• 4.9

    QC Information Systems / Sr. Analyst

    Astrazeneca
    Information Systems Analyst Job in Frederick, MD
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    Our Frederick Manufacturing Center (FMC) is one of 30 production facilities in 18 countries that creates life-changing medicines for people around the world. Analyst* in Frederick, MD, you'll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients' lives. The FMC is also an award-winning employer and has been recognized as a Top 50' Business in Frederick and awarded Frederick County's Best Place to Work' distinction in 2015 and 2019. At *AstraZeneca* we work together across global boundaries to make an impact and find answers to challenges.
    Mid Level
    Senior Level
    Doctorate Required
    New
    6d ago
    Opens new tab
  • 4.9

    Production Lead Technician - Day Shift

    Astrazeneca
    Technical Production Lead Job in Frederick, MD
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    Our Frederick Manufacturing Center (FMC) is one of 30 production facilities in 18 countries that creates life-changing medicines for people around the world. The FMC is also an award-winning employer and has been recognized as a Top 50' Business in Frederick and awarded Frederick County's Best Place to Work' distinction in 2015 and 2019. At *AstraZeneca* we work together across global boundaries to make an impact and find answers to challenges. Production Lead Technician - Day Shift:
    Senior Level
    New
    3d ago
    Opens new tab
  • 4.9

    Validation Associate Scientist I

    Astrazeneca
    Associate Scientist Job in Frederick, MD
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    We continuously forge partnerships that help pursue world-class medicines in new ways, combining our people's outstanding skills with those of people from all over the globe.Our Frederick Manufacturing Center (FMC) is one of 30 production facilities in 18 countries that creates life-changing medicines for people around the world. *Validation Associate Scientist I*At AstraZeneca, we work together across global boundaries to make an impact and find answers to challenges. Come join our award-wining team and support the manufacture of life-changing medicines for patients across the world.As a *Validation* *Associate Scientist I*, you are expected to provide technical solutions to a wide range of critical issues in compliance with organizational objectives. The FMC is also an award-winning employer and has been recognized as a Top 50' Business in Frederick and awarded Frederick County's Best Place to Work' distinction in 2015 and 2019.
    Mid Level
    Bachelors Required
    New
    1d ago
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  • 4.9

    Director, Business Process Optimization - Cambridge, MA or Remote

    Takeda Pharmaceutical
    Business Director Job, Remote or Elizabeth, NJ
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    This includes driving and leading overall management, direction, coordination, and implementation of high priority change initiatives designed to optimize business processes critical to the operational effectiveness of Takeda. Oversee and mentor direct reports, providing leadership and training to support professional development and responsible for demonstration of Takeda Leadership Behaviors will report to the Head of Business Optimization and Regulatory Chief of Staff and lead Takeda Global Regulatory Affair optimization group. Provide leadership, direction, and overall oversight for the continuous improvement of products and processes as well as new initiatives aligned with Takeda strategy
    Senior Level
    Executive
    12d ago
    Opens new tab
  • 4.9

    Production Technician III - Day Shift- Operations

    Astrazeneca
    Production Operations Technician Job in Frederick, MD
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    Our Frederick Manufacturing Center (FMC) is one of 30 production facilities in 18 countries that creates life-changing medicines for people around the world. At *AstraZeneca* we work together across global boundaries to make an impact and find answers to challenges. As a *Production Technician III- Day Shift* in the Manufacturing group at Frederick, MD, you'll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients' lives. * Proven ability to perform all process steps of upstream / downstream / central services production operations and act as the primary trainer of those with less experience (and may act as interim Lead as required) * At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big.
    Senior Level
    Bachelors Preferred
    High School Diploma Required
    New
    1d ago
    Opens new tab
  • 4.9

    Senior Program Manager, Clinical Quality Assurance, Rare Genetic and Hematology (Remote)

