Quality Assurance Specialist I - cGMP Lab

SGS; Fairfield (NJ); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Health Insurance

401(k) with company match

Tuition reimbursement

Job summary

SGS in Fairfield, NJ is seeking a Specialist I in Quality Assurance to support the maintenance of Quality Systems in a pharmaceutical testing laboratory, under supervision of a Team Leader or Manager. The role focuses on timely testing, ensuring compliance with cGMP, issuing Certificates of Analysis, and participating in SOP training and equipment calibration.

Candidates should have a B.S. in Chemistry, Biology or related field and 0-2 years' Life Sciences experience; strong scientific

Qualifications

• 0-2 years of experience preferably in Life Sciences supporting cGMP Operations
• Thorough knowledge of scientific principles is requires

Responsibilities

• Provides support to technical staff in their efforts to ensure that routine testing submitted by clients is completed within established parameters governing turnaround time, quality specifications, etc.
• Performs routine testing in conjunction with client-specific projects
• Approves and issues Certificate of Analysis and signs on cGMP related reports
• Participates in departmental and/or company-wide projects designed to improve the nature of SGS client services
• Demonstrates willingness and ability to train on applicable general SOPs pertaining to the Analytical Laboratory
• Participates in general staff training sessions as these are scheduled
• Participates in departmental efforts directed toward equipment maintenance and calibration
• Adheres to relevant SGS SOPs governing official records and documentation.
• Compliance with applicable SOPs related to the handling of customer complaints

Education

B.S. in Chemistry, Biology, Microbiology, or equivalent experience

Job description

SGS in Fairfield, NJ is seeking a Specialist I in Quality Assurance to support the maintenance of Quality Systems in a pharmaceutical testing laboratory, under supervision of a Team Leader or Manager. The role focuses on timely testing, ensuring compliance with cGMP, issuing Certificates of Analysis, and participating in SOP training and equipment calibration.

Candidates should have a B.S. in Chemistry, Biology or related field and 0-2 years' Life Sciences experience; strong scientific