Job Description

Contract – 12 Months with a possibility of extension

Night Shift:- This is a 12-hour night shift role following the 2-2-3 manufacturing schedule (6 PM to 6 AM).

Summary :

The Analyst, Quality Control, assists and supports the organization with compliance and ongoing preparation, testing and monitoring of conformance to established quality processes and standards for manufacturing and production.

Key Responsibilities:

• Executes routine and non-routine analysis for cGMP release and characterization testing using techniques including but not limited to PCR (ddPCR, qPCR), ELISAs, NGS, Western Blot, PCC, and Bioburden.
• Responsible for a limited range of laboratory support functions and procedures as assigned, developing capability in basic technical skills, disciplines, and procedures within assigned discipline area(s).
• May be assigned to specific disciplines, but will support all necessary laboratory and assay functions, including housekeeping, safety, logbook/equipment use and maintenance, and updates to existing operating procedures.
• Capable of delivering to the assigned work schedule with attention to detail and accuracy.
• Notifies management and initiates events (such as Laboratory Investigations) in the quality systems, with guidance from senior analysts or management.
• Assist in special projects on analytical and instrument problem-solving by executing assays.
• Gain familiarity with basic process improvement methodologies, learning and applying concepts of lean lab and six sigma that are applicable to the QC lab environment.
• Other related job duties as assigned.

Requirements :

• Bachelor's degree in scientific disciplines such as Biochemistry, Biology, Microbiology or related field.
• Learns to use professional concepts.
• Applies company policies and procedures to resolve routine issues.
• Ability to communicate and work in a team environment.
• Normally receives detailed instructions on all work.

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