    Takeda Pharmaceutical
    Senior Project Manager Job, Remote or Westford, MA
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    Assist with management of GCP health authority inspections; lead clinical development teams in preparation for announced inspections and provide GCP compliance technical support during inspections of investigator sites and Takeda. Develop and implement program-specific risk-based audit and compliance strategy and manage audits of sites, documents, databases, vendors or internal systems in compliance with GCP and Takeda policies and procedures. Collaborate with Quality Compliance and Systems team to identify and mitigate GCP quality and compliance issues with potential impact across multiple compounds, Takeda sites, or functional groups. Manage domestic and international audits of sites, documents, databases, vendors or internal systems in compliance with GCP and Takeda policies and procedures; assess impact of audit findings on subject safety, data integrity, and business operations. Senior Program Manager, Clinical Quality Assurance, Rare Genetic and Hematology
    Senior Level
    Management
    13d ago
    Opens new tab
  • 4.9

    Senior Director of Statistics

    Takeda Pharmaceutical
    Senior Director Job, Remote or Swarthmore, PA
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    Such roles will have a connection to a Takeda R&D center. As part of DSI, the Statistics and Quantitative Sciences (SQS) at Takeda is looking to add individuals to our team that are team oriented, collaborative, strong understanding of the statistical programming function, exceptional leaders and innovators. To attract and retain the very best talent, we in Takeda SQS are open to flexible or remote working for some roles. Takeda is a global, values-based, R&D-driven, top 10 biopharmaceutical leader committed to discover and deliver life-transforming treatments, guided by our commitment to patients, our people and the planet. At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. Serve as leader, expert, mentor and manager of group supporting translational and exploratory statistical analyses in support of Takeda R&D assets across Therapeutic Area Units (TAUs)
    Senior Level
    Executive
    13d ago
    Opens new tab
  • 4.9

    Associate Director, GCP Supplier Quality Lead, Clinical Operations (Remote)

    Takeda Pharmaceutical
    Director Of Clinical Operations Job, Remote or Hamilton, MA
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    Liaise and collaborate with internal Takeda and external business partners to provide guidance and support pertaining to compliance and supplier quality oversight initiatives What you bring to Takeda: Lead the development and implementation of risk-based GCP supplier audit and compliance strategy and manage supplier audits in compliance with GCP and Takeda policies and procedures.
    Senior Level
    Executive
    Bachelors Preferred
    11d ago
    Opens new tab
  • 4.9

    Associate Director, Programming

    Takeda Pharmaceutical
    Associate Program Director Job, Remote or Helmetta, NJ
    Opens new tab
    Such roles will have a connection to a Takeda R&D center. OBJECTIVES/PURPOSE: Takeda SQS is looking to add individuals to our team that are team oriented, collaborative, strong understanding of the statistical programming function, exceptional leaders and innovators. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To attract and retain the very best talent, we in Takeda SQS are open to flexible or remote working for some roles. Takeda is a global, values-based, R&D-driven, top 10 biopharmaceutical leader committed to discover and deliver life-transforming treatments, guided by our commitment to patients, our people and the planet. Join us as an Associate Director, Programming, in our Cambridge, MA office.
    Executive
    13d ago
    Opens new tab
  • 4.9

    Territory Business Manager, Oncology (Frederick/Fairfax)

    Bristol Myers Squibb
    Territory Business Manager Job in Arlington, VA
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    Candidates with 5+ years of pharmaceutical sales experience will be considered at the Senior Territory Business Manager, Oncology level and title This position covers: Fredericksburg, VA, Harrisonburg, VA, Cumberland, MD and Frederick/Hagerstown, MD, Arlington, VA The Territory Business Manager is a business leader who represents the integrity of the company by providing approved disease and product information and resources to key decision makers and stakeholders within the oncology community practice setting. At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science. The Territory Business Manager builds and maintains strong professional relationships with community-based physicians/HCPs in private practice, medical groups practices, office staff and others in the patient care continuum. Candidates with 3+ years of pharmaceutical sales experience will be considered at the Territory Business Manager, Oncology level and title
    Mid Level
    Management
    Bachelors Preferred
    9d ago
    Opens new tab
  • 4.9

    Clinical Quality Assurance, Senior Manager - Oncology (Remote)

