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    US Tech Solutions

    Staffing and Recruiting

    Senior Scientist

    Wilmington, United StatesOn-SiteContractPosted 3w ago
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    Job description

    The Senior Scientist role is responsible for aiding in the supply of strategic drug product technical expertise and support to a portfolio of established products. The products are manufactured either internally at an CLIENT’S manufacturing site or externally at a contractor. The technical expertise and support is used in problem solving as well as in continuous improvement activities.

    This a great opportunity to learn about CLIENT’S’s exciting and diverse established product portfolio and to gain experience working in a Global function and with external suppliers.

    Responsibilities:

    Support License to Operate activities:

    -Provide technical expertise and problem solving support to the manufacturing sites.

    -Provide technical expertise and support in creating regulatory documentation and responses to regulatory questions in a way that ensures maximum flexibility for Operations.

    Support manufacturing and supply chain changes:

    -Perform technical risk assessments for proposed changes, e.g. to excipients, packaging/device components, manufacturing processes and/or analytical testing methods.

    -Propose experimental work to support changes

    -Review generated data and make recommendations on whether to proceed with changes or not.

    Maintain product knowledge:

    -Write reports and memos to record technical investigations or recommendations, ensuring data integrity.

    -Contribute to and/or coordinate Quality Risk Assessments and Technical Opportunity and Risk Assessments (TORAs) as required.

    -Produce and maintain information in the Product Knowledge Management tool.

    Coordinate, lead or support product improvement initiatives:

    -As required, ensure delivery of product and process improvements that will deliver business benefits.

    -Develop or support the manufacturing sites in developing business cases.

    -Co-ordinate appropriate support teams if required

    Maintain communication to product stakeholders:

    -Work with Product Champions to receive work requests, perform priority assessments and agree level of effort on each activity

    -Establish networks between sites who manufacture the same or similar products to ensure effective collaboration.

    -Effectively communicate product performance and product issues to the manufacturing sites.

    Build technical understanding and capability:

    -Train manufacturing sites in, e.g. pharmaceutical technologies, formulation and packaging design, manufacturing and testing control strategies and analytical techniques as appropriate.

    Minimum Requirements - Education and Experience (Required)

    -BSc degree in a relevant discipline, e.g. analytical chemistry, chemical engineering or pharmaceutics

    -Experience of pharmaceutical manufacturing/QC testing and/or research and development

    -Knowledge of the overall drug development and commercialization process from development, launch and through life cycle management

    -Experience working in one of the following disciplines: Analytical Science, Chemical Science, Formulation Science, Physical Science, Pharmaceutical Manufacturing and Supply Chain Management

    -Knowledge of international GMP and SHE requirements and their applicability to pharmaceutical manufacturing, research and development

    -Knowledge of Quality Management Systems and their applicability to pharmaceutical manufacturing

    Minimum Requirements - Education and Experience (Desired)

    -Masters Degree or PhD in a relevant discipline, e.g. analytical chemistry, chemical engineering or pharmaceutics

    -Experience working in Global function and/or with external parties

    -Experience working in more than one area of the overall drug development and commercialization process from development, launch and through life cycle management

    -Experience working in two or more disciplines such as Analytical Science, Chemical Science, Formulation Science, Physical Science, Pharmaceutical Manufacturing and Supply Chain Management

    -Extensive knowledge of international GMP and SHE requirements and their applicability to pharmaceutical manufacturing, research and development

    -Extensive knowledge of Quality Management Systems and their applicability to pharmaceutical

    Manufacturing

    Sneha Shrivastava

    Sr Technical Recruiter

    sneha.s(at)ustechsolutionsinc.com

    862 - 579 - 4236

    Job details are sourced from the employer's original posting.

    Open job posting
    US

    About the company

    US Tech Solutions

    USTECH is a global firm providing a wide-range of talent on-demand and total workforce solutions. Through the USTECH Talent Network of 100% company-owned and managed offices, we provide highly-skilled professionals whose education, skills and experience are vetted and matched to your unique hiring needs, work environment and company requirements. Our 24x7 global service delivery drives time and cost out of any recruiting and staffing process (15-30% cost reduction in most cases) across all of our services and solutions, providing you with the talent you need on-demand when, where and how you need it.

    View all US Tech Solutions jobs
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