Our Lot Disposition Specialist 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 performing review activities of finished good products to ensure compliance with applicable SOPs and regulatory requirements are adhered to prior to final release of 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 - 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 Lot Disposition Specialist Does Each Day
- Reviews completed Batch Records for compliance to Regulatory and QuVa SOPs and to ensure product quality and safety standards are met
- Promptly communicates with Operations and Manufacturing Quality Assurance regarding batch record discrepancies, product issues/variances
- Escalates procedural deviations or discrepancies that have product impact to the Quality Investigations Team for review
- Reviews Variances associated with batch records for impact to the product disposition.
- Reviews QC testing results, and EMPM monitoring data, are within specifications
- Enters QC testing results into Management System to generate product Certificate of Analysis (COA)
Our Most Successful Lot Disposition Specialist
- Works to create an environment of open communication, participation, and information-sharing within and between teams within Quality Assurance and throughout facility
- Works closely with the department supervisor to ensure alignment on day-to-day priorities
- Has knowledge of sterile pharmaceutical manufacturing technologies and FDA and other applicable GMP regulations for Sterile Product
- Is detail-oriented with strong verbal and written communications skills
- Supports the development of a climate of quality and safety within the teams, by identifying and monitoring quality and safety standards
- Drives achievement, expresses energy, shows accountability, ability to multi-task and work in a fast-paced, quality-rich environment
- Motivates others, shares knowledge, builds high performing team, shows respect towards others, gives constructive feedback
Minimum Requirements For This Role
- A High School diploma or equivalent
- Able to successfully complete a drug and background check
- 2-4 years of experience in Quality Assurance, Sterile Compounding and/or FDA regulated industry
- Prior batch record/document review
- Strong Microsoft Word and Excel skills
- Must be currently authorized to work in the United States on a full-time basis; QuVa is not able to sponsor applicants for work visas
Any Of The Following Will Give You An Edge
- Bachelor’s Degree in life science or related field
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
- A minimum of 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.”
