Production Technician I - ILP 2nd Shift

Quva • Bloomsbury, NJ

4d • Onsite

About The Position

The Production Technician I supports visual inspection, labeling, and packaging (ILP) operations at Quva’s Bloomsbury, New Jersey facility after completing training. The role helps ensure medications meet safety, efficacy, and quality standards by following established processes, procedures, and documentation requirements. This is a full-time, on-site position with a set Monday–Friday second-shift schedule of 3:00 PM–11:30 PM and minimum overtime requirements. The position is safety-sensitive and may be subject to random drug testing in accordance with applicable laws.

Requirements

• High school diploma or GED from a recognized institution or organization.
• Pass a color perception exam.
• Pass a vision exam demonstrating 20/20 vision, with or without correction.
• Successfully complete a drug and background check.
• Be at least 18 years of age.
• Be currently authorized to work in the United States on a full-time basis; Quva will not sponsor work visas.
• Demonstrate strong attention to detail.
• Have strong verbal and written communication skills and the ability to work effectively with other departments and people at all organizational levels.
• Be flexible and able to adapt to support multiple production areas and shifts as needed.
• Follow policies and procedures and complete administrative tasks correctly and on time.

Nice To Haves

• Pharmaceutical experience.
• Mechanical aptitude.

Responsibilities

• Prepare inspection and packaging room materials and supplies.
• Label and process production materials as required.
• Clean rooms and equipment on daily, bi-weekly, and monthly schedules, and complete applicable preventive-maintenance forms and checklists in accordance with SOPs.
• Conduct and complete line and room clearances according to established procedures.
• Complete product accountability and traceability documents using Good Documentation Practices (GDPs), and comply with cGMPs and company ISO standards.
• Comply with 503B guidelines, cGMPs, standard operating procedures, and company policies.
• Perform equipment calibration checks and troubleshoot production equipment as needed.
• Document activities according to established procedures.
• Notify production management immediately of deviations from established processes or procedures.
• Assist other areas as needed, including cleaning, non-sterile filling, kitting, and preparation operations.
• Perform primary, secondary, and tertiary product labeling.
• Complete secondary and final product packaging.
• Visually inspect products.
• Maintain an inspection-ready environment and support internal and external audits.

Benefits

• Medical, dental, and vision benefits.
• 401(k) retirement program with company match.
• 17 paid days off plus 8 paid holidays per year.
• Occasional weekend and overtime opportunities with advance notice.
• Career advancement opportunities at a national, industry-leading high-growth company.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED