Junior Formulation & GMP Manufacturing Chemist

Aptar Italia S.P.A.; Boonton (NJ); On-site; USD 61,000 - 83,000; Full time

Job summary

Aptar Pharma in New Jersey seeks a Formulation & Manufacturing Chemist I to support early-phase development and cGMP manufacturing of orally inhaled and nasal drug products. You will mix formulations, perform line setup, and ensure thorough documentation while collaborating with R&D, Engineering, and Quality teams.

This role requires strong attention to detail, lab discipline, and willingness to learn GMP practices in a fast-paced production environment.

Qualifications

• Bachelor of Science in Chemistry, Biology, Biochemistry, or Engineering.
• 0–5 years of relevant experience (laboratory, manufacturing, or engineering).
• GMP experience preferred but not required; willingness to learn GMP.

Responsibilities

• Execute GMP manufacturing activities (formulation preparation, device filling, assembly).
• Perform line setup, in-process checks, and equipment cleaning per SOPs.
• Document all activities in batch records with high accuracy.
• Maintain compliance with cGMP, data integrity, and safety requirements.
• Support cleanroom operations and material control.
• Prepare and evaluate lab-scale formulations.
• Design and execute controlled formulation experiments.
• Document procedures, observations, and results with precision.
• Troubleshoot formulation and process issues.
• Support scale-up of lab processes into GMP manufacturing.
• Collaborate with R&D, Engineering, and Quality teams.
• Support technology transfer and clinical supply production.
• Escalate deviations and inconsistencies in a structured manner.

Skills

Attention to detail

Documentation accuracy

Formulation execution

Troubleshooting

Lab equipment operation

Team communication

Process equipment understanding

Hands-on problem solving

Education

BS in Chemistry, Biology, Biochemistry, or Engineering

Job description

Aptar Pharma in New Jersey seeks a Formulation & Manufacturing Chemist I to support early-phase development and cGMP manufacturing of orally inhaled and nasal drug products. You will mix formulations, perform line setup, and ensure thorough documentation while collaborating with R&D, Engineering, and Quality teams.

This role requires strong attention to detail, lab discipline, and willingness to learn GMP practices in a fast-paced production environment.