Senior Quality Systems Analyst

Cynet systems Inc; Irvine; On-site; GBP 80,000 - 100,000; Full time

Job summary

A medical device manufacturing company in Scotland seeks a candidate for a role that requires analyzing product changes and collaborating across departments. The ideal applicant will have a Bachelor's Degree in a related field, 5-7 years of experience in a quality or manufacturing environment, and excellent communication skills. Responsibilities include processing change packages, leading projects, and maintaining high attention to detail. The salary range is competitive, reflecting the complexity of the role.

Qualifications

• Experience in a quality and/or manufacturing environment is required.
• Proven expertise in MS Office Suite.
• Strong problem-solving and critical thinking skills.

Responsibilities

• Analyze complex changes and collaborate across departments.
• Support and process change packages against governing procedures.
• Lead small-scale projects requiring an in-depth evaluation.

Skills

Quality and/or manufacturing experience

MS Office Suite expertise

Knowledge of Windchill PLM

Written and verbal communication skills

Problem-solving skills

Attention to detail

Education

Bachelor's Degree in a related field

5-7 years of experience in medical device industry

Job description

Job Description

Pay Range: $51.90hr – $56.90hr

Responsibilities

• Analyze varying complexity of changes and resolve issues with collaboration from cross-functional departments.
• Understand Product Lifecycle Management, ERP, and other Change Control processes and relationships.
• Able to multi-task and handle variable loads independently within multiple systems (Windchill PLM, JDE).
• High attention to detail and robust understanding of document control and GDP.
• Proactive, quick learner with strong communication and decision-making skills.
• Support and process change packages against governing procedures interact with departments to complete the change package, and release final change package.
• Perform incorporation of approved changes to documentation (e.g., JDE data entry and verify correct implementation)
• Participate in special projects, complete assigned tasks, and deliverables
• Evaluate changes proposed by initiators and provide feedback.
• Other incidental duties assigned by Leadership
• Works independently without close supervision
• Compares and evaluates possible courses of action after considering various possibilities
• Applies Candidate's or Candidate's knowledge in following procedures or in determining which procedures to follow or determining whether specified standards are met
• Considers the cause and effect of activities
• Determines or effectively recommends course of action after considering potential risks of alternatives
• May provide guidance to lower-level personnel
• Makes decisions in the face of different alternatives and without formulas or guidelines, or with guidelines that are not complete and exhaustive, and which allow room for creativity and judgment
• Direction tends to be high-level and focused on end results, with means of accomplishment left to the incumbent
• Lead small-scale projects where analysis of situations requires an in-depth evaluation of multiple factors and/or requires an in-depth knowledge of organizational objectives.
• Drive to resolve these issues completely and with speed by leveraging your network of key contacts outside your own area of expertise.
• Drive improvement of current practices and work with the appropriate functions to implement changes or participate in their implementation

Additional Skills

• Experience in a quality and/or manufacturing environment in the medical device industry is required.
• Proven expertise in MS Office Suite.
• Knowledge of Windchill PLM preferred.
• Excellent written and verbal communication skills, including negotiating and relationship management skills.
• Strong problem-solving and critical thinking skills.
• Good understanding of medical device documentation development activities
• Ability to manage confidential information with discretion.
• Strict attention to detail.
• Ability to interact professionally with all organizational levels.
• Ability to manage competing priorities in a fast paced environment.
• Adhere to compliance with internal procedures.

Education and Experience

• Bachelor's Degree or equivalent in a related field of study.
• Experience in a quality and/or manufacturing environment in the medical device industry is required.
• 5-7 years of experience required.