Quality Assurance Technician 2nd Shift
QuVa Pharma
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. Watch this video to learn more. 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
- 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
- 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
- 0 to 2 years’ experience with FDA-regulated operations (cGMP processes) or Quality Assurance
- 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
- The base compensation for this role is estimated to be within the range described below. The compensation offered may vary depending on relevant factors such as experience, skills, training, education, certifications, geographic location, and market condition
- Range: $18.00 - $21.00 / Hour + $2.50/Hr shift differential
- About Quva
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.
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