Production Technician I - Clean Room Support 3rd Shift

Quva

Sugar Land (TX)

On-site

USD 52,000 - 68,000

Full time

7 hours ago
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Benefits offered by this job

Health benefits
401k plan
Paid time off

Job summary

QuVa Pharma in Sugar Land, TX, seeks a Production Technician I – Prep/Clean Room Support to join our 3rd shift. After training, you will assist in prep, cleanroom operations, formulations, ILP, and compounding in a GMP environment.

You will perform routine cleaning, maintain aseptic gowning qualification, document activities per GDPs, and manage chemicals FEFO. The role is safety sensitive and requires lifting up to 50 lbs and adherence to strict sterile operating procedures.

Qualifications

  • High School diploma or equivalent is required.
  • Background check will be conducted.
  • Able to lift up to 50 lbs. and stand/walk for long periods.
  • Comfortable using mobile devices (smartphones, tablets, handhelds).
  • Must be authorized to work in the United States full-time; visa sponsorship is not available.

Responsibilities

  • Support cleanrooms, formulations, ILP, and compounding.
  • Assist in preparation, transportation, labeling, production, and processing of materials.
  • Daily/weekly/monthly cleaning of rooms and equipment following standards.
  • Maintain Aseptic Gowning Qualification to support cleaning.
  • Document activities per GDPs for accountability and traceability.
  • Manage FEFO of chemicals and pull expired items monthly.
  • Document activities in accordance with procedures.
  • Perform sterile filter integrity testing as required.

Skills

Attention to detail
Team collaboration
Customer oriented
Safety conscious

Education

High School diploma or equivalent

Job 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 3rd shift, working Monday through Friday from 10:00 PM to 6:30 AM. 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
Our Most Successful Production Technicians I – Prep/Clean Room Support
  • 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
  • Set, full-time, consistent work schedule
  • 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 medicines and 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 BrightStream partners with health-systems to analyze large amounts of data and through AI and machine learning, develops software solutions 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.”

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