Chemist I

Viltis; Scarborough (ME); On-site; USD 55,000 - 75,000; Full time

Job summary

Viltis is seeking a Technical Manufacturing Chemist I to join their team in Scarborough, Maine. This role involves producing materials for immunology-based tests, supporting quality systems, and ensuring compliance with established safety and production procedures.

Ideal candidates will have a Bachelor’s degree in Chemistry or related fields and experience with laboratory techniques such as HPLC and ELISA. The position offers an opportunity to contribute to innovative diagnostic solutions while working in a collaborative environment.

Qualifications

• Bachelor’s degree in Chemistry, Life Sciences, or a related scientific discipline.
• Experience with laboratory techniques such as HPLC and ELISA.
• Proven ability to follow detailed procedures and maintain documentation.

Responsibilities

• Support and maintain manufacturing production schedules.
• Manufacture bioreagents according to Standard Operating Procedures (SOPs).
• Perform in-process quality control testing and maintain compliance with GMP and GLP.

Skills

Pipetting techniques

Spectrophotometry

High-Performance Liquid Chromatography (HPLC)

pH meter operation

Gel Electrophoresis

SDS-PAGE

ELISA assays

Education

Bachelor’s degree in Chemistry, Life Sciences, or a related scientific discipline

Tools

Microsoft Excel

Database systems

Manufacturing software systems

Word processing applications

Job description

Abbott Rapid Diagnostics is part of Abbott’s Diagnostics family of businesses, bringing together exceptional teams of experts and industry-leading technologies to support diagnostic testing that provides critical information for the treatment and management of diseases and other health conditions.

Position Summary

Technical Manufacturing Chemist I

We are seeking a Technical Manufacturing Chemist I to join our Infectious Disease Developed Markets business unit in Scarborough, Maine. In this role, you will produce materials used in immunology-based chromatography and enzyme tests while supporting manufacturing operations, quality systems, and continuous improvement initiatives.

Location

Abbott Rapid Diagnostics
10 Southgate Road
Scarborough, ME 04074, USA

Key Responsibilities

• Support and maintain manufacturing production schedules.
• Manufacture critical and non-critical bioreagents according to Standard Operating Procedures (SOPs).
• Perform in-process quality control testing, including qualifications, inspections, and titrations.
• Maintain compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
• Investigate production issues and identify opportunities for process improvements.
• Develop, create, and execute protocols focused on product and process enhancement.
• Follow established laboratory procedures and safety requirements.
• Coordinate manufacturing activities within a team environment to ensure uninterrupted production and bioreagent supply.
• Document manufacturing activities accurately and maintain required records.
• Assist in maintaining inventory and raw material availability to support production demands.

Required Qualifications

• Education: Bachelor’s degree in Chemistry, Life Sciences, or a related scientific discipline; or an equivalent combination of education and relevant experience.

Technical Skills & Experience

Experience with the following laboratory techniques and equipment is preferred:

• Pipetting techniques
• Spectrophotometry
• High-Performance Liquid Chromatography (HPLC)
• pH meter operation
• Gel Electrophoresis
• SDS-PAGE
• ELISA assays

Competencies

• Ability to work effectively both independently and within a collaborative team environment.
• Strong attention to detail and commitment to quality.
• Excellent organizational and problem-solving skills.
• Ability to follow detailed procedures and maintain accurate documentation.
• Proficiency with computer applications, including:
  • Microsoft Excel or similar spreadsheet software
  • Database systems
  • Manufacturing software systems
  • Word processing applications

Work Environment

This position is based in a laboratory and manufacturing environment and requires adherence to established safety procedures, quality standards, and regulatory requirements.

Viltis is an equal opportunity employer committed to fostering an inclusive workplace where all employees can contribute and succeed.