Quality Manual
Quality Manual
Quality Manual
1. PURPOSE
This document defines the requirements, processes, structure and documentation for the
Teledyne DGO Quality Management System.
2. SCOPE
The Teledyne DGO Quality Management System has been designed and implemented for
effective management, customer satisfaction, and continual improvement. It has been
implemented to meet the requirements of ISO 9001:2008, external and internal interested
parties and applicable regulatory agencies. The QMS governs the design, development and
manufacture of electrical and optical connectors, cable assemblies, penetrators, and servo
control devices used in hostile environments for military and commercial applications,
including sales, testing and technical services.
3. REFERENCES
ISO 9001:2008 Quality Management Systems - Requirements
4. TABLE OF CONTENTS
Section Topic ISO 9001:2008 ISO Teledyne DGO
9001:2015 Document
5 Definitions - - -
6 Process Approach Quality 4.1 4-4.4 -
Management System
7 Document Control 4.2.1, 4.2.3 7.5 SOP-QMS-001
8 Records Control 4.2.4 7.5 Legal 02-001,
Current Teledyne
Technologies
Approved
Retention
Schedule
5. DEFINITIONS
Unless otherwise specified, all terms used in this document are defined in ISO 9001-2008
Term Definition
TDGO Teledyne D G O’Brien
TM Teledyne Marine
Concession A special approval that is granted to release a nonconforming
product for use or delivery
PPM Policy and Procedure Manual
QMS Quality Management System
SOP Standard Operating Procedure
7. DOCUMENT CONTROL
TDGO shall determine which documents shall be controlled and which shall be managed. The
document control process shall ensure that only the correct revision of controlled documents
are available for use and that obsolete documents are not available for use.
To align with industry standard documentation structure, TDGO has adopted QMS SOPs as
Level 2 documents and Work Instructions as Level 3 documents. During the transition from
PPM’s to SOP’s, and PPM’s to Work Instructions, all new released documents shall adopt the
new document labels. All other documents with PPM labels shall be renamed at their next
revision. An electronic link will be established for any PPM document that has been renamed or
superseded to facilitate document user’s in locating renamed or superseded documents.
L1
Manual
Policy
L2
SOP (Standard
Operating
Procedures)
L3
PPM & WI (Work instruction)
L4
Forms & Records
These requirements and process are further defined in the document(s) listed for this section in the
Table of Contents.
8. RECORDS CONTROL
Records established to provide evidence of conformity to requirements and of the effective
operation of the QMS shall be controlled. Records shall remain legible, readily identifiable and
retrievable.
Where customer requirements for records retention conflict with the Teledyne Approved
Retention Schedule, the longer retention requirement shall take precedence.
These requirements and process are further defined in the document(s) listed for this section in the
Table of Contents.
Quality Policy: TDGO management shall establish a quality policy that shall be communicated
and implemented across the organization to describe management’s intentions with respect to
Quality. As a part of TM, TDGO implements the TM Quality Policy and reviews it for adequacy at
each Management Review.
These requirements and process are further defined in the document(s) listed for this section in the
Table of Contents.
Quality Objectives: TDGO management shall establish Quality objectives that define the specific
quality goals that the organization is committed to achieving. The Quality Objectives shall be
measurable and consistent with the Quality Policy. TDGO is provided annual Quality Objectives.
Management Representative: TDGO shall appoint a management representative who has the
responsibility and authority to:
a) Ensure that processes needed for the QMS are established and maintained.
b) Report on the performance of the QMS and needs for improvement.
c) Ensure the promotion of awareness of customer requirements throughout the
organization.
Management Review: TDGO management with executive responsibility shall review the
effectiveness of the quality management system at least annually.
Attendees:
a) All members of the general manager’s staff (top management) participate and attend
management reviews. Where a member is unable to attend, advance written notice
must be provided to the ISO Management representative and a delegate named to
participate in the review.
b) Assemble and forward all required and relevant data to the Management
Representative(s) prior to the scheduled meeting for inclusion into the summary to be
presented at the Management Review.
c) Complete any assigned actions resulting from the Management Review.
These requirements and process are further defined in the document(s) listed for this section in the
Table of Contents.
These requirements and process are further defined in the document(s) listed for this section in the
Table of Contents.
12. INFRASTRUCTURE
TDGO shall ensure that infrastructure, including buildings, workspaces, utilities, process
equipment and supporting services are sufficient to ensure conformity to product requirements
is consistently achieved.
Equipment: TDGO shall ensure that all equipment used in the manufacturing process, including
inspection and test equipment, meets specified requirements and is appropriately designed,
constructed, placed and installed to facilitate maintenance, adjustment, cleaning and use. TDGO
shall ensure that equipment maintenance schedules are established and maintained, periodic
equipment inspections are conducted and documented, and that adjustments are made
correctly as needed.
