Visual Inspection Technician I - 2nd Shift

Alcami Corporation•Charleston, SC

6d•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 Visual Inspection Technician I is accountable for results in a fast-paced environment and responsible to perform tasks for the quality inspection of sterile injectable products for commercial distribution and clinical trials. The Visual Inspection Technician handles and inspects manufactured products by following standard operation procedures (SOPs) and batch records in accordance with current Good Manufacturing Practices (cGMPs). In addition, the Visual Inspection Technician employs acceptable techniques while working in manufacturing environments, including PPE gowning. On-Site Expectations 100% on-site position. 2nd Shift: Monday - Friday, 2:00pm - 10:30pm.

Requirements

High school diploma or GED required.
Entry level, 1+ years of relevant work experience strongly preferred.
Relevant work experience in roles with visual inspection in regulated environments (i.e. medical field, electronics, aerospace, automotive production) are applicable.
20/20 correctable near-sighted vision in both eyes, tested annually required.
Ability to see and distinguish colors required.
Ability to perform basic math calculations, including product accountability calculations and rounding required.
Ability to read and comprehend detailed written instructions required.
Ability to move materials throughout the facility using appropriate methods and equipment required.
Excellent verbal and written communication, documentation, detail orientation and organizational skills required.
Proficiency in basic computing skills required.

Nice To Haves

Associate degree preferred.
cGMP or prior work experience in a regulated environment preferred.
Prior pharmaceutical or CDMO experience 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.
Conducts visual inspection of sterile liquids in accordance with regulatory agency guidelines.
Visually identifies debris, air lines, and other defects in sterile liquids.
Documents activities in real time on controlled documentation and legibly, per SOPs and cGMPs.
Performs component counting and basic math calculations.
Performs cleaning of rooms, tools, and equipment.
Performs specific visual inspections per SOPs.
Ensures product meets appearance specifications before sending the product for packaging.
Performs bulk packaging for product vials for shipment to another facility.
Operates material handling equipment.
Other duties as assigned.