What are the responsibilities and job description for the Specialist, Associate Process Engineer - Devens MA position at VetJobs?
Job Description
ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post.
At Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team.
The Specialist, Associate Process Engineer, Cell Therapy provides technical support to the Devens Cell Therapy Facility (CTF) Manufacturing processes in a GMP environment. Technical support includes troubleshooting process and equipment related issues that occur during the Manufacturing process. The Associate Process Engineer works closely with the Manufacturing and Quality teams to determine immediate corrective actions for deviations, identifies root cause, and implements long-term preventive actions. Other responsibilities include participation in process tech transfer, supports incoming process changes by communicating the changes to applicable departments, and participates in process improvement projects at the site. The process engineer works to identify and drive continuous improvements to the manufacturing process.
Shifts Available
TBD
Responsibilities
Provides on-the-floor and on-site troubleshooting and technical support to Manufacturing
Facilitates deviation prevention and deviation closure through site quality systems
Analyze and summarize manufacturing data to support impact assessments and investigations
Owner of change controls for routine process and procedure changes
CAPA owner for Manufacturing improvements
Author and revise manufacturing SOPs and provide technical content and direction for electronic batch records
Participates in technology transfer efforts for new processes and product implementation
Train and support GMP operators on new procedures, processes, and changes
Applies continuous improvement tools to identify and close procedural and compliance gaps
Identify opportunities for process improvements and operational efficiencies, and lead implementation efforts.
Interfaces with other functions such as Scheduling, Global MSAT, Supply Chain, Quality, and Facilities & Engineering
Support equipment and systems validation activities, including review of equipment qualification documents, drafting user requirements, and participating on impact assessments
Ability to perform gowning activities and enter the manufacturing plant. Exposure to strong magnetic fields is commonplace in the manufacturing areas.
Auto req ID
472473BR
Minimum Education Required
High School/GED
Job_Category
Analyst
Additional Qualifications/Responsibilities
Minimum Requirements:
BSc and/or MSc degree in Science or Chem/Bio Engineering
Minimum 0-3 years of industry experience. cGMP and/or Cell Therapy manufacturing experience preferred.
This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job.
This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management.
BMSCART
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.
Compensation Overview
Devens - MA - US: $79,150 - $95,914
City*
Devens
State*
Massachusetts
Job Code
Pharmaceutical Pharmaceutical
Affiliate Sponsor
Bristol Myers Sqibb BMS
Salary Range
$75,000-$100,000
ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post.
At Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team.
The Specialist, Associate Process Engineer, Cell Therapy provides technical support to the Devens Cell Therapy Facility (CTF) Manufacturing processes in a GMP environment. Technical support includes troubleshooting process and equipment related issues that occur during the Manufacturing process. The Associate Process Engineer works closely with the Manufacturing and Quality teams to determine immediate corrective actions for deviations, identifies root cause, and implements long-term preventive actions. Other responsibilities include participation in process tech transfer, supports incoming process changes by communicating the changes to applicable departments, and participates in process improvement projects at the site. The process engineer works to identify and drive continuous improvements to the manufacturing process.
Shifts Available
TBD
Responsibilities
Provides on-the-floor and on-site troubleshooting and technical support to Manufacturing
Facilitates deviation prevention and deviation closure through site quality systems
Analyze and summarize manufacturing data to support impact assessments and investigations
Owner of change controls for routine process and procedure changes
CAPA owner for Manufacturing improvements
Author and revise manufacturing SOPs and provide technical content and direction for electronic batch records
Participates in technology transfer efforts for new processes and product implementation
Train and support GMP operators on new procedures, processes, and changes
Applies continuous improvement tools to identify and close procedural and compliance gaps
Identify opportunities for process improvements and operational efficiencies, and lead implementation efforts.
Interfaces with other functions such as Scheduling, Global MSAT, Supply Chain, Quality, and Facilities & Engineering
Support equipment and systems validation activities, including review of equipment qualification documents, drafting user requirements, and participating on impact assessments
Ability to perform gowning activities and enter the manufacturing plant. Exposure to strong magnetic fields is commonplace in the manufacturing areas.
Auto req ID
472473BR
Minimum Education Required
High School/GED
Job_Category
Analyst
Additional Qualifications/Responsibilities
Minimum Requirements:
BSc and/or MSc degree in Science or Chem/Bio Engineering
Minimum 0-3 years of industry experience. cGMP and/or Cell Therapy manufacturing experience preferred.
This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job.
This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management.
BMSCART
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.
Compensation Overview
Devens - MA - US: $79,150 - $95,914
City*
Devens
State*
Massachusetts
Job Code
Pharmaceutical Pharmaceutical
Affiliate Sponsor
Bristol Myers Sqibb BMS
Salary Range
$75,000-$100,000
Salary : $75,000 - $100,000