Production Technician I - Clean Room Support 2nd Shift

Quva • Sugar Land, TX

11d • Onsite

About The Position

The Production Technician I – Prep/Cleanroom Support Technician supports preparation and cleanroom operations at QuVa Pharma, following established processes and procedures to maintain the safety, efficacy, and quality of pharmaceutical products. After completing training, the technician assists with cleanroom, formulation, ILP, and compounding activities, as well as preparation, transportation, labeling, production, and processing of materials. The role also includes cleaning rooms and equipment, maintaining required aseptic gowning qualifications, completing traceability documentation, managing chemical inventory, and conducting sterile filter integrity testing as required.

This is a full-time, on-site role at QuVa Pharma’s Sugar Land, Texas location, working a consistent second-shift schedule Monday through Friday, 2:00 PM to 10:30 PM. Minimum overtime requirements apply; occasional weekend and overtime opportunities may be available with advance notice. This is a safety-sensitive position and may be subject to random drug testing in accordance with applicable laws.

QuVa is a national provider of compounded injectable medicines and software solutions for hospital and health-system pharmacy. The company states that it is an equal opportunity employer and maintains an at-will employment relationship.

Requirements

• High school diploma or equivalent.
• Successfully complete a background check.
• Able and willing to walk, stoop, stand, bend, and lift up to 50 lbs. throughout each shift, with or without reasonable accommodation.
• Familiarity with and comfort using mobile devices such as smartphones, tablets, and handhelds.
• Able and willing to follow strict clothing and accessory rules to support a sterile operating environment.
• At least 18 years of age.
• Currently authorized to work in the United States on a full-time basis; QuVa will not sponsor applicants for work visas.
• Promote active listening and collaboration with team members.
• Engage effectively and productively with others and establish trust, credibility, and confidence.
• Be customer oriented.
• Take initiative to identify problems and opportunities.

Nice To Haves

• Experience in a role requiring repetitive tasks.
• Experience in a pharmaceutical manufacturing environment.
• Experience with Good Documentation Practices (GDPs).
• One year of pharmaceutical manufacturing experience.
• CPhT Certification.
• ACPE Sterile Certification.

Responsibilities

• Support cleanrooms, formulations, ILP, and compounding.
• Assist with the preparation, transportation, labeling, production, and processing of materials.
• Clean rooms and equipment daily, weekly, and monthly in accordance with applicable standards.
• Maintain Aseptic Gowning Qualification to support cleaning activities.
• Complete required documents to support product accountability and traceability, following Good Documentation Practices (GDPs).
• Manage FEFO of chemicals and remove expired chemicals monthly.
• Document activities in accordance with established procedures.
• Perform sterile filter integrity testing as required.

Benefits

• Comprehensive health and wellness benefits, including medical, dental, and vision.
• 401k 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