Top 8 Hplc Jobs in Milwaukee Wi

Quality Control Manager - ChemRite
Lewis & Clark Capital —Lannon, WI
- $90,000 - $110,000 a year
- Spanish
- Microsoft Excel
- 5 years
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Chemist I
Eurofins USA Food Testing —New Berlin, WI
- Full-time
- Bachelor of Science
- Bachelor's degree
- Entry level
- Paid holidays
- Disability insurance
Quick Apply
Research Scholar in Medicinal Chemistry
Concordia University Wisconsin/Ann Arbor —Mequon, WI
- Online Application
- University
- Doctor of Philosophy
- Senior level
- Health savings account
- AD&D insurance
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Manufacturing Chemist
Sterling Pharma Solutions —Germantown, WI
- 12 hour shift
- Mid-level
- 3 years
- High school diploma or GED
- Health insurance
- Dental insurance
Senior/Principal Chemical R&D Scientist
Sterling Pharma Solutions —Germantown, WI
- Microsoft Excel
- Microsoft Outlook
- 5 years
1d

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Water Sampling Technician (Part-Time) – Milwaukee & Green Bay Location
I-2-I Solutions, Inc. —Milwaukee, WI
Valid driver’s license and reliable vehicle for local travel and sample drop-off. Record required field information, including sample location, date and time of…
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2d
Scientific Laboratory Technician
Three Point Solutions, Inc. —Milwaukee, WI
Comfortable in hot/dusty manufacturing environments. Seeking a Laboratory Technician to support food safety, quality control, and laboratory testing operations…
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14d

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QC Chemist I
American Regent, Inc. —Columbus, OH
B.S. in Chemistry, Pharmaceutical Science or related field required. Perform analytical analysis using HPLC, GC, UV/VIS and FTIR.
7d
Pharmaceutical Laboratory Analyst
Ashland —Columbus, OH
Associate's degree in Chemistry or related field. In this exciting role you would be exposed to and learn about chemical manufacturing and associated testing in…

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hplc jobs near milwaukee wi

Quality Control Manager - ChemRite

Lewis & Clark Capital
Lannon, WI

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Job Details

$90,000 - $110,000 a year

Qualifications

Quality control within consumer goods industry
Data compliance
Microsoft Excel
Laboratory equipment performance testing and validation
Team leadership
Pharmaceutical regulatory compliance
Laboratory instrument validation
Microbiology testing
Word embeddings
GMP
Manufacturing facility
Team development
Production validation processes
Bachelor's degree
Materials analysis (analytical chemistry specialty)
Quality control within pharmaceutical industry
Microbiological analysis
Productivity software
Chemical testing
Managing product quality assurance teams
Test validation method
Cleaning and sanitation quality assurance
FDA regulations
Pharmaceutical manufacturing facility experience
Team building

Full Job Description

ChemRite CoPac is looking for a Quality Control Manager responsible for supporting a GMP-regulated liquid blending and filling manufacturing operation that provides contract packaging, blending, and filling services for OTC, cosmetic, and specialty chemical products. ChemRite CoPac partners with customers to manufacture high-quality liquid products across a variety of package types while maintaining strict adherence to FDA, GMP, and customer-specific quality requirements.

The Quality Control Manager manages the daily activities and job functions of the personnel of the QC Department, the analytical laboratory, and the plant microbiological plan. The Quality Control Manager works closely with Quality Assurance leadership to ensure that all incoming raw materials, batch mixes, and finished goods meet established standards while maintaining adherence to the Quality Systems Manual (QSM), supporting customer audits, and driving continuous improvement in a fast-paced production environment.

Responsible for planning, coordination, and execution of QC activities across raw material testing, finished product testing, stability, method transfers, cleaning and process validations. Accountable for achieving QC targets and KPIs, managing budgets, and developing a high-performing, cross-trained QC organization with robust succession and backup coverage for critical roles.

Specific responsibilities include, but are not limited to:

Manages the daily activities and job functions of the personnel of the QC Department, including resource planning and scheduling.
Manage quality control testing on incoming raw materials, batch mixes, finished goods and stability, per established standards.
Maintain proficiency on all QSM (Quality Systems Manual) procedures, and create and update QSM specifications (i.e., Raw Materials, Packaging Materials, Finished Goods, Test Methods, and Validations).
Identify gaps and make necessary modifications to QC documents.
Lead laboratory investigations, deviations, OOS/OOT investigations, and recommend corrective and preventive actions (CAPAs)
Leads project management of laboratory activities, ensuring alignment with manufacturing schedules, regulatory commitments, and product launch timelines.
Ensures accurate documentation, review, and submission of raw data and results.
Ensures data integrity and compliance through robust data review
Support and sustains a continuous audit readiness program to ensure inspection-ready state at all times for customer audits and governmental agency inspections.
Complete accurate documentation for tests, inspection results, and defects related to chemical raw materials, packaging materials, or finished packaging.
Maintains SDS files.
Orders all lab supplies and ensures all reagents and standards are current.
Maintains the cleanliness of the QC labs, and retain room, and checks calibration of lab equipment per established standards.

Basic Qualifications – Required

Bachelor’s degree in Chemistry or related field of study.
At least 5 years of previous Quality Control experience in a cGMP and FDA-regulated manufacturing environment.
Experience with various analytical instrumentation (HPLC, GC, FTIR, TOC, etc.).
Strong written, verbal and interpersonal communication skills
Strong attention to detail with consistent focus on data integrity and compliance
Leadership capabilities such as building effective teams, problem solving and decision making
Proficiency with Microsoft Word, Excel, PowerPoint
A working knowledge of how to develop and validate analytical methods.
A working knowledge of microbiological testing.
A working knowledge of IQ/OQ/PQ.
A working knowledge of how to plan and execute cleaning validations.
A working knowledge of FDA regulations for the manufacturing of pharmaceuticals and OTC products.
Provides clear direction and accountability for team performance.

Basic Qualifications – Preferred

Reinforces safety culture and operational standards.
Liquid fill manufacturing experience (e.g., hand soaps, sanitizers, cosmetics).
Has a background with adjusting formulations to meet specifications.
Bilingual in both English and Spanish.
Demonstrates strong technical writing and communication skills relating to quality procedures.

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hplc jobs in milwaukee wi

Quality Control Manager - ChemRite

Chemist I

Research Scholar in Medicinal Chemistry

Manufacturing Chemist

Senior/Principal Chemical R&D Scientist

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