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Quality Engineering Supervisor Jobs

Company

Berry Global, Inc

Address , Franklin, 46131, In
Employment type FULL_TIME
Salary
Expires 2023-07-27
Posted at 10 months ago
Job Description
Overview:
Berry Global Berry Global, headquartered in Evansville, Indiana, is committed to its mission of ‘Always Advancing to Protect What’s Important.’ With $13 billion in revenue for fiscal year 2019 on a combined pro forma basis from operations, Berry is a leading global supplier of a broad range of innovative nonwoven, flexible, and rigid products used every day within consumer and industrial end markets. Berry operates over 290 manufacturing facilities worldwide, on six continents, and employs over 48,000 individuals.

At Berry, we pursue excellence in all that we do and are always advancing to improve the way we work along with the products and services we provide. Our culture fosters trust and partnerships through appreciation, acknowledgement, and inclusion. At Berry, we are continuously improving to support our mission and exemplify our values of partnerships, excellence, growth, and safety. To learn more about Berry, visit berryglobal.com
Responsibilities:
Under the direction of the Quality Manager, the Quality Engineer is responsible to understand the
principles of product and service quality through evaluation and control. Body of knowledge and
applied technologies include, but are not limited to, validation, development and operation of
quality control systems, application and analysis of testing and inspection procedures, the ability
to use metrology and statistical methods to diagnose and correct improper quality control
practices, an understanding of human factors and motivation, proper application of
business/quality/safety cost concepts and techniques, knowledge and ability to develop and
administer management systems and to audit quality systems for deficiency identificaticin,
correction and improvement.
Primary quality signatory responsible for providing leadership, guidance and oversight of
commissioning, qualifications and validations related to molding, equipment, and software at
the Franklin facility.
  • Writes validation documents, as needed (e.g. URS, FAT, IQ, OQ, PQ), executes protocols,
analyzes and writes summary reports, deviation resolution and CAPA's.
  • Assists in the implementation of, and adheres to, company policies and procedures to ensure
compliance to applicable federal, state, and local laws and regulating the industry.
  • Manages continuous improvement activities regarding quality of all products, as determined
by manufacturing production events, heldware, scrap and customer complaints.
  • Investigates internal and external concerns related to the plant quality system.
  • Possesses and maintains an ongoing thorough knowledge of cGMP requirements and
  • Supports customer needs in coordination with plant management.
regulatory expectations.
  • Responsible for Qualification of Change (Change Control). Reviews and approves
manufacturing changes to ensure that quality requirements are met.
  • May assist in other areas or perform other duties as reauired by fluctuatinq business needs.
  • Assists with Internal Audits and Supplier Quality Audits, as needed.
Qualifications:
  • Should possess a strong understanding of qualification and validation requirements for
  • Ability to work in a team based, high paced and multi-task environment.
  • Blackbelt training/certification preferred
  • 5-10 years experience in an FDA regulated industry preferred
  • Possesses strong technical, verbal and written communication and interpersonal skills.
  • Bachelors Degree in an Engineering discipline required. CQE preferred.
    • Blackbelt training/certification preferred
    • Addresses inquiries and resolves problems by leading or working with appropriate
    resources/other departments to achieve results/answers.
    • Ability to work in a team based, high paced and multi-task environment.
    • Ability to interact closely with other departments to support quality focus.
    • Ability to interact professionally with external customers.
    • Demonstrated proficiency in Microsoft Word, Excel, MS PowerPoint, and applicable statistical
    software (MiniTab, lnfinityQS).
    • Must possess a working knowledge of statistical process control, Lean Manufacturing, and
    other quality systems (e.g. FMEA, DOE, Gauge R&R, Capability Studies, etc.).
    • Maintains working knowledge of ISO quality standards (specifically 9001, 13485, 15378),
    US medical device regulations and guidelines (21 CFR 820, QSR, GAMP4).
    • Should possess a strong understanding of qualification and validation requirements for
    healthcare/medical device products and equipment.
    • Ability to communicate throughout all levels and functions of the organization
    • Demonstrates excellent data analysis and presentation skills
    • Demonstrates excellent analytical decision making and problem solving skills
    • Possesses strong technical, verbal and written communication and interpersonal skills.
    • High attention to detail, initiative, self-motivated, and independent decision making ability.
  • High attention to detail, initiative, self-motivated, and independent decision making ability.
  • Must possess a working knowledge of statistical process control, Lean Manufacturing, and
  • Demonstrates excellent analytical decision making and problem solving skills
  • Ability to interact professionally with external customers.
  • Demonstrated proficiency in Microsoft Word, Excel, MS PowerPoint, and applicable statistical
  • Demonstrates excellent data analysis and presentation skills
  • Maintains working knowledge of ISO quality standards (specifically 9001, 13485, 15378),
  • Addresses inquiries and resolves problems by leading or working with appropriate
  • Ability to interact closely with other departments to support quality focus.
  • Ability to communicate throughout all levels and functions of the organization