Quality Assurance Technician 2nd Shift

QuVa Pharma, Inc.; Northern (KY); Hybrid; USD 45,000 - 65,000; Full time

Benefits offered by this job

Health benefits

401k match

Paid time off

Job summary

QuVa Pharma, Inc. is seeking a Quality Assurance Technician for the Bloomsbury, NJ site. After training, you will perform basic QA functions, verify incoming materials, and oversee label printing to ensure manufacturing readiness and patient safety.

The role is full-time on the 2nd shift, 3:00 PM–11:30 PM, with a consistent rotating schedule and potential overtime. This safety-sensitive position may involve random drug testing and requires compliance with applicable laws.

Qualifications

• High school diploma or equivalent.
• Able to successfully complete a drug and background check.
• Able to walk, stand, and lift up to 50 lbs. throughout shift.
• 18+ years of age.
• Must be authorized to work in the United States without visa sponsorship.

Responsibilities

• Ensure US Regulatory requirements are met within procedures and practices.
• Quality review/verification of information related to incoming goods or distribution of finished goods.
• Ensure compliance of incoming materials prior to use in Manufacturing Operations.
• Verify labels against batch record requirements.
• Maintain cleanliness levels for components and equipment used in manufacturing.

Skills

Detail oriented

Communication skills

Teamwork

Interpersonal skills

Physical ability

Education

High School diploma

Job description

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

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 2nd shift, working rotating Monday through Friday from 3pm to 11:30pm. This is a set, consistent schedule with minimum overtime requirements and based on site in our Bloomsbury location. 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