Pharmaceutical Lab Analyst - Day Shift, Onsite

Catalent Pharma Solutions

South Carolina

On-site

USD 42,000 - 56,000

Full time

14 days+
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Benefits offered by this job

Competitive PTO
8 paid holidays
Medical, dental, and vision benefits
Tuition reimbursement
Site-based activities

Job summary

Catalent’s Greenville, North Carolina site is a leading facility for oral solid dose development and manufacturing. The Laboratory Analyst will perform routine non-chromatographic analytical testing and ensure data integrity in accordance with safety, quality, and regulatory standards.

The role involves working on site, following SOPs, and supporting development and manufacturing of pharmaceutical products.

Qualifications

  • Associate degree in Biotechnology, Chemistry, or an equivalent science degree
  • Ability to lift 10-40 lbs, unassisted
  • Majority of the workday involves standing, walking, lifting, pulling, and pushing
  • Requires bending, squatting, crawling, climbing, and reaching
  • Some exposure to hazardous chemicals and other active chemical ingredients

Responsibilities

  • Maintain data integrity and employ good documentation practices when performing experiments
  • Compare laboratory data against specifications and trend data where applicable to determine if results meet requirements
  • Ensure proper usage, care, and return of calibration standards including, but not limited to, reference standards, timers, thermometers, and instrumentation
  • Ensure accuracy of testing by following method/standard instructions and adhering to internal SOPs to eliminate the potential for repeat testing, deviations, and investigations
  • Under general supervision, perform primarily routine testing for non-chromatographic methods of analysis in support of pharmaceutical API and/or drug product
  • Enter data into established reports/templates or software-based systems
  • Other Duties as assigned

Education

Associate degree in Biotechnology, Chemistry, or an equivalent science degree

Job description

Catalent’s Greenville, North Carolina site is a leading facility for oral solid dose development and manufacturing. The Laboratory Analyst will perform routine non-chromatographic analytical testing and ensure data integrity in accordance with safety, quality, and regulatory standards.

The role involves working on site, following SOPs, and supporting development and manufacturing of pharmaceutical products.

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