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Production Technician III ILP

Quva


Job Location:

Hunterdon County, NJ - USA

Monthly Salary: Not provided by the employer
Posted: 11 October 2026 (9 hours ago)
Application Deadline: 8 January 2027
Vacancies: 1 Vacancy

Job Summary

The Production Technician III ILP position is responsible for supporting the 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.

Key Duties and Responsibilities:

Will directly support the ILP operation to include but not limited to:

Visual Inspection of product or label printing operations

Assist preparation of inspection and packaging room materials supplies

Safely transport product and materials from warehouse to designated areas in accordance with Standard Operating Procedures (SOP) and EH&S requirements

Conduct labeling and the processing of production materials as required

Investigate and resolve reconciliation issues to advance batches towards closure.

Daily/ Bi-Weekly/Monthly cleaning of room and equipment and fill out appropriate preventative maintenance forms and checklists in accordance with SOPs

Conduct and complete line and room clearances as per established procedures

Complete necessary documents for accountability and traceability of product following Good Documentation Practices (GDPs); comply with cGMPs and company ISO standards

Daily Supply list for respective area turned into receiving by scheduled time

Comply with 503B guidelines; cGMPs and company standards

Perform equipment calibration checks and troubleshoot equipment as needed

Complete documentation of activities in accordance with established procedures

Immediate notification of production management of deviations to established processes or procedures

Assist other areas as needed (cleaning; non-sterile filling; kitting and preparation operations etc.)

Primary secondary and tertiary labeling of product

Other duties as assigned

Competencies / Skills:

Communication: Promotes active listening with team members; Contributes appropriately to conversations; Strong verbal and written communication skills with the ability to work effectively with other departments within the organization and with people at all levels of the organization

Problem Solving: Understands 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

Interpersonal Skills: Effectively and productively engages with others and establishes trust credibility and confidence with others

Customer Orientation: Listens to internal customers ensures commitments are met sets appropriate internal customer expectations

Preferred working knowledge of cGMPs and regulatory requirements as well as all applicable SOPs

Follows policies and procedures; completes administrative tasks correctly and on time

Approaches others in a tactful manner; reacts well under pressure; treats others with respect and consideration regardless of their status or position; accepts responsibility for own actions; follows through on commitments

Work Environment:

Ability to sit and/or stand 8 hours or more per day if needed

Ability to manipulate necessary office equipment computer software hardware & equipment

Ability to perform the following physical activities: stooping reaching standing grasping walking feeling talking and hearing

Ability to exert up to 50 pounds of force frequently or constantly to lift carry push pull or otherwise move objects

Ability to tolerate a work environment that uses cleaning chemicals in order to maintain a sterile manufacturing facility

Work environment is a registered 503B facility and requires compliance with many federal regulations including but not limited to the following:

Required to wear neat and clean scrubs (preferably pocketless)

Required to wear PPE

You must wear hosiery/socks

Legs must be covered at all times

You must wear flat shoes with closed-toes and closed-heels (no crocs)

No makeup

Nails should be kept short and well maintained no nail polish (gel or acrylic)

No personal electronic device usage in the production area

No hair gels hair sprays or perfumes/colognes

No food/drink in the production area

Hours:

You will be scheduled to work an 8-hour shift during the hours of operation

Ability to come in prior to scheduled shift hours to support production needs

Due to the nature of our work working beyond the scheduled end of your shift is often necessary to complete a production batch and can be required with little or no notice

Saturdays are expected to be worked when scheduled

You may specifically be hired to work a later shift than we currently have available if so you will be assigned to work an existing shift as determined by your manager

Training may not be scheduled during your normal shift flexibility to work the hours necessary to complete training is required

Qualifications:

Legally authorized to work in the job posting country

High school Diploma or GED from recognized institution or organization required

Minimum of 2 years reliable and sustained performance as a Production Technician II ILP or pharmaceutical manufacturing experience

Ability to work competently on all lines including equipment: Equipment CA (PacMac Labelers)

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

To be considered:

In order to be considered for this position you must complete the entire application process which includes answering all prescreening questions and providing your eSignature on or before the requisition closing date.

Candidates for regular U.S. positions must be a U.S. citizen or national or an alien admitted as permanent resident refugee asylee or temporary resident under 8 U.S.C. 1160(a) or 1255(a)(1). Individuals with temporary visas such as E F-1 H-1 H-2 L B J or TN or who need sponsorship for work authorization now or in the future are not eligible for hire.

It is the policy of Quva to afford equal opportunity for employment to all individuals regardless of race color age national origin physical or mental disability history of disability ancestry citizenship status political affiliation religion gender transgender gender identity marital status status as a parent sexual orientation veteran status genetic information or other factors prohibited by law and to prohibit harassment or retaliation based on any of these factors.


Required Experience:

IC


About Company

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Transform healthcare decisions with Quva BrightStream – where data becomes intelligence, complexity becomes clarity, and uncertainty becomes decisive action that drives improved performance and patient outcomes.

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