Qc Sample Technician 3Rd Shift

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 3rd Shift, working Monday through Friday from 10:00 PM to 6:30 PM. This is a set, consistent schedule with minimum overtime requirements and based on site in our Sugar Land 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 Pharma is a national, industry-leading, FDA registered 503B outsourcing services company that provides hospitals with essential medications in ready-to-administer injectable formats that are critical for effective patient care. We are leading the way with unmatched expertise in current Good Manufacturing Practices and sterile pharmaceutical manufacturing, and the highest quality and safety standards so hospitals can more confidently and reliably focus on patient care nationwide. As a leader in sterile compounding, we continue to invest in automation and integrated technologies to improve our production processes, safety, consistency, and product quality.
As part of our team, you'll experience being at the forefront of groundbreaking solutions, collaborating with brilliant minds, and making a tangible impact in healthcare delivery.
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."