Quality Assurance Technician 2nd Shift

About the role

Our Quality Assurance Technician plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. 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.

Responsibilities

• Perform 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
• 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
• Ensure compliance of incoming materials prior to use in Manufacturing Operations
• Ensure verification of labels against batch record requirements complies with company standards
• Ensure levels of cleanliness for components and equipment used in the manufacturing process meet the company standards

Qualifications

• 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

Skills

• 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
• Good interpersonal skills and the ability to work effectively and efficiently in a team environment to accomplish goals

Preferred experience

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

Pay

• $18.00 - $21.00 / Hour + $2.50/Hr shift differential

Schedule

• Full-time, 2nd shift, rotating Monday through Friday from 3pm to 11:30pm
• Set, consistent schedule with minimum overtime requirements
• Based on site in Bloomsbury location

Benefits

• Set, full-time, consistent work schedule
• 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