Devens, Massachusetts, United States · On-site
$90k–$109k/yr
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 …
Skills: Quality Assurance, cGMP Compliance, Deviation Management, CAPA, Change Control
Shrewsbury, Massachusetts, United States · On-site
We are ready for you to join our team! Deciding on a new career at Valmet can be an exciting opportunity! Every day there are teams of Valmet employees around the world who share the feeling of achieving something great …
Skills: HSE Management, Risk Assessment, ISO 14001, ISO 45001, Regulatory Compliance
Danvers, Massachusetts, United States · On-site
$65k–$104k/yr
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less in…
Skills: Manufacturing Engineering, Lean Manufacturing, Six Sigma, Root Cause Investigation, Process Validation
Raynham, Massachusetts, United States · On-site
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less in…
Skills: Agile Manufacturing, Developing Others, Good Manufacturing Practices (GMP), Inclusive Leadership, Leadership
Boston, Massachusetts, United States · Hybrid
$155k–$200k/yr
About this role Pickle is looking for an experienced Senior Technical Program Manager (TPM) to join our Software Engineering organization and help drive the execution of complex, cross-functional initiatives that power o…
Skills: Technical Program Management, Software Engineering, Agile Methodologies, Cross-functional Coordination, Risk Management
Milford, Massachusetts, United States · On-site
$125k–$208k/yr
OverviewJoin a high-impact team at the forefront of bioprocess innovation, where you will lead the development of next-generation LC/MS-based process analytical technologies. This role offers a unique blend of cutting-ed…
Skills: LC/MS System Design, Bioprocess Innovation, System Architecture, System Integration, Verification Strategies
Boston, Massachusetts, United States · On-site
$117k–$146k/yr
At DraftKings, AI is becoming an integral part of both our present and future, powering how work gets done today, guiding smarter decisions, and sparking bold ideas. It’s transforming how we enhance customer experiences,…
Skills: Python, SQL, Snowflake, Databricks, Kafka
Boston, Massachusetts, United States · On-site
$116k–$182k/yr
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice an…
Skills: CMC Data Standards, Data Modeling, Data Governance, Ontologies, Taxonomies
Boston, Massachusetts, United States · On-site
$154k–$243k/yr
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice an…
Skills: Product Lifecycle Management, Electronic Lab Notebooks, Continued Process Verification, Stakeholder Management, Roadmap Planning
Boston, Massachusetts, United States · On-site
$116k–$182k/yr
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice an…
Skills: CMC Data Standards, Taxonomies, Ontologies, Data Modeling, Data Governance
Boston, Massachusetts, United States · On-site
$85k–$110k/yr
Overview What You’ll Be Doing As Environmental Project Manager, you will support Cadmus’ rapidly growing portfolio of task orders under federal and state contracts, including work with the EPA and other government client…
Skills: Project Management, Regulatory Compliance, Stakeholder Engagement, Risk Management, Budget Management
Cambridge, Massachusetts, United States · Hybrid
$149k–$215k/yr
Job title: CMC dossier leader Location: Framingham, MA About the job Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their familie…
Skills: CMC Dossier Preparation, Regulatory Submissions, Pharmaceutical Development, AI-Powered Solutions, Cross-functional Leadership
Boston, Massachusetts, United States · On-site
$100k–$200k/yr
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Skills: Quantitative Portfolio Construction, Portfolio Analysis, Optimization Software, Python, R
Pittsfield, Massachusetts, United States · On-site
Basic Qualifications Education: High school diploma or general education degree (GED) required. Minimum of 2 years of testing of electrical / electronics and associated measurement equipment or equivalent technical train…
Skills: Electrical Testing, Electronics Troubleshooting, Schematic Interpretation, MS Windows, Data Logging
Lexington, Massachusetts, United States · On-site
$177k–$278k/yr
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice an…
Skills: Project Management, CAPEX Management, Contract Management, GxP Compliance, Pharmaceutical Engineering
Boston, Massachusetts, United States · Remote OK
$178k–$230k/yr
Senior Database Engineer (State Street Bank and Trust Company; Boston, Massachusetts): Will contribute to the development and certification of Azure DB and Managed Instance of State Street's Charles River Investment Mana…
