Assistant Manager - QMS Job at Nordex Group (Chennai)

Process Engineering Specialist

This is a multi-faceted position providing process engineering support to the fa...

Location

United States , Sudbury

Salary:

100000.00 - 115000.00 USD / Year

Nestlé Purina

Expiration Date

Until further notice

Requirements

BS Degree in Chemical, Mechanical Engineering or a related field
3+ years of experience in process engineering & projects field
Experience in a food, dairy, pharmaceutical, etc manufacturing plant environment (preferably in infant formula and/or medical nutritional, dairy processing, spray drying process, or food / fluid products). Aseptic experience is a plus Preferred.
Ability to work flexible hours
Above average communication skills (written and oral)
Above average project management skills preferably in handling large scale projects (< $750,000)
Problem-solving skills
Ability to prioritize
Knowledge of Microsoft Word, Project and Excel required
SAP, AutoCAD experience is preferred

Job Responsibility

Provide process engineering support to the factory in capital project execution and process line support.
Responsible for project management, production line trouble shooting, administering budgeting, design, installation, qualification, and commissioning of new/modified process systems.
Assist Production and Quality Departments to resolve non-maintenance related production and quality issues.
Conduct training, maintain and update documentation relating to job.
Assist in training and mentoring of new engineering staff.
Follow up investigation using root cause analysis tools such as GSTD and/or DMAIC on process related issues
Provide resolution of process line quality deviations thru formal requests such as ODIR, process deviations, and NCR's
Investigation feasibility and scope analysis to determine potential operational improvements
Independently develop and design process systems for manufacturing of food products including liquid and powder
Conduct budget estimation, planning, and execution of projects.

What we offer

performance-based incentives
401k with company match
healthcare coverage
broad range of other benefits
physical, financial, and emotional wellbeing support
professional growth opportunities
dynamic career paths
robust development
opportunities to learn from talented colleagues around the globe

Fulltime

Electrical Quality Control Inspector

The Quality Control Inspector is responsible for following the M.C. Dean Quality...

Location

United States , Caroline County

Salary:

Not provided

M.C. Dean, Inc

Expiration Date

Until further notice

Requirements

Associates Degree in Technical Discipline (may be substituted for quality related experience)
At least 4 years hands-on experience in the electrical industry
To possess or have the ability to obtain a state issued Journeyman License within 6 months of hire
Experience with reading and interpreting contractual requirements, drawings, BIM models, specifications, current NEC codes, NETA and other applicable standards
Experience with receiving, production, shipping and quality processes
Excellent communication skills (written, and verbal)
Strong attention to details, highly organized and computer literate
Ability to work well in a fast-paced manufacturing environment

Job Responsibility

Conduct inspections to ensure compliance and conformance with project or contract specifications
Conduct inspections in accordance with Quality Control Plan
Conduct inspections to ensure adherence to applicable legal requirements
Confer with Quality Assurance, Manager as appropriate
Read blueprints and specifications
Monitor operations to ensure that they meet specifications
Recommend adjustments to the assembly or installation process
Inspect, identify, and submit material, components, or products for testing and measurement
Operate electronic inspection equipment and software
Document approval or rejection of inspected material, components, or products

What we offer

A competitive salary
Medical, dental, vision, life, and disability insurance
Paid-time off
Tuition reimbursement
401k Retirement Plan
Military Reserve pay offset
Paid maternity leave

Fulltime

Quality Manager

The Quality Manager is a critical leadership role responsible for stewarding and...

