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. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.
The following positions will require the employees to work with chemical, radiological, or biological agents that may be hazardous to health if mishandled (including Agents which may potentially affect reproduction or the fetus). Employees will be required to follow all safety procedures and use personal protective clothing/Equipment where specified. Inquires for further information should be directed to the hiring manager.
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Permanent Position – Pharmaceutical Development Technician – 25
Shift: 7:00am-3:30pm Site:NBR Bldg #105 (excluded)
Manager: Limin Zhang Rate: $38.47
JOB FUNCTION:
Carries out assigned laboratory responsibilities which may include performance of a variety of tests or analysis. Assists in development, execution and validation of analytical methods and routine sample analysis under the direct supervision of a professional/scientist or laboratory supervisor. Able to work independently in the analysis of routine pharmaceutical development samples. Assignments will be based upon the laboratory supervisor's assessment of technical abilities of the individual technician, project demand for the specific analysis and priorities critical to the business not based on seniority.
Technicians are expected to follow a written procedures and/or carry out verbal instructions with appropriate supervision, both independently or as part of a team. Familiarity and demonstrated competency (after training) is required with test equipment that includes but is not limited to the following: high performance liquid chromatography (HPLC), gas chromatography (GC), spectrophotometers, IR/Raman spectrometers, fluorimeters, polarimeters, dissolution instruments, volumetric and gravimetric analyzers, balances, pH meters, and other analytical instruments including computers and automated systems, is required. Common equipment will be used by technicians and scientists dependent upon the requirements of the assay as determined by the laboratory supervisor. Laboratory responsibilities include, but are not limited to the following: preparation and proper labeling of standards, samples, reagents, including mobile phases for HPLC analysis and dissolution media, sorting glassware for storage or cleaning, collecting waste solvents for disposal, and general laboratory housekeeping. Some projects will require working in high containment areas using established handling procedures. Assignments will be based upon supervisor’s assessment of technical abilities of the individual technician, demand for analysis, and priorities critical to the business, independent of seniority.
Laboratory skills training will be implemented to ensure PDT employees receive relevant training to facilitate the performance of their job responsibilities. Interactive training modules (i.e. On-The-Job Training) will be used for training on specific competencies. Competency check after training specific to an area will be conducted to evaluate proficiency of the new skill (or module). If required proficiency is not obtained the interactive learning and testing will be repeated. A pass/repeat summary of all testing on each module will be kept to assess the performance of the module. Pharmaceutical development technicians will be required to demonstrate competence after training as assessed by their management. In the event competence is not demonstrated, re-training will be provided. Required refresher training including laboratory safety and compliance must be kept up to date.
Responsibilities include maintaining laboratory documentation and equipment in strict compliance with safety, GLP, GMP, federal, state, and local regulations. Make adjustments and/or minor repairs to instruments and equipment as dictated by Instrument Operating Procedures (IOPs). Responsible for reporting to supervisor any anomalies or irregularities that may occur during the performance of any and all assigned assays. Maintain laboratory notebooks (paper or electronic) record/capture raw data, calculate results and submit results for supervisor review/approval.
EDUCATION REQUIREMENTS:
Two-year Associate Degree in Science related to pharmaceutical development or equivalent. Proficiency in use of computer programs/systems is essential. Technicians must maintain their skills and knowledge to stay current with advances in the field of pharmaceutical development analysis. Pharmaceutical development technicians may attend internal or external training courses as approved by management.
If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
On-site Protocol
Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Bristol Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.
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