Pharmaceutical Manufacturing Technician - 2nd Shift

Alcami Corporation•Charleston, SC

4d•Onsite

About The Position

At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record. Are you interested in joining our team? Job Summary The Manufacturing Technician I is accountable for results in a fast-paced environment and assists with the manufacturing of drug products (parenteral or solid dosage) for commercial distribution and clinical trials. The Manufacturing Technician I assists with the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). The Manufacturing Technician I employ acceptable techniques while working in manufacturing environments, including PPE gowning. The Manufacturing Technician I works collaboratively to support other manufacturing areas as required. On-Site Expectations 100% on-site position. 2nd Shift: Monday - Friday, 3:00pm - 11:30pm. 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. Other duties as assigned. Manufacturing Technologies for Sterile Liquids: Equipment and component preparation and sterilization Compounding Aseptic filling Capping

Requirements

High school diploma or GED required.
1+ years of GMP and prior pharmaceutical work experience required.
Excellent verbal and written communication and documentation skills required.
Excellent detail orientation and organizational skills required.
Excellent problem-solving and basic trouble-shooting ability required.
Ability to perform basic math calculations.
Ability to read and comprehend detailed written instructions required.
Ability to move materials throughout the facility using appropriate methods and equipment required.
Proficiency in basic computing skills required.

Nice To Haves

Associate’s degree preferred.
Awareness of or prior experience with cGMP practices and procedures 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.
Other duties as assigned.
Manufacturing Technologies for Sterile Liquids: Equipment and component preparation and sterilization Compounding Aseptic filling Capping