Pharma Granulation & Coating Operator – 1st Shift

Linked Professional Services; Piscataway Township (NJ); Presencial; USD 55.000 - 75.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Medical Insurance

Vision Insurance

401(k)

Descripción de la vacante

Linked, LLC is seeking an experienced Pharmaceutical Production Operator for Granulation, Compression, and Coating operations in a fast-paced, regulated environment. This role requires solid oral dosage manufacturing experience and strict adherence to cGMP standards.

You will operate and monitor equipment, follow BMRs and SOPs, document production activity, and collaborate with QA and maintenance. Overtime and Saturdays may be required.

Formación

• 3–5+ years of hands-on pharmaceutical manufacturing experience.
• Direct experience in solid oral dosage production essential.
• Experience with Granulation, Compression, and Coating equipment.
• Familiar with cGMP, SOPs, and BMRs.
• Ability to work overtime and Saturdays if needed.

Responsabilidades

• Operate, monitor, set up, and clean Granulation, Compression, and Coating equipment.
• Perform daily manufacturing operations per cGMP and SOPs.
• Follow Batch Manufacturing Records (BMRs) to ensure accuracy.
• Monitor equipment performance and maintain product quality.
• Identify deviations, document issues, and report promptly.
• Perform line clearance, cleaning, and changeover between batches.
• Maintain accurate production documentation and records.
• Adhere to FDA regulations and safety standards.
• Collaborate with production, QA, and maintenance teams.
• Maintain a clean, compliant production environment.

Conocimientos

Granulation

Compression

Coating

Solid dosage

cGMP

SOPs

BMRs

FDA regulations

Quality documentation

Team collaboration

Descripción del empleo

Linked, LLC is seeking an experienced Pharmaceutical Production Operator for Granulation, Compression, and Coating operations in a fast-paced, regulated environment. This role requires solid oral dosage manufacturing experience and strict adherence to cGMP standards.

You will operate and monitor equipment, follow BMRs and SOPs, document production activity, and collaborate with QA and maintenance. Overtime and Saturdays may be required.