Production Technician I - ILP 2nd Shift

Quva • Sugar Land, TX

2d • Onsite

About The Position

The Production Technician I – ILP supports 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. This is a full-time, onsite, second-shift role with a set Monday–Friday schedule from 1:00 PM to 9:30 PM CST, minimum overtime requirements, and possible occasional weekend or overtime opportunities with advance notice. 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 required color perception exam.
• Pass a required 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 full-time in the United States; Quva will not sponsor work visas.
• Strong verbal and written communication skills and ability to work effectively with other departments and people at all levels.
• Working knowledge of cGMPs, regulatory requirements, and applicable SOPs.
• Strong attention to detail; ability to follow policies and procedures and complete administrative tasks correctly and on time.
• Ability to adapt and support multiple production areas and shifts as needed.
• Ability to work effectively with others, listen to internal customers, meet commitments, and respond tactfully and respectfully under pressure.

Nice To Haves

• Pharmaceutical experience.
• Mechanical aptitude.

Responsibilities

• Assist with preparing materials and supplies for inspection and packaging rooms.
• Label and process production materials as required, including primary, secondary, and tertiary product labeling.
• Perform secondary and final product packaging and visually inspect products.
• Clean rooms and equipment daily, bi-weekly, or monthly; 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; 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 and promptly 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.
• Set, full-time, consistent work schedule.
• Occasional weekend and overtime opportunities with advance notice.
• Career advancement opportunities at a national, industry-leading high-growth company.

What This Job Offers

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