Compounds sterile preparations as per work instructions under pharmacist supervision. Assists in cleaning and maintenance of the work environment.
Responsibilities may include:
Complies with all state and federal laws, rules, and regulations governing the practice of pharmacy
Ensures cleansing and garbing policy is performed exactly per sterile preparations
Compounds all required types of sterile preparations accurately and in compliance with master worksheets
Operates all compounding equipment accurately and according to policy and procedure
Utilizes correct and appropriate aseptic techniques at all times
Prepares work area and products thoroughly prior to compounding
Compounds daily without fingertip growth during compounding
Performs cleaning of the clean room areas thoroughly and according to policy without viable particle growth
Maintains a high degree of productivity within recommended guidelines
Conducts oneself in a professional manner and continually strive to improve efficiency
Demonstrates thorough knowledge of the job, completing all annual competencies and skills validations
Passes all initial and on-going validations and advanced complex media-fill verification
Effectively integrates knowledge into job and continuously attains new knowledge
Maintains accurate records of all assignments
Completes any other duties designated by the pharmacist and/or supervisor
Cooperates with team members to accomplish departmental goals
Understands and adheres to policies and procedures
Arrives at work as scheduled and notifies supervisors in a timely manner of any absences
Recognizes priorities and takes action; makes productive use of time
Legally authorized to work in the job posting country
High School diploma or general education degree (GED) required
Licensed as a Pharmacy Technician (CPhT) preferred
Registered as a Pharmacy Technician with the state of NJ is preferred
ACPE Sterile products certification preferred
IV compounding experience preferred, but not required
To be considered:
In order to be considered for this position you must complete the entire application process, which includes answering all prescreening questions and providing your eSignature on or before the requisition closing date.
Candidates for regular U.S. positions must be a U.S. citizen or national, or an alien admitted as permanent resident, refugee, asylee or temporary resident under 8 U.S.C. 1160(a) or 1255(a)(1). Individuals with temporary visas such as E, F-1, H-1, H-2, L, B, J, or TN or who need sponsorship for work authorization now or in the future, are not eligible for hire.
It is the policy of QuVa Pharma to afford equal opportunity for employment to all individuals regardless of race, color, age, national origin, physical or mental disability, history of disability, ancestry, citizenship status, political affiliation, religion, gender, transgender, gender identity, marital status, status as a parent, sexual orientation, veteran status, genetic information or other factors prohibited by law, and to prohibit harassment or retaliation based on any of these factors.
Internal Number: 9090
About QuVa Pharma
QuVa Pharma is a nationally recognized industry leading state-of-the-art cGMP compliant 503B FDA registered manufacturing platform and partner of choice for compliance-oriented healthcare facilities looking to ensure a quality, safe and consistent supply of medications. The Company offers a broad portfolio of ready-to-use products across Pain Management, Anti-infective, OR Syringes, Labor and Delivery therapeutic areas amongst others, all of which are released only once sterility and potency testing is successfully complete, and with validation supporting appropriate Beyond Use Dating (BUD). The company is committed to having a patient-first orientation, as well as a robust product portfolio, leading safety standards, and collaborative, partnership-oriented customer service.