Manager, Cell Therapy Manufacturing in Devens, MA
for each section heading.
We must use - for any list of duties/requirements/benefits. Use
for prose.
We must preserve all substantive info; do not invent or summarize away detail.
We need to extract content.
Let's parse the posting.
Intro: "At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it. 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."
That's about the role/company. Could be "About the role". We'll put that in
.
Then: "The Manager, Cell Therapy Manufacturing supports the commercial operations of the facility. The Manager will be responsible for the people manufacturing both clinical and commercial product with oversight of shifts that cover 24/7 cell therapy manufacturing unit operations such as media preparation, cell selection, cell processing, or product fill, all of which are executed in accordance with Current Good Manufacturing Practices (cGMP’s). Shifts Available 6am – 6pm, rotating schedule including holidays and weekends"
That's part of role description; maybe we can include in About the role or Responsibilities. But we have a Responsibilities section later.
Responsibilities list: many bullet-like sentences separated by periods. We need to extract each duty as list items.
Let's list responsibilities from the text:
- Supporting the development, implementation and compliance of manufacturing documentation, procedures and policies.
- Operating within the requirements of a validated manufacturing systems, plan, assign and oversee daily operational activities associated with assigned areas of responsibility.
- Maintaining operating and storage areas that are compliant, efficient, effective and safe.
- Identifying strategic and operational issues to prevent deviations and maintain a compliant environment.
- Leading and managing the development of corrective and preventative actions, deviation responses and investigations.
- Creating an environment of teamwork, open communication, and a sense of urgency.
- Foster a culture of safety and compliance that embraces safety in the work environment and the safety of the patients by compliance with company procedures and policies, and cGMP requirements.
- Efficiently coordinating, communicating, and providing Operations project information and activities status to Planning, Manufacturing, Quality Assurance / Operations, Global Supply and other associated functions in a timely manner in accordance to schedules and defined implementation timelines.
- Overseeing operators on daily basis as they:
- Perform unit operations and support operations described in standard operating procedures and batch records in a safe and GMP compliant manner.
- Complete documentation required by process transfer protocols, validation protocols, standard operating procedures, and batch records.
- Maintain training assignments to ensure the necessary technical skills and knowledge.
- Assist in the setup of manufacturing areas and equipment/fixtures and perform facility and equipment commissioning, qualification and validation activities.
- Hiring, mentoring and developing exceptional people
- Conducting performance reviews and identifying opportunities for career growth for manufacturing associates.
We need to format as
- . For nested list under overseeing operators, we could have sublist.
Now Requirements: "Minimum Requirements 5+ years of experience in cGMP bioprocessing manufacturing, cell therapy manufacturing or relevant experience.Bachelors in relevant science or engineering discipline, or equivalent in work experience."
Also "BMSCART We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway." That's more about hiring philosophy; could be part of About or Requirements but not needed as separate.
Qualifications: maybe education? Already covered.
Skills: "Knowledge, Skills & Abilities Experience in cell therapy manufacturing techniques, including cell washing processes, cell separation processes, cryopreservation processes, cell expansion processes using incubators and bioreactors, and automated equipment is highly preferred.Experience with aseptic processing in ISO 5 biosafety cabinets, universal precautions for handling human derived materials in BSL-2 containment areas is highly preferred."
We can list as bullet points.
Benefits: The posting includes a Benefits paragraph: "Benefits Subject to the terms and conditions of the applicable plans then in effect, you may be eligible to participate in our comprehensive benefit plans – including wellbeing support, retirement and financial protection benefits, and insurance offerings (medical, dental, vision, life and disability). U.S.-based exempt employees are eligible for Flexible Time Off (FTO), which provides paid time off without a set accrual limit, subject to manager approval, along with 11 paid company holidays each year. Non-exempt employees, RayzeBio employees, and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires (subject to manager approval), 11 paid company holidays, and 3 optional holidays. Depending on eligibility, employees may also have access to additional time-off benefits, including paid sick leave, up to two paid volunteer days per year, summer hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs. Eligible employees also enjoy an annual Global Shutdown between Christmas Day and New Year's Day. U.S.-based job seekers can explore full benefit offerings at https://careers.bms.com/benefits"
We need to preserve all substantive info; we can list benefits as bullet points.
Pay: "Compensation Overview Devens - MA - US: $104,975 - $127,205 The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully – carefully considering the nature of the role, required skills, work location, schedule and the knowledge and experience you bring. Final compensation is guided by pay equity principles and applicable employment laws. Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors, and individual, team or Company performance."
We can summarize as pay range and note discretionary incentive.
Schedule: "Shifts Available 6am – 6pm, rotating schedule including holidays and weekends" plus "Working Conditions This position will require shift work, including holidays and weekends.This position will require you to work in a clean room environment, with exposure to human blood components and in close proximity to strong magnets."
We can include schedule info: shift work 6am-6pm rotating, holidays, weekends. Also note clean room environment etc maybe as part of Working Conditions but not required as separate section; we could include in About or Responsibilities but maybe better to include in Schedule section? The instruction: include Schedule section only if posting actually states them. It does state shift schedule. So we can include schedule details.