Skills: Azure DB, Azure Managed Instance, Transact-SQL, PL/SQL, SQL
Cambridge, Massachusetts, United States · On-site
$122k–$177k/yr
Job Title: CMC Demand & Supply Leader Location: Framingham, MA About the Job Within CMC function, in the Global CMC Project Management department, the ambition is to expand a strong End to End R&D Supply Demand integrati…
Skills: Demand Management, CMC, Forecasting, Project Management, Data Analytics
Cambridge, Massachusetts, United States · On-site
$122k–$177k/yr
Job Title: CMC Demand & Supply Leader Location: Framingham, MA About the Job Within CMC function, in the Global CMC Project Management department, the ambition is to expand a strong End to End R&D Supply Demand integrati…
Skills: Demand Management, Supply Chain Planning, CMC, Project Management, Data Analytics
Boston, Massachusetts, United States · Hybrid
$178k–$196k/yr
Software Engineering & Development – Development Lead (State Street Bank and Trust Company; Boston, Massachusetts): Will contribute to the development, enhancement, and maintenance of our internal platform as a member of…
Skills: Python, Java, Spring Boot, SQL, Kafka
Woburn, Massachusetts, United States · On-site
$80k–$90k/yr
Spear Bio, founded in 2021, is a well-funded and rapidly growing biotech start-up headquartered in Woburn, Massachusetts. Our proprietary technology, Successive Proximity Extension Amplification Reaction (SPEAR), is a no…
Skills: Immunoassays, qPCR, Molecular biology, Assay development, Data management
Devens, Massachusetts, United States • On-site
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Provide Quality Assurance oversight for Manufacturing, QC, and Warehouse operations to ensure compliance with Global cGMP and company policies. Monitor process performance through data analytics and approve GxP records including deviations, CAPAs, and change controls.
Requires 4+ years of relevant cGMP experience, preferably with manufacturing site experience in biopharmaceuticals or cell therapy. A Bachelor's degree in a STEM field is preferred, along with proficiency in Quality Management Systems and digital tools.
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: careers.bms.com/working-with-us.
The Quality Assurance Shop Floor team is responsible for 24x7 Quality collaboration and oversight of site operations, including but not limited to Manufacturing, Quality Control laboratories, and Warehouse Operations.
This position works a Monday to Friday schedule, Day shift. This position will oversee and partner with operational areas to ensure compliance with Bristol-Myers Squibb policies, standards, procedures, and Global cGMP.
In the capacity of Shop Floor QA, the Senior Specialist shall serve as one of the Shop Floor Representatives interacting with Manufacturing, Supply Chaing, Quality Control and other supporting teams.
The Senior Specialist, Shop Floor QA, is accountable to monitor and track process performance related to key Shop Floor quality assurance quality tasks and other operational tasks through data and analytics; to own, review or approve Floor Quality GxP records including but not limited to procedures, CAPAs, change controls, impact assessments, documentation, or deviations; and represents SFQA at relevant governance forums. Additionally, the incumbent shall to support deviation approval, alarm approval, other Quality System Records, or batch record review as requested by management. Effective communication, critical thinking, and a thirst for knowledge are foundational skills for members of the Shop Floor Quality Assurance team to succeed.
This position reports to the Senior Manager, Quality Assurance Shop Floor Monday to Friday Team. This is an individual contributor role working Monday to Friday.
Provide Quality oversight to Manufacturing/QC/Warehouse/ Packout operations. Identify departures from approved procedures & respond to complex issues independently & escalate critical issues to management.
May perform and document operational verification per approved procedures.
Develops, reviews and/ or approves temporary and non routine procedure for event response.
Observe manufacturing operations and identify departures from clean room behaviors and aseptic techniques.
Coordinate and lead area walkthroughs to identify quality issues. Negotiate remediations and drive alignment of implementation plans.
Own actions for departmental programs and propose improvements to programs.
Participate in Gemba walks.
Communicate and resolve discrepancies independently and escalate as required.
Author, review, and approve procedural documents.
Maintain compliance with assigned learning plan. Provide guidance and training for QA personnel.
