Senior Cryogenics Process Associate
Working with UsChallenging.
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 Senior Cryogenics Process Associate will perform Drug Substance handling activities across the site which include freezing and storage of Drug Substance (DS), packaging and shipping of Drug substance, and Quality Control (cold chain and/or ambient) samples in accordance with the defined process parameters and the business requirements.
This role will be assigned to support Cryogenics Warehouse Operations.
This role is required to work standard M-F schedule but may include night, weekend and/or holidays.
Support of warehouse or manufacturing operations may be required.
Key
Responsibilities:
Performs Drug Substance handling activities, including receipt, freezing, storage and transfers, to GMP manufacturing facility and finished product from production to interim storage (cold and frozen storage).
Performs Cell bank handling activities, including receipt, shipping, storage and transfers, to GMP manufacturing facility and to interim storage (frozen storage).
Performs Quality Control (cold chain and/or ambient) samples handling activities, including transfers and shipment to GMP contract labs.
Maintains DS inventory levels using required systems and equipment.
Packs/ships materials to both domestic and international markets, including HazMat.
Works on routine assignments per written procedures with little to no instruction, where ability to recognize deviation from accepted practice is required.
Adheres to good manufacturing practices and standard operating procedures.
Completes GMP forms and/or batch records as required for material receiving, shipping, and freezing activities.
Maintains a safe work environment by following all safety processes, procedures, and guidelines.
Assists with reviewing work throughout the process and at completion to ensure that it has been performed properly.
Revises and creates process documents with little to no instruction, assists with process related investigations.
Assists with reviewing batch records associated with each manufacturing lot, in conjunction with supervisor and Quality representative.
Able to drive small projects associated with improving safety and compliance.
Effectively uses in process automation systems (i.
e.
Delta V and OSI/Pi Historian) and some supporting business systems (i.
e.
SAP.
Infinity, Maximo etc.
) to maintain production records.
Requirements &
Qualifications:
High school diploma is required; Associates Degree preferred with 2 to 4 years of relevant experience.
Knowledge of science generally attained through studies resulting in a B.
S.
, in science, engineering, biochemistry or related discipline, is a plus.
A minimum of 2
years of operations experience in a facility subject to Good Manufacturing Practices (GMP) regulations.
Practical knowledge of regulations such as GMP and company Standard Operating Procedures (SOP).
Previous manufacturing or GMP warehouse experience preferred.
Previous work experience where attention to detail and personal accountability were critical to success.
Prior evidence of successful participation on work teams where combined contribution, collaboration, and results were expected.
Maintains a professional and productive relationship with area management and co-workers.
Demonstrates good interpersonal skills, is attentive and approachable.
Demonstrated proficiency in common computer tools such as word processing, spreadsheet and web based applications.
Working knowledge of standard computer based business systems such as SAP, Syncade, DeltaV strongly desired.
Mechanical aptitude to operate cryogenics and material handling equipment.
Previous use of personal protection equipment (PPE) preferred.
A valid Drivers License is required.
#BMSBLDMA #LI-ONSITE 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 CareersWith 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 ProtocolPhysical 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.
Recommended Skills Attention To Detail Automation Biochemistry Business Requirements Business Systems Delta V Distributed Control System Estimated Salary: $20 to $28 per hour based on qualifications.
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 Senior Cryogenics Process Associate will perform Drug Substance handling activities across the site which include freezing and storage of Drug Substance (DS), packaging and shipping of Drug substance, and Quality Control (cold chain and/or ambient) samples in accordance with the defined process parameters and the business requirements.
This role will be assigned to support Cryogenics Warehouse Operations.
This role is required to work standard M-F schedule but may include night, weekend and/or holidays.
Support of warehouse or manufacturing operations may be required.
Key
Responsibilities:
Performs Drug Substance handling activities, including receipt, freezing, storage and transfers, to GMP manufacturing facility and finished product from production to interim storage (cold and frozen storage).
Performs Cell bank handling activities, including receipt, shipping, storage and transfers, to GMP manufacturing facility and to interim storage (frozen storage).
Performs Quality Control (cold chain and/or ambient) samples handling activities, including transfers and shipment to GMP contract labs.
Maintains DS inventory levels using required systems and equipment.
Packs/ships materials to both domestic and international markets, including HazMat.
Works on routine assignments per written procedures with little to no instruction, where ability to recognize deviation from accepted practice is required.
Adheres to good manufacturing practices and standard operating procedures.
Completes GMP forms and/or batch records as required for material receiving, shipping, and freezing activities.
Maintains a safe work environment by following all safety processes, procedures, and guidelines.
Assists with reviewing work throughout the process and at completion to ensure that it has been performed properly.
Revises and creates process documents with little to no instruction, assists with process related investigations.
Assists with reviewing batch records associated with each manufacturing lot, in conjunction with supervisor and Quality representative.
Able to drive small projects associated with improving safety and compliance.
Effectively uses in process automation systems (i.
e.
Delta V and OSI/Pi Historian) and some supporting business systems (i.
e.
SAP.
Infinity, Maximo etc.
) to maintain production records.
Requirements &
Qualifications:
High school diploma is required; Associates Degree preferred with 2 to 4 years of relevant experience.
Knowledge of science generally attained through studies resulting in a B.
S.
, in science, engineering, biochemistry or related discipline, is a plus.
A minimum of 2
years of operations experience in a facility subject to Good Manufacturing Practices (GMP) regulations.
Practical knowledge of regulations such as GMP and company Standard Operating Procedures (SOP).
Previous manufacturing or GMP warehouse experience preferred.
Previous work experience where attention to detail and personal accountability were critical to success.
Prior evidence of successful participation on work teams where combined contribution, collaboration, and results were expected.
Maintains a professional and productive relationship with area management and co-workers.
Demonstrates good interpersonal skills, is attentive and approachable.
Demonstrated proficiency in common computer tools such as word processing, spreadsheet and web based applications.
Working knowledge of standard computer based business systems such as SAP, Syncade, DeltaV strongly desired.
Mechanical aptitude to operate cryogenics and material handling equipment.
Previous use of personal protection equipment (PPE) preferred.
A valid Drivers License is required.
#BMSBLDMA #LI-ONSITE 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 CareersWith 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 ProtocolPhysical 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.
Recommended Skills Attention To Detail Automation Biochemistry Business Requirements Business Systems Delta V Distributed Control System Estimated Salary: $20 to $28 per hour based on qualifications.
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