Manufacturing Technician IV, Lead - DAP (Nights)

National Resilience; United States; On-site; USD 36,000 - 56,000; Full time

Benefits offered by this job

401(k) plan with company match

Comprehensive health insurance (med, d

Paid vacation

Paid holidays

Tuition reimbursement

Family-building benefits

Life and disability insurance

Caregiving support

Job summary

Resilience in the United States seeks an experienced manufacturing professional to oversee operations on the production floor in a pharmaceutical/biotech cGMP setting. You will lead complex process activities, start-up, equipment operation, packaging, and line clearances, while ensuring SOPs and data integrity.

The role emphasizes training, documentation, continuous improvement, lean practices, and performance in a fast-paced environment.

Qualifications

• Significant experience in pharmaceutical, biotechnology, or cGMP manufacturing.
• Advanced knowledge of cGMP requirements and quality systems.
• Ability to train peers and read/write English technical information.

Responsibilities

• Lead and monitor complex process activities on the production floor.
• Perform start-up, equipment operation, packaging, and line clearances.
• Manage inventory control using SAP and run process validation tasks.
• Maintain GMP documentation and batch records with accuracy.
• Serve as a technical resource and OJT trainer for the team.

Skills

Process monitoring

Documentation

OJT trainer

Education

High school diploma or equivalent

Tools

SAP

Veeva Vault

Claude AI

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

Job Responsibilities

Operations

• Lead and monitor complex process activities to ensure successful operations on the production floor.
• Perform technician tasks as required including start-up, equipment operation, manual packaging, and line clearances.
• Perform inventory control and reconciliation activities using SAP and WES.
• Execute protocols as required as part of equipment qualification and process validation work.
• Ensure work requirements are followed on the production floor in accordance with SOPs and cGMPs.
• Support lean activities including 5S, problem-solving, and serving as CI project resource.

Documentation & Compliance

• Perform advanced-level batch record and GMP documentation entries on the production floor, including complex or non-routine documentation; provide guidance to team members on documentation accuracy.
• Review process documents such as operational SOPs, forms, and batch records for accuracy; propose revisions and update documents where needed .
• Maintain all required certifications and qualifications for the assigned work area.

Training & Development

• Serve as a technical resource for the team, providing subject-matter support to production and mechanical technicians.
• Act as a certified OJT trainer on assigned equipment and process tasks, training and supporting team members.
• Collaborate with Management and Engineers on packaging floor initiatives.
• Apply strong problem-solving and prioritization skills to make independent decisions and provide guidance to team members on daily operational activities.
• Acquire and maintain all required certifications and qualifications for the assigned work area.
• Prepare and lead daily Tier 0 meetings.

Experience & Education

Minimum Qualifications

• Significant experience in a pharmaceutical, biotechnology, or cGMP-regulated manufacturing environment.
• Advanced knowledge of cGMP requirements and quality systems, including deviations, change control, and data integrity.
• Demonstrated ability to work independently and resourcefully to resolve complex production issues and provide guidance to team members in a fast-paced production environment.
• Proven ability to review and ensure accuracy of critical GMP documentation and batch records.
• Demonstrated ability to work with limited supervision and independently determine daily priorities, with strong organizational, analytical, and problem-solving skills to make informed decisions under pressure.
• Applied quantitative skills sufficient to interpret production data, evaluate trends, and support investigations and continuous improvement work.
• Experience providing on-the-job training to peers in a manufacturing environment.
• Ability to effectively read, write, speak, and understand English to communicate technical information cross-functionally.
• 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.
• 4+ years of experience in a pharmaceutical, biotechnology, or cGMP-regulated manufacturing environment.
• Prior experience serving as a subject-matter resource or trainer on the production floor.
• Experience in a lean manufacturing environment.
• Working knowledge of Microsoft applications, SAP and/or Veeva Vault and generative AI language tools such as Claude.

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

[examples: 8 hours - Monday- Friday; 10 hours – Monday-Thursday; 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.

Resilience offers employees a robust total rewards program including an annual cash bonus program, a 401(k) plan with a generous company match and our benefits package which is thoughtfully designed to support our employees with 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 and support for caregiving needs. Our target base pay hiring range for this position is $26.00 - $40.50 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.