RFP 202606109 Proposed Services Response Form.docx
DOCX document 43 KB Posted
- Attached to
- Forensic Chemistry Quality Assurance Services
- Solicitation number
- RFP - 10A - 202606109
- Issued by
- Maine
About this file
This is a Proposed Services Response Form for RFP #202606109 issued by the State of Maine Department of Health and Human Services (DHHS) for Forensic Chemistry Quality Assurance Services. The RFP requests support for the Department's Health and Environmental Testing Laboratory (HETL) Forensic Chemistry Section on a remote basis for up to forty hours per month. The scope of work encompasses development and review of Standard Operating Procedures and quality management documentation, coordination and conduct of annual internal audits, preparation for ANAB onsite assessments, monitoring of nonconforming work and corrective actions, implementation of risk-based thinking and preventive actions, maintenance of quality records, administration of proficiency testing and personnel monitoring programs, validation and verification of new methods and equipment, assistance with annual management reviews, and maintenance of all communications with the accrediting body regarding ISO/IEC 17025 and ANAB AR 3125 compliance requirements.
The position requires a minimum of a bachelor's degree in chemistry, biology, or forensic science and six years of analytical laboratory experience, including specific experience in forensic testing laboratories, ISO 17025 accredited environments, quality assurance practices, validations, and advanced analytical instrumentation such as GC/MS, FTIR, and LC-MS/MS, with prior supervisory experience preferred. Bidders must submit six required reports on specified timelines: Internal Audit Reports and Management Review Reports due annually by April 1st, Corrective Action Reports, Nonconforming Work Reports, and Improvement Reports submitted as needed with timelines to be determined between the Department and awarded bidder, and a Conformance File Report due annually by April 1st. The RFP document provided is a response form template that bidders must complete to describe their proposed methods, resources, how tasks will be accomplished, and how desired outcomes will be achieved, with provisions for identifying any subcontractor work.
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Other files
| File | Type | Posted |
|---|---|---|
| RFP# 202606109 - Forensic Chemistry Quality Assurance Services_FINAL.docx | DOCX document | |
| Rate Base (All-Inclusive) Cost Form.xlsx | XLSX spreadsheet |
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Text version
RFP # 202606109
Forensic Chemistry Quality Assurance Services
PROPOSED SERVICES RESPONSE FORM
Bidder Name:
INSTRUCTIONS: Bidder must complete this form to discuss the Services to be Provided referenced in Part II of the RFP and what the Bidder will offer, including:
· A description of the methods and resources the Bidder will use and how each task involved will be accomplished.
· A description of how the expectations and/or desired outcomes as a result of these services will be achieved.
· If subcontractors are involved, Bidders must clearly identify the work each will perform.
Bidders may expand each of the response (white) spaces within this document in order to provide a full response to each requirement.
A. Forensic Chemistry Quality Assurance Services
1. The awarded bidder will support the Department’s Health and Environmental Testing Laboratory (HETL) Forensic Chemistry Section, in a remote capacity for up to forty (40) hours per month by:
a. Assisting with the development, review, and approval of Standard Operating Procedures and other documents that make up the quality management system and administer the document control system, including maintaining and updating the quality manual.
b. Coordinating and conducting annual internal audits onsite:
i. Select internal auditors to participate and ensure proper training and understanding of the audit process.
ii. Prepare and distribute a detailed report of findings and opportunities for improvement.
c. Preparing and coordinating for annual ANAB onsite assessments.
d. Monitoring nonconforming work and conducting and coordinating corrective actions.
e. Implementing risk-based thinking approach and ensuring the initiation of preventive actions to reduce risk.
f. Maintaining all quality records according to established policies and procedures (such as authorizations to perform casework, list of approved vendors, training and professional development of personnel, courtroom testimony evaluations, improvement measures, internal audits, external assessments, and management reviews).
g. Administering the proficiency testing and personnel monitoring program according to accreditation criteria.
h. Ensuring new methods and equipment are properly validated and/or verified, and records maintained.
i. Assisting with the annual management reviews.
j. Maintaining responsibility for all communications with the accrediting body, including responding to findings of nonconformance, requests for various documents and records, surveillance and external assessment planning and submission of information, annual reports, and disclosure of significant changes, events, and nonconformities.
k. Ensuring management and technical operations conform to the ISO/IEC 17025 standard and the ANAB AR 3125 requirements.
l. Staying abreast of any changes in accreditation requirements, providing guidance regarding quality issues, and proposing improvements to the quality system.
m. Overseeing training programs and maintaining training records.
n. Ensuring courtroom testimony provided by HETL staff is monitored.
o. Creating and maintaining a detailed conformance file or checklist that demonstrates how the laboratory has determined compliance with accreditation requirements.
B. Staffing Requirements
1. Quality Assurance Staff must have at minimum a bachelor’s degree in chemistry, biology, or forensic science, and six (6) years of experience in an analytical laboratory, including experience:
a. Working in a forensic testing laboratory;
b. Working in an ISO 17025 accredited laboratory;
c. Working with quality assurance and control practices and procedures, including but not limited to, audits, proficiency tests, corrective actions and document control;
d. Performing validations;
e. Using advanced analytical instrumentation, including but not limited to GC/MS, FTIR and LC-MS/MS.
f. Previous supervisory experience preferred but not required.
C. Reports
1. Track and record all data/information necessary to complete the required reports listed in Table 1:
Table 1 – Required Reports
| Name of Report |
| Description |
| a. |
| Internal Audit Report |
| Audit of laboratory operations and policies and procedures required for ANAB accreditation |
| b. |
| Management Review Report |
| Review of management system required for ANAB accreditation |
| c. |
| Corrective Action Reports |
| Reports detailing laboratory issues and plans for remediation |
| d. |
| Nonconforming Work Reports |
| Reports detailing laboratory issues |
| e. |
| Improvement Reports |
| Reports detailing areas for improvement to laboratory policies and procedures |
| f. |
| Conformance File Report |
| Report demonstrating laboratory’s compliance with ANAB accreditation criteria |
2. Submit all the required reports to the Department in accordance with the timelines established in Table 2:
Table 2 – Required Reports Timelines
| Name of Report |
| Period Captured by Report |
| Due Date |
| a. |
| Internal Audit Report |
| Annual |
| April 1st |
| b. |
| Management Review Report |
| Annual |
| April 1st |
| c. |
| Corrective Action Reports |
| As needed |
| To be determined between the Department and awarded Bidder |
| d. |
| Nonconforming Work Reports |
| As needed |
| To be determined between the Department and awarded Bidder |
| e. |
| Improvement Reports |
| As needed |
| To be determined between the Department and awarded Bidder |
| f. |
| Conformance File Report |
| Annual |
| April 1st |
DHHS RFP Proposed Services Response Form (Rev. 10/2025)
File details come from the government source that posted it. Updated .