GMP Manufacturing Technician - Sterile Fill & Assembly

Alcami Corporation; South Carolina; On-site; USD 42,000 - 54,000; Full time

Job summary

Alcami Corporation in South Carolina is seeking a Manufacturing Technician I to support the production of drug products in a fast-paced, cGMP environment. The role requires following SOPs, batch records, and PPE gowning to ensure quality and regulatory compliance.

On-site 1st shift, Monday through Friday, with occasional weekend work as business needs dictate. Responsibilities include performing in-process testing, documentation, and assisting with equipment operation and maintenance.

Qualifications

• High school diploma or GED required; Associate’s degree preferred.
• 1+ years of GMP and prior pharmaceutical work experience required.

Responsibilities

• Follows applicable SOPs and cGMPs to perform assigned duties and tasks.
• Ensures timely completion and compliance with cGMP and all other relevant company training requirements.
• Assists with applicable manufacturing techniques and technologies per SOPs and cGMPs.
• Assists with manufacturing technologies and operation of manufacturing and material handling equipment.
• Documents activities in real time on controlled documentation and legibly, per SOPs and cGMPs.
• Performs in-process testing, weight checks, component counting and basic math calculations.
• Performs cleaning of rooms, tools and equipment.
• Assists with other manufacturing areas as required.
• Works occasional hours outside of scheduled shift based on business needs, which may include weekend work.
• Other duties as assigned.

Skills

Verbal and written communication

Documentation skills

Detail orientation

Organizational skills

Problem-solving

Basic math calculations

Reading comprehension

Computing basics

Education

High school diploma or GED

Associate’s degree preferred

Job description

Alcami Corporation in South Carolina is seeking a Manufacturing Technician I to support the production of drug products in a fast-paced, cGMP environment. The role requires following SOPs, batch records, and PPE gowning to ensure quality and regulatory compliance.

On-site 1st shift, Monday through Friday, with occasional weekend work as business needs dictate. Responsibilities include performing in-process testing, documentation, and assisting with equipment operation and maintenance.