Scientist Jobs

About The Position

Requirements

• Demonstrates foundational knowledge and basic understanding of pharmaceutical manufacturing processes.
• Demonstrates attention to detail and commitment to accuracy and quality.
• Demonstrates ownership and accountability for assigned tasks and minor decisions.
• Follows technical instructions and documentation.
• Demonstrates decision-making ability using basic problem-solving and structured logic.
• Proficiency in basic mathematics.
• Communicates clearly and effectively, both verbally and in writing.
• Basic computer skills (Word, Excel, documentation systems).
• Works effectively in a team environment.
• Accepts and seeks feedback and guidance to build technical and communication skill.
• Manages time and workload effectively to meet deadlines.

Nice To Haves

• Oral liquid manufacturing experience preferred.
• cGMP knowledge preferred.

Responsibilities

• Provides technical support as related to commercial manufacturing of oral liquid pharmaceutical drug products.
• Works under moderate supervision, demonstrating efficient, effective, and proficient ability to: Perform troubleshooting and investigating process and equipment-related issues, Perform optimizations of manufacturing processes and applicable procedures, Gather, analyze, and communicate outcomes of historical data to support investigations, Oversee exhibit and scale-up batch manufacturing, technology transfer, and equipment trials for commercial products, Lead the modification, enhancement, and qualification of new and existing processes, equipment, and procedures, Assist with execution of validation protocols and data collection, Execute generated protocols.
• Generate and review Manufacturing Batch Records (MBRs), Protocols/Reports, SOPs, and documentation to support submissions (Common Technical Document (CTD) sections with justifications).
• Provides knowledgeable support and effective communication to cross-functional teams (Validation, QA, QC, Engineering, Operations, RA, and Supply Chain).
• Design and deliver technical training for batch manufacturing and in-process sampling.
• Adheres to company policies, cGMP regulations, industry standards, SOPs/WIs, and supervisory directives.
• Supports safe and compliant pharmaceutical manufacturing processes.
• Performs additional responsibilities as assigned to support team and project objectives.