Quality Control Scientist - HPLC & Stability

Planet Pharma; Painesville (OH); On-site; USD 65,000 - 95,000; Full time

Job summary

Planet Pharma seeks an Associate Scientist, QC to perform analytical testing of raw materials, in-process samples, finished products, and stability samples in a cGMP-regulated lab. You will generate and review analytical data, support investigations, and ensure regulatory compliance.

The role requires a strong HPLC background, experience in GMP/GLP environments, and collaboration with QA, manufacturing, and clients.

Qualifications

• Bachelor's degree in Chemistry or a related scientific discipline required.
• Minimum of 3 years of related pharmaceutical analytical laboratory experience with a B.S. degree, or 1 year with an M.S. degree, or an equivalent combination of education and experience.
• Relevant experience in a Quality Control laboratory is required.
• Experience working in a cGMP and/or GLP-regulated environment is required.

Responsibilities

• Perform analytical testing of raw materials, in-process samples, finished products, and stability samples using techniques such as HPLC, GC, KF, FTIR, XRD, DSC, TGA, PSD, NMR, ICP-MS, ICP-OES, and other laboratory instrumentation as required.
• Support stability programs through sample management, stability chamber monitoring, testing, and generation of stability data.
• Coordinate timely and compliant generation of analytical data to support client projects and manufacturing operations.
• Review laboratory data for technical accuracy, completeness, compliance, and adherence to good documentation practices.
• Conduct OOS, OOT, and laboratory investigations and support implementation of corrective and preventive actions (CAPAs).
• Author and review protocols, reports, specifications, analytical methods, and related laboratory documentation.
• Perform raw material sampling, testing, inspection, and coordination activities as required.
• Manage laboratory inventory, retained samples, reagents, standards, chemicals, and associated laboratory systems.
• Collaborate with Quality Assurance, Manufacturing, and Clients to support analytical testing, batch release, and stability studies.
• Maintain compliance with cGMP, GLP, ICH, FDA, EMA, and other applicable regulatory requirements.
• Other duties as assigned.

Skills

HPLC

GMP/GLP

data analysis

Good documentation practices

analytical testing

troubleshooting

team collaboration

chemistry fundamentals

Education

Bachelor's degree in Chemistry

3+ years pharmaceutical analytical lab experience

GMP/GLP-regulated environment experience

Tools

HPLC

GC

KF

FTIR

XRD

DSC

TGA

NMR

ICP-MS

ICP-OES

PSD

pH meter

titration systems

Job description

Planet Pharma seeks an Associate Scientist, QC to perform analytical testing of raw materials, in-process samples, finished products, and stability samples in a cGMP-regulated lab. You will generate and review analytical data, support investigations, and ensure regulatory compliance.

The role requires a strong HPLC background, experience in GMP/GLP environments, and collaboration with QA, manufacturing, and clients.