Engineer - II (Associate)

Nesco Resource, LLC

West Point, PA

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JOB DETAILS

SALARY

$50–$52 Per Hour

SKILLS

Automation, Biology, Biotech and Pharmaceutical, Change Control, Chemistry, Communication Skills, Continuous Improvement, Corrective Action, Corrective and Preventative Action (CAPA) Systems, Cost Control, Cross-Functional, Documentation, GMP (Good Manufacturing Practices), Identify Issues, Leadership, Maintain Compliance, Manufacturing, Manufacturing Operations, Multitasking, Operational Audit, Operational Support, Operations Processes, Power BI, Problem Solving Skills, Process Engineering, Process Improvement, Production Systems, Project Schedule, Project/Program Management, Quality Management, Regulatory Compliance, Root Cause Analysis, SAP, Safety Compliance, Safety/Work Safety, Schedule Development, Standard Operating Procedures (SOP), Support Documentation, Team Player, Technical Operations, Technical Support, Technical Writing, Time Management, Validation Documentation, Writing Skills

LOCATION

West Point, PA

POSTED

10 days ago

Position Summary

We are seeking a motivated Process Engineer / Technical Operations Engineer to support manufacturing operations within a sterile production environment. This role will be responsible for investigating deviations, supporting continuous improvement initiatives, authoring GMP documentation, and partnering with cross-functional teams to drive compliance, operational excellence, and process reliability.

The ideal candidate possesses strong technical writing abilities, excellent communication skills, and the ability to manage multiple priorities in a fast-paced manufacturing environment.

Key Responsibilities

Support deviation investigations, including product impact assessments, root cause analysis, and development of corrective and preventative actions (CAPAs).
Assist with authoring and managing quality investigations and quality event documentation.
Create, revise, and maintain GMP documentation including:
- Standard Operating Procedures (SOPs)
- Batch records
- Change controls
- Validation documents
- Technical protocols
- Supporting manufacturing documentation
Provide technical support for equipment and facility projects within Sterile Supply operations.
Drive continuous improvement initiatives focused on increasing compliance, improving efficiency, reducing costs, and standardizing processes.
Analyze operational issues from multiple perspectives including safety, compliance, equipment, automation, process, and personnel to identify and resolve root causes.
Design, execute, review, and support experimental protocols as required.
Provide on-the-floor support for manufacturing operations and troubleshooting of process and equipment issues.
Lead or support projects aimed at:
- Improving Right-First-Time performance
- Reducing deviations
- Implementing CAPAs
- Enhancing operational efficiency
- Increasing regulatory compliance
Support site safety, environmental, and quality objectives.
Manage project schedules and ensure key milestones and compliance deadlines are achieved.
Communicate potential delays and develop mitigation plans when necessary.
Collaborate closely with Operations, Quality, Planning, Automation, Maintenance, Engineering teams, project stakeholders, and external vendors.

Required Qualifications

Education

Bachelor's Degree (B.S. or B.A.) in:
- Engineering
- Life Sciences
- Biological Sciences
- Chemistry
- Or a related technical discipline

Experience

2-4 years of relevant experience (co-op, internship, and industry experience combined will be considered).
Strong technical writing and documentation skills.
Excellent communication, leadership, and teamwork abilities.
Demonstrated ability to manage projects and meet aggressive deadlines.
Ability to work effectively in a fast-paced manufacturing environment.

Preferred Qualifications

Experience with deviation investigations and deviation management systems.
Root Cause Analysis (RCA) experience.
Change Control experience.
Experience supporting biologics, vaccine, pharmaceutical, or sterile manufacturing operations.
Familiarity with GMP-regulated environments.
Experience in manufacturing operations or technical support roles.
SAP experience.
Power BI experience.
Experience supporting CAPAs and continuous improvement initiatives.

Key Skills

Technical Writing
GMP Documentation
Root Cause Analysis
CAPA Management
Change Control
Problem Solving
Cross-Functional Collaboration
Project Management
Process Improvement
Manufacturing Support
Compliance and Quality Systems

Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.

Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

About the Company

Nesco Resource, LLC

Companies need talent. You want job opportunities.

That’s where we come in. We create meaningful connections between companies and candidates, and we’ve been doing it for over 65 years.
Our national workforce solutions include contract, contract-to-hire, direct placement services, and managed services for a variety of industries.

We employ specialized recruiters focused in Engineering, Information Technology, Accounting & Finance, Administrative & Customer Service, and Manufacturing & Distribution.

When you need to find a job, we're your partner.

COMPANY SIZE

10,000 employees or more

INDUSTRY

Staffing/Employment Agencies

EMPLOYEE BENEFITS

Paid Sick Days, Parking, Performance Bonus, Employee Referral Program

FOUNDED

1956

WEBSITE

https://nescoresource.com/

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