GMP QC Chemist I — Bioreagent & SOP Specialist

The Fountain Group; Scarborough (ME); On-site; USD 40,000 - 43,000; Full time

Benefits offered by this job

Referral Bonus

Job summary

The Fountain Group is seeking a Chemist for a 6-month contract located in Scarborough, ME, 04074. The role focuses on production scheduling, in-process QC testing, and supporting GMP/GLP quality systems onsite.

Qualifications include a Bachelor/Master/PhD and experience with GLP/GMP regulations and analytical methods such as HPLC, ELISA, and spectrophotometry. SOP compliance and batch records are required. Onsite day shift with potential extension or conversion based on performance.

Qualifications

• Bachelor or Master, or PhD is required.
• Experience with GLP or GMP regulations is highly preferred.
• Experience with analytical testing such as HPLC, SDS- Page, ELISA, Spectrophotometry, pH meters, Gel electrophoresis, or Pipetting is required.
• Experience with blood, urine, or diagnostic product testing is preferred.
• Experience with SOP compliance is required.
• Experience with preparing buffers or reagents and batch production and batch records is preferred.

Responsibilities

• Maintain production schedules and perform in-process QC testing.
• Support qualifications and quality inspections and GMP/GLP quality systems.
• Investigate problems, implement procedures, and ensure safety compliance.
• Prepare critical and non-critical bioreagents according to SOPs.
• Coordinate manufacturing activities and maintain raw bioreagents.

Skills

GLP/GMP experience

SOP compliance

Blood/urine testing

HPLC

SDS-PAGE

ELISA

Spectrophotometry

pH meters

Gel electrophoresis

Pipetting

Diagnostic product testing

Education

Bachelor/Master/PhD

Job description

The Fountain Group is seeking a Chemist for a 6-month contract located in Scarborough, ME, 04074. The role focuses on production scheduling, in-process QC testing, and supporting GMP/GLP quality systems onsite.

Qualifications include a Bachelor/Master/PhD and experience with GLP/GMP regulations and analytical methods such as HPLC, ELISA, and spectrophotometry. SOP compliance and batch records are required. Onsite day shift with potential extension or conversion based on performance.