Quality Engineer

at  Celeros Flow Technology

Glasgow G44, Scotland, United Kingdom -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate29 Nov, 2024Not Specified01 Sep, 2024N/AProfessional Conduct,Powerpoint,Disabilities,Preparation,Iso,Training Programs,Excel,Technical Competence,Interpersonal SkillsNoNo
Add to Wishlist Apply All Jobs
Required Visa Status:
CitizenGC
US CitizenStudent Visa
H1BCPT
OPTH4 Spouse of H1B
GC Green Card
Employment Type:
Full TimePart Time
PermanentIndependent - 1099
Contract – W2C2H Independent
C2H W2Contract – Corp 2 Corp
Contract to Hire – Corp 2 Corp

Description:

For over 140 years our products have helped ensure the safe, reliable operations of key industries. With a passion for precision and partnership, Celeros Flow Technology continues this heritage of high performance and dependability, providing mission critical, sustainable flow control solutions for our customers around the globe.
Celeros Flow Technology is looking for individuals with a voice and a vision. We embrace change, diversity and promote new ways of looking at old ideas. We seek talented professionals to join our world-class team of innovators in a global, collaborative & multi-cultural environment, where you will be challenged, supported, and inspired to be extraordinary.

GENERAL SUMMARY

The Quality Engineer shall manage, and coordinate Quality Assurance activities support of project execution in accordance with the company’s quality management system, across product lines that are manufactured, assembled, and serviced within the Glasgow (Cathcart) facility. Working in accordance with company policies and procedures to meet external regulations to deliver standards such as: ISO 9001& ASME Certificates of Authorisation.

EDUCATION AND EXPERIENCE

  • University or College Degree in Engineering or Quality Management. Or significant relevant Industry experience
  • Experience of ISO 9001, API, DEF-STAN`s,NQA-1, ASME Codes and Standards, RCC-M,ASNT-TC-1A and EN ISO 9712
  • Technical competence for review of ISO/ASTM Standards and customer specifications
  • Process risk management and RCFA experience
  • High level of computer proficiency (WORD, Excel and Powerpoint)
  • Experience in preparation, development, and delivery of training programs
  • Wide ranging auditing experience Internal and External
  • Basic knowledge of HSEQ Company Standards
  • Continual Improvement experience in an engineering / manufacturing environment’
  • Yellow/Green Belt in Lean 6-Sigma
  • Excellent communication (both written and oral), influencing and interpersonal skills
  • High degree of commercial acumen
  • Highly professional conduct
  • Must be willing to occasionally travel and able to spend time away from home, full UK Driving Licence

Responsibilities:

PRINCIPLE DUTIES AND RESPONSIBILITIES

  • Lead Quality reviews of contract specific requirements at tender and order execution phase.
  • Communicate effectively Quality requirements and expectation to functional areas through formal communication with internal and external stakeholders i.e., Review meetings, Order Review Documents and Quality Plans.
  • Coordinating with internal departments to define and resolve product quality problems and provide advice, guidance and support on all aspects and matters concerning Quality.
  • Leading negotiation of Quality standards with customers and promoting the external image of the Company through effective Quality management.
  • Coordinating with external customers and vendors to ensure clear and concise understanding of Quality requirements.
  • Support Quality initiatives to ensure the appropriate culture, knowledge, understanding and attitude towards Quality matters, and support continuous improvement as well as widespread acceptance and adoption of best practice.
  • Issuing of technical documentation for customers, aimed at verifying organisation’s products’ reliability, safety, and guarantee.
  • Supporting the development of Quality procedures and standards and updating quality procedures as Standard or best practice changes occur.
  • Ensuring Clyde Union Ltd maintains and surpasses the necessary Group, Company, Industry, National and International standards, regulations, statutes, compliance, and other governmental guidance to ensure as far as is reasonably practicable, that best practices in the field of Quality are exercised.
  • Conducting audits in accordance with the applicable audit programs for Cathcart site in line with ISO9001:2015, NQA-1 and any other industry standards supporting the business functions, including the completion of supporting documents.
  • Leading product or process related incident investigations, ensuring that methods of investigationLead Quality reviews of contract specific requirements at tender and order execution phase.
  • Communicate effectively Quality requirements and expectation to functional areas through formal communication with internal and external stakeholders i.e., Review meetings, Order Review Documents and Quality Plans.
  • Coordinating with internal departments to define and resolve product quality problems and provide advice, guidance and support on all aspects and matters concerning Quality.
  • Leading negotiation of Quality standards with customers and promoting the external image of the Company through effective Quality management.
  • Coordinating with external customers and vendors to ensure clear and concise understanding of Quality requirements.
  • Support Quality initiatives to ensure the appropriate culture, knowledge, understanding and attitude towards Quality matters, and support continuous improvement as well as widespread acceptance and adoption of best practice.
  • Issuing of technical documentation for customers, aimed at verifying organisation’s products’ reliability, safety, and guarantee.
  • Supporting the development of Quality procedures and standards and updating quality procedures as Standard or best practice changes occur.
  • Ensuring Clyde Union Ltd maintains and surpasses the necessary Group, Company, Industry, National and International standards, regulations, statutes, compliance, and other governmental guidance to ensure as far as is reasonably practicable, that best practices in the field of Quality are exercised.
  • Conducting audits in accordance with the applicable audit programs for Cathcart site in line with ISO9001:2015, NQA-1 and any other industry standards supporting the business functions, including the completion of supporting documents.
  • Leading product or process related incident investigations, ensuring that methods of investigation and reporting appropriate to the incident are utilised; ensuring that lessons are established, learned, and implemented such that all parties benefit from these lessons.
  • Develop efficient and effective processes and controls with respect to Quality performance.
  • Ownership of project NCR`s through to closure, prior to goods shipment.
  • Application of Root Cause Failure Analysis (RCFA) techniques on identified product and processes to eliminate repeat errors.
  • Support EHS requirements as applicable through project execution and facility needs.

ADDITIONAL RESPONSIBILITIES

  • Promoting Clyde Union Ltd Health and Safety policies to reduce potential harm to self and others.
  • Maintenance of Human Resource activities in relation to attendance, holidays, and performance.
  • Perform all duties in accordance with the Company’s Procedures to deliver and maintain the highest standards of ethical behaviors and be a role model for others.
  • Developing self within role and participate in and develop from training and developmental activities assigned to oneself.
  • Understanding Clyde Union Ltd service and product offerings
  • Establishing self as a subject matter expert with customer and expert in designated technical/professional discipline
  • Creating and maintaining good working relationships
  • Understanding and using of the correct reporting lines
  • Employees are expected to work whatever reasonable hours are necessary to meet the requirements of their job.
  • Travel and additional duties may be required on an ad hoc basis, so a degree of flexibility is required.

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  • Required daily to stand, sit, walk, talk, hear, and see (specific close vision abilities are required to perform computer work)
  • Required occasionally to stoop, kneel, crouch and crawl
  • Required daily to use hands and fingers and arms to reach (to operate a computer and telephone)
  • Required occasionally to lift and/or move objects that are light to moderate
  • Required occasionally to travel (usually by air or road so may be required to sit for extended periods

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  • Ability to work with moderate noise (i.e. business office with computers, phone, and printers, etc.)
  • Ability to work in an open planned office / individual office
  • Ability to sit at a computer terminal for extended periods
  • Ability to sit in a car or on a plane for extended period


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Production / Maintenance / Quality

Clinical Pharmacy

Graduate

Proficient

1

Glasgow G44, United Kingdom