Our QC Sample 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 providing support and subject matter expertise within areas of the Quality Management System (QMS). This position is responsible for collecting samples for testing to ensure they conform to all applicable laws and company quality standards. Operates within the legal and regulatory compliance, producing a quality product. 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 QC Sample Technician Does Each Day
- The ability to learn and understand cGMP requirements
- Collect, inspect, and label QC Samples in accordance with procedures and production needs
- Review and verify critical batch record information related to the QC samples sections in the batch record
- Interact with other departments to assist in maintaining production flow following QC Sample collection and if supervision deemed necessary
- Assist in the submission and shipping of QC samples to internal and external laboratories on a daily basis
- Assist in the participation of process improvement projects within the company
Our Most Successful QC Sample Technicians
- Are attentive to all aspects of the system while working to monitor and solve routine activities/issues
- Work effectively in a team environment with great organization skills
- Demonstrate initiative and accountability in a fast-paced environment
- Have excellent verbal and written communication skills
- Maintain a mature problem-solving attitude while dealing with interpersonal conflict, complex environments, or time demands
- Work independently and follow good documentation practices
- Demonstrate leadership skills through example
- Start and persist with specific courses of action while exhibiting high motivation and a sense of urgency to exceed internal customer satisfaction
Minimum Requirements For This Role
- High school Diploma or GED required
- Able to successfully complete a drug and background check
- Familiarity with and comfortable using mobile devices such as smartphones, tablets, handhelds
- Able and willing to walk, stoop, stand, bend, and lift throughout each shift, with or without accommodation
- 18+ years of age
- Proficient in the use of office applications such as MS Word, Excel, PowerPoint
- 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
- Bachelor’s Degree in Business, Engineering, or related field
- Experience managing documents and records in a regulatory or controlled environment
- Knowledge in business computer applications (e.g., MasterControl, Documentum, SAP, LIMS, Track wise, etc.)
- 2 years’ experience in Quality Assurance / cGMP / FDA regulated industry
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 pharmacy services, including ready-to-administer sterile outsourcing and advanced AI-generated insights providing clarity for revenue capture and inventory management. QuVa Pharma delivers essential medications in injectable formats critical for effective patient care. LogicStream, a QuVa company, partners with health systems to aggregate, normalize, and analyze large amounts of complex data through AI and machine learning tools that generate actionable insights supporting revenue optimization, inventory management, and inventory-related workflows. Through QuVa’s integrated solutions, health systems can transform pharmacy management to achieve greater value by operating more efficiently and effectively as they deliver high-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.”
