Manufacturing Pharmaceutical Technician

Katalyst CRO; Wilson (NC); Presencial; USD 42.000 - 62.000; Jornada completa

Descripción de la vacante

Katalyst CRO in Wilson, NC is seeking a Pharmaceutical Technician to efficiently clean, set up, and operate manufacturing equipment in the controlled production area, while adhering to cGMPs, SOPs, FDA and DEA guidelines.

You will follow Master Batch Records for oral solid dose production, prepare materials, perform in-process testing and weight checks, maintain accurate documentation, and participate in production team meetings; weekend/overtime work may be required.

Formación

• High School Diploma or equivalent.
• Up to three years pharmaceutical industry experience preferred.
• General ability to perform basic to complex mathematical computations and understanding of the Metric System.
• Preferred experience in oral solid dose (OSD) pharmaceutical manufacturing Granulation/Blending and Bead Coating operations.
• Familiarity with cGMPs, SOPs, FDA and DEA guidelines.

Responsabilidades

• Follow Master Batch Records for the manufacturing of controlled, oral solid dose (OSD) and other dosage forms when required.
• Prepare raw materials, blends, and bulk accountability throughout manufacturing processes.
• Performs weight checks for incoming and dispensed materials ensuring compliance with established procedures.
• Identify, report, and resolve quality issues.
• Safely set up, operate, and clean manufacturing equipment per batch records and SOPs.
• Perform in-process testing and inspections as required by Master Batch Record.
• Clean and sanitize manufacturing rooms including walls, floors, and ceilings per SOPs.
• Report accidents and unsafe conditions or unusual circumstances to supervisor.
• Complete accurate and timely documentation and follow good documentation practices in GMP.
• Actively participate in Production team and Site communication meetings.
• Maintain regular and punctual attendance; work overtime as required.
• Support GMP investigations and events.
• Identify and report potential GMP impacting situations.
• Contribute to SOP writing in your technical area.

Conocimientos

Mathematical calculations

Metric system understanding

Educación

High School Diploma or equivalent

Descripción del empleo

Job Description

The Pharmaceutical Technician will efficiently, effectively, and safely clean, set-up, and operate machinery in the manufacturing area while adhering to applicable cGMPs, SOPs, FDA, and DEA guidelines.

Job Description

The Pharmaceutical Technician will efficiently, effectively, and safely clean, set-up, and operate machinery in the manufacturing area while adhering to applicable cGMPs, SOPs, FDA, and DEA guidelines.

Primary Responsibilities

• Follow Master Batch Records for the manufacturing of controlled, oral solid dose (OSD) and other dosage forms when required.
• Prepare raw materials, blends, and bulk accountability throughout manufacturing processes.
• Performs weight checks for incoming and dispensed materials ensuring compliance with established procedures. Operates scales including set-up, verification, leveling and challenging.
• Identify, report, and resolve quality issues.
• Safely and in compliance with batch records and SOPs, set up, operate, and clean manufacturing equipment (oral solid dose manufacturing may include rotor sieves, granulators, blenders, coaters, encapsulators, compression machines, etc.).
• Perform in-process testing and inspections as required by Master Batch Record (weighing, tablet thickness, tablet hardness, friability, visual inspection, etc.).
• Clean and sanitize manufacturing rooms including walls, floors, and ceilings per SOPs.
• Report accidents and unsafe conditions or unusual circumstances to supervisor.
• Complete accurate and timely documentation. Follow good documentation practices in accordance with GMP.
• Actively participate in Production team and Site communication meetings.
• Maintain regular and punctual attendance; work overtime as required.
• Support GMP investigations and events.
• Identify and report potential GMP impacting situations.
• Contribute to Standard Operating Procedure (SOP) writing in your technical area.
• Education and Experience Requirements
• High School Diploma or equivalent.
• Up to three years pharmaceutical industry experience preferred or an equivalent combination of education, demonstrated mechanical skill, and experience in a similar industry.
• Necessary Knowledge, Skills, and Abilities
• General ability to perform basic to complex mathematical computations of addition, subtraction, multiplication, and division. Understanding of the Metric System of Measurement.
• Preferred experience in oral solid dose (OSD) pharmaceutical manufacturing Granulation/Blending and Bead Coating operations.