Pharmaceutical Manufacturing Technician — 3rd Shift

Pfizer Inc; McPherson (KS); Presencial; USD 26 000 - 44 000; Tempo integral

Resumo da oferta

Pfizer is seeking dedicated manufacturing staff in McPherson, Kansas, to support the preparation and operation of components, materials, equipment and processes essential to producing medicines for patients.

The role focuses on accurate documentation, room setup, sanitation and strict adherence to cGMPs, batch records, SOPs and related quality controls. You will work rotating shifts, with potential overtime while collaborating closely with cross-functional teams.

Qualificações

• High School Diploma or GED with 1+ year of experience.
• Self-motivated problem solver able to work effectively both independently and as part of a team.
• Ability to communicate effectively across departments and follow written and verbal instructions.
• Competence in troubleshooting and performing quality checks
• Demonstrated ability to follow established procedures and guidelines
• Analytical, detail-oriented problem solver with strong organizational skills

Responsabilidades

• Maintain batch records, check sheets, logbooks.
• Perform fill room setup and room/equipment sanitation.
• Ensures environmental excursions are kept at an acceptable level.
• Stay current with training requirements and follow SOPs, cGMPs, batch records, TCPs, BOMs and POPs.
• Communicates openly and clearly with line personnel and supervision to accomplish manufacturing goals.
• Promote a positive team environment.
• Notifies Group Leader/Supervisor of all safety issues.

Conhecimentos

Self-motivated

Teamwork

Communication

Troubleshooting

Quality checks

Follow procedures

Analytical thinking

Organizational skills

Formação académica

High School Diploma or GED

Descrição da oferta de emprego

Pfizer is seeking dedicated manufacturing staff in McPherson, Kansas, to support the preparation and operation of components, materials, equipment and processes essential to producing medicines for patients.

The role focuses on accurate documentation, room setup, sanitation and strict adherence to cGMPs, batch records, SOPs and related quality controls. You will work rotating shifts, with potential overtime while collaborating closely with cross-functional teams.