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Analytical Chemist

Job in Minnetonka, Hennepin County, Minnesota, 55345, USA
Listing for: Actalent
Full Time position
Listed on 2026-07-12
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, QA Specialist - Analyst/Manager
Salary/Wage Range or Industry Benchmark: 39 - 43 USD Hourly USD 39.00 43.00 HOUR
Job Description & How to Apply Below
Position: Analytical Chemist 2

Analytical Chemist II

Long-Term Opportunity | Excellent Industry Experience | Day Shift | Offers Benefits

Job Description

The Analytical Chemist II plays a key role in ensuring that raw materials, bulk products, and finished goods consistently meet customer and regulatory analytical requirements. This position supports a fast-growing manufacturing operation by validating analytical methods, performing complex testing, and maintaining high standards of quality in a cGMP laboratory environment. The role is part of the quality team at the Eden Prairie facility and serves as a senior technical resource within the lab.

Responsibilities

  • Validate analytical procedures, test methods, chemical assays, and laboratory processes used to detect and identify active ingredients to ensure compliance with customer and regulatory guidelines.
  • Validate analytical test methods for testing controlled articles, including raw materials, bulk product, and filled product, to ensure methods are robust, reliable, and compliant.
  • Calibrate, monitor, and maintain laboratory test equipment to ensure accurate and reliable analytical results.
  • Accurately record all data and pertinent information in accordance with current Good Manufacturing Practices (cGMP).
  • Create and maintain monthly Key Quality Indicators (KQI) in a timely and accurate manner to support continuous improvement and quality reporting.
  • Conduct detailed batch record reviews to verify compliance with cGMP practices and identify potential issues or deviations.
  • Document out-of-specification (OOS) situations, determine root causes, and recommend or support corrective and preventive actions (CAPA).
  • Lead OOS investigations, review findings, and approve analytical data and product release (ADPRs) for fill and stability studies.
  • Ensure analytical specifications are met for raw materials, bulk product, and finished goods, and that all results are documented and maintained to meet customer expectations.
  • Report test results clearly and promptly, and ensure accurate and timely transition of quarantined raw materials, bulk product, and finished products based on those results.
  • Troubleshoot out-of-specification situations by identifying potential causes, recommending solutions, and implementing corrective actions where appropriate.
  • Ensure Good Laboratory Practices (GLP) are followed and align with applicable regulatory guidelines.
  • Work closely with Analytical Chemists and QC Chemists in a collaborative team setting to support testing, investigations, and continuous improvement initiatives.
  • Serve as leader in technical resource within the laboratory by providing mentorship, training, work review, troubleshooting support, and quality control assistance to other team members.
  • Support a high-volume, fast-paced production environment by adapting to changing priorities and workloads while maintaining quality and safety standards.

Essential Skills

  • Bachelor's degree in Chemistry or a related scientific discipline.
  • 3+ years of industry analytical chemistry experience, including hands-on work with HPLC, GC, and USP methods.
  • 2+ years of experience with analytical method development or optimization.
  • Demonstrated experience working in a cGMP laboratory environment.
  • Strong practical knowledge of analytical chemistry techniques, including HPLC and GC.
  • Experience with gas chromatography (GC) and related instrumentation.
  • Experience with HPLC and GC method development in a quality control or analytical laboratory setting.

Additional Skills & Qualifications

  • Previous experience with method validation is a plus.
  • Experience using Empower or similar chromatography data systems is beneficial.
  • Experience working with Key Quality Indicators (KQI) or similar quality metrics.
  • Familiarity with 5S or other continuous improvement methodologies.

Work Environment

This is an on-site role. The position follows a Monday–Friday, first-shift schedule, with typical start times between 7:00 a.m. and 9:00 a.m.

Job Type & Location

This is a Contract to Hire position based out of Minnetonka, MN.

Pay and Benefits

The pay range for this position is $39.00 - $43.00/hr eligibility requirements apply to some benefits and may depend on your job…

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