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14 job opportunities

  • |  Posted On: Feb 04, 2026

    location: Cambridge, MA 02139

    mode of work:On-site

    duration: 0 Month, Direct Hire (Full Time)

    The Senior Associate Scientist role focuses on in vivo pharmacology within the Preclinical In Vivo Pharmacology group. Responsibilities include designing studies, evaluating therapeutic efficacy, and performing ex vivo analyses. Requires expertise in in vivo techniques, immunocompromised mice handl ...

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  • |  Posted On: Feb 04, 2026

    location: Cambridge, MA 02139

    mode of work:On-site

    duration: 0 Month, Direct Hire (Full Time)

    The role of Senior Associate Scientist requires expertise in in vivo pharmacology, focusing on neuroinflammation research. Key duties include immunohistology and in vivo studies, requiring skills like drug formulation and data analysis. Candidates should have a Bachelor's or Master's in Science. Ex ...

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  • |  Posted On: Jan 30, 2026

    location: Tampa, FL 33601

    mode of work:On-site

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  • |  Posted On: Jan 30, 2026

    location: Tampa, FL 33601

    mode of work:On-site

    The Senior Associate - Software Engineer at a leading pharmaceutical company will leverage technology to drive digital solutions across functions. Key responsibilities include developing software solutions, collaborating with teams, mentoring juniors, and translating business needs into technical s ...

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  • |  Posted On: Jan 30, 2026

    location: Sanford, NC 27330

    mode of work:On-site

    duration: 0 Month, Direct Hire (Full Time)

    The Bioprocess Technician at Pfizer is responsible for producing drug substances, assisting in various manufacturing functions, and ensuring equipment functionality. The role requires 2+ years of experience in a manufacturing environment, proficiency in manufacturing equipment, and a basic understa ...

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  • |  Posted On: Jan 30, 2026

    location: Sanford, NC 27330

    mode of work:On-site

    The QA Specialist provides Quality Assurance oversight for the QC Department, ensuring compliance with regulations and procedures. Key responsibilities include technical reviews, approval of QA documents, and facilitating process improvements. Candidates need experience in QA/QC, applied statistics ...

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  • |  Posted On: Jan 29, 2026

    location: Andover, MA 01810

    mode of work:On-site

    The role of Process Engineer/Scientist II involves executing production activities, ensuring compliance with regulatory guidelines, and assisting in troubleshooting and technology transfer. Key responsibilities include overseeing technical documentation and process approvals. Candidates should poss ...

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  • |  Posted On: Jan 28, 2026

    location: Sanford, NC 27330

    mode of work:On-site

    duration: 0 Month, Contract

    Seeking a Bioprocess Technician IV for night shifts in the pharmaceutical industry. Key responsibilities include executing manufacturing operations, troubleshooting equipment, and driving continuous improvement. The role demands cGMP knowledge, proficiency in enterprise systems, and effective commu ...

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  • |  Posted On: Jan 26, 2026

    location: Louisville, KY 40229

    mode of work:On-site

    The role of Transaction Specialist involves transcribing confidential information from scanned paper documents, maintaining accuracy, and processing transactions through workflows. No prior experience is required, but proficiency in data entry and handling confidential information is crucial. The p ...

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  • |  Posted On: Jan 26, 2026

    location: Louisville, KY 40229

    mode of work:On-site

    Seeking a Transaction Specialist for a seasonal role focusing on confidential data transcription and document processing. Responsibilities include ensuring accuracy, handling mail, and operating scanning machines. Requires data entry accuracy, technical skills, and a team-oriented attitude. Ideal f ...

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  • |  Posted On: Jan 23, 2026

    location: Rochester, MI 48307

    mode of work:On-site

    The Sterile Manufacturing Operator role involves supporting engineers, preparing documentation, and conducting preliminary analyses in a pharmaceutical setting. Key competencies include cGMP adherence, problem-solving, and communication. The operator must manage time effectively and contribute to t ...

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