QC Chemist I

Scorpion Therapeutics

Covington (OH)

On-site

USD 42,000 - 60,000

Full time

14 days+

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Benefits offered by this job

Competitive benefits

Job summary

Scorpion Therapeutics in Covington, OH is seeking a detail-oriented Laboratory Technician to collect samples, test materials, and operate lab equipment in a GMP environment. You will participate in quality audits and maintain clean work areas.

The role requires a B.S. in a scientific discipline and 1–2 years of GMP/FDA experience, with strong communication, documentation, and teamwork skills. Overtime may be required.

Qualifications

  • B.S. in a scientific discipline with academic lab experience.
  • 1–2 years’ GMP/FDA manufacturing experience preferred.
  • Excellent written and verbal communication, documentation, and organization.

Responsibilities

  • Collect samples including raw material, finished product, process equipment and environmental.
  • Test purchased materials and Perrigo manufactured products per cGMP requirements.
  • Operate laboratory equipment.
  • Participate in internal and external quality audits.
  • Maintain personal laboratory work area and assist with general cleaning.
  • Participate in training and development.

Skills

Communication skills
Documentation
Organizational skills

Education

B.S. in Chemistry / Food Science / Biology

Job description

Scope of the Role
  • Collect samples including raw material, finished product, process equipment and environmental.
  • Test purchased materials and/or Perrigo manufactured products per cGMP requirements and participate in laboratory investigations.
  • Operate laboratory equipment.
  • Participate in internal and external quality audits.
  • Maintain personal laboratory work area and assist with general laboratory cleaning.
  • Participate in training and development.
Experience Required
  • Bachelor of Science degree in a scientific discipline (Chemistry or Food Science preferred, Biology) required; includes academic lab experience.
  • 1–2 years’ experience working in a GMP/FDA regulated manufacturing environment preferred.
  • Good written and verbal communication skills; excellent documentation and organizational skills.
  • Demonstrated critical thinking skills, attention to detail, and ability to work independently and with others.
  • Ability to take ownership of assigned tasks and responsibility for results.
  • Ability to work overtime as required.
Benefits
  • Competitive compensation, benefits tailored to supporting you and your family, and career development opportunities.
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