Production Technician I - Clean Room Support 2nd Shift

Quva-Pharma; Sugar Land (TX); On-site; USD 42,000 - 64,000; Full time

Benefits offered by this job

Health benefits

401k retirement program

Paid time off

Overtime opportunities

Career advancement

Job summary

Quva Pharma in Sugar Land, TX is seeking a Production Technician I – Prep/Clean Room Support for the 2nd shift, 2:00 PM–10:30 PM. You will support cleanrooms, formulations, ILP, and compounding while ensuring GDP compliance and aseptic practices to help deliver safe, high-quality injectable medicines across the US.

This on-site role requires a high school diploma, ability to lift 50 lbs, and training, with potential overtime.

Qualifications

• High School diploma or equivalent required.
• Able to lift up to 50 lbs. and stand for long periods.
• Familiarity with mobile devices and sterile environment rules.

Responsibilities

• Support cleanrooms, formulations, ILP, and compounding.
• Assist in preparation, labeling, production, and processing of materials.
• Daily/weekly/monthly cleaning of rooms and equipment per standards.
• Maintain aseptic gowning qualification to support cleaning.
• Document activities per GDPs and established procedures.
• Manage FEFO of chemicals and remove expired items monthly.

Skills

Attention to detail

Team collaboration

Customer oriented

Initiative

Education

High School diploma or equivalent

Job description

Production Technician I - Clean Room Support 2nd Shift

Job Category : 6000-Manufacturing

Requisition Number : PRODU006074

• Full-Time
• On-site

Locations

Showing 1 location

TX - Sugar Land 1075 1075 W Park One Dr #100 Sugar Land, TX 77478, USA

Description

Our Production Technician I – Prep/Cleanroom Support Technician plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, your responsibilities will include assisting in Prep/Cleanroom operations at QuVa Pharma in accordance with established processes and procedures. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US.

This is a full-time role for our 2nd shift, working Monday through Friday from 2:00 PM to 10:30 PM. This is a set, consistent schedule with minimum overtime requirements and based on site in our Sugar Land, TX location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws.

What the Production Technician I – Prep/Clean Room Support Does Each Day:

• Support cleanrooms, formulations, ILP, and compounding
• Assist in preparation, transportation, labeling, production, and processing of materials
• Daily/weekly/monthly cleaning of rooms and equipment while adhering to standards
• Maintain Aseptic Gowning Qualification to support cleaning
• Complete necessary documents for accountability and traceability of product following Good Documentation Practices (GDPs)
• Manage FEFO of chemicals, pulling expired ones monthly
• Complete documentation of activities in accordance with established procedures
• Perform sterile filter integrity testing as required
• Promote active listening with team members and enjoys collaboration
• Effectively and productively engages with others and establishes trust, credibility, and confidence with others
• Are Customer Oriented
• Take initiative to identify problems and opportunities

Minimum Requirements for this Role:

A High School diploma or equivalent

Able to 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 comfortable using mobile devices such as smartphones, tablets, handhelds

Able and willing to follow strict clothing and accessory rules to support our sterile operating environment

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

Any of the Following Will Give You an Edge:

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

Benefits of Working at Quva:

• 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
• National, industry-leading high growth company with future career advancement opportunities

About Quva:

Quva is a national, industry-leading provider of compounded injectable medicinesand software solutions that help power the business of hospital and health-system pharmacy. Quva Pharma produces and distributes injectable medicines required by health care providers and critical to patient care. Quva BrightStreampartners with health-systems to analyze large amounts of data and through AI and machine learning,develops softwaresolutions that turns the data into insights that are used to better run their pharmacy operation. Quva’s overall product and technology offerings help health-systems achieve greater value and deliver the highest-quality patient care.

Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is “at will.”

Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.For further information, please review the Know Your Rights notice from the Department of Labor.