Technical Manufacturing Chemist I — GMP & QC Focus

Abbott (abbottcareers2 board); United States; On-site; USD 58,741,000 - 117,482,000; Full time

Benefits offered by this job

HIP PPO medical plan

Generous retirement plan

Tuition reimbursement

FreeU education benefit

Job summary

Abbott is seeking a Technical Manufacturing Chemist in Scarborough, Maine. You will produce materials for immunology-based chromatography and enzyme tests, supporting the ID Infectious Disease division and ensuring safe, compliant manufacturing.

Responsibilities include maintaining the production schedule, investigating issues, performing in-process QC, following GMP/GLP, creating SOP-based protocols, and coordinating bioreagent supply with the team.

Qualifications

• Bachelor's Degree in Chemistry, Life Sciences, or related field.

Responsibilities

• Maintains and supports the production schedule
• Investigates problem areas and areas of desirable improvement
• Undertakes new procedures and observes proper safety precautions
• Responsible for in-process QC testing of manufacturing material as it relates to qualifications, quality inspections and titration
• Maintains quality systems and proper GMP/GLP
• Creates and follows protocols designed around product improvement
• Responsible for making critical and non-critical bioreagents for use in product and manufacturing processes using Standard Operating Procedures (SOPs)
• Works in a team setting and coordinates manufacturing efforts based upon a set production schedule and maintaining the raw bioreagent supply as needed to support this schedule

Education

Bachelor's Degree in Chemistry, Life Sciences, or related field

Tools

Pipette

Spectrophotometry

HPLC

pH meters

Gel Electrophoresis / SDS Page

ELISA assays

Job description

Abbott is seeking a Technical Manufacturing Chemist in Scarborough, Maine. You will produce materials for immunology-based chromatography and enzyme tests, supporting the ID Infectious Disease division and ensuring safe, compliant manufacturing.

Responsibilities include maintaining the production schedule, investigating issues, performing in-process QC, following GMP/GLP, creating SOP-based protocols, and coordinating bioreagent supply with the team.