• Administrative Assistant IV

    US Tech Solutions (North Chicago, IL)
    **Length of Contract :** 6 months-1 year (starting with six months; may go longer than a year if all works out for the candidate/STAR Team. Supporting: VPs, SVPs, ... the face of the STAR Program, retains clients and meets expectations consistently. + The Contract Admin Assistant will be hired on an as need basis to fulfill Admin… more
    US Tech Solutions (09/13/25)
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  • 340B Analyst

    Rochester Regional Health (Rochester, NY)
    SUMMARY As a 340B Analyst you ensure all 340B contract pharmacies are overseen and in compliance with the program. Your strong attention to detail, accuracy and ... LOCATION: DEPARTMENT: SCHEDULE: ATTRIBUTES + At least one (1) year of contract management experience is strongly preferred + Demonstrated analytical and critical… more
    Rochester Regional Health (07/25/25)
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  • Materials Processing Machine Operator (Day, Night…

    Contract Pharmacal Corp (Hauppauge, NY)
    …or GED diploma preferred. + Operator Level I: 6 months+ experience in pharmaceutical blending, granulation and/or compounding + Operator Level II: 2+ years of work ... experience in pharmaceutical blending, granulation and/or compounding + Operator Level III:...operations sites/areas to complete job functions. + Responsible for compliance with all rules and regulations pertaining to safety… more
    Contract Pharmacal Corp (09/24/25)
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  • Clinical Study Manager

    Takeda Pharmaceuticals (Boston, MA)
    …the Clinical Operations Leadership team. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led ... + Oversee the execution of studies in assigned clinical program(s) in compliance with quality standards (including ICH GCP, local regulations and Takeda SOPs),… more
    Takeda Pharmaceuticals (09/27/25)
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  • Facilities Engineer

    Catalent Pharma Solutions (San Diego, CA)
    **Facilities Engineer** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to ... annually. Catalent Pharma Solutions in San Diego is a premier pharmaceutical chemistry development and manufacturing organization supporting the pharmaceutical more
    Catalent Pharma Solutions (09/27/25)
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  • Validation Engineer

    Actalent (Franksville, WI)
    …evaluating the operations of Manufacturing and Quality activities to ensure compliance with Quality Standards and Regulations, and recommending necessary corrections ... suppliers. + Identify new quality improvement initiatives/projects to enhance compliance , quality levels, and operational efficiencies. + Support training programs… more
    Actalent (09/27/25)
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  • Facilities Coordinator

    Mentor Technical Group (Carolina, PR)
    …SOP's (Quality, EHS and Facilities Maintenance). + Audit facilities areas for compliance with standards set by the Maintenance, Quality & EHS Owner's Departments. ... audit should be, as a minimum, Housekeeping, Pest Control, Work Order Compliance , Maintenance Program, Contractor Safety Program, Refrigerants Program (RCM) and Gap… more
    Mentor Technical Group (09/25/25)
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  • Senior Quality Systems Specialist

    Catalent Pharma Solutions (Greendale, IN)
    …Systems Specialist** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, ... Quality Systems and will be responsible for managing and supporting key compliance and quality system activities such as Change Controls, Deviations, Complaints,… more
    Catalent Pharma Solutions (09/24/25)
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  • Research Analyst I - Formulations 1

    Charles River Laboratories (Mattawan, MI)
    …Efficiently perform and document all procedures, materials and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, ... the disposal and transport of residual dosing material, non-regulated pharmaceutical solids, accumulated single-use containers to designated waste receiving areas.… more
    Charles River Laboratories (09/24/25)
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  • Pharma Technical Writer

    System One (New Brunswick, NJ)
    …NJ Hours/Schedule: Mon-Friday (normal business hours) Compensation: $34.87- $44.29 Type: Contract Overview Leading pharmaceutical company looking for an ... of experience specifically for Regulatory CMC documentation within the pharmaceutical or biotechnology industry. Responsibilities + Co-authors/ authors scientific… more
    System One (09/23/25)
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