Formulation GMP Manufacturing Associate

Automatic Data Processing, Inc.; Aguadilla (PR); On-site; USD 25,000 - 39,000; Full time

Job summary

OcyonBio in Aguadilla, PR, is seeking a Manufacturing Associate – Formulation at levels I, II, III, or Senior to support startup manufacturing activities, including preparation, formulation, mixing, filtration, and transfer of sterile products.

The role requires strict adherence to cGMP, meticulous documentation, and the ability to work in cleanroom environments while collaborating with Manufacturing, Quality, Engineering, and Facilities to ensure readiness and continuous improvement.

Qualifications

• High school diploma or equivalent required; an associate or bachelor's degree in a related field is preferred.
• Previous experience in pharmaceutical manufacturing or regulated production environment is preferred.
• Entry-level candidates may be considered for Manufacturing Associate I positions.
• Placement at higher levels depends on experience and competencies.

Responsibilities

• Execute routine formulation operations including dispensing, solution preparation, mixing, filtration, and bulk transfer per SOPs and batch records.
• Prepare, weigh, dispense, and verify raw materials and drug substances for formulation activities.
• Operate and monitor formulation equipment such as mixing vessels, single-use systems, pumps, and filtration assemblies.
• Set up, clean, and changeover formulation equipment and related systems.
• Document batch records, equipment logs, and GDP-compliant paperwork accurately.

Skills

Pharmaceutical manufacturing

cGMP compliance

Formulation processes

Equipment operation

GDP documentation

Education

High school diploma or equivalent

Job description

OcyonBio in Aguadilla, PR, is seeking a Manufacturing Associate – Formulation at levels I, II, III, or Senior to support startup manufacturing activities, including preparation, formulation, mixing, filtration, and transfer of sterile products.

The role requires strict adherence to cGMP, meticulous documentation, and the ability to work in cleanroom environments while collaborating with Manufacturing, Quality, Engineering, and Facilities to ensure readiness and continuous improvement.