Bristol Myers Squibb
Join to apply for the
Manager, Site Support
role at
Bristol Myers Squibb .
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. 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 at careers.bms.com/working-with-us.
Principal Objective of the Position Support Devens site through review and approval of investigations and change controls. Provide Quality oversight and support for Technology Transfer, Automation, Cell Bank Disposition, Validation, Manufacturing Science and Technology, Master Data and Site Engineering programs. Assure the quality of manufactured products are in compliance with all applicable regulations and guidelines. May assist in preparing for and hosting of regulatory audits.
Major Duties and Responsibilities
Supports and provides quality oversight to technical transfer sub‑teams and the review and approval of technology transfer documentation.
Leads and provides quality oversight to automation forums. Provides review and approval of automation change management.
Assures consistent, effective use of the site change control system for all change requests. Ensures supporting documentation and change deliverables meet external regulatory and internal Global BMS guidelines and requirements.
Leads the cell bank disposition program and program management. Tracks and reviews deliverables for disposition and re‑evaluation.
Supports and provides quality oversight to projects and incoming transfers for cell banking operations.
Provides quality oversight, review and approves Master Data for SAP and Syncade in support of tech transfer and projects.
Provides quality oversight, review and approves Maximo work orders, OOTs, extensions for PMs and Cals.
May support projects interfacing with Site Engineering.
Provides quality support and oversight for Manufacturing Science and Technology and Validation protocols and reports and periodic assessments.
Provides quality support to Devens Site through quality review and approval of deviations or change controls.
Participates as requested in the response team for audits and inspections by World Health authorities.
Receives little supervision and identifies and reports discrepancies from normal practices or procedures to management, recommending and implementing corrective actions.
Drives opportunities for continuous improvement through project leadership, Quality systems program ownership, and group engagement.
Represents QA in cross‑functional meetings.
Provides training on QA‑owned procedures.
May provide guidance to less experienced staff.
May have direct supervision of non‑exempt and/or exempt staff.
Knowledge and Skills
Knowledge of biotech bulk and finished product manufacturing, analytical testing is highly desirable.
Extensive knowledge of US and EU cGMP regulations and guidance.
Knowledge of Quality Risk Management principles preferred.
Knowledge of electronic systems including any of the following SAP, LIMS, Infinity (Veeva Vault), LES, Maximo, Vault and Syncade desirable.
Experience working in a team‑based environment with a diverse group of people.
Excellent writing and oral communication skills are required.
Qualifications
Knowledge of science generally attained through studies resulting in a B.S. in science, engineering, biochemistry or related discipline, or its equivalent is preferred.
A minimum of 6 years of relevant experience in a regulated environment with at least 4 years focused on product quality.
Compensation Overview Devens, MA – US $100,480 – $121,756. The starting compensation range(s) for this role are listed above for a full‑time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. Final, individual compensation will be decided based on demonstrated experience.
Benefits
Health Coverage – Medical, pharmacy, dental and vision care.
Wellbeing Support Programs such as BMS Well‑Being Account, BMS Living Life Better and Employee Assistance Programs (EAP).
Financial Well‑being and Protection – 401(k) plan, short‑ and long‑term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
Work‑life Benefits
US Exempt Employees flexible time off (unlimited, with manager approval), 11 paid national holidays (excluding Phoenix, AZ, Puerto Rico or Rayzebio).
Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non‑Exempt, Hourly Employees 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays.
Seniority Level Mid‑Senior level
Employment Type Full‑time
Job Function Information Technology
Industries Pharmaceutical Manufacturing
#J-18808-Ljbffr
Manager, Site Support
role at
Bristol Myers Squibb .
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. 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 at careers.bms.com/working-with-us.
Principal Objective of the Position Support Devens site through review and approval of investigations and change controls. Provide Quality oversight and support for Technology Transfer, Automation, Cell Bank Disposition, Validation, Manufacturing Science and Technology, Master Data and Site Engineering programs. Assure the quality of manufactured products are in compliance with all applicable regulations and guidelines. May assist in preparing for and hosting of regulatory audits.
Major Duties and Responsibilities
Supports and provides quality oversight to technical transfer sub‑teams and the review and approval of technology transfer documentation.
Leads and provides quality oversight to automation forums. Provides review and approval of automation change management.
Assures consistent, effective use of the site change control system for all change requests. Ensures supporting documentation and change deliverables meet external regulatory and internal Global BMS guidelines and requirements.
Leads the cell bank disposition program and program management. Tracks and reviews deliverables for disposition and re‑evaluation.
Supports and provides quality oversight to projects and incoming transfers for cell banking operations.
Provides quality oversight, review and approves Master Data for SAP and Syncade in support of tech transfer and projects.
Provides quality oversight, review and approves Maximo work orders, OOTs, extensions for PMs and Cals.
May support projects interfacing with Site Engineering.
Provides quality support and oversight for Manufacturing Science and Technology and Validation protocols and reports and periodic assessments.
Provides quality support to Devens Site through quality review and approval of deviations or change controls.
Participates as requested in the response team for audits and inspections by World Health authorities.
Receives little supervision and identifies and reports discrepancies from normal practices or procedures to management, recommending and implementing corrective actions.
Drives opportunities for continuous improvement through project leadership, Quality systems program ownership, and group engagement.
Represents QA in cross‑functional meetings.
Provides training on QA‑owned procedures.
May provide guidance to less experienced staff.
May have direct supervision of non‑exempt and/or exempt staff.
Knowledge and Skills
Knowledge of biotech bulk and finished product manufacturing, analytical testing is highly desirable.
Extensive knowledge of US and EU cGMP regulations and guidance.
Knowledge of Quality Risk Management principles preferred.
Knowledge of electronic systems including any of the following SAP, LIMS, Infinity (Veeva Vault), LES, Maximo, Vault and Syncade desirable.
Experience working in a team‑based environment with a diverse group of people.
Excellent writing and oral communication skills are required.
Qualifications
Knowledge of science generally attained through studies resulting in a B.S. in science, engineering, biochemistry or related discipline, or its equivalent is preferred.
A minimum of 6 years of relevant experience in a regulated environment with at least 4 years focused on product quality.
Compensation Overview Devens, MA – US $100,480 – $121,756. The starting compensation range(s) for this role are listed above for a full‑time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. Final, individual compensation will be decided based on demonstrated experience.
Benefits
Health Coverage – Medical, pharmacy, dental and vision care.
Wellbeing Support Programs such as BMS Well‑Being Account, BMS Living Life Better and Employee Assistance Programs (EAP).
Financial Well‑being and Protection – 401(k) plan, short‑ and long‑term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
Work‑life Benefits
US Exempt Employees flexible time off (unlimited, with manager approval), 11 paid national holidays (excluding Phoenix, AZ, Puerto Rico or Rayzebio).
Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non‑Exempt, Hourly Employees 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays.
Seniority Level Mid‑Senior level
Employment Type Full‑time
Job Function Information Technology
Industries Pharmaceutical Manufacturing
#J-18808-Ljbffr