R&D Intern

Job Summary:

We are seeking a motivated and detail-oriented R&D Intern to join our pharmaceutical manufacturing team in our Bridgewater, New Jersey location. The intern will support the Research & Development group in conducting both qualitative and quantitative studies, analyzing data, and contributing to innovative product and process development. This is a hands-on opportunity to gain valuable experience in a regulated environment while working alongside experienced scientists and engineers.

Key Responsibilities:

• Assist in the design and execution of qualitative and quantitative laboratory studies to support pharmaceutical development.
• Perform data analysis using appropriate statistical tools; evaluate and interpret experimental results to draw valid scientific conclusions.
• Maintain accurate and organized laboratory records and documentation in compliance with cGMP (Current Good Manufacturing Practices).
• Apply basic laboratory techniques and follow established protocols for sample preparation, testing, and analysis.
• Demonstrate working knowledge of pharmaceutical industry regulations, including FDA and ICH guidelines.
• Participate in team meetings, contribute to technical discussions, and prepare summaries or presentations of experimental findings.
• Follow all safety procedures and assist in maintaining a clean and compliant lab environment.

Qualifications:

• Currently pursuing a Bachelor’s in Pharmaceutical Sciences, Chemistry, Biochemistry, Chemical Engineering, or a related scientific discipline.
• Familiarity with laboratory techniques and basic instrumentation (e.g., HPLC, UV-Vis, dissolution testing, etc.).
• Strong understanding of cGMP requirements and regulatory standards in the pharmaceutical industry.
• Analytical mindset with attention to detail and a passion for scientific exploration.
• Proficiency in Microsoft Office and data analysis tools (e.g., Excel, GraphPad Prism, JMP, etc.).
• Excellent written and verbal communication skills.

What You'll Gain:

• Practical experience in a regulated pharmaceutical R&D environment.
• Exposure to real-world challenges in drug formulation and process development.
• Mentorship from industry professionals.
• Opportunities to contribute to ongoing research projects with potential real-world impact.

To perform this job successfully, an individual must be able to perform the essential job functions satisfactorily. PAI is an Equal Opportunity Employer. In compliance with the Americans with Disabilities Act, PAI will provide reasonable accommodations to qualified individuals with disabilities and encourages both prospective and current employees to discuss potential accommodations with the employer. PAI uses E-Verify.

PAI Pharma is a nicotine-free campus, meaning the use of nicotine products—including cigarettes, vaping, chewing tobacco, and any other nicotine-containing substances—is strictly prohibited on company property. All employees should be able to complete their full shift without the need to use nicotine. By joining PAI Pharma, you agree to adhere to our nicotine-free workplace policy, which supports a healthier environment for all employees.

EEO Employer / Veteran / Disabled