Science - Chemist I

Randstad Life Sciences US; Fort Snelling Unorganized Territory (MN); On-site; USD 60,000 - 80,000; Full time

Job summary

A leading company in pharmaceutical manufacturing is seeking a Chemist I to support chemical characterization testing of medical devices. The role involves hands-on testing in the analytical lab, developing methods, and ensuring compliance with ISO and FDA standards. Candidates should possess a BS in Chemistry and be eager to engage in a dynamic lab environment.

Benefits

Comprehensive benefits package

401K plan

Qualifications

• 0-2 years of experience in analytical chemistry.
• Experience in preparation of samples, standards, and laboratory solutions.

Responsibilities

• Perform hands-on testing in the analytical chemistry laboratory.
• Support development, validation, and qualification of analytical methods.
• Prepare analysis summary reports/documentation.

Skills

HPLC

Chemistry

Chromatography

Sample Preparation

Education

BS in Chemistry

Job description

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Job Purpose:

Support chemical characterization testing of medical devices. Apply chemistry skills in standard and sample preparation. Initiate instrumental testing using FTIR, GCMS, LCMS, or ICPMS techniques.

Job Summary

Job Purpose:

Support chemical characterization testing of medical devices. Apply chemistry skills in standard and sample preparation. Initiate instrumental testing using FTIR, GCMS, LCMS, or ICPMS techniques.

location: Saint Paul, Minnesota

job type: Contract

salary: $30.00 - 39.75 per hour

work hours: 9 to 5

education: Bachelors

Responsibilities

Key responsibilities:

• Perform hands-on testing in the analytical chemistry laboratory, including sample preparation (extractions, solvent exchange, concentration), gravimetric determination of non-volatile residue, and standard preparation
• Support development, validation, and qualification of analytical methods
• Prepare analysis summary reports/documentation to communicate results to lab customers and the technical community
• Complete tasks on analytical lab documentation and quality records
• Support qualification and maintenance of analytical instrumentation
• Complete lab maintenance activities such as ordering, glassware washing, and other lab monitoring activities
• Familiarity with ISO 10993, ISO 17025, FDA, and other regulatory agency requirements for chemical characterization of medical device and combination products
• Apply scientific principles and company policies and procedures, analyzes data or situations, and exercises judgment to recommend solutions to solve problems.
• Demonstrate a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures
  
  

Quality Systems Duties And Responsibilities

• Build Quality into all aspects of their work by maintaining compliance to all quality requirements.
  
  

Qualifications

Required Qualifications:

• BS in Chemistry with aptitude for analytical chemistry.
• 0-2 years of experience - post graduate with internship(s) count!
• Experience in preparation of samples, standards, and laboratory solutions
  
  

Preferred Qualifications

• Exposure to Chromatography Data Systems
• Experience with chemical characterization analysis per ISO 10993
• Experience with HPLC or GC instrument analysis and troubleshooting
• Experience applying ISO 10993 and ISO 17025 requirements to laboratory work
• Working experience in performing analyses and preparing documentation within FDA, ISO 17025, and other regulatory environments
• Medical device or pharmaceutical company analytical chemistry lab work experience, especially in chromatography characterization and investigative analyses.
• Strong organizational, communication, and collaboration skills
• Strong technical writing and scientific laboratory documentation skills
  
  

skills: HPLC, Chemistry, Chromatography, Sample Preparation

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact [e-mail].

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).

This posting is open for thirty (30) days.

u50000030026

Seniority level

• Seniority level

  Not Applicable

Employment type

• Employment type

  Contract

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  Pharmaceutical Manufacturing

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