    Takeda Pharmaceutical
    Quality Assurance Manager Job, Remote or Wakefield, MA
    Opens new tab
    Assist with management of GCP health authority inspections; lead clinical development teams in preparation for announced inspections and provide GCP compliance technical support during inspections of investigator sites and Takeda. Develop and implement program-specific risk-based audit and compliance strategy and manage audits of sites, documents, databases, vendors or internal systems in compliance with GCP and Takeda policies and procedures. Collaborate with Quality Compliance and Systems team to identify and mitigate GCP quality and compliance issues with potential impact across multiple compounds, Takeda sites, or functional groups. Responsible for leading Clinical Quality Assurance (CQA) activities for assigned clinical development programs, including the management of audits, quality issues and investigations, and inspections. Senior Program Manager, Clinical Quality Assurance, Oncology Manage domestic and international audits of sites, documents, databases, vendors or internal systems in compliance with GCP and Takeda policies and procedures; assess impact of audit findings on subject safety, data integrity, and business operations.
    Senior Level
    Management
    13d ago
    Opens new tab
  • 4.9

    Associate Manager, Programming

    Takeda Pharmaceutical
    Associate Program Manager Job, Remote or Pittsburgh, PA
    Opens new tab
    Such roles will have a connection to a Takeda R&D center. Takeda SQS is looking to add individuals to our team that are team oriented, collaborative, strong understanding of the statistical programming function, exceptional leaders and innovators. This individual will also have an opportunity to work on ISS studies and contribute to broader improvement of submissions (adhoc regulatory work such, BIMO, define) at Takeda. To attract and retain the very best talent, we in Takeda SQS are open to flexible or remote working for some roles. Takeda is a global, values-based, R&D-driven, top 10 biopharmaceutical leader committed to discover and deliver life-transforming treatments, guided by our commitment to patients, our people and the planet.
    Entry Level
    Management
    13d ago
    Opens new tab
  • 4.9

    Product Manager, Operations Data - Alta Petens - REMOTE

    Takeda Pharmaceutical
    Data Product Manager Job, Remote or Point, PA
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    OBJECTIVES/PURPOSE: Takeda is advancing an exciting product pipeline and wants to ensure that we have the infrastructure and talent in place to support it. Oversee development, testing, validation, and support vendors & ensure compliance with all Takeda processes and procedures. The product manager will contribute to Takeda's mission by leading the development and implementation of one or more product strategies within a transformational R&D trial data program.
    Management
    11d ago
    Opens new tab
  • 4.9

    Qc Information Systems / Sr. Analyst

    Astrazeneca
    Information Systems Analyst Job in Frederick, MD
    Opens new tab
    Our Frederick Manufacturing Center (FMC) is one of 30 production facilities in 18 countries that creates life-changing medicines for people around the world. Analyst* in Frederick, MD, you'll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients' lives. The FMC is also an award-winning employer and has been recognized as a Top 50' Business in Frederick and awarded Frederick County's Best Place to Work' distinction in 2015 and 2019. At *AstraZeneca* we work together across global boundaries to make an impact and find answers to challenges.
    Mid Level
    Senior Level
    Doctorate Required
    New
    1d ago
    Opens new tab
  • 4.9

    Production Lead Technician - Night Shift

    Astrazeneca
    Technical Production Lead Job in Frederick, MD
    Opens new tab
    Our *Frederick Manufacturing Center (FMC) *is one of 30 production facilities in 18 countries that creates life-changing medicines for people around the world. As a *Production Lead Technician-Night Shift* in the Manufacturing group at Frederick, MD, you'll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients' lives. You will be responsible for the Production Lead Technician duties, which will include: At *AstraZeneca* we work together across global boundaries to make an impact and find answers to challenges. * At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big.
    Mid Level
    Senior Level
    Bachelors Preferred
    High School Diploma Required
    11d ago
    Opens new tab
  • 4.9

