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RTP QC Chemistry Lab Tech 2026

Job Overview

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Employment Type

Temporary
Hourly
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Compensation

Hourly
Exact $23.00
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Work Schedule

Rotating Shifts
Weekend Shifts
Night Shifts
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Benefits

competitive hourly wage
On-site role
Experience in GMP environment
skill development opportunities
collaborative work environment
night shift differential
Potential for contract extension or conversion

Job Description

Our client, located in Research Triangle Park (RTP), North Carolina, is a leading player in the pharmaceutical manufacturing industry with a strong commitment to quality and innovation. Specializing in the production of parenteral drug products, the company operates within a highly regulated GMP (Good Manufacturing Practices) environment to ensure the highest standards of quality and safety. With a focus on scientific excellence and operational efficiency, the organization fosters a culture of continuous improvement and collaboration among its workforce.

The company is seeking a skilled Chemistry Lab Technician for a 6-month contract position situated on-site in RTP, NC. The ... Show More

Job Requirements

  • high school diploma or equivalent
  • associate's degree in chemistry, biology, or microbiology preferred
  • experience with analytical testing techniques
  • familiarity with GMP and laboratory safety standards
  • ability to work night shifts and weekends
  • strong written and verbal communication skills
  • ability to work independently and as part of a team
  • attention to detail and accuracy in documentation
  • problem-solving and critical thinking skills
  • willingness to comply with EHS guidelines
  • availability for 6-month contract with possibility of extension or conversion

Job Qualifications

  • high school diploma with relevant chemistry lab experience or associate's degree in chemistry, biology, or microbiology
  • experience performing analytical techniques (e.g., UV-VIS, TOC, pH, conductivity, color, clarity, osmolality, visual/functional inspection)
  • familiarity with GMP and safety guidelines in a laboratory setting
  • experience with laboratory information management systems (LIMS) preferred
  • GMP QC laboratory experience preferred
  • strong problem-solving and analytical thinking skills
  • excellent written and verbal communication skills
  • high attention to detail and ability to accurately document data
  • ability to manage and prioritize multiple tasks in a fast-paced environment
  • ability to work independently and collaboratively within a team
  • strong interpersonal and collaboration skills
  • ability to follow environmental, health, and safety (EHS) guidelines
  • willingness to work 12-hour night shifts on a 2-2-3 schedule, including weekends and outside standard hours
  • willingness to provide on-call support if needed

Job Duties

  • perform analytical testing and related laboratory activities in accordance with approved procedures and protocols
  • accurately document and record data in reports and/or LIMS in compliance with GMP standards
  • identify and escalate deviations from procedures or methods
  • support investigations as needed
  • review analytical data generated by other analysts and perform second-person verification activities as required
  • follow all environmental, health, and safety (EHS) guidelines
  • troubleshoot laboratory equipment and test methods as needed
  • maintain laboratory inventory, including supplies and consumables
  • support lean lab and 5S initiatives and identify process improvement opportunities
  • apply scientific principles related to drug substance and drug product testing
  • work 12-hour night shifts on a 2-2-3 schedule, including weekends and outside standard hours as required to support 24/7 manufacturing operations
  • work in multiple areas of the site, with possible exposure to allergens in a parenteral manufacturing environment
  • perform tasks that may involve repetitive motion (e.g., keyboarding)

Job Criteria

Experience

Mid Level (3-7 years)


Job Location

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