Role details

Contract type

Permanent contract

Employment type

Full-time (> 32 hours)

Experience required

0 years minimum

Working hours

Regular working hours

Job source

www.indeed.com

Tech stack

Microsoft Word Microsoft Excel Document Management Systems Microsoft PowerPoint Model Validation

Job description

• Perform routine and non-routine analytical testing using of analytical techniques such as: Ligand binding assay (ELISA, MSD) and Nab Assay for ADA
• Perform bioanalytical method development and validation for PK and ADA.
• Operate plate reader (Molecular device, MSD) for method development, method validation and sample analysis.
• Demonstrate initiative to perform routine laboratory responsibilities such as sample coordination, lab equipment maintenance, document management, inventory control, and reconciliation of sample requests/documents as needed.
• Following cGMP/GLP regulations when executing his/her daily work load.
• Update supervisor his/her work progress at scheduled intervals.
• Apply his/her scientific expertise for analytical methods/instruments troubleshooting, laboratory investigations, etc.
• Required to work in the laboratory that has a certain level of noise and contains hazardous chemicals

Requirements

• BS or MS (preferred) in a related science such as Biology or Pharmacology.
• BS requires 1-5 years and a MS requires 0-3 years of previous related experience
• Basic working knowledge of cGMP/GLP regulations is required.
• Ability to work independently and achieve problem resolution with minimal supervision. Attentive to detail.
• Excellent teamwork and communication skills.
• Good computer skills, profound knowledge with Microsoft word, Excel, and PowerPoint.

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