Production Technician I - ILP 2nd Shift

Quva•Sugar Land, TX

2d•Onsite

About The Position

The Production Technician I – ILP supports product visual inspection, labeling, and packaging operations at Quva’s Sugar Land facility, following established processes and procedures. The role helps ensure medications meet standards for safety, efficacy, and quality. It is a full-time, onsite, second-shift position with a consistent Monday–Friday schedule from 1:00 PM to 9:30 PM CST and minimum overtime requirements. The position is safety-sensitive and may be subject to random drug testing in accordance with applicable laws. After completing training, the technician supports inspection and packaging operations, maintains rooms and equipment, completes production documentation, and follows applicable standard operating procedures, cGMPs, 503B guidelines, and company ISO standards. The technician may also assist other production areas as needed.

Requirements

High school diploma or GED from a recognized institution or organization.
Must pass a color perception exam.
Must pass a vision exam demonstrating 20/20 vision, with or without correction.
Must successfully complete a drug and background check.
Must be at least 18 years of age.
Must be currently authorized to work in the United States on a full-time basis; Quva will not sponsor applicants for work visas.
Strong verbal and written communication skills and ability to work effectively with other departments and people at all organizational levels.
Strong attention to detail and mechanical aptitude.
Working knowledge of cGMPs, regulatory requirements, and applicable SOPs.
Ability to follow policies and procedures and complete administrative tasks correctly and on time.
Ability to respond tactfully and respectfully, work well under pressure, accept responsibility, and follow through on commitments.
Ability to adapt and support multiple production areas and shifts as needed.

Nice To Haves

Pharmaceutical experience.

Responsibilities

Assist with preparing materials and supplies for inspection and packaging rooms.
Conduct labeling and process production materials as required, including primary, secondary, and tertiary labeling.
Perform secondary and final product packaging and visually inspect products.
Clean rooms and equipment on daily, bi-weekly, and monthly schedules, and complete applicable preventive maintenance forms and checklists in accordance with SOPs.
Conduct and complete line and room clearances according to established procedures.
Complete documentation for product accountability and traceability in accordance with Good Documentation Practices and established procedures.
Follow 503B guidelines, cGMPs, SOPs, company policies, and company ISO standards.
Perform equipment calibration checks and troubleshoot production equipment as needed.
Immediately notify production management of deviations from established processes or procedures.
Assist other areas as needed, including cleaning, non-sterile filling, kitting, and preparation operations.
Maintain an inspection-ready environment and support internal and external audits.