We must not include boilerplate like EEO, scam warning, legal, application instructions, etc. So we need to remove those paragraphs.
Now construct HTML.
We'll have:
About the role
...
Responsibilities
- ...
...
Requirements
- 5+ years of experience in cGMP bioprocessing manufacturing, cell therapy manufacturing or relevant experience.
- Bachelor’s degree in a relevant science or engineering discipline, or equivalent work experience.
Maybe also include "BMSCART We hire for skills and capabilities..." but that's not a requirement; could be part of About.
Skills
- Experience in cell therapy manufacturing techniques, including cell washing processes, cell separation processes, cryopreservation processes, cell expansion processes using incubators and bioreactors, and automated equipment (highly preferred).
- Experience with aseptic processing in ISO 5 biosafety cabinets, universal precautions for handling human derived materials in BSL-2 containment areas (highly preferred).
Benefits
- Comprehensive benefit plans including wellbeing support, retirement and financial protection benefits, and insurance offerings (medical, dental, vision, life, disability).
- Flexible Time Off (FTO) for U.S.-based exempt employees: paid time off without a set accrual limit, subject to manager approval, plus 11 paid company holidays each year.
- Non-exempt employees, RayzeBio employees, and Puerto Rico-based employees: 160 hours of paid vacation annually for new hires (subject to manager approval), 11 paid company holidays, and 3 optional holidays.
- Additional time-off benefits where eligible: paid sick leave, up to two paid volunteer days per year, summer hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs.
- Annual Global Shutdown between Christmas Day and New Year's Day for eligible employees.
- Full benefit details available at https://careers.bms.com/benefits
But we must not add extra links? The instruction: preserve ALL substantive information; we can include the link as part of benefits description. It's okay to include inside - . Not prohibited.
Pay
Pay range for this full‑time position in Devens, MA: $104,975 – $127,205 per year. Additional discretionary incentive cash and stock opportunities may be available. Starting pay is determined based on role requirements, skills, location, schedule, and experience, guided by pay equity principles and applicable employment laws.
Schedule
Shifts are 6 am – 6 pm on a rotating schedule that includes holidays and weekends. The role requires shift work, including holidays and weekends, in a clean‑room environment with exposure to human blood components and proximity to strong magnets.
We need to ensure we didn't miss any substantive info: The "Working Conditions" also mentions clean room environment, exposure to human blood components, proximity to strong magnets. We included that in Schedule section. Could also be a separate Working Conditions but not required; we can include in Schedule.
We must not repeat job title as heading. We didn't.
We must not put Job ID/requisition numbers as headings; we omitted.
We must not include boilerplate like EEO, scam
for prose. We must preserve all substantive info; do not invent or summarize away detail. We need to extract content. Let's parse the posting. Intro: "At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it. 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." That's about the role/company. Could be "About the role". We'll put that in
. Then: "The Manager, Cell Therapy Manufacturing supports the commercial operations of the facility. The Manager will be responsible for the people manufacturing both clinical and commercial product with oversight of shifts that cover 24/7 cell therapy manufacturing unit operations such as media preparation, cell selection, cell processing, or product fill, all of which are executed in accordance with Current Good Manufacturing Practices (cGMP’s). Shifts Available 6am – 6pm, rotating schedule including holidays and weekends" That's part of role description; maybe we can include in About the role or Responsibilities. But we have a Responsibilities section later. Responsibilities list: many bullet-like sentences separated by periods. We need to extract each duty as list items. Let's list responsibilities from the text: - Supporting the development, implementation and compliance of manufacturing documentation, procedures and policies. - Operating within the requirements of a validated manufacturing systems, plan, assign and oversee daily operational activities associated with assigned areas of responsibility. - Maintaining operating and storage areas that are compliant, efficient, effective and safe. - Identifying strategic and operational issues to prevent deviations and maintain a compliant environment. - Leading and managing the development of corrective and preventative actions, deviation responses and investigations. - Creating an environment of teamwork, open communication, and a sense of urgency. - Foster a culture of safety and compliance that embraces safety in the work environment and the safety of the patients by compliance with company procedures and policies, and cGMP requirements. - Efficiently coordinating, communicating, and providing Operations project information and activities status to Planning, Manufacturing, Quality Assurance / Operations, Global Supply and other associated functions in a timely manner in accordance to schedules and defined implementation timelines. - Overseeing operators on daily basis as they: - Perform unit operations and support operations described in standard operating procedures and batch records in a safe and GMP compliant manner. - Complete documentation required by process transfer protocols, validation protocols, standard operating procedures, and batch records. - Maintain training assignments to ensure the necessary technical skills and knowledge. - Assist in the setup of manufacturing areas and equipment/fixtures and perform facility and equipment commissioning, qualification and validation activities. - Hiring, mentoring and developing exceptional people - Conducting performance reviews and identifying opportunities for career growth for manufacturing associates. We need to format as
- . For nested list under overseeing operators, we could have sublist.
