Analytical Chemist I

Safetec of America Inc. is your trusted source for infection control first aid and compliance products for over 30 years. We are a fast-growing OTC pharmaceutical company located in Buffalo NY. We are a family-owned local business with a reputation for retaining employees because we treat them like family.

Come work for a company that is diverse a WNY Best Place to Work and is recognized for excellence in manufacturing!

If you have the ambition and drive to take on new challenges apply today!

Role Overview

The Chemist I is an entry-level professional responsible for performing routine analytical testing in support of OTC manufacturing operations. This role works under direct supervision and follows established procedures to ensure laboratory testing is conducted in compliance with cGMP USP FDA and company quality standards.

Responsibilities

• Perform routine analytical testing of raw materials in-process samples stability samples and finished OTC products according to approved methods
• The testing may include but is not limited to: HPLC/GC IR UV wet chemistry Auto-titrator etc. for raw materials bulk liquids and finished products
• Accurately document test results in appropriate laboratory notebooks worksheets logs or other designated forms in compliance with cGMP requirements
• Operate basic laboratory instrumentation including pH meters balances pipettes UV-Vis FTIR and titration equipment
• Follow approved SOPs test methods compendial testing and safety procedures at all times.
• Notify supervisor of atypical results or laboratory issues
• Participate in training to develop proficiency in chromatographic techniques (HPLC and/or GC)
• Perform testing and review of raw materials in-process samples and finished products to adhere to required timeframes

Requirements

• Associate or bachelors degree in chemistry Analytical Chemistry or other related field
• 1-2 years of laboratory experience (GMP experience preferred but not required)
• Basic understanding of chemistry principles and analytical techniques
• Familiarity with GMP concepts preferred
• Strong attention to detail and documentation accuracy
• Ability to follow detailed written procedures
• Good organizational and time management skills
• Basic proficiency with the Microsoft Suite
• Good interpersonal skills that support working in a team environment

Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position.

This job description is not intended to be an exhaustive list of all duties responsibilities or qualifications associated with the position.