Immunocore

Manufacturing Engineer / Quality Specialist

Immunocore$70K — $95K *
Manufacturing & Automotive
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Associate's degree in industrial engineering, manufacturing engineering technology, or equivalent (Bachelor's preferred).
  • 3-5 years of experience in a manufacturing engineering role.
  • Pragmatic and entrepreneurial personality with a strong initiative.
  • Ability to work independently with minimal supervision.
  • Familiarity with ISO 9001:2015 Quality Management System.

Responsibilities

  • Support manufacturing processes and conduct failure analysis.
  • Ensure compliance with QMS during manufacturing activities.
  • Develop and execute process validation plans and protocols.
  • Perform PPAP inspections and verify product compliance.
  • Lead initiatives for continuous improvement in quality processes.
  • Maintain and improve the Quality Management System (QMS) compliance.
  • Track KPIs related to quality, delivery, and customer satisfaction.

Benefits

  • Health/Prescription Coverage
  • FSA or HSA
  • Dental and Vision insurance
  • Life Insurance
  • Company-match 401(k) Plan
  • Vacation, Sick Leave, and Paid Holidays.
Full Job Description
Vacancy Name
Manufacturing Engineer / Quality Specialist

Vacancy No
VN849

Employment Type
Full-Time

Shift

Duration (if temporary)

Location Country
United States

Location State
New Jersey
Location City
South Plainfield

Description
The Manufacturing Engineer / Quality Specialist will play a key role in implementing process improvements within an efficient ISO-9001:2015 compliant environment: The Mechanical Engineer / Quality Specialist will report directly to the Plant Manager with dotted line reporting to the company president. An elevated level of independent activity is expected. This position is on-site.

Key Responsibilities
The employee is required to perform all or a combination of the following essential responsibilities as determined by business objectives
Manufacturing support:
• Support manufacturing processes, including failure analysis, documentation review and approval, equipment qualification/calibration, and defect containments.
• Ensure manufacturing activities follow QMS.
• Support development and execution of process validation and verification test plans, protocols, and reports.
• Perform and coordinate PPAP inspections and product verification activities.
• Ensure compliance with drawings, specifications, and customer requirements.
• Administer and improve quality processes, with a focus on Lean process management.
• Assist manufacturing and product development with documentation, guidance, and execution of design verification/validation and process validation.
• Lead implementation and improvement of manufacturing-related quality processes.
Continuous Improvement:
• Lead and manage initiatives in multiple product and process quality areas.
• Ensure successful, on-time completion of continuous improvement and capex projects.
• Support internal and external audits, prepare and review back-room documentation.
• Full responsibility of change order and deviation processes.
• Lead timely investigation (root cause analysis), disposition (including corrective and preventative actions), tracking, and reporting of non-conformances (NCP), both internal and supplier related.
• Track KPIs including delivery performance, NCPs, cost of quality, and customer satisfaction.
• Ensure QMS integrity during changes and process improvements.
• Maintain technical documentation in support of QMS
Quality Management System (QMS)
• Maintain and improve the ISO 9001:2015 Quality Management System.
• Control and update the Quality Manual, procedures, and work instructions.
• Maintain and administer IQM (Ideagen Quality Management) system including document control, audits, assets, and workflow processes
• Perform, Coordinate and Support internal and external (including customer) audits.
• Identify risks and opportunities and support QMS planning and improvements.
• Ensure controlled implementation of QMS changes and improvements in compliance with ISO standards.
The employee may be required to perform other non-essential functions, follow any other job-related instructions, and perform any other job-related duties requested by their supervisor.

Key Requirements
EDUCATION - associate's degree in industrial engineering (IE), manufacturing engineering technology (MET), or equivalent (bachelor's degree preferred).
SKILLS - Pragmatic, entrepreneurial personality, and strong initiative-taker. Continually strives to improve.
EXPERIENCE - A minimum of 3-5 years of working experience in a manufacturing engineering capacity

Education Level
Associates or equivalent

Experience Level
3-5 years

Benefits
• Health/Prescription Coverage
• FSA or HSA
• Dental
• Vision
• Life Insurance
• Company-match 401(k) Plan
• Vacation/Sick/Paid Holidays
*All benefits start on date of hire

Physical Requirements

About Immunocore

Immunocore is a biotechnology company that specializes in the development of novel cancer therapies. The company's proprietary technology platform, called ImmTACs, is designed to activate the immune system to target and destroy cancer cells. Immunocore's lead product candidate, IMCgp100, is currently in clinical trials for the treatment of melanoma and other solid tumors. The company was founded in 2008 and is headquartered in Abingdon, UK.
Learn more about Immunocore
Size
300 employees
Market Cap
$2.5 billion
Industry

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