Pharmaceutical Manufacturing Technician I - 3rd Shift

Alcami Corporation•North Charleston, SC

3d•Onsite

About The Position

The Manufacturing Technician I assists with manufacturing drug products (parenteral or solid dosage) for commercial distribution and clinical trials. The role operates manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory requirements and current Good Manufacturing Practices (cGMPs). The technician uses appropriate techniques in manufacturing environments, including PPE gowning, and collaborates with other manufacturing areas as needed. This is a 100% on-site position on the third shift, Sunday through Thursday, 11:00 p.m. to 7:30 a.m. Occasional hours outside the scheduled shift may be needed based on business requirements, including weekend work. Domestic travel is up to 5%. For sterile liquids manufacturing, technologies and processes include equipment and component preparation and sterilization, compounding, aseptic filling, and capping. The work environment includes exposure to moving mechanical parts, fumes or airborne particles, and toxic or caustic chemicals. Appropriate personal protective equipment is required for specific duties; elevated work may require a body harness and lanyard. The employee may also be required to operate an industrial vehicle.

Requirements

High school diploma or GED.
At least 1 year of GMP and prior pharmaceutical work experience.
Excellent verbal and written communication and documentation skills.
Excellent attention to detail and organizational skills.
Problem-solving and basic troubleshooting ability.
Ability to perform basic math calculations.
Ability to read and understand detailed written instructions.
Ability to move materials throughout the facility using appropriate methods and equipment.
Basic computing proficiency.

Nice To Haves

Associate’s degree.
Awareness of or prior experience with cGMP practices and procedures.

Responsibilities

Follow applicable SOPs and cGMPs to perform assigned duties and tasks.
Complete required cGMP and other relevant company training in a timely manner and remain compliant.
Assist with manufacturing techniques and technologies according to SOPs and cGMPs.
Assist with manufacturing technologies and operation of manufacturing and material-handling equipment.
Document activities legibly and in real time on controlled documentation, according to SOPs and cGMPs.
Perform in-process testing, weight checks, component counting, and basic math calculations.
Clean rooms, tools, and equipment.
Assist other manufacturing areas as required.
Work occasional hours outside the scheduled shift based on business needs, which may include weekends.
Perform other duties as assigned.