Qualifications

• Bachelor's degree in Chemistry or related field.
• 2+ years of supervisory experience in a pharmaceutical QC lab.
• Experience with Empower 3, HPLC, GC, and wet chemistry techniques.
• Knowledge of cGMP, ICH, CFR, and USP requirements.
• Background in method development, validation, and stability testing.
• Strong leadership and coaching abilities.
• Excellent problem-solving and communication skills.

Responsibilities

• Supervise and lead a team of QC chemists and analysts.
• Oversee all analytical testing for manufacturing, release, and stability.
• Review and interpret data from HPLC, GC, and wet chemistry in cGMP compliance.
• Author and review SOPs, analytical methods, and validation protocols.
• Conduct and support laboratory investigations and CAPA activities.
• Manage lab workloads to meet production timelines.
• Ensure lab safety and adherence to FDA and ICH guidelines.
• Collaborate cross-functionally to resolve quality-related issues.
• Develop and mentor QC staff while supporting continuous improvement initiatives.

Benefits

• Opportunity to lead a dedicated QC team.
• Hands-on involvement in technical operations.
• Focus on compliance and quality assurance in a regulated environment.
• Professional development through training and mentoring.
• Engagement in continuous improvement initiatives.