May own training curriculum and content.
May present individual topics during audits as needed.
Independently assess discrepancies for entry into quality system and approve deviations as applicable.
May serve as quality subject matter expert for risk assessments, change controls, etc.
Lead meetings and represent function at cross functional meetings.
Share data/knowledge within and across team. Build & maintain strong relationships with partner functions.
May prioritize and assign tasks for the team.
Periodically observe operations occurring on the floor and proactively identify risks and drive improvements.
Establish and maintain key performance indicators and standard work databases in alignment with departmental and product supply goals.
Functions as a project manager able to influence others based on time and task commitments, organize/run meetings.
Obtain access to, and develop as an SME for, various electronic systems utilized by Shop Floor Quality (BMSDocs, CELabs, MES, SAP, ValG, DeltaV, Maximo, Infinity, etc.).
Should be familiar with GMP-related systems including Quality Risk Management, Document and Data Governance, Monitoring and Reporting.
Share data/knowledge within and across teams by acting as a champion for quality-culture and learning.
Ability to research, understand, interpret and apply internal SOP’s, policies and regulatory guidelines.
Proficient computer skills with knowledge of digital tools such as MS Office, etc. and ability to learn and work with new software applications.
Ability to interpret data & results, understand complex problems with multiple variables, and articulate practical solutions.
Excellent written and verbal skills and ability to present technical data effectively based on target audience.
Ability to work in a fast-paced team environment and lead peers through changing priorities.
Detail oriented and task focused with ability to meet deadlines and support work prioritization.
Ability to negotiate and influence to craft mutually beneficial solutions.
Ability to motivate and foster a positive team environment.
Exhibit strong decision-making ability and think creatively while maintaining compliance and quality.
Pioneering mindset and ability to create innovative solutions.
Demonstrated experience with quality management systems for handling of records such as change control, product complaints, deviations, investigations, and CAPA management.
Demonstrated ability to learn and work with analytical computer/digital tools like Microsoft Power Automate, Smartsheet, Tableau, etc.
Bachelor's degree in STEM field preferred. High school diploma/ Associates degree with equivalent combination of education and work experience may be considered.
4+ years of relevant cGMP experience, preferably with 1+ year of manufacturing site experience. Experience in FDA/EMA regulations in biopharmaceuticals or cell therapy manufacturing is preferred.
Demonstrated experience with quality management systems
Demonstrated experience in GxP electronic systems such as Quality Management Systems (QMS); Manufacturing Execution Systems (MES) for electronic batch records; Enterprise Resource Planning (ERP) such as SAP; laboratory information management systems; or electronic logbooks/forms.
Able to gown for ISO 8 rooms (medical scrubs, safety shoes, safety glasses, gloves, etc.).
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:
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. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.
Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:
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 include:
Paid Time Off
US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
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
Based on eligibility, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.
Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.
Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science™ ”, 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 a supportive culture, promoting global participation 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.
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
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 will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/
We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at [email protected]. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.
R1603742 : Senior Specialist, QA Shop Floor M-F, Cell TherapyAt Bristol Myers Squibb, we work every day to transform patients’ lives through science. That work inspires some of the most interesting, meaningful, and life-changing careers you’ll experience. Join us and pursue innovative ideas alongside some of the brightest minds in biopharma, collaborating with a team rich in diversity of experiences, and perspectives. We have built a sustainable pipeline of potential therapies and are leveraging translational medicine and data analytics to understand how we can deliver the right medicine to the right patient, at the right time, to achieve the best outcome. Whether in a scientific, business or supporting function, a career at BMS means you’ll be inspired every day to grow and thrive through opportunities that are uncommon in scale and scope. Here, you’ll be on the cutting edge of powerful innovation in oncology, hematology, immunology, cardiovascular disease, and fibrosis, with colleagues united in the mission to help patients. Through the Bristol Myers Squibb Foundation, we also promote health equity and seek to improve health outcomes of populations disproportionately affected by serious diseases and conditions. Our mission is to give new hope to help patients prevail over serious disease – it drives everything we do. Review our Social Media Community Guidelines at: https://www.bms.com/social-media-community-guidelines.html
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