We are seeking a skilled QC/Lab Deviation Investigator to assist with a backlog of OOS-related deviations in a fast-paced pharmaceutical production environment. The ideal candidate will have a strong background in quality control, chemistry, and raw materials, and will provide investigation support for deviations from open to close.

Key Responsibilities:

• Manage and investigate deviations related to quality control (QC), chemistry, raw materials, and stability processes.
• Provide writing support to document investigations thoroughly, including root cause analysis, corrective actions, and follow-ups.
• Assist the team in closing out the backlog of deviations, helping to meet production deadlines during peak production season.
• Collaborate with other team members to ensure timely resolution of deviations and compliance with industry standards.

Required Skills:

• Strong experience in deviations and investigations.
• Excellent writing skills to document investigations clearly and effectively.
• Proficiency in QC, chemistry, raw materials, and stability.
• Ability to work independently and efficiently to resolve issues.

Experience:

• 5-6 years of experience in the pharmaceutical industry.