Location

United States , White River Junction

Salary:

80000.00 - 115000.00 USD / Year

Concepts NREC

Expiration Date

Until further notice

Requirements

A degree in Quality Engineering, Aerospace Engineering, Industrial Engineering, or a related technical discipline is preferred
equivalent combination of education and experience will be considered.
Preference given to candidates with a minimum of 5 years of AS9100 or similar quality system experience in an aerospace, defense, or precision manufacturing environment.
Preference given to candidates with demonstrated leadership of a team.
AS9100 Lead Auditor certification preferred. Experience managing third-party registrar and OEM customer audits is preferred.
Working knowledge of FAR/DFAR requirements and experience navigating quality requirements of government contracts in collaboration with DCMA strongly preferred.
Proficiency in MS Office products required.
Experience with or desire to leverage AI in support organizational quality objectives strongly preferred.
Exceptional communicator in both written and verbal interactions.
High degree of emotional intelligence with the ability to develop trust with customers, leaders, and team members.

Job Responsibility

Manage all QMS certifications including AS9100, ISO 9001, and OEM approvals. Schedule and host onsite audits with OEM customers and third-party registrars.
Manage and maintain internal audit programs. Drive change and improvement from audit findings.
Manage the corrective action (CAR) system to ensure action plans are appropriate, complete, and closed in a timely manner.
Manage the non-conformance (NCM) system to drive disposition, verification and identify corrective actions to prevent recurrence.
Manage and monitor QMS performance metrics to identify trends and develop effective mitigation plans.
Manage a team of experienced Quality Technicians and Quality Engineers in support of inspection activities, including but not limited to CMM, hard-gauging, visual, receiving and documentation.
Manage and ensure the calibration system is current and documented, including oversight of suppliers that support calibrations.
Manage QMS document control and implement a QMS document auditing program to ensure the most current revision levels are in use and that work instructions, processes, and procedures meet the latest applicable requirements.
Conduct employee performance reviews and performance planning for direct reports.
Serve as a trusted quality liaison for operations leadership and customers by communicating quality issues, trends, and improvement opportunities.

Fulltime

Qa Gcp Manager

Proclinical is looking for a Quality Assurance Manager to join a dynamic organiz...

Location

United Kingdom , City of London

Salary:

Not provided

Proclinical

Expiration Date

Until further notice

Requirements

Training and proven years of working experience in Good Clinical Practice (GCP)
Professional working years of relevant QA experience, preferably within the life sciences sector
Expert knowledge of UK, EU, and US clinical trial legislation
Strong ability to communicate effectively and influence across and within the organization
Excellent written and verbal communication skills
Exceptional interpersonal and negotiation skills

Job Responsibility

Manage the Quality Management System (QMS)
Contribute to the generation and management of the internal audit schedule
Independently conduct and report audits in accordance with the internal audit schedule
Conduct vendor audits as instructed
Lead, manage, and coordinate client audits and regulatory inspections
Respond to and follow up on audit reports and vendor questionnaires
Review and provide QA approval of SOPs and other controlled documents
Effectively monitor compliance with processes
Provide input for and maintain oversight of CAPAs and quality issues
Generate quality metrics reports to update the management team on quality-related issues and initiatives

What we offer

Flexible home and/or office working
Industry leading training
Competitive total reward package

Fulltime

Senior Manager, Patient Safety

The Senior Manager, Medical Device end to end Management is a leadership role re...

Location

India , Hyderabad

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Experience in Patient Safety Services
demonstrated success in clinical, medical, or scientific domains
People management capabilities with experience leading teams
Experience in client relationship management
Understanding of pharmacovigilance operations, clinical research methodologies, and regulatory frameworks
Clinical experience with progressive responsibilities
Strong clinical, regulatory, and medical Patient Safety Services knowledge
Good understanding of ICH, CIOMS, GVP, and pharmacovigilance requirements
Familiarity with automation/AI in pharmacovigilance
Adaptable mindset with enthusiasm for learning

Job Responsibility

Lead the complete lifecycle of medical device complaint handling and post-market surveillance
Oversee FDA MDR reporting including 5-Day, 30-Day, and Supplemental Reports
Ensure high-quality investigations, root cause analysis, and CAPA linkage
Maintain compliance with 21 CFR 803, 820, ISO 13485, and internal QMS standards
Partner with Regulatory, Quality, R&D, and Manufacturing teams to manage product performance and patient safety insights
Support FDA inspections and internal/external audits
Manage and mentor a high-performing complaint operations team
Delegate work to Patient Safety staff according to allocated budget/hours
Coordinate with Solutions Consultant and/or regional Head of Safety Services as appropriate to assign resources to the project, and to assess staffing needs for current and future activities
Conduct interviews for recruitment of new personnel as necessary

