Associate Scientist, Sample and Data Management
4.
1 New Brunswick, NJ New Brunswick, NJ Estimated:
$85.
9K - $109K a year Estimated:
$85.
9K - $109K a year 4 days ago 4 days ago 4 days ago 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.
Position Summary This position is part of the Sample and Data Management group, and as such requires the handling of clinical biologics materials/samples, including monoclonal antibodies, fusion proteins, antibody-drug conjugates and fixed drug ration combination products to support clinical therapies, particularly immuno-oncology and oncology agents.
In this role, personnel are responsible for sample submission/distribution/tracking activities, sample inventory, maintain accurate and complete records for samples and other GLP/GMP compliance activities as assigned.
Key Responsibilities Processes Clinical Biologics samples that are classified as Band 4 and 5 materials, and the safety and handling requirements, thereof.
Due to the nature of Biologics samples, specialized training is required for the handling of Band 4 and 5 materials.
Attends designated meetings for management as needed and is empowered to make decisions for the group in those meetings, relaying back to the team any pertinent information.
Responds to audit comments for GLP samples comments which are received and proposes potential corrections for future samples, training his direct reports on the required corrections.
Point person for certain functional areas during GMP/GLP audits, which includes answering questions as a Subject Matter Expert (SME) for both Inventory and PD LIMS tasks related to sample processing, as well as investigations/discrepancies involving samples related to GMP/GLP.
Process incoming and outgoing samples, for release, re-assay, stability, validation and development testing including reagents and reference materials to support clinical development activities.
Administration of sample tracking activities and sample documentation for receipts, shipping and inventory of samples and reference standards.
Maintain shipping documentation for all samples for both incoming and outgoing shipments.
Support department analysts by providing sample and reference standard retrievals and inventory reports utilizing Inventory.
Release samples for testing using departmental notification procedures.
Submit and log in samples in PDLIMS and Inventory for such materials as; Clinical release and re-assay, IND, IMP, and BLA submissions, Analytical Method Development, and Validation of Analytical Methods.
Adhere to cGMP/GLP, good documentation practices, departmental procedures and safety requirements, maintaining control of incoming and outgoing samples and other materials for validation work, development projects and outsourced testing.
Provide support to personnel in generating and extracting sample information and documentation.
Document relevant activities in equipment log books that includes equipment performance, review of calibration, maintenance and inventory of all freezers and refrigerators used to store materials.
Clearly and accurately document work reflecting movement, handling and aliquoting of samples on worksheets and logbooks.
Maintain records to ensure accurate inventory and traceability.
Qualifications & Experience 2-4 years of experience working in a regulated environment, i.
e.
pharmaceutical/medical setting.
preferred degree in a Medical/Scientific Field of Study.
Proficient in Use of Electronic Systems:
PC based software, such as Inventory management, PDLIMS, Infinity, and Microsoft Office suite of applications.
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(TM) , 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 email protected .
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.
.
Estimated Salary: $20 to $28 per hour based on qualifications.
1 New Brunswick, NJ New Brunswick, NJ Estimated:
$85.
9K - $109K a year Estimated:
$85.
9K - $109K a year 4 days ago 4 days ago 4 days ago 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.
Position Summary This position is part of the Sample and Data Management group, and as such requires the handling of clinical biologics materials/samples, including monoclonal antibodies, fusion proteins, antibody-drug conjugates and fixed drug ration combination products to support clinical therapies, particularly immuno-oncology and oncology agents.
In this role, personnel are responsible for sample submission/distribution/tracking activities, sample inventory, maintain accurate and complete records for samples and other GLP/GMP compliance activities as assigned.
Key Responsibilities Processes Clinical Biologics samples that are classified as Band 4 and 5 materials, and the safety and handling requirements, thereof.
Due to the nature of Biologics samples, specialized training is required for the handling of Band 4 and 5 materials.
Attends designated meetings for management as needed and is empowered to make decisions for the group in those meetings, relaying back to the team any pertinent information.
Responds to audit comments for GLP samples comments which are received and proposes potential corrections for future samples, training his direct reports on the required corrections.
Point person for certain functional areas during GMP/GLP audits, which includes answering questions as a Subject Matter Expert (SME) for both Inventory and PD LIMS tasks related to sample processing, as well as investigations/discrepancies involving samples related to GMP/GLP.
Process incoming and outgoing samples, for release, re-assay, stability, validation and development testing including reagents and reference materials to support clinical development activities.
Administration of sample tracking activities and sample documentation for receipts, shipping and inventory of samples and reference standards.
Maintain shipping documentation for all samples for both incoming and outgoing shipments.
Support department analysts by providing sample and reference standard retrievals and inventory reports utilizing Inventory.
Release samples for testing using departmental notification procedures.
Submit and log in samples in PDLIMS and Inventory for such materials as; Clinical release and re-assay, IND, IMP, and BLA submissions, Analytical Method Development, and Validation of Analytical Methods.
Adhere to cGMP/GLP, good documentation practices, departmental procedures and safety requirements, maintaining control of incoming and outgoing samples and other materials for validation work, development projects and outsourced testing.
Provide support to personnel in generating and extracting sample information and documentation.
Document relevant activities in equipment log books that includes equipment performance, review of calibration, maintenance and inventory of all freezers and refrigerators used to store materials.
Clearly and accurately document work reflecting movement, handling and aliquoting of samples on worksheets and logbooks.
Maintain records to ensure accurate inventory and traceability.
Qualifications & Experience 2-4 years of experience working in a regulated environment, i.
e.
pharmaceutical/medical setting.
preferred degree in a Medical/Scientific Field of Study.
Proficient in Use of Electronic Systems:
PC based software, such as Inventory management, PDLIMS, Infinity, and Microsoft Office suite of applications.
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(TM) , 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 email protected .
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.
.
Estimated Salary: $20 to $28 per hour based on qualifications.
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