Associate Scientist

About the Role

Join us as an Associate Scientist at Thermo Fisher Scientific, contributing to meaningful work that makes a positive impact globally. You will be part of the Synthetic Molecule Pharmaceutics (SMP) team, responsible for delivering clinical supplies and developing robust, scalable manufacturing processes for quality products.

Key Responsibilities

• Powder Processing: Conduct hands-on powder handling operations for solid dosage form development, including weighing, sieving, blending, granulation, milling, powder compaction, and film coating using bench-scale and at-scale equipment.
• In-Process Testing & Characterization: Perform routine assessments of powder and compact properties, such as flowability, density, mechanical characterization, disintegration testing, and other relevant characterizations.
• Drug Product Manufacturing: Execute manufacturing operations for solid oral dosage forms (tablets and capsules) following Batch Records and SOPs.
• Documentation: Maintain accurate, real-time documentation in Electronic Lab Notebooks (ELNs), batch records, and other data management systems.
• Data Analysis: Process and analyze data using tools such as Excel, statistical software, or Python scripts.
• Safety & Compliance: Adhere to laboratory safety protocols, equipment handling procedures, and SOPs.

Requirements & Tech Stack

• Microsoft Office suite (including Excel, Word, and PowerPoint)
• Python scripts (advantageous)
• Excel spreadsheets

Qualifications

• Bachelor's degree or equivalent in Chemical Engineering, Mechanical Engineering, Materials Science, Pharmaceutical Sciences, or a related field.
• Previous experience equivalent to 0-1 years providing the necessary knowledge, skills, and abilities.
• Demonstrated proficiency in following complex experimental protocols and batch records without deviation.
• Knowledge and hands-on experience in powder processing, handling, and characterization is highly desired.
• Strong background in applied mathematics and core engineering principles is advantageous.
• Excellent organizational skills and time management abilities.
• Clear written and verbal communication skills.
• Ability to thrive in collaborative, fast-paced settings.

Preferred Qualifications

• Hands-on experience with solid dosage form development and powder characterization.
• Solid mathematical and engineering background.
• Prior hands-on experience in a 100% lab-based operational environment.

Working Conditions and Environment

• Laboratory and/or clinical environment.
• Exposure to electrical office equipment.
• Occasional drives to site locations, occasional domestic travel.
• Exposure to biological fluids with potential for infectious organisms.
• Rare exposure to skin and lung irritants, radiation, toxic materials, and hazardous waste.
• Personal protective equipment required (e.g., protective eyewear, garments, gloves).
• Exposure to fluctuating and/or extreme temperatures on rare occasions.

Physical Requirements

• Ability to work in an upright and/or stationary position for 6-8 hours per day.
• Repetitive hand movement of both hands.
• Occasional mobility.
• Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
• Light to moderate lifting and carrying (up to 15-20 lbs).
• Ability to access and use various computer software.
• Ability to communicate and understand information.
• Frequent interaction with diverse groups.
• Ability to work independently with little guidance and plan work schedules.
• Ability to perform under stress and multi-task.
• Regular and consistent attendance.