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Parexel

End-to-end clinical trials and regulatory consulting

Depot Technician

Picking & PackingConfirmed live in the last 24 hours
Full-timeSingaporeNo salary listedIn-person

About the Job

Requirements

  • Proficiency in Microsoft Office, including Word, Excel, and PowerPoint.
  • Good hand-eye coordination.
  • Knowledge of GxP guidance, or willingness to be educated in GxP regulations.
  • Basic understanding of the drug development and regulatory framework.
  • Knowledge of a warehouse management system and/or inventory system.
  • Experience in warehouse support.
  • High school or vocational degree, or 2–4 years of relevant work experience.
  • Proficiency in the local language, spoken and written.

Responsibilities

  • Receive and stock materials.
  • Pick, pack, and perform quality control of clinical trial materials according to instructions.
  • Perform quality control checks.
  • Prepare study documents.
  • Dispatch materials.
  • Assist with and execute packaging and labeling, including relabeling procedures.
  • Assist with and execute clinical trial materials destruction, recalls, reconciliation, and returns.
  • Execute regular cycle counts and physical inventory.
  • Perform warehouse management tasks, including production activities.
  • Assist with and execute general premises and equipment management.
  • Report any issue affecting quality and/or any deviation.
  • Handle filing and archiving activities.
  • Follow internal and external, including client, workflows and processes.
  • Complete required training on time.
  • Manage multiple tasks effectively and efficiently.

Desired Qualifications

  • Packaging and labeling experience in the pharmaceutical or biological industry is preferred.

About the Company

Parexel

End-to-end clinical trials and regulatory consulting

Parexel provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device clients from Phase I to Phase IV. Its offerings include clinical trial management, regulatory consulting, and biostatistical analysis to support the design, execution, and analysis of clinical studies. The company operates as a CRO, partnering with sponsors to manage trials, ensure regulatory compliance, and generate robust data for drug development. What sets Parexel apart is its breadth of services across the trial lifecycle, emphasis on quality and reliability, and industry recognition, along with a focus on patient-centric approaches and leadership in gender partnership. The company’s goal is to help clients bring new therapies to market efficiently and safely by delivering high-quality, compliant trial outcomes and data that support regulatory submissions.

Company size
10,001+
Company stage
Acquired
Total funding
$8.5B
Headquarters
Durham, NC
Founded
1982

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