Quality control chemist

Us tech Solutions; Myerstown (PA); On-site; USD 50,000 - 70,000; Full time

Job summary

Us tech Solutions is seeking a Quality Control Chemist for the 2nd shift in Myerstown, PA. The role involves ensuring the quality of raw materials through rigorous testing and analysis using advanced analytical techniques.

The ideal candidate will have a Bachelor's degree in Chemistry or a related field, along with 1-3 years of experience in a GMP laboratory. Responsibilities include performing qualitative and quantitative analyses and maintaining compliance with industry standards.

Qualifications

• Bachelor’s degree in Chemistry, Biology, Pharmacy, or related 4-year science degree is required.
• 1-3 years of experience in a GMP laboratory environment preferred.
• Knowledge of analytical chemistry essential for job functions.

Responsibilities

• Perform qualitative and quantitative analysis on raw materials.
• Document and maintain records of all analysis information.
• Assist in troubleshooting analytical methodology and instrumentation malfunctions.

Skills

Analytical chemistry

Problem-solving

Team collaboration

Communication skills

Education

Bachelor’s degree in Chemistry, Biology, Pharmacy or related

Tools

HPLC

GC

UV

FT-IR

Job description

Job Description

Title: Quality control chemist- 2nd shift

Duration: 12 Months

Location: Myerstown, PA 17067

Description: The Raw Material testing team is responsible for Quality Control testing of APIs and excipients used in the manufacture of pharmaceutical and nutritional products. This is a fast‑paced, energetic team that works together across two shifts to meet aggressive throughput times to support a lean manufacturing operation.

Position Summary

In this position, the incumbent will be expected to draw upon previous analytical experience, as well as continuously learn Quality Control systems and effectively engage in relationships with peers in the laboratories, Manufacturing/Production, and personnel in other departments as needed. The incumbent will perform analysis on raw materials following prescribed procedures to provide the information base leading to material disposition, as well as assist in troubleshooting and problem solving as directed. Once the incumbent is assigned specific materials on which to perform the quality control tests, or provide development or troubleshooting, the incumbent will have a considerable impact on results from his/her work. Material can be rejected and manufacturing procedures can be altered significantly either in schedule changes or in process itself.

Position Duties & Responsibilities

• Perform standard qualitative and quantitative analysis.
• Utilize standard analytical chemistry techniques: wet analytical methods, HPLC, UV, GC, AA, polarimeter, FT‑IR, NIR, RAMAN, etc. to test raw materials in accordance with approved testing procedures, including those from company, the National Formulary (NF), the United States Pharmacopoeia (USP), the European Pharmacopoeia (EP), and the FDA.
• Properly document and maintain records of all analysis information of assigned materials on data sheets and laboratory notebooks for permanent file.
• Evaluate all data obtained from analysis; if discrepancy or deviation occurs, consult with Supervisor and recommend additional testing if necessary.
• Communicate to supervision in a timely manner all non‑compliance situations, and assist in investigations.
• Assist with troubleshooting analytical methodology and instrumentation malfunctions.
• Perform special assignments as directed by supervisor, for example, revise existing analytical testing monographs to comply with compendia changes or other specific needs.
• Accurate, complete and timely fulfillment of the job responsibilities will, in part, ensure GMP compliance as outlined in various Bayer and U.S. government rules and regulations.
• Documentation Review: review testing documentation performed by other analysts for compliance with BAYER, FDA, National Formulary (NF), United States Pharmacopoeia (USP), and European Pharmacopoeia (EP) procedures.
• Safety: adhere to the pertinent aspects of Corporate and plant safety programs and adhere to GMP’s, ISO standards or other regulations.

Qualifications

• Bachelor’s degree in Chemistry, Biology, Pharmacy, or related 4‑year science degree required. Chemistry degree is preferred.
• At least 1–3 years of experience in a GMP laboratory environment. Master’s degree in a related field with 1 year of experience may be considered.
• Knowledge, practical application, and understanding of analytical chemistry is required to perform the functions of this position.
• Basic experience with Personal Computer (PC).
• Demonstrated capability for communicating ideas, concepts, and work results effectively to colleagues and supervision.
• Demonstrated ability to be self‑motivated as well as to work collaboratively in a team‑based environment is required.
• Must demonstrate initiative and a willingness to learn.
• Good working knowledge of advanced laboratory instrumentation and personal computer skills are required.
• Strong troubleshooting skills for assigned area such as HPLC, GC, AA, UV, TOC, NIR and/or dissolution and low error rates with microbiology or chemistry techniques for defined area.
• A working knowledge of organic chemistry, statistics, data processing and good manufacturing practices is required.
• Demonstrated ability to clearly communicate technical information in writing required.
• Demonstrated ability to manage key projects and display area of expertise; i.e. clear/consistent notebook skills and function as an independent worker.
• A thorough understanding of National Formulary (NF), United States Pharmacopeia (USP), and European Pharmacopeia (EP) testing procedures, as well as US Pharmaceutical Industry Good Manufacturing Practices (GMP’s), quality control methods and procedures is required.
• Competencies required: analytical problem solving, alertness, work within established policies and procedures, commitment to task, decisiveness, effective written and interpretive communication skills, and organization and planning skills.
• Travel Requirements: None

Additional Information

All your information will be kept confidential according to EEO guidelines.

Job Location

Myerstown, PA 17067