SPECIALIST QUALITY (5178)

NICE-PAK PRODUCTS LLC•Overland, MO

12d•Onsite

About The Position

The QC Specialist (Chemist) is responsible for prioritizing daily sample testing and performing a variety of laboratory tests on raw materials, in-process samples, and finished products. This role reviews compounding and laboratory records for accuracy and completeness, investigates customer complaints, and handles out of spec (OOS) or out of trend (OOT) results including implementing any corrective action as directed by QC leadership.

Requirements

Bachelor’s degree (BS/BA) degree in Chemistry or related science.
Must have a thorough understanding of FDA regulations and strong working knowledge of laboratory testing procedures.
Must demonstrate the ability to use laboratory equipment safely and efficiently.
1-2 years of progressive Quality Control experience in a laboratory environment.
Must be proficient in analytical testing techniques and demonstrate strong attention to detail.
Must have interpersonal skills and the ability to work well independently while making sound decisions under pressure.

Nice To Haves

Proficient in analytical testing techniques
Strong attention to detail
Interpersonal skills
Ability to work well independently
Ability to make sound decisions under pressure

Responsibilities

Perform laboratory analysis on incoming raw materials, in-process samples, and finished products per established procedures, including wet chemistry, GC & HPLC.
Prepare samples for chromatographic analysis.
Maintain a clean, safe, and organized laboratory environment at all times.
Coordinate information flow within the laboratory and to internal customers.
Access, input, and retrieve information from the QC computer systems.
Approve or reject raw materials, process samples, and finished products for release or sale.
Be thoroughly versed in GMP regulations and ensure that all laboratory documentation meets standards for completeness and accuracy.
Demonstrate a complete understanding of safe procedures for handling, processing, and storing hazardous and/or flammable products and raw materials in compliance with local, state, and federal guidelines.
Document and report deviations in performance not anticipated or indicated in test procedures.
Maintain a thorough understanding of QC procedures, manufacturing processes, workflow, the QC retain program, and documentation procedures.
Work with minimal supervision while effectively re-prioritizing work schedules to meet production demands.
Be proficient in performing routine GC and HPLC analysis in an efficient and accurate manner.
Perform all assigned laboratory tasks accurately, efficiently, and within established timelines.
Provide timely, accurate information to production personnel.
Participate in department meetings as required.
Complete all assigned training assignments within established deadlines.
Perform other related duties as assigned by QC leadership.
Exhibit team player qualities of cooperation, coordination, and professional interaction in all business contacts.
Presence at work on time when scheduled is a mandatory function.
Compliance with all company safety rules, procedures, and guidelines is mandatory.