Sterile Pharma Manufacturing Operator - 3rd Shift

Alcami Corporation; Charleston (SC); On-site; USD 45,000 - 60,000; Full time

Job summary

Alcami Corporation is seeking a Manufacturing Technician I to support commercial and clinical production in a fast-paced pharmaceutical environment. You will follow SOPs and cGMPs, operate manufacturing equipment, document activity in real time, and assist multiple manufacturing areas as needed.

The role requires basic high school education with GMP experience and may include weekend hours; 3rd shift Sunday to Thursday, 11:00pm–7:30am, on-site only.

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 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.
• Manufacturing Technologies for Sterile Liquids: Equipment and component preparation and sterilization; Compounding; Aseptic filling; Capping

Skills

Verbal communication

Written communication

Detail oriented

Problem solving

Basic math

Reading comprehension

Material handling

Computing basics

cGMP awareness

Education

High school diploma or GED

Associate’s degree

Job description

Alcami Corporation is seeking a Manufacturing Technician I to support commercial and clinical production in a fast-paced pharmaceutical environment. You will follow SOPs and cGMPs, operate manufacturing equipment, document activity in real time, and assist multiple manufacturing areas as needed.

The role requires basic high school education with GMP experience and may include weekend hours; 3rd shift Sunday to Thursday, 11:00pm–7:30am, on-site only.