Summary:

This role supports the timely and accurate investigation and documentation of operational events in an Oral Solid Dosage (OSD) manufacturing environment, specifically involving tablets and capsules

Key Responsibilities:

• Conduct thorough investigations of events occurring in OSD operations.
• Document findings clearly and accurately in accordance with regulatory and internal standards.
• Collaborate with cross-functional teams to gather relevant data and insights.
• Ensure all documentation is completed within required timelines to avoid delays.
• Observe equipment and processes directly to support investigation accuracy.

Qualifications:

• Bachelor’s degree in a scientific discipline (e.g., Chemistry, Biology, Microbiology).
• 3-5 years of relevant experience in pharmaceutical manufacturing or quality documentation.
• Proven ability to manage documentation workflows under tight deadlines.
• Strong analytical and communication skills.
• Experience working in OSD environments is highly preferred.

Work Methodology:

• 100% On-site 
• 2-3 months (1st Contract)
• Administrative Shift. Weekends and overtime may also be required.
• Professional Service Contract