Senior GMP Manufacturing Technician (Parenteral)

Alcami Corporation; South Carolina; On-site; USD 60,000 - 80,000; Full time

Job summary

Alcami Corporation in Charleston, SC is seeking a Senior Manufacturing Technician to support sterile liquids and solid dosage production for commercial distribution and clinical trials. You will follow SOPs and cGMPs, operate manufacturing equipment, and document activities in real time.

This 3rd shift role (Sunday–Thursday, 11:00pm–7:30am) is on-site and requires high school diploma or GED, 5+ years GMP/pharma experience, and strong attention to detail.

Qualifications

• High school diploma or GED; associate degree preferred.
• 5+ years of GMP and pharmaceutical experience.
• Awareness of or prior experience with cGMP practices preferred.

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

GMP experience

cGMP knowledge

Documentation skills

Attention to detail

Basic math skills

Reading SOPs

Computing skills

Education

High school diploma or GED

Associate's degree or technical certification

Job description

Alcami Corporation in Charleston, SC is seeking a Senior Manufacturing Technician to support sterile liquids and solid dosage production for commercial distribution and clinical trials. You will follow SOPs and cGMPs, operate manufacturing equipment, and document activities in real time.

This 3rd shift role (Sunday–Thursday, 11:00pm–7:30am) is on-site and requires high school diploma or GED, 5+ years GMP/pharma experience, and strong attention to detail.