Our Medication Safety Clinical Pharmacist 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 ensuring and improving medication safety across all of QuVa. These services will be provided in compliance with federal and state regulations and QuVa’s policies 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 safety sensitive position that may be subject to random drug testing, in accordance with applicable laws.

What the Medication Safety Clinical Pharmacist Does Each Day:

• Conducts evaluations of inquiries, complaints, and adverse events to identify areas for improvement and implement interventions to reduce risk
• Monitors and analyzes inquiries, complaints and adverse events and continuous quality-improvement data to identify trends and patterns, and work with interdisciplinary teams to prioritize safety issues and develop risk-reduction strategies
• Correctly identifies customer product inquiry cases requiring targeted follow-up, determine relevant follow-up required and prepare follow-up queries
• Coordinates complaint investigations
• Remains current with cases handling SOPs, guidance documents and database technology
• Maintains records of customer complaints and documentation in the complaint management system to ensure complaints are adequately resolved on time
• Escalates complaints as per SOP, FDA, and BOP laws
• Retrieves and ensures accurate and consistent information, including but not limited to, adverse event verbatim descriptions and medication data received from customers
• Supports audits related to customer complaints

Our Most Successful Medication Safety Clinical Pharmacist:

• Is customer service and customer focus driven
• Has excellent verbal and written communication
• Has product/industry knowledge – pharmaceutical, large production compounding, medical, hospital environment
• Works independently and as part of a team
• Is proactive and demonstrated initiative and accountability; uses time wisely
• Is proficient with computers and word processing software (i.e., Microsoft Office products)

Minimum Requirements for this Role:

• S. in Pharmacy or Pharm D
• 2 years’ relevant work experience
• Knowledge of medication use-safe practices; Process Improvement methodologies (Lean and Six Sigma)
• Excellent technical writing and verbal/written communication skills
• Knowledge of cGMP (Current Good Manufacturing Processes)
• Able to successfully complete a drug and background check
• 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: 

• Clinical environment experience

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 

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.”