Chemist I

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

Job summary

Viltis Consulting is looking for a Technical Manufacturing Chemist I in Scarborough, Maine. In this role, you will be responsible for manufacturing critical and non-critical bioreagents used in diagnostic products, ensuring compliance with GMP/GLP standards and supporting production schedules.

The ideal candidate should hold a Bachelor’s degree in a relevant scientific discipline and have experience with laboratory techniques such as pipetting and spectrophotometry. A commitment to quality and attention to detail are essential for success in this laboratory setting.

Qualifications

• Bachelor's degree in Chemistry, Life Sciences, or related scientific discipline.
• Ability to work effectively both independently and within a team.
• Strong attention to detail and commitment to quality.

Responsibilities

• Support and maintain manufacturing production schedules.
• Manufacture bioreagents according to SOPs.
• Perform quality control testing.
• Maintain compliance with GMP and GLP.

Skills

Pipetting techniques

Spectrophotometry

pH meter operation

SDS-PAGE

Microsoft Excel or similar software

Database systems

Manufacturing software systems

Word processing applications

Education

Bachelor’s degree in Chemistry, Life Sciences, or related

Job description

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

About Abbott Rapid Diagnostics

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.

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.

Position Summary

The Technical Manufacturing Chemist I is responsible for manufacturing critical and non‑critical bioreagents used in diagnostic products and processes. This position supports production schedules, performs quality control testing, maintains compliance with GMP/GLP standards, and contributes to process improvements in a regulated laboratory manufacturing environment.

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
• pH meter operation
• SDS-PAGE
• 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

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.