Job Description

Technical Manufacturing Chemist I

We are seeking a detail-oriented Technical Manufacturing Chemist to join a leading healthcare diagnostics organization. This laboratory-based role focuses on manufacturing and testing biological reagents used in infectious disease diagnostic products, including immunology-based chromatography and enzyme assays. The ideal candidate will have a background in chemistry or life sciences, hands-on laboratory experience, and a strong commitment to quality and manufacturing standards.

Key Responsibilities:

• Manufacture critical and non-critical biological reagents according to established Standard Operating Procedures (SOPs).
• Perform in-process quality control testing, inspections, titrations, and material qualifications.
• Conduct laboratory testing using pipettes, spectrophotometers, pH meters, and other analytical instruments.
• Support manufacturing production schedules and maintain an adequate supply of biological reagents.
• Follow Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and established quality systems.
• Investigate manufacturing issues, troubleshoot laboratory processes, and identify opportunities for improvement.
• Develop and follow laboratory protocols to support product improvements and process optimization.
• Maintain accurate laboratory records, test results, and manufacturing documentation.
• Collaborate with cross-functional teams to achieve production targets and maintain product quality.
• Follow laboratory safety procedures and support the implementation of new manufacturing processes.

Required Qualifications:

• Bachelor's degree in Chemistry, Biology, Biochemistry, Life Sciences, or a related scientific discipline, or an equivalent combination of education and experience.
• Hands-on laboratory experience through academic research, internships, or professional employment.
• Familiarity with laboratory techniques such as Pipetting, Spectrophotometry, pH Measurement, and analytical testing.
• Basic understanding of laboratory safety, quality control procedures, and scientific documentation.
• Ability to follow established SOPs and perform laboratory tasks with accuracy and consistency.
• Strong attention to detail, analytical thinking, and problem-solving skills.
• Ability to work independently with moderate supervision and collaborate effectively in a team environment.
• Proficiency in MS Office applications, spreadsheets, and basic laboratory data management.
• Ability to work onsite in Scarborough, Maine, during the assigned schedule.

Preferred Qualifications:

• Master's degree or PhD in Chemistry, Biology, Biochemistry, or a related scientific discipline.
• Experience with High-Performance Liquid Chromatography (HPLC), Gel Electrophoresis, SDS-PAGE, or ELISA Assays.
• Previous laboratory experience in pharmaceutical, biotechnology, medical device, or diagnostic manufacturing environments.
• Familiarity with GMP, GLP, and regulated laboratory manufacturing processes.
• Experience in biological reagent preparation, immunology-based testing, or enzyme assays.
• Exposure to Polymerase Chain Reaction (PCR) and ultraviolet-based analytical testing.
• Experience performing product testing, quality inspections, or analytical testing of biological samples.
• Prior experience supporting production schedules and manufacturing quality systems.

Benefits:

The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, paid time off, paid sick and safe time, hours of paid vacation time, weeks of paid parental leave, and paid holidays annually – as applicable.

Pay Range: $25/hr to $30/hr

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