Fulltime

Quality Control Officer - Microbiology

Location

United Kingdom , Stirling

Salary:

Not provided

SRG

Expiration Date

Until further notice

Requirements

Knowledge of and experience in regulated industrial microbiology/cleanroom environments
Experience of working in a GMP regulated environment would be beneficial
Experience of helping manage a QMS and assist with investigations

Fulltime

Technical Quality Specialist

The Technical Quality Specialist is responsible for providing technical support ...

Location

Canada , Cambridge

Salary:

76000.00 - 104500.00 USD / Year

ATS Automation Tooling Systems Inc.

Expiration Date

Until further notice

Requirements

A post-secondary technology diploma or engineering degree or equivalent, specializing in electronics, electrical or mechanical engineering or equivalent work experience is required
A minimum of five years of quality assurance experience is required
Demonstrated technical problem solving
the ability to analyze and solve problems is essential
Strong communication skills are required to communicate with people at all levels within the organization, both orally and in writing
Ability to work cooperatively in a team environment
Strong data analysis skills

Job Responsibility

Assist process owners in the interpretation of quality, technical performance and business requirements
Develop, recommend and facilitate implementation changes to workflow
improve quality management system, review operational performance and provide solutions
Support the deployment of N299/ISO 9001 program and perform audits with associated RCCA activities
Inspection of incoming parts and associated supplier documentation
Review incoming unqualified/qualified source material for compliance with the Purchase Order and code requirements
Manage assigned projects in accordance with applicable standards, procedures and the gate review process
Analyze and prepare statistical data to determine capability of processes and measurement systems
Analyze test data as evidence to the degree of compliance to customer specifications
Investigate product/process/system quality issues, develop and initiate improvement, preventative actions and/or corrective actions

What we offer

Eligible for Annual Incentive Bonus
Stock Purchase Plan
3 Weeks Vacation
Health Care Benefits + $600 Health Care Spending Account
Employee Engagement Events (Employee BBQ’s and lunches, weekly snack day, etc.)
Employee Development Programs

Fulltime

Quality Management Systems Coordinator

Location

United Kingdom , Newcastle

Salary:

35000.00 GBP / Year

Gillespie Recruitment

Expiration Date

Until further notice

Requirements

Minimum 3 years’ experience implementing and managing ISO 9001 Quality Management Systems
Strong understanding of quality, environmental, and health & safety standards
Experience supporting audits and maintaining compliance post-accreditation
Excellent organisational and planning skills
Strong communication skills (both written and verbal)
Ability to analyse information and present clear, actionable insights
Confident using Microsoft Office packages (Excel, Word, PowerPoint)
Ability to prioritise workload and manage multiple tasks effectively
Experience working both independently and as part of a team

Job Responsibility

Supporting the development and implementation of a robust QMS framework aligned to ISO standards
Assisting in achieving ISO 9001 accreditation and ensuring ongoing compliance
Maintaining and updating policies, procedures, and standards in line with business needs
Supporting internal and external audits and ensuring follow-up actions are completed
Assisting with company-wide risk management and objectives programmes
Preparing performance dashboards and management reports
Supporting leadership with data, insights, and compliance tracking
Advising and supporting colleagues on QMS processes and best practices
Providing training on management systems and compliance requirements
Working collaboratively across departments to embed standards

What we offer

Salary of £35,000
Opportunity to play a key role in achieving ISO accreditation
Involvement in shaping and embedding business-wide processes
Collaborative working environment with senior stakeholder exposure
Ongoing professional development opportunities
A role with real impact on organisational performance and compliance

Fulltime

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Assistant Manager - QMS

Job Description

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