year

Location: USA
Full Job Descriptions:-

Set of working responsibilities

Working with Us

Testing. Significant. Groundbreaking. Those aren't words that are normally connected with a task. Yet, working at Bristol Myers Squibb is everything except regular. Here, particularly fascinating work happens consistently, in each office. From upgrading a creation line to the most recent leap forwards in cell treatment, this is work that changes the existences of patients, and the vocations of the people who make it happen. You'll be able to develop and flourish through open doors unprecedented in scale and degree, close by successful groups wealthy in variety. Take your vocation farther than you expected.

Bristol Myers Squibb perceives the significance of equilibrium and adaptability in our workplace. We offer a wide assortment of serious advantages, administrations and projects that give our representatives the assets to seek after their objectives, both at work and in their own lives. Understand more: /working-with-us.

RayzeBio is a powerful biotechnology organization settled in San Diego, CA. Sent off in late 2020 and as of late procured by Bristol Myers Squibb (BMS) as an entirely possessed auxiliary, the organization is centered around further developing endurance of individuals with disease by tackling the force of designated radioisotopes. RayzeBio will work as an independent element inside the BMS association, keeping up with its biotech culture with the chance to use the top tier oncology capacities of BMS. RayzeBio is creating inventive medications against focuses of strong growths. The lead resource, RYZ101, is in Stage 3 testing for patients with gastroenteropancreatic neuroendocrine growths (GEP-NETs), as well as prior stage testing for patients with little cell cellular breakdown in the lungs (SCLC). Driven by an effective and experienced enterprising group, RayzeBio means to be the worldwide forerunner in radiopharmaceuticals.

RayzeBio, a Bristol Myers Squibb organization, is looking for candidates for a Quality Control Information Commentator. We are looking for a conscientious Quality Control Information Commentator to assume a critical part in the turn of events and commercialization of RayzeBio's designated alpha treatment (TAT) radiopharmaceuticals. In a perfect world, the competitor will have earlier research center and specialized insight in the radiopharmaceutical business. Extra obligations might incorporate archiving as well as leading research facility examinations.
? *This is an on location position situated at Rayzebio's Indianapolis, IN site*

Key Liabilities:

Audit Quality Control information for exactness, culmination and consistence with laid out systems and administrative prerequisites.

Guarantee Quality Control information is surveyed as soon a possible.

Direct occasional survey and updates of Value Control Standard Working Systems, as the need might arise.

Direct Examinations ? Lead and direct top to bottom examinations observing guideline working systems for out of detail results and other quality issues in the quality control lab.

Archive Discoveries of examinations ? compose itemized examination reports and work with QA and QC the board to propose give restorative activity and remedial preparation to forestall rehash occasions.

Guarantee information honesty all through information audit and examinations as required.

Proactively recognize valuable open doors for upgrades to the two examinations and the information audit processes.

Position is salaried position, by and large first shift, however expanded hours or end of the week work in light of radiopharmaceutical producing timetable might be required

This position will require the candidate to work with and around ionizing radiation, biohazardous materials, and perilous synthetic compounds.

Up to 10% of movement might be required.

Different obligations as alloted by the board.

Instruction and Experience:

BS in Science, Science, Science, or applicable field with five to seven years of involvement with drug or other cGMP experience. Postgraduate educations might be satisfactory with less experience, but direct involvement in cGMP specialized composing is required.

Careful comprehension of cGMP guidelines, ICH rules, FDA and other administrative cycle examination process

Experience with injectable drugs or radiopharmaceuticals emphatically liked.

Experience following upkeep of research center gear liked.

Abilities and Capabilities:

Capacity to perform various tasks, and focus on work in view of different work processes is an unquestionable necessity

Capacity to securely deal with unsafe materials

Great hierarchical practices are required

Solid scientific and critical thinking abilities.

Capacity to function admirably and discuss really with different partners

Solid composed and oral relational abilities

Work with PC programs, including however not restricted to Microsoft Office

Profoundly energetic with the capacity to work freely, without bearing, or with others in a group climate

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