Laboratory Assistant

Found in: Appcast Linkedin GBL C2 - 2 weeks ago

Round Lake, United States Randstad Life Sciences US Full time

Job Details:

Quality Lab Associate I in Round Lake, IL

12 Years Contract

General Shift (Mon - Fri)

The candidate must not be allergic to Penicillin and Cephalosporin or their related products and /or materials.

This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.

Job Summary:

  • The position may be responsible for analytical testing, validation/verification, and/or transfer of test methods supporting parenteral products. The position will be in the Round Lake, IL Stability Laboratories within Product Quality serving multiple global businesses.
  • This role is essential for supporting the global commercial product teams and/or product development teams. The position may interface with multiple functions. The individual in this position must:
  • Effectively demonstrate working technical knowledge and skills to support a variety of projects within the relevant discipline with minimal assistance.
  • Display basic technical understanding of related disciplines.
  • Conduct routine/non-routine experiments with minimal assistance.
  • A candidate must not be allergic to Penicillin and Cephalosporin or their related products and /or materials.

Essential Duties and Responsibilities:

  • Under direction, conduct critical chemical, physical, and biological analyses on finished product stability samples. May also support testing of raw materials, initial, in-process, and final product samples from the manufacturing facility, as required. Work under minimum supervision.
  • Use sophisticated laboratory instrumentation and computer systems to collect and record data. May be required to conduct validations.
  • Complete all testing, including special project/protocol testing in a timely and appropriate manner to meet project schedules.
  • Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, cGxP, and QSR regulations.
  • Participate with management to investigate deviations and write exception documents.
  • May perform advanced biological and chemical assays requiring precise analytical skills and an understanding of chemistry principles.
  • May review test data, which includes overall documentation practices. May perform review functions in LIMS or other computerized systems.
  • May participate in cross-functional teams, which impact production, increase efficiency, solve problems, generate cost savings and improve quality, and provide new product support.
  • Maintain laboratory supplies and laboratory safety requirements to ensure audit readiness at all times.
  • Perform equipment maintenance and calibrations as required. Troubleshoot and resolve instrument problems with some assistance.

Qualifications:

  • Proficient in advanced wet chemistry, volumetric preparation techniques, and instrumental methods of analysis
  • Must demonstrate effectiveness in attention to detail, organization, teamwork/interpersonal skills, results orientation, and task completion.
  • Must be able to handle multiple tasks concurrently and in a timely fashion.
  • Possess writing and computer skills.
  • Must communicate effectively with managers and peers.
  • Interpret available information and make recommendations to resolve technical challenges.

Education and/or Experience:

  • Bachelor’s degree in Chemistry or biological science with analytical chemistry laboratory coursework and 0-1 years experience.
  • Analytical chemistry instrumentation experience (e.g. HPLC, pH, KF, AA, GFAA, titrations, etc.) preferred.
  • Pharmaceutical GMP/QC laboratory experience is desired.

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