Chemist III

JOB SUMMARY: The position exists to provide a technical chemistry team leader that serves as the lead trainer and works alongside other chemists in the lab to ensure the highest quality in testing and the development of said chemists. The Chemist III performs manual and automated titration test methods and compendial methods for measuring characteristics of raw materials, stability samples, and finished goods. The Chemist III is responsible for managing the inventory for the chemistry lab. They are responsible for ensuring the equipment is functioning and compliant through equipment qualifications in accordance with USP, ISO, ASTM, and industry standards. They may provide technical advice to site management interpreting investigations problems throughout the facility. The Chemist III performs test method validations and test method transfers in accordance with USP and industry standards. The Chemist III also supports the QC LAB Manager with administrative tasks such as data review, data archival, and provide feedback on performance of others. They will perform Lab audits. They review and update documents associated with general lab operations and chemistry. The Chemist III assists higher level chemists designing processes and technical writing. The Chemist III may have direct customer interactions to explain technical and sensitive information regarding product quality.

ESSENTIAL ACCOUNTABILITIES:
*Chemical testing tasks
Titrations, pH, routine batch testing, and TOC analysis
ID testing by FTIR
ID testing following USP or other compendial standards
Gas Chromatography testing of finished goods and raw materials
High Performance Liquid Chromatography testing of finished goods and raw materials

*Administrative support of the lab
Ordering and maintaining levels of laboratory supplies and consumables
Ensuring chemicals are monitored for proper receipt and labeling
Organization of paperwork flow
Archiving data
Reviewing logs for completion and accuracy
Authoring and reviewing specifications, procedures, work instructions, forms
Compiling data for Key Performance Indicators
JD Template Revised - 1/12/2023
Completing housekeeping responsibilities monitoring for both laboratories

*Chemical team leader
Lead trainer
Direct Chemist I & II to construct development plan
Talk directly with management & customers to explain testing problems or differences
Review data for accuracy and compliance to Good Documentation Practices
Lead OOS investigations
Provide performance feedback to chemists and QC Lab Manager

*Run the calibration system for the plant.
*Lead or assist method validation design, execute and report
*Participate with other Rockline plants in the Global Laboratory Working Group to align chemistry testing between sites
*Demonstrate commitment to the company's RRITE Values of Renew, Respect, Integrity, Teamwork, and Excellence.
*Associates have a direct and important role in ensuring that all work is performed in a safe manner. Effectiveness in carrying out this responsibility is part of each associate's essential accountabilities.
*Contribute to a cooperative working effort by demonstrating a willingness to perform other job-related work, as needed or requested.

This position is designated as a Safety-Sensitive (A safety-sensitive position is one in which the associate's inability or impaired ability to perform their job-related tasks could result in a direct threat to the associate's safety or the safety of others).

QUALIFICATION REQUIREMENTS: (To perform this job successfully, an individual must be able to perform each of the essential accountabilities satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required.)
*Bachelor's degree in chemistry
*5+ years of experience in a QC lab and professionally demonstrated understanding of titration, GC, and HPLC
*Must be familiar with interpreting USP General chapters related to reagent preparation and general ID tests
*Must have experience in method validation and transfers following USP and ICH guidelines to meet FDA expectations
*Must understand analytical instrument qualifications following USP guidelines
*External training in current Chemistry topics will be required to become a Chemist III. Training could be in the form of traditional classroom training, webinars, or scientific conferences as provided by such organizations as AOAC, Pittconn, ACS, USP, etc.

*Other training that is desirable for the position:
Graduate degree or certificate in analytical chemistry
Experience with ISO and ASTM standards for testing labs, cosmetic testing, and drug testing
Internal auditing experience
ASQ certification in metrology or auditing
Understanding of general microbiological test methods

PHYSICAL AND MENTAL REQUIREMENTS: (The physical demands described here are representatives of those that must be met by an associate to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions)
JD Template Revised - 1/12/2023
*Standing, sitting, reading, writing, reasoning/analyzing, and social interaction.
*Frequent carrying and lifting 0-10 pounds, repetitive hand movement, reading, writing, reasoning/analyzing, and social interaction
*Occasional carrying and lifting 10-30 pounds, standing/walking, bending/twisting, pushing/pulling, reaching above shoulder, and calculating

WORK ENVIRONMENT: (The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.)
*This role takes place mostly in a Laboratory office setting. Moderate exposure to noise, fumes, odors, and hazards.
*Environmental Monitoring and Plant Validation duties will require working in the Plant environment to collect samples.

FLSA Status - Exempt
Grade - 9