top of page

Quality Control Specialist - 1662918

🔬 Specialist Quality Control 32809🧪

📍 Location: Juncos, PR (Only for local candidates with W-2 contract. No C2C agreements)

📅 Shift: Administrative shift, Onsite Work

⏳ Period: Eight (8) months starting 12/11/2023

💰 Rate: $28 to $33 hourly

🔬 Business Unit: AML QC Technical Resources


📚 Education/Software Requirements:

  • Doctorate degree or Master's degree & 3 years of directly related experience
  • Bachelor's degree & 5 years of directly related experience
  • Associate degree & 10 years of directly related experience
  • High school diploma / GED & 12 years of directly related experience


🧪 Degree Requirements:

  • Degree in Chemistry/Biochemistry preferred. Degrees in other scientific fields with quality control experience may be applicable.
  • Degree in Microbiology preferred. Degrees in other scientific fields with quality control experience may be applicable.


🌟 Preferred Qualifications:

  • Experienced in providing technical support to the quality control laboratory
  • Proficient in Transfer/validation of analytical methods for new product introduction
  • Skilled in routine/non-routine testing lifecycle at the QC laboratories
  • Proficient in method trending and invalid tracking for QC laboratories
  • Strong in writing and reviewing technical reports
  • Demonstrates strong analytical skills and logical critical thinking
  • Fully fluent in English, both verbal and written


📃 Description:

Under general direction, you will serve as the technical specialist for testing & development in the areas of molecular biology and microbiology. Your focus will be on complex technical issues with a multi-organizational and/or multi-site scope and/or involving outside resources.


Functions:

  • Provide technical guidance
  • Generate reports and conduct data analysis
  • Ensure the flow of communication between technical groups, resolving arising issues
  • Troubleshoot assays when necessary
  • Ensure lab compliance, implementing procedures enhancing GMP, GLP, and safety
  • Manage existing and/or develop and implement new programs, processes, and methodologies
  • Develop, revise, and audit various complex controlled documents that may have multi-organizational and/or multi-site impact
  • Approve lab investigations
  • Lead audit teams
  • Serve as a subject matter expert to develop technical training
  • May perform routine work in a specific area of responsibility as necessary
  • Represent the department/organization on various teams
  • Independently responsible for following through on multi-site action items
  • Interact with regulatory agencies regarding area(s) of responsibility, including written responses
  • Resolve issues with outside resources
  • Perform special projects as requested by the supervisor
  • May supervise employees as necessary to meet technical requirements


Join us in this exciting role and make a significant impact in the field of quality control! 💼🔬


Thank you. We will be in contact soon.

bottom of page