2nd Shift Manufacturing Operations Supervisor

RXinsider LTD.; Bloomsbury (NJ); On-site; USD 57,000 - 78,000; Full time

Benefits offered by this job

Health and wellness benefits

401k retirement program with company/

22 paid days off + 8 paid holidays per

Job summary

Quva is seeking a Supervisor, Manufacturing Operations (ILP) based at our Bloomsbury, NJ site for 2nd shift (Wed-Sat 3:30PM–1:30AM). The role focuses on coordinating ILP labeling, packaging operations, and label printing, ensuring compliance with cGMP and QA standards.

You will supervise frontline staff, oversee production and scheduling, drive quality system tasks, train personnel, and prepare daily and monthly reports.

Qualifications

• High school Diploma or GED from recognized institution required.
• 2-3 years prior experience in cGMP / FDA regulated industry.
• 1 year of supervisory or management experience required.
• Successful completion of certified in-house qualification programs.
• Experience training personnel on aseptic techniques and appropriate gowning techniques.
• Able and willing to walk, stoop, stand, bend, and lift up to 50 lbs. throughout each shift, with or without reasonable accommodation.
• Well versed in the compliance & quality requirements of 503B pharmaceutical industry and CGMP's and have demonstrated strength in problem solving and resolution.
• Must be currently authorized to work in the United States on a full-time basis; Quva is not able to sponsor applicants for work visas

Responsibilities

• Supervise ILP operations and label printing activities
• Supervises ILP schedule in accordance with production schedule and customer demand
• Prepares and submits daily/weekly/monthly reports, prepares metrics and trends data to identify and prioritize continuous improvement opportunities
• Participates in safety meetings, investigates accidents, and takes appropriate corrective action to eliminate
• Oversee production activities to assure performance to plan is achieved
• Effectively arranges for work to be completed, schedules workflow and assignments to ensure delivery performance objectives for product or projects are met or exceeded
• Manages front line leadership in completion of daily operational tasks and assignments
• Drives Quality Management System assignments
• Reviews documentation such as batch records and logs to assure accurate recording of processes in conformance to policies and procedures and in compliance with Good Documentation Practices
• Develops training programs & assures training is conducted
• Reports & initiates production schedule changes, requests equipment and facility repairs, or modifications

Skills

cGMP experience

FDA regulated industry

Supervisory experience

Training personnel

Aseptic techniques

Record keeping

Education

High school diploma or GED

Bachelor's degree in Life Science

Job description

Quva is seeking a Supervisor, Manufacturing Operations (ILP) based at our Bloomsbury, NJ site for 2nd shift (Wed-Sat 3:30PM–1:30AM). The role focuses on coordinating ILP labeling, packaging operations, and label printing, ensuring compliance with cGMP and QA standards.

You will supervise frontline staff, oversee production and scheduling, drive quality system tasks, train personnel, and prepare daily and monthly reports.