Quality Assurance Technician 2nd Shift

QuVa Pharma; Bloomsbury (NJ); On-site; USD 52,000 - 70,000; Full time

Benefits offered by this job

Comprehensive health and wellness (med

401k retirement program with company

17 paid days off plus 8 paid holidays

Overtime opportunities with advance

Career advancement opportunities

Job summary

QuVa Pharma in Bloomsbury, NJ is seeking a Quality Assurance Technician to ensure quality and patient safety. After training, you’ll verify incoming materials, check labels, and oversee prep and labeling tasks on the floor.

This full-time second-shift role (Mon–Fri, 3:00 PM–11:30 PM) is on-site with a safety-sensitive environment. Responsibilities include regulatory compliance, record checks, and ensuring cleanliness and accuracy in manufacturing.

Qualifications

• High School diploma or equivalent is required.
• Drug and background checks must be successfully completed.
• Able to walk, stand, lift up to 50 lbs. throughout shift.
• Authorized to work in the United States full-time; visa sponsorship is not offered.
• Edge: 0–2 years’ experience in FDA-regulated operations or QA.

Responsibilities

• Verify incoming materials and distribution of finished goods per batch records.
• Perform label verification against batch record requirements.
• Ensure cleanliness and proper handling of components and equipment.
• Maintain compliance with US regulatory requirements and company standards.
• Support on-floor QA functions and ensure documentation accuracy.

Skills

Detail-oriented

Verbal communication

Written communication

Team collaboration

Education

High School diploma or equivalent

Job description

NJ - Bloomsbury Site 519 NJ-173 Bloomsbury, NJ 08804, USA

• On-site
• 8000-Quality
• Full-Time
• Requisition #: QUALI006202

Description

Our Quality Assurance Technician 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 performs basic QA functions related to verification of incoming materials, label checks, and oversight of support areas (i.e. prep and/or label printing) to ensure the manufacturing areas are set up for success. The on-the-floor quality team is responsible for making sure the process and documentation records are compliant with patient safety in mind, executing with efficiency always. Quality, safety, and on-time delivery is a must to be successful in this role!

This is a full-time role for our second shift, working Monday through Friday from 3:00 PM-11:30 PM. This is a set, consistent schedule with minimum overtime requirements and based on site in our Bloomsbury, NJlocation. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws.

What the Quality Assurance Technician Does Each Day:

• Ensure that all applicable US Regulatory requirements are being met within the procedures and practices
• Quality review / verification of critical information related to the receipt of incoming goods or the distribution of finished goods for customer orders
• Ensures compliance of incoming materials prior to use in Manufacturing Operations
• Ensures verification of labels against batch record requirements complies with company standards
• Ensures levels of cleanliness for components and equipment used in the manufacturing process meet the company standards

Our Most Successful Quality Assurance Technicians:

• Are detail-oriented with strong verbal and written communications skills
• Express energy, show accountability, and multi-task
• Fulfill expectations, establish sustainable relationships with team members, maintain effective and meaningful communication channels
• Have good interpersonal skills and the ability to work effectively and efficiently in a team environment to accomplish goals

Minimum Requirements for this Role:

• A High School diploma or equivalent
• Able to successfully complete a drug and background check
• Able and willing to walk, stoop, stand, bend, and lift up to 50 lbs. throughout each shift, with or without reasonable accommodation
• 18+ years of age
• 20/20 vision (with or without corrective lenses) and the ability to successfully pass a color vision test
• Familiarity with and comfortable using mobile devices such as smartphones, tablets, handhelds
• Must 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:

• 0 to 2 years’ experience with FDA-regulated operations (cGMP processes) or Quality Assurance

Benefits of Working at Quva:

• Comprehensive health and wellness benefits including medical, dental and vision
• 401k retirement program with company match
• 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 compounded injectable medicinesand software solutions that help power the business of hospital and health-system pharmacy. Quva Pharma produces and distributes injectable medicines required by health care providers and critical to patient care. Quva BrightStreampartners with health-systems to analyze large amounts of data and through AI and machine learning,develops softwaresolutions that turns the data into insights that are used to better run their pharmacy operation. Quva’s overall product and technology offerings help health-systems achieve greater value and deliver the highest-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.”

Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.For further information, please review the Know Your Rights notice from the Department of Labor.