Manufacturing Technician II - DAP (Nights)

Resilience; Blue Ash (OH); On-site; USD 29,000 - 44,000; Full time

Benefits offered by this job

Annual bonus

401(k) plan

Healthcare benefits

Paid vacation

Paid holidays

Tuition reimbursement

Caregiving support

Job summary

Resilience is a technology-focused biomanufacturing company innovating how medicine is made. The Manufacturing Technician II will operate packaging equipment, perform in-process monitoring, and maintain batch records in a cGMP environment at the Blue Ash site during the night shift.

Responsibilities include material handling, line clearances, quality inspection, and basic troubleshooting. Candidates should have regulated manufacturing experience and be able to work in a fast-paced team setting

Qualifications

• Prior experience in a regulated manufacturing environment.
• Working knowledge of product security controls and material handling equipment.
• Demonstrated documentation and data entry skills, including accurate completion of batch records and logbooks.
• Basic mathematics for weights, measures, conversions.
• Ability to read, write, speak, and understand English to interpret SOPs, batch records, and work instructions.
• Ability to follow written procedures and work instructions with minimal supervision, escalating issues as needed.
• Basic problem-solving skills and ability to identify deviations or inconsistencies in processes or documentation.
• Proficiency with SAP and/or Veeva Vault.
• High school graduate or equivalent.
• 1+ years in pharmaceutical/biotechnology, or cGMP-regulated manufacturing.
• Experience with lean manufacturing and SAP/Veeva Vault.

Responsibilities

• Operate packaging equipment and monitor line status.
• Perform in-process monitoring and line clearances.
• Inspect and sample in-process materials; escalate concerns.
• Handle light material transfers and palletize materials.
• Perform cleaning and line clearance to maintain cGMP environment.
• Record batch data and complete GMP documentation.
• Follow safety procedures and PPE usage.
• Support lean and process improvements including 5S.
• Assist with equipment qualification and calibration activities.

Skills

Basic mathematical skills

Documentation

English literacy

Teamwork

Problem solving

Education

High school diploma or equivalent

1+ years pharma/biotech/cGMP manufacturing

Vocational training (preferred)

Tools

SAP

WES

SCADA / HMI

Job description

A career at Resilience is more than just a job – it’s an opportunity to change the future. Resilience is a technology-focused biomanufacturing company that’s changing the way medicine is made. We’re building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need. For more information, please visit www.resilience.com

The Manufacturing Technician II reports to a Supervisor/Manager, Manufacturing and performs a variety of manufacturing tasks in Controlled/Non-Classified areas in accordance with cGMPs, supporting Packaging operations. Responsibilities include operating packaging equipment, performing in-process monitoring, line clearances, cosmetic inspection, cleaning, and completing batch record entries. Note: Blue Ash, Device Assembly, Night Shift

Operations

• Perform the duties of operating assigned machinery: service machines with materials, monitor equipment status, reintroduce materials, manually palletize finished materials, and ensure smooth product flow.
• Start-up machinery including equipment setup, recipe selection, data entry on SCADA and HMI; make minor adjustments and perform critical sensor challenges.
• Perform manual packaging tasks as required including hand packaging and rework of in-process and finished material.
• Operate light material handling equipment (motorized and manual pallet jacks, non-motorized lifts) to safely move, store, or deliver material.
• Perform visual quality inspection and sampling of in-process materials; promptly escalated concerns to Lead and Management as needed.
• Perform minor troubleshooting including clearing minor jams and identifying equipment defects; escalating to the Lead and Management as needed.
• Perform inventory control and reconciliation activities using SAP and WES.
• Perform cleaning, housekeeping, and line clearance activities for assigned areas to maintain a cGMP environment.

Documentation & Compliance

• Perform batch record and GMP documentation entries; perform mathematical computations as required.
• Follow job-related safety procedures including PPEs, LOTO, ergonomics, and material/chemical/waste handling, spill controls and human safety.
• Support lean activities and process improvement work including 5S, problem-solving, and manual data collection.
• Execute protocols as required as part of equipment qualification and process validation work.

Training & Development

Provide flexible support to other areas of the Manufacturing Team as needed. Acquire and maintain all required certifications and qualifications for the assigned work area. Attend and actively participate in daily Tier 0 meetings.

Experience & Education

Minimum Qualifications

• Prior experience in a regulated manufacturing environment.
• Working knowledge of product security controls and material handling equipment.
• Demonstrated documentation and data entry skills, including accurate completion of batch records and logbooks.
• Basic mathematical skills, including the ability to perform routine calculations (e.g., weights, measures, conversions).
• Ability to effectively read, write, speak, and understand English to interpret SOPs, batch records, and work instructions.
• Ability to follow written procedures and work instructions with minimal supervision, escalating issues as needed.
• Basic problem-solving skills and the ability to identify deviations or inconsistencies in processes or documentation.
• Ability to work effectively as part of a team in a fast-paced production environment.

Preferred Qualifications

• High school graduate, vocational school graduate, or equivalent.
• 1+ years of experience in a pharmaceutical, biotechnology, or cGMP-regulated manufacturing environment.
• Experience working in a lean manufacturing environment.
• Working knowledge of cGMP principles, including documentation practices, safety procedures, and compliance expectations.
• Experience working in a lean manufacturing environment.
• Working knowledge of Microsoft applications, SAP and/or Veeva Vault.

Physical & Work Environment

This role is primarily a non-Sedentary role. This can include climbing, kneeling, repetitive motion, temperature changes, and exerting up to 100 pounds of force to move objects. Visual acuity such as working with data & figures, viewing computer terminal, extensive reading, operating machinery, operating motor vehicles, general observations of facilities, etc. Participation in an occupational health program, which can include medical assessment, surveillance, vaccination, and testing. Use of personal protective equipment, which can include respirators, Personal Air Purifying Respirators [PAPR], gowns, gloves, face protection, other barrier equipment, etc. All employees are expected to adhere to the Quality Management System established in the Quality Manual, Quality Policy, Standard Operating Procedures, Current Good Manufacturing Practices, and any other applicable regulations and standards to the duties within their role. Ability to pass eye exam during onboarding.

Work Schedule

Work Schedule [12 hour - 2/2/3] The work schedule listed reflects the employee’s expected schedule at the time of hire. The Company reserves the right to modify work schedules at any time, including a request to work overtime, with or without notice, based on business needs, operational requirements, or other considerations. Nothing in this description creates a guarantee of specific hours, days, or shift assignments.

Sponsorship or support for work authorization, including visas, is not available for this position.

Resilience is an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, physical or mental disability, genetic information, or characteristic, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state, and local laws.

Requests for reasonable accommodation can be made at any stage of the recruitment process.

Benefits

• annual cash bonus program
• 401(k) plan with a generous company match
• great healthcare (including medical, dental and vision)
• family building benefits
• life and disability insurance
• paid vacation
• paid holidays
• other paid leaves of absence
• tuition reimbursement
• support for caregiving needs

Our target base pay hiring range for this position is $21.50 - $32.00 per hour. Actual base pay is dependent upon a number of factors, including but not limited to, the candidate’s geographical location, relevant experience, qualifications, skills and knowledge.