Pharma Manufacturing Tech I - Sterile Liquids (2nd Shift)

Alcami Corporation; North Charleston (SC); Sur place; USD 25 000 - 36 000; Plein temps

Résumé du poste

Alcami Corporation is seeking a Manufacturing Technician I to support parenteral or solid dosage product manufacturing in a fast-paced, GMP-regulated environment. You will follow SOPs, batch records, and operate manufacturing equipment while wearing PPE.

This on-site, second-shift role requires a high school diploma (associate degree preferred) and 1+ year GMP/pharma experience. You will perform in-process tests, document results, and assist multiple manufacturing areas.

Qualifications

• High school diploma or GED required; Associate’s degree preferred.
• 1+ years of GMP and prior pharmaceutical work experience required.
• Excellent communication and documentation skills.
• Ability to perform basic math calculations.

Responsabilités

• Follows applicable SOPs and cGMPs to perform assigned duties and tasks.
• Ensures timely completion and compliance with cGMP and training requirements.
• Assists with manufacturing techniques and operation of equipment per SOPs.
• Documents activities in real time on controlled documentation per SOPs.
• Performs in-process testing, weight checks, component counting and basic math.
• Performs cleaning of rooms, tools and equipment.
• Assists with other manufacturing areas as required.
• Occasional weekend work may be required.

Connaissances

Communication skills

Attention to detail

Problem solving

Basic math

Computer skills

Formation

High school diploma or GED

Associate’s degree preferred

Description du poste

Alcami Corporation is seeking a Manufacturing Technician I to support parenteral or solid dosage product manufacturing in a fast-paced, GMP-regulated environment. You will follow SOPs, batch records, and operate manufacturing equipment while wearing PPE.

This on-site, second-shift role requires a high school diploma (associate degree preferred) and 1+ year GMP/pharma experience. You will perform in-process tests, document results, and assist multiple manufacturing areas.