Quality Documentation Specialist

at  Emerson

Cluj-Napoca, Cluj, Romania -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate22 Jan, 2025Not Specified23 Oct, 20242 year(s) or aboveCommunication Skills,ResistanceNoNo
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Description:

If you are a professional looking for an opportunity to grow, Emerson has an appealing role for you! Based in Cluj Napoca, Romania, Quality Documentation Specialist will be responsible to verify, validate & approve the quality documents received from suppliers for the critical components used in assembly of the product, including the material certificates for pressure retaining parts.

PREFERRED QUALIFICATIONS THAT SET YOU APART:

  • Ability to prioritize and coordinate tasks and work on several objectives at the same time
  • Thoroughness, logical thinking, autonomy, ability to react, resistance to stress, oriented towards the client and towards objectives, oral and verbal communication skills;
  • Good communication and relationship skills.

Responsibilities:

IN THIS ROLE, YOUR RESPONSIBILITIES WILL BE:

  • Verify, validate & approve the quality documents received from suppliers for the critical components used in assembly of the product, including the material certificates for pressure retaining parts
  • Ensure traceability for critical components and associated documentation respecting specific rules
  • Perform the final verification and validation for the products for validation of product conformity
  • Generate the documentation package for the qualified tested products as per customer and defined requirements
  • Collaborate with manufacturing department, shipping department and receiving inspectors to ensure that delivered product is according to defined requirements.

FOR THIS ROLE, YOU WILL NEED:

  • Knowledge and experience in working with MRP system;
  • Knowledge of PC operation, MS Office;
  • Knowledge of industrial technical drawing (reading drawings, geometric / tolerant dimensions);
  • Practical knowledge of the use of measuring and monitoring devices;
  • Ability to work in a team and autonomously;
  • Experience of at least 2 years in production or quality;
  • College / Technical University graduate;
  • Good knowledge of MS Office
  • English language skills - verbal and written


REQUIREMENT SUMMARY

Min:2.0Max:7.0 year(s)

Other Industry

Pharma / Biotech / Healthcare / Medical / R&D

Other

Trade Certificate

Verify validate & approve the quality documents received from suppliers for the critical components used in assembly of the product including the material certificates for pressure retaining parts

Proficient

1

Cluj-Napoca, Romania