Intern, Quality Control

QuVa Pharma is excited to support the growth and development of Quality Control Intern.  This person will support laboratory operations at the QuVa location. The learning plan will support the student's academic program and provide hands-on opportunities to perform analytical testing and documentation with a clearly stated start and end period. The intern will be exposed to analytical chemistry, microbiology, R&D, and quality compliance as needs and aptitudes develop. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US.

This is a role working Monday through Friday based on site in our Bloomsbury, NJ location.

What the QC Intern Does Each Day:

• Sample management, including logging samples into the laboratory, archiving data, and supporting documentation of controlled substances.
• Learn and perform various analytical test methods
• Support laboratory investigations, and investigative experiments
• Order/receive lab supplies
• Prepare solutions or reagents for lab use.
• The Supervisor/Mentor will provide periodic feedback to the Intern on the overall progress, and work with the intern to ensure that their expectations regarding the work are being met
• Consistently at work and on time; ensures work responsibilities are covered when absent and that absences are appropriately communicated and approved in advance

Our Most Successful QC Interns:

• Are detail-oriented with strong verbal and written communications skills
• Motivates others, shares knowledge, builds high performing team, shows respect towards others, gives constructive feedback
• Display eagerness to learn and continuously improve, adapt quickly to change, and apply sound judgment
• Foster team environment, invest in team members and peers by inclusion and listening, recognize employees effectively, demonstrate trust

Minimum Requirements for this Role: 

• Legally authorized to work in the job posting country
• High school diploma or GED from recognized institution or organization required
• Must be actively pursuing a bachelor's degree from an accredited institution, with an anticipated graduation date within the next two years
• Must be in good standing with accredited institution where pursuing degree
• Microsoft Word and Excel skills

Any of the Following Will Give You an Edge: 

• MS Office (Outlook, Excel, PowerPoint, Word) skills. Understanding other technology platforms, a plus
• Problem solving, project management and communication skills are necessary, as is the ability to operate in a team
• Preferred working knowledge of cGMPs and regulatory requirements as well as all applicable SOPs

Benefits of Working at QuVa: 

• Set, full-time, consistent work schedule
• 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.”