Chemist I – Technical Manufacturing

Viltis; Scarborough (ME); On-site; USD 42,000 - 64,000; Full time

Job summary

Viltis seeks an entry-level Chemist I to support production of materials for immunology-based chromatography and enzyme diagnostic tests. You will manufacture bioreagents, perform in-process QC testing, and maintain lab documentation in a regulated environment.

This on-site contract role is ideal for recent chemistry or life sciences graduates, or an associate-degree candidate with relevant lab experience, aiming to gain hands-on experience in diagnostics manufacturing.

Qualifications

• Bachelor’s degree in Chemistry, Biochemistry, Biology, Life Sciences, or related field; recent graduates encouraged to apply.
• Associate degree with 1–2 years of lab experience or equivalent.
• Equivalent combination of education and laboratory experience.

Responsibilities

• Support and maintain established manufacturing and production schedules.
• Prepare bioreagents used in diagnostic products and processes.
• Follow SOPs, manufacturing instructions, and laboratory protocols.
• Perform in-process quality control testing and materials qualifications.

Skills

Chemistry

Laboratory skills

GMP/GLP

Documentation

Education

BSc in Chemistry

Associate degree (lab)

Equivalent experience

Tools

Pipettes

pH meters

Spectrophotometer

Chromatography system

Job description

Chemist I – Technical Manufacturing
Scientific Contract Aug 5, 2026

Chemist I – Technical Manufacturing

Location: Scarborough, Maine
Work Arrangement: On-site
Employment Type: Contract

Position Overview

Viltis is seeking an entry-level Chemist I to support the production of materials used in immunology-based chromatography and enzyme diagnostic tests for a leading global diagnostics organization.

The Technical Manufacturing Chemist will manufacture bioreagents, perform in-process quality control testing, maintain laboratory documentation, and help ensure that production activities are completed according to established schedules, Standard Operating Procedures, and GMP/GLP requirements.

This is an excellent opportunity for a recent chemistry or life sciences graduate, or an associate-degree candidate with relevant laboratory experience, to gain hands-on experience in a regulated diagnostic manufacturing environment.

Key Responsibilities

• Support and maintain established manufacturing and production schedules.
• Prepare critical and non-critical bioreagents used in diagnostic products and manufacturing processes.
• Follow approved Standard Operating Procedures, manufacturing instructions, and laboratory protocols.
• Perform in-process quality control testing, including material qualifications, quality inspections, and titrations.
• Use laboratory equipment such as pipettes, pH meters, spectrophotometers, and chromatography systems.
• Coordinate manufacturing activities with team members to maintain an adequate supply of raw bioreagents.
• Investigate production problems and identify opportunities for process or product improvement.
• Assist with new laboratory procedures and product improvement protocols.
• Maintain accurate and complete laboratory and manufacturing documentation.
• Follow applicable GMP, GLP, quality system, and safety requirements.
• Properly handle laboratory materials and observe all required safety precautions.
• Communicate production issues, testing results, and material needs to appropriate team members.

Basic Qualifications

Candidates must meet one of the following education and experience combinations:

• Bachelor’s degree in Chemistry, Biochemistry, Biology, Life Sciences, or a related scientific field; recent graduates are encouraged to apply, or
• Associate degree in a relevant scientific field with one to two years of related laboratory experience, or
• An equivalent combination of education and laboratory experience.

Preferred Laboratory Experience

Experience or academic exposure involving one or more of the following is preferred:

• Wet-bench laboratory techniques
• Pipetting
• pH meters
• Titrations
• Spectrophotometry
• SDS-PAGE
• Analytical chemistry principles
• In-process quality control testing
• GMP or GLP environments

Skills and Competencies

• Ability to carefully follow written procedures, protocols, and manufacturing instructions.
• Strong attention to detail and commitment to producing accurate, high-quality work.
• Ability to work effectively both independently and as part of a collaborative team.
• Strong organizational and time-management skills.
• Basic understanding of analytical chemistry theories and laboratory practices.
• Ability to recognize and communicate testing or production discrepancies.
• Proficiency with common computer applications, including spreadsheet, database, word-processing, and manufacturing software.
• Ability to work with moderate supervision in a regulated laboratory and manufacturing environment.

About Viltis

Viltis connects skilled scientific, engineering, quality, clinical, and regulatory professionals with opportunities at leading organizations in the life sciences and healthcare industries.

Viltis is an equal opportunity employer. We welcome and encourage diversity in the workforce and provide reasonable accommodations to qualified individuals with disabilities.