Now Requirements: "Minimum Requirements 5+ years of experience in cGMP bioprocessing manufacturing, cell therapy manufacturing or relevant experience.Bachelors in relevant science or engineering discipline, or equivalent in work experience."
Also "BMSCART We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway." That's more about hiring philosophy; could be part of About or Requirements but not needed as separate.
Qualifications: maybe education? Already covered.
Skills: "Knowledge, Skills & Abilities Experience in cell therapy manufacturing techniques, including cell washing processes, cell separation processes, cryopreservation processes, cell expansion processes using incubators and bioreactors, and automated equipment is highly preferred.Experience with aseptic processing in ISO 5 biosafety cabinets, universal precautions for handling human derived materials in BSL-2 containment areas is highly preferred."
We can list as bullet points.
Benefits: The posting includes a Benefits paragraph: "Benefits Subject to the terms and conditions of the applicable plans then in effect, you may be eligible to participate in our comprehensive benefit plans – including wellbeing support, retirement and financial protection benefits, and insurance offerings (medical, dental, vision, life and disability). U.S.-based exempt employees are eligible for Flexible Time Off (FTO), which provides paid time off without a set accrual limit, subject to manager approval, along with 11 paid company holidays each year. Non-exempt employees, RayzeBio employees, and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires (subject to manager approval), 11 paid company holidays, and 3 optional holidays. Depending on eligibility, employees may also have access to additional time-off benefits, including paid sick leave, up to two paid volunteer days per year, summer hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs. Eligible employees also enjoy an annual Global Shutdown between Christmas Day and New Year's Day. U.S.-based job seekers can explore full benefit offerings at https://careers.bms.com/benefits"
We need to preserve all substantive info; we can list benefits as bullet points.
Pay: "Compensation Overview Devens - MA - US: $104,975 - $127,205 The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully – carefully considering the nature of the role, required skills, work location, schedule and the knowledge and experience you bring. Final compensation is guided by pay equity principles and applicable employment laws. Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors, and individual, team or Company performance."
We can summarize as pay range and note discretionary incentive.
Schedule: "Shifts Available 6am – 6pm, rotating schedule including holidays and weekends" plus "Working Conditions This position will require shift work, including holidays and weekends.This position will require you to work in a clean room environment, with exposure to human blood components and in close proximity to strong magnets."
We can include schedule info: shift work 6am-6pm rotating, holidays, weekends. Also note clean room environment etc maybe as part of Working Conditions but not required as separate section; we could include in About or Responsibilities but maybe better to include in Schedule section? The instruction: include Schedule section only if posting actually states them. It does state shift schedule. So we can include schedule details.
We must not include boilerplate like EEO, scam warning, legal, application instructions, etc. So we need to remove those paragraphs.
Now construct HTML.
We'll have:
About the role
...
Responsibilities
- ... ...
Requirements
- 5+ years of experience in cGMP bioprocessing manufacturing, cell therapy manufacturing or relevant experience.
- Bachelor’s degree in a relevant science or engineering discipline, or equivalent work experience.
Skills
- Experience in cell therapy manufacturing techniques, including cell washing processes, cell separation processes, cryopreservation processes, cell expansion processes using incubators and bioreactors, and automated equipment (highly preferred).
- Experience with aseptic processing in ISO 5 biosafety cabinets, universal precautions for handling human derived materials in BSL-2 containment areas (highly preferred).
Benefits
- Comprehensive benefit plans including wellbeing support, retirement and financial protection benefits, and insurance offerings (medical, dental, vision, life, disability).
- Flexible Time Off (FTO) for U.S.-based exempt employees: paid time off without a set accrual limit, subject to manager approval, plus 11 paid company holidays each year.
- Non-exempt employees, RayzeBio employees, and Puerto Rico-based employees: 160 hours of paid vacation annually for new hires (subject to manager approval), 11 paid company holidays, and 3 optional holidays.
- Additional time-off benefits where eligible: paid sick leave, up to two paid volunteer days per year, summer hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs.
- Annual Global Shutdown between Christmas Day and New Year's Day for eligible employees.
- Full benefit details available at https://careers.bms.com/benefits
- . Not prohibited.
Pay
Pay range for this full‑time position in Devens, MA: $104,975 – $127,205 per year. Additional discretionary incentive cash and stock opportunities may be available. Starting pay is determined based on role requirements, skills, location, schedule, and experience, guided by pay equity principles and applicable employment laws.
Schedule
Shifts are 6 am – 6 pm on a rotating schedule that includes holidays and weekends. The role requires shift work, including holidays and weekends, in a clean‑room environment with exposure to human blood components and proximity to strong magnets.
We need to ensure we didn't miss any substantive info: The "Working Conditions" also mentions clean room environment, exposure to human blood components, proximity to strong magnets. We included that in Schedule section. Could also be a separate Working Conditions but not required; we can include in Schedule. We must not repeat job title as heading. We didn't. We must not put Job ID/requisition numbers as headings; we omitted. We must not include boilerplate like EEO, scam