Astrix is the unrivaled market-leader in creating & delivering innovative strategies, solutions, and people to the life science community.  

Through world class people, process, and technology, Astrix works with clients to fundamentally improve business & scientific outcomes across many domains including the laboratory, clinical & regulatory, pharmacovigilance, R&D, and manufacturing. 

Founded by scientists to solve the unique challenges of the life science community, Astrix offers a growing array of strategic, application & platform, data transformation & analytics, change management, and staffing services designed to deliver immediate value to clients and solve their most complex technical and staffing challenges.

Industry: IT Services and IT Consulting
Company Size: 1,001-5,000 employees

Astrix

Savvy Admin PROD

Pay Rate Low: 75000 | Pay Rate High: 90000

**We’re hiring an Associate Scientist with analytical experience to join a global leader in the development and production of active pharmaceutical ingredients (APIs) for CDMO partners and generic drugs. This is a great opportunity to work with an industry leader that focuses on their expertise and competence in all of the companies processes!**

**Schedule: ** M-F 8a-5p

**Location: ** Lake County, OH

- Benefits include*** PTO, health/vision/dental insurance, HSA, 401(k) with match, and holiday pay!

**Responsibilities**

- Perform routine HPLC and GC analysis to support API method transfers, including data generation, interpretation, and documentation in compliance with GMP standards

- May perform other analytical testing (e.g., FTIR, KF, NMR)

- Support GMP method transfers, including protocol/report preparation

- Conduct release testing for raw materials, intermediates, and APIs

- Investigate out-of-specification (OOS) results and document findings

- Ensure timely and compliant data generation to meet project timelines

- Review analytical data for accuracy and GDP compliance

**Qualifications**

- Bachelor’s degree in chemistry or related field

- Minimum of 3 years’ hands-on experience performing HPLC and GC analysis within GMP pharmaceutical manufacturing

- Demonstrated experience in analytical method transfers

- Strong working knowledge of GLP/GMP standards, quality control procedures, and laboratory documentation practices

- This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!***

INDBH

QC Associate Scientist

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