ACL Digital
Senior Executive – US TAG at ACL (Pharmaceuticals, Life Sciences and Medical Devices)
Job Title:
Research Associate
Location:
Foster City, CA
Duration:
12 Months
Responsibilities
Plan and successfully execute experiments and activities to support formulation and drug product process development work packages including molecular assessment, First‑in‑Human formulation development, Drug Product manufacturing process development, and clinical in‑use evaluations
With general guidance, select and run or operate scientific equipment and tools such as HPLCs, UV‑Vis, CE‑SDS, ICIEF etc. to ensure applicable methods and techniques are followed
Clearly, timely, and accurately document data in appropriate repositories such as lab notebooks, reports, protocols etc.
Analyze, interpret, draw conclusions, and present or share data from experiments executed including preparation of appropriate documents such as reports and memos
Fully embrace a lean‑agile mindset, matrix working environment, and continuous improvement
Help support key project or department stakeholders as needed to ensure that company objectives are met
Use established data, reports and previous results to identify inappropriate variances and concerns as well as identify and report inconsistent results to manager or supervisor
Participate in group meetings and efforts by presenting data or preparing information for others to present
Support team initiative to drive business process excellence, scientific innovation, laboratory and work safety etc.
Working Hours Location: 5 days a week onsite at FC
Seniority level Mid‑Senior level
Employment type Contract
Job function Research
Industries: Pharmaceutical Manufacturing and Biotechnology Research
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Research Associate
Location:
Foster City, CA
Duration:
12 Months
Responsibilities
Plan and successfully execute experiments and activities to support formulation and drug product process development work packages including molecular assessment, First‑in‑Human formulation development, Drug Product manufacturing process development, and clinical in‑use evaluations
With general guidance, select and run or operate scientific equipment and tools such as HPLCs, UV‑Vis, CE‑SDS, ICIEF etc. to ensure applicable methods and techniques are followed
Clearly, timely, and accurately document data in appropriate repositories such as lab notebooks, reports, protocols etc.
Analyze, interpret, draw conclusions, and present or share data from experiments executed including preparation of appropriate documents such as reports and memos
Fully embrace a lean‑agile mindset, matrix working environment, and continuous improvement
Help support key project or department stakeholders as needed to ensure that company objectives are met
Use established data, reports and previous results to identify inappropriate variances and concerns as well as identify and report inconsistent results to manager or supervisor
Participate in group meetings and efforts by presenting data or preparing information for others to present
Support team initiative to drive business process excellence, scientific innovation, laboratory and work safety etc.
Working Hours Location: 5 days a week onsite at FC
Seniority level Mid‑Senior level
Employment type Contract
Job function Research
Industries: Pharmaceutical Manufacturing and Biotechnology Research
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