Job Description

Duties and Responsibilities:

• Uses basic to moderately complex applicable test and measurement equipment and instruments to complete quality control tasks to ensure acceptability of raw materials, intermediate, in-process, and finished products.
• Calibrates test and measurement equipment and devices to ensure accuracy in their use.
• Prepares samples and solutions for tests per established methodologies and protocols.
• Identifies material, product,t and/or methodology issues impacting acceptance and/or quality and reports same to appropriate senior QC personnel and/or management as directed.
• Documents all tests and measurements according to GMP guidelines.
• Assists and supports the development of corrective measures and/or actions to correct quality issues or problems.
• May perform basic troubleshooting of tests and measurement equipment.
• Is responsible for maintaining high housekeeping and cleanliness standards.
• May support the development of standard operating procedures (SOPs) and certain protocols for the proper testing and measurement of materials and products.
• Performs all additional duties as required for this position.

Qualifications:

• BS degree in Chemistry or Biochemistry or equivalent
• 1+ years experience in a cGMP pharmaceutical/biotechnology laboratory
• Proficient use of Microsoft Office suite of applications (Outlook, Excel, Word, PowerPoint, Teams, etc.)
• Ability to work as part of a team and also independently with minimal to no supervision
• Proficient use of analytical techniques/instruments, such as HPLC, GC, MS, etc.
• Ability to rapidly change focus during times of shifting or changing priorities
• Impeccable technical writing skills with extreme attention to detail, specifically the lexicology and grammatology of written English text as applied to technical writing
• Excellent organizational, multitasking, and communication skills

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