Customer Related Processes: TDGO shall define product, customer, statutory and regulatory
requirements and shall establish processes to review and understand these requirements. This
review shall be conducted prior to the organizations commitment to supply a product to the
customer and shall ensure that:
a) Product requirements are defined
b) Contract or order requirements differing from those previously expressed are resolved
c) The organization has the ability to meet the defined requirements
Records of the results of the review and actions arising from the review shall be maintained.
Where product requirements are changed, the organization shall ensure that relevant document
is amended and that the relevant personnel are made aware of the changed requirements.
Design Inputs: The organization shall plan and control the design and development of the
product. These inputs shall include:
a) Functional and performance requirements
b) Applicable statutory and regulatory requirements
c) Where applicable, information derived from previous similar designs
d) Other requirements essential for design and development
Design Outputs: The outputs of design and development are provided in a form that enables
verification against the design and development input and shall be approved prior to release.
These outputs shall:
©Teledyne Marine 2017
These requirements and process are further defined in the document(s) listed for this section in the
Table of Contents.
Design Review: At suitable stages, systematic reviews of design and development shall be
performed in accordance with planned arrangements. Participants in such reviews shall
include representatives of functions concerned with the design and development stage(s) being
reviewed. Records of the results of the review shall be maintained.
Design and Development Verification: Verification shall be performed to ensure that the design
and development outputs have satisfied the input requirements. Records of the verification and
any necessary actions shall be maintained.
Design and Development Validation: Validation shall be performed in accordance with planned
arrangements to ensure that the resulting product is capable of fulfilling the requirements for
the specified or known intended use or application. When practical, validation shall be
completed prior to delivery of the product. Records of the results of the validation or any
necessary actions shall be maintained.
Control of Design and Development Changes: Design and development changes shall be
identified and records maintained.
These requirements and process are further defined in the document(s) listed for this section in the
Table of Contents.
Purchasing Data: TDGO shall ensure that suppliers are provided with accurate and complete
requirements, including quality requirements and that changes to these requirements are
delivered to the supplier in writing, and records of these changes shall be retained in
accordance with Records Control requirements.
Verification of Purchased Product: The organization shall establish and implement the
inspection or other activities necessary for ensuring that purchased product meets specified
purchase requirements.
These requirements and process are further defined in the document(s) listed for this section in the
Table of Contents.
Production and Process Changes: TDGO shall ensure that process changes are reviewed,
approved and verified or validated, as appropriate, prior to implementation.
Process Control Data: TDGO shall ensure that validated processes are monitored and controlled
to ensure requirements are consistently met on an ongoing basis. The data collected as a result
of ongoing monitoring shall be documented.
Revalidation: TDGO shall ensure that when changes or process deviations occur that processes
are reviewed and evaluated and where appropriate, revalidation is performed and documented.
Traceability: TDGO, directly or through its suppliers, contractors and service providers, shall
establish, document, and maintain procedures for identifying each unit, lot, or batch of finished
products and components, where appropriate, with a unique control number. These controls
shall be used to facilitate corrective action when and if required.
These requirements and process are further defined in the document(s) listed for this section in the
Table of Contents.
The audit schedule shall be defined by the designated Quality Audit Leader. The schedule shall
be planned taking into consideration the status and importance of the processes and areas to be
audited, as well as the results of previous audits. The audit criteria, scope, frequency and
methods shall be defined. Audits shall be conducted by trained auditors who are independent of
the work being audited.
Audit Documentation: Audit reports are company confidential. Additional audit records that
provide objective evidence of audit execution shall be maintained and available for outside
review as needed.
These requirements and process are further defined in the document(s) listed for this section in the
Table of Contents.
TDGO shall ensure that product that is nonconforming or is suspected of being nonconforming
is identified, and controlled to prevent its unintended use or delivery.
TDGO shall ensure that procedures are established for review and disposition of
nonconforming product and that responsibility and authority for disposition is defined within
these procedures.
TDGO shall also ensure that actions are taken to identify, document and eliminate the root
cause of nonconforming product.
These requirements and process are further defined in the document(s) listed for this section in the
Table of Contents.
This shall include data generated as a result of monitoring and measurement and from other
relevant sources. The analysis of data shall provide information relating to:
a) Customer satisfaction
b) Conformity to product requirements
c) Characteristics and trends of processes and products, including opportunities for
preventive action
d) Suppliers
These requirements and process are further defined in the document(s) listed for this section in the
Table of Contents.