    Associate Director, Programming

    Takeda Pharmaceutical
    Associate Program Director Job, Remote or Dumont, NJ
    Opens new tab
    Such roles will have a connection to a Takeda R&D center. OBJECTIVES/PURPOSE: Takeda SQS is looking to add individuals to our team that are team oriented, collaborative, strong understanding of the statistical programming function, exceptional leaders and innovators. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To attract and retain the very best talent, we in Takeda SQS are open to flexible or remote working for some roles. Takeda is a global, values-based, R&D-driven, top 10 biopharmaceutical leader committed to discover and deliver life-transforming treatments, guided by our commitment to patients, our people and the planet. Join us as an Associate Director, Programming, in our Cambridge, MA office.
    Executive
    13d ago
    Opens new tab
  • 4.9

    Associate Director/Sr. Manager Clinical Data Standards - Remote US

    Takeda Pharmaceutical
    Associate Director Job, Remote or Boston, MA
    Opens new tab
    Join us as a Senior Manager/Associate Director, Clinical Data Standards in our Cambridge office. Ensures CROs/strategic service providers and Takeda are deploying standards and leveraging them across the organization at an enterprise level. Builds relationships across the global Takeda organization and with CROs/strategic service providers in support of the standards vision and implementation. Conducts standards compliance review and works with functional areas and CROs/strategic service providers to reinforce content and interpretation of Takeda standards. Participates with and influences at industry standards forums in support of Takeda's Standards. If so, be empowered to take charge of your future at Takeda. Collaborates closely with CROs/Strategic service providers to ensure appropriate management, training and deployment of Takeda's standards within the service provider's infrastructure. Represents Takeda and Global Development Operations as a member of Standards Development Organization or Standard Support Groups (e.g. CDISC, PhUSE).
    Senior Level
    Management
    Executive
    10d ago
    Opens new tab
  • 4.9

    Director, Business Process Optimization - Cambridge, MA or Remote

    Takeda Pharmaceutical
    Business Director Job, Remote or Tappan, NY
    Opens new tab
    This includes driving and leading overall management, direction, coordination, and implementation of high priority change initiatives designed to optimize business processes critical to the operational effectiveness of Takeda. Oversee and mentor direct reports, providing leadership and training to support professional development and responsible for demonstration of Takeda Leadership Behaviors will report to the Head of Business Optimization and Regulatory Chief of Staff and lead Takeda Global Regulatory Affair optimization group. Provide leadership, direction, and overall oversight for the continuous improvement of products and processes as well as new initiatives aligned with Takeda strategy
    Senior Level
    Executive
    12d ago
    Opens new tab
  • 4.9

    Associate Director, GCP Supplier Quality Lead, Clinical Operations (Remote)

    Takeda Pharmaceutical
    Director Of Clinical Operations Job, Remote or Boston, MA
    Opens new tab
    Liaise and collaborate with internal Takeda and external business partners to provide guidance and support pertaining to compliance and supplier quality oversight initiatives What you bring to Takeda: Lead the development and implementation of risk-based GCP supplier audit and compliance strategy and manage supplier audits in compliance with GCP and Takeda policies and procedures.
    Senior Level
    Executive
    Bachelors Preferred
    11d ago
    Opens new tab
  • 4.9

    Senior Manager, Programming

    Takeda Pharmaceutical
    Senior Project Manager Job, Remote or Merrick, NY
    Opens new tab
    Takeda SQS is looking to add individuals to our team that are team oriented, collaborative, strong understanding of the statistical programming function, exceptional leaders and innovators. To attract and retain the very best talent, we in Takeda SQS are open to flexible or remote working for some roles. Takeda is a global, values-based, R&D-driven, top 10 biopharmaceutical leader committed to discover and deliver life-transforming treatments, guided by our commitment to patients, our people and the planet. Such roles will have a connection to a Takeda R&D center.
    Senior Level
    Management
    13d ago
    Opens new tab

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AstraZeneca may also be known as or be related to AstraZeneca, AstraZeneca LP, AstraZeneca plc, Astrazeneca Biotech AB and Astrazeneca Pharmaceuticals Lp.