Production Technician I - ILP 3rd Shift

Quva • Sugar Land, TX

54d • Onsite

About The Position

The Production Technician I supports execution of product visual inspection, labeling, and packaging (ILP) operations at Quva’s Sugar Land facility, following established processes and procedures. After completing training, the technician helps ensure medications meet standards for safety, efficacy, and quality. This is a full-time, onsite third-shift role, Monday through Friday from 10:00 PM to 6:30 AM CST, with a set schedule and minimum overtime requirements. The position is safety-sensitive and may be subject to random drug testing in accordance with applicable laws.

Requirements

• High school diploma or GED from a recognized institution or organization.
• Pass a color perception exam.
• Pass a vision exam demonstrating 20/20 vision with or without correction.
• Successfully complete a drug and background check.
• Be at least 18 years of age.
• 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.
• Working knowledge of cGMPs, regulatory requirements, and applicable SOPs.
• Strong attention to detail, flexibility, and ability to adapt to support multiple production areas and shifts as needed.

Nice To Haves

• Pharmaceutical experience.
• Mechanical aptitude.

Responsibilities

• Assist with preparation of inspection and packaging room materials and supplies.
• Conduct labeling and process production materials as required, including primary, secondary, and tertiary product labeling.
• Perform secondary and final packaging of products.
• Visually inspect products.
• Clean rooms and equipment on daily, bi-weekly, and monthly schedules; 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 following Good Documentation Practices (GDPs), cGMPs, and company ISO standards.
• Comply with 503B guidelines, cGMPs, standard operating procedures, and company policies.
• Perform equipment calibration checks and troubleshoot production equipment as needed.
• Document activities in accordance with established procedures.
• 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.

Benefits

• Comprehensive health and wellness benefits, including medical, dental, and vision.
• 401(k) retirement program with company match.
• 17 paid days off plus 8 paid holidays per year.
• Occasional weekend and overtime opportunities with advance notice.
• Career advancement opportunities.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED