Production Technician I - ILP 1st Shift

Quva • Sugar Land, TX

4d • 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. After completing training, the technician helps ensure medications meet safety, efficacy, and quality standards while supporting a mission-driven organization focused on access to affordable medication and data insights.

This is a full-time, onsite position on a set first-shift schedule, Monday through Friday from 6:00 AM to 2:30 PM CST. Minimum overtime requirements apply. 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 old.
• 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.
• Attention to detail and ability to follow policies, procedures, and applicable SOPs.
• Working knowledge of cGMPs and regulatory requirements.
• Ability to complete administrative tasks correctly and on time.
• Ability to adapt and support multiple production areas and shifts as needed.

Nice To Haves

• Pharmaceutical experience.
• Mechanical aptitude.

Responsibilities

• Prepare inspection and packaging room materials and supplies.
• Perform labeling and process production materials as required, including primary, secondary, and tertiary labeling.
• Perform secondary and final product packaging.
• Visually inspect products.
• Clean rooms and equipment daily, bi-weekly, and monthly, and complete related preventative maintenance forms and checklists according to SOPs.
• Conduct and complete line and room clearances according to established procedures.
• Complete product accountability and traceability documentation using Good Documentation Practices (GDPs), and comply with 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 according to 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 coverage.
• 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.
• Future career advancement opportunities.

What This Job Offers

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