Cleanroom Material Handler 1st Shift

Our Cleanroom Material Handler 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 supporting handling and processing of materials within operations at the QuVa facility in accordance with established processes and procedures. Your attention to detail and adherence to precise procedures will guarantee that our medications reach patients accurately and securely. 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 1st shift, working Monday through Friday from 6:00 AM to 2:30 PM. This is a set, consistent schedule with minimum overtime requirements and based on site in our Bloomsbury, NJ location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws.

What The Cleanroom Material Handler Does Each Day

Will directly support Cleanroom Compounding operations, Picking, and Batch PreparationStaging of compounding materials in cleanrooms in preparation of compoundingSafely transport and transfer materials in and out of cleanroomsCompletes Daily/Weekly/Monthly cleaning of cleanroom and equipment in compliance with appropriate Standard Operating Procedures (SOP) and EH&S requirementsSafely transport product and materials from warehouse to designated areas in accordance with Standard Operating Procedures (SOP) and EH&S requirementsOpen and empty glass vials into measurement containers in accordance with Standard Operating Procedures (SOP) and EH&S requirementsComplete necessary documents for accountability and traceability of product following Good Documentation Practices (GDPs); Comply with cGMPs, and company procedures and work instructionsSafely transport product and materials to designated areas for disposal in accordance with Standard Operating Procedures (SOP) and EH&S requirementsDaily/ Bi-Weekly/Monthly cleaning of room and equipment and fill out appropriate preventative maintenance forms and checklists in accordance with SOP'sConduct and complete line and room clearances as per established proceduresDaily Supply list for respective area turned into receiving by scheduled timeComply with 503B guidelines; cGMPs, and company standardsPerform equipment calibration checks and troubleshoot equipment as neededComplete documentation of activities in accordance with established proceduresImmediate notification of production management of deviations to established processes or proceduresAssist other areas as needed (non-sterile filling, picking and preparation operations, etc.)

Our Most Successful Cleanroom Material Handler

Promotes active listening with team members; Contributes appropriately to conversations; Has strong verbal and written communication skills with the ability to work effectively with other departments within the organization and with people at all levels of the organizationUnderstands how various issues affect each other and the outcome of projects; Improves upon existing approaches by seeking opportunities to creatively transform; mechanical aptitude a plusEffectively and productively engages with others and establishes trust, credibility, and confidence with othersListens to internal customers, ensures commitments are met, sets appropriate internal customer expectations

Minimum Requirements For This Role

A High School diploma or equivalentAble to successfully complete a drug and background check18+ years of ageFamiliarity with and comfortable using mobile devices such as smartphones, tablets, handheldsAble and willing to walk, stoop, stand, bend, and lift throughout each shift, with or without accommodationAble and willing to follow “garb and gown” requirements from head to toe in order to maintain a sterile, clean room environment. This includes:Hand washingWearing hair net, shoe covers, facemask, sterile gown, and gloves, etc. Stringent regulations concerning, for example, the carrying of cellphones, the wearing of jewelry and makeup, and the length / type of fingernailsMust 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

Pharmaceutical experienceAt least 1-year regulated manufacturingExperience in a role requiring repetitive tasks, attention to detail and individualized work - such as working in a warehouse or manufacturing environment

Benefits Of Working At QuVa

Set, full-time, consistent work scheduleComprehensive health and wellness benefits including medical, dental and vision401k retirement program with company match17 paid days off plus 8 paid holidays per yearOccasional weekend and overtime opportunities with advance noticeNational, 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.”