Chemist

Job Title: Quality Control Chemist II

Location: Johns Creek GA Onsite
Duration: 12 months with potential for extension
Work Schedule: MondayFriday 8:00 AM5:00 PM (40 hours/week)
Interview Process: Two rounds Phone Interview and Panel Interview

Position Summary

We are seeking an experienced Quality Control Chemist II to support analytical chemistry activities within a regulated manufacturing environment. The successful candidate will be responsible for analytical method development validation and transfer instrument qualification laboratory troubleshooting and technical investigations.

This role will work closely with Quality Control Manufacturing Quality Assurance and other cross-functional teams to ensure analytical methods and laboratory systems remain compliant reliable and fit for intended use.

Key Responsibilities

• Develop optimize and improve analytical test methods to support laboratory and manufacturing requirements.
• Execute analytical method validations method transfers and periodic method reviews in accordance with applicable procedures and regulatory requirements.
• Support method transfers between internal sites and external suppliers.
• Perform compendial assessments and evaluate changes to applicable compendial requirements.
• Execute and support analytical instrument qualifications periodic validation reviews and instrument lifecycle activities.
• Lead and manage complex technical projects including developing project plans resolving technical challenges and making sound technical decisions.
• Provide technical troubleshooting and support for analytical instruments methods and laboratory processes.
• Support laboratory investigations deviations root-cause analysis and corrective and preventive actions (CAPA).
• Prepare and review technical documentation protocols reports and other quality-related records.
• Collaborate with cross-functional teams to ensure analytical activities are completed within established timelines and quality requirements.

Top 3 Must-Have Qualifications

1. Strong experience in analytical method development and validation
2. Hands-on experience with analytical instrument qualification
3. Industry experience in pharmaceutical medical device or other highly regulated environments

Basic Qualifications

• Bachelors degree in Chemistry or a related scientific field.
• Demonstrated experience with analytical method validation and instrument qualification.
• Strong computer skills including proficiency with Microsoft Office Suite.
• Excellent written and verbal communication skills.
• Strong analytical troubleshooting and problem-solving abilities.
• Ability to manage multiple priorities and work effectively in a cross-functional regulated environment.

Preferred Qualifications

• Masters or Ph.D. in Chemistry or a related scientific discipline.
• Experience with LabVantage LIMS or a similar Laboratory Information Management System (LIMS).
• Experience with Empower 3 or a similar chromatography/data acquisition system.
• Experience supporting laboratory investigations CAPA and analytical lifecycle management.
• Experience working in a GMP/GLP-regulated laboratory environment.

Qualifications :

1. Strong experience in analytical method development and validation
2. Hands-on experience with analytical instrument qualification
3. Industry experience in pharmaceutical medical device or other highly regulated environments

Additional Information :

All your information will be kept confidential according to EEO guidelines.

Remote Work :

No

Employment Type :

Full-time