Production Technician I - ILP 2nd Shift

About the role

The Production Technician I – ILP plays a vital role within our organization. Once you complete our training, your responsibilities will include supporting execution of product visual inspection, labeling and packaging (ILP) operations at the Quva facility in accordance with established processes and procedures. At Quva, you will be an essential part of a mission-driven organization dedicated to expanding critical access to quality, affordable medication and data insights while promoting a culture of innovation, collaboration, and continuous improvement.

Responsibilities

• Aids in the preparation of inspection and packaging room materials and supplies.
• Conducts labeling and the processing of production materials as required.
• Daily/ Bi-Weekly/Monthly cleaning of room and equipment and fills out appropriate preventative maintenance forms and checklists in accordance with SOP’s.
• Conducts and completes line and room clearances as per established procedures.
• Completes necessary documents for accountability and traceability of products following Good Documentation Practices (GDPs); comply with cGMPs, and company ISO standards.
• Complies with 503B guidelines; cGMPs, standard operating procedures and company policies.
• Performs equipment calibration checks and troubleshoots production equipment as needed.
• Completes documentation of activities in accordance with established procedures.
• Immediately notifies production management of deviations to established processes or procedures.
• Affords assistance to other areas as needed (cleaning; non-sterile filling; kitting and preparation operations, etc.).
• Primary, secondary, and tertiary labeling of products.
• Secondary and final packaging of product.
• Maintains visual inspection of product.
• Maintains inspection ready environment and supports internal / external audits.

Requirements

• High school Diploma or GED from recognized institution or organization required.
• Will be required to undergo a color perception exam and must be able to produce a passing test result.
• Will be required to undergo a vision exam and must be able to produce 20/20 vision with or without correction.
• Able to successfully complete a drug and background check.
• Must be currently authorized to work in the United States on a full-time basis; Quva will not sponsor applicants for work visas.
• Minimum age requirement: 18+

Qualifications

• Strong attention to detail.
• Flexible and can adapt to support multiple production areas and shifts as needed.

Skills

• Effective verbal and written communication skills.
• Active listening with team members.
• Understanding of how various issues affect each other and the outcome of projects.
• Improves upon existing approaches by seeking opportunities to creatively transform.
• Mechanical aptitude a plus.

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.

Pay

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 conditions.

Raise: $18.00 - $21.00 / Hour + $2.50 shift differential

Schedule

This is a full-time role for our 2nd Shift, working Wednesday - Saturday from 3:00PM to 1:30AM. This is a set, consistent schedule with minimum overtime requirements and based on site in our Bloomsbury, NJ location.