Analytical Chemist I

Boston Analytical; Salem (NH); On-site; USD 52,000 - 78,000; Full time

Job summary

Boston Analytical is seeking a Chemist to conduct quantitative and qualitative analysis of pharmaceutical products in line with FDA, cGMP, and BA Sciences SOPs. Primary duties include analysis using HPLC, GC, Dissolution, AA, UV-Vis and method development.

Qualifications require a bachelor's degree in chemistry or related science and 0–2 years of related experience; knowledge of cGMPs is preferred. The role emphasizes compliant practices, data integrity and teamwork.

Qualifications

• Bachelor’s degree in chemistry or related science required, 0–2 years of experience preferred.
• Knowledge of cGMPs and related compliance guidance preferred.

Responsibilities

• Prepare and analyze products to determine chemical and physical properties.
• Confer with chemists and client personnel regarding procedures and results.
• Receive training to become proficient and subject matter expert.
• Perform routine data generation and solve problems with minimal rework.
• Comply with SOPs, cGMPs, and FDA regulations.
• Maintain calibrations and operation of equipment.
• Document work clearly and safely.

Skills

Interpersonal skills

Organizational skills

Verbal communication

Technical documentation

Computer skills

Lab safety

Team player

Education

Bachelor’s degree in chemistry or related science

Tools

HPLC

GC

Dissolution

AAS

UV-Vis

Wet chemistry

Job description

JOB SUMMARY

The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and BA Sciences Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development.

PRIMARY DUTIES AND RESPONSIBILITIES

• Prepares and analyzes products to determine chemical and physical properties.
• Under close supervision confers with chemists and other client personnel regarding research, procedures performed, related results and prepares reports.
• Under close supervision will be trained to become proficient at assigned tasks in order to become subject matter experts.
• Performs routine data generation and problem solving with a minimal rework.
• Works under close supervision to ensure all work performed is performed in compliance with standard operating procedures, good manufacturing practices, and the regulations of the Food and Drug Administration.
• Ensures all work performed strictly adheres to company, client and pharmacopeial methodologies.
• Performs system maintenance and calibrations to ensure equipment is operating with specified requirements.
• Learns proper handling of hazardous waste in compliance with the company and DES hazardous waste rules.
• Documents work in a clear and organized manner.
• Follows all safety rules and regulations and conducts periodic safety audits.
• Follows all cGMP rules and regulations.

REQUIREMENTS AND QUALIFICATIONS

Qualification include a bachelor’s degree in chemistry or a related science discipline is required with 0-2 years of related experience. Knowledge of cGMPs and related compliance regulations and guidances is preferred.

MINIMUM SKILLS REQUIREMENTS

• Must have the ability and skill to perform the detailed job requirements noted above competently, safely and proficiently.
• A self-starter, motivated person who possesses good interpersonal skills capable of effectively interacting with all departments and client personnel.
• Must have excellent organizational, verbal communication and technical documentation skills.
• Solid computer skills.
• Knowledge of safe laboratory practices, including the proper procedures in handling chemicals and samples.
• Must be a team player with integrity and concern for the quality of company products, services and staff members.