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HomeCompaniesQualdocMid-Level Project Engineer

Mid-Level Project Engineer

Qualdoc · Richmond, VA · On Site · Deleted · $105,000 / year · Lever

Job facts

FieldValue
CompanyQualdoc
TitleMid-Level Project Engineer
Normalized title-
Department / teamQualdoc Staffing
LocationRichmond, VA, United States
Work modelOn Site
Employment typeDirect Hire
Salary$105,000 / year
Statusdeleted
ATS providerLever
Posted / first seen2026-05-29 / 2026-05-29
Changed / last seen2026-06-04 / 2026-06-02

Related slices

PageWhat it containsOpen
Company jobsActive postings from Qualdoc.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through Lever.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Richmond.Open
Work model jobsActive On Site postings.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyQualdoc
Sourceaca8c915-0193-4d06-bdaf-d0dce8ce7a85
ATS providerLever

Description

Packaging Equipment Project Engineer Location: Richmond, Virginia Job Type: Direct Hire | Full-Time Starting Salary: $105,000+ depending on experience Overview An established manufacturing organization is seeking an experienced engineering professional to support capital projects and packaging system initiatives within a regulated production environment. This role will oversee packaging equipment projects from planning and design through installation, startup, qualification, and operational support. The ideal candidate will have strong project ownership skills, technical engineering expertise, and the ability to collaborate effectively with operations and support teams in a fast-paced manufacturing setting. Primary Responsibilities Technical & Project Execution Provide engineering support for packaging equipment projects for new and existing products Design and develop packaging equipment lines and support systems integration Lead or support installation, commissioning, and verification of equipment Develop and execute equipment testing and qualification protocols Assist with vendor testing, factory acceptance testing (FAT), and site acceptance testing (SAT) Project Management Initiate, plan, and manage multiple projects simultaneously, including scope, schedule, and budget Perform cost estimation and track project expenses Support capital project planning, budgeting, and long-range planning initiatives Conduct project status updates and present progress to stakeholders Review and approve contractor bids, RFIs, and change requests Cross-Functional Collaboration Work with Operations, Quality, Regulatory Affairs, Engineering, Purchasing, and vendors to resolve challenges Coordinate multi-disciplinary teams to ensure successful project execution Ensure alignment with site standards, best practices, and regulatory requirements Compliance & Continuous Improvement Ensure all activities comply with FDA cGMP and company policies Support change control processes for new equipment and process changes Manage or support equipment validation Identify opportunities for process improvements and standardization Promote and exemplify cGMP compliance in all activities Documentation & Training Prepare and maintain project documentation including SOPs, job aids, and technical reports Maintain accurate project records and history files Train production staff on new equipment and processes Serve as a technical resource and mentor to junior team members Qualifications Education & Experience Bachelor’s degree in Mechanical Engineering or related field 5+ years of experience in a manufacturing environment (pharmaceutical, personal care, or similar preferred) Experience with equipment design, installation, commissioning, and validation in a cGMP environment Skills & Abilities Strong project management and organizational skills Ability to manage multiple projects independently Analytical, troubleshooting, and problem-solving skills Effective communication and technical writing abilities Working knowledge of FDA cGMP requirements Ability to read and interpret P&IDs, process flow diagrams, and technical drawings Experience with CAD or similar design software preferred Ability to lead cross-functional teams and influence stakeholders Benefits & Compensation Competitive compensation package beginning at $105,000 annually Medical, dental, and vision insurance options Company-paid life and disability coverage 401(k) retirement savings plan Additional employee benefit programs and resources

Full job record

Job ID00b980ac1cbd1132578286848e8aa303ceb0e0b1
Org ID67e84269-fc5f-4905-aa1b-394afa709294
Source IDaca8c915-0193-4d06-bdaf-d0dce8ce7a85
Board IDaca8c915-0193-4d06-bdaf-d0dce8ce7a85
Providerlever
Provider Job Keycc64728d-1852-41c7-b30f-6705f49e0234
TitleMid-Level Project Engineer
Normalized Title
Statusdeleted
Activeno
Location TextRichmond, VA
Department
TeamQualdoc Staffing
Employment TypeDirect Hire
Workplace Typeon_site
Remote Policy
CountryUnited States
RegionVA
CityRichmond
Salary RawCompensation Competitive compensation package beginning at $105,000 annually Medical, dental, and vision insurance options Company-paid life and di
Salary Min105,000
Salary Max
Salary CurrencyUSD
Salary Periodyear
Source URLhttps://jobs.lever.co/qualdoc/cc64728d-1852-41c7-b30f-6705f49e0234
Apply URLhttps://jobs.lever.co/qualdoc/cc64728d-1852-41c7-b30f-6705f49e0234/apply
First Seen At2026-05-29 07:06:00Z
Last Seen At2026-06-02 10:40:36Z
Last Checked At2026-06-04 11:33:24Z
Last Changed At2026-06-04 11:33:24Z
Inactive At2026-06-04 11:33:24Z
Source Posted At2026-05-29 03:41:08Z
Source Updated At
Raw Payload Uris3://bluework-jobs-prod-raw-590183727216/raw/provider=lever/board=qualdoc/date=2026-06-02/2026-06-02T10-40-35-902Z-3d116f3827bd8e6fe6614f242f1c58c81159561b127cc07674e218a797ead266.json
Event Fields
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  "last_changed_at": "2026-06-04T11:33:24.197Z",
  "active_status": "deleted"
}
Parsed Structured
{
  "language": "en",
  "location": {
    "raw": "Richmond, VA",
    "city": "Richmond",
    "region": "VA",
    "country": "United States",
    "is_remote": false,
    "confidence": 0.9
  },
  "salary_max": null,
  "salary_min": 105000,
  "inferred_at": "2026-06-02T10:40:36.793Z",
  "launch_scope": {
    "reason": "english_us_canada",
    "included": true,
    "language": "en",
    "location": {
      "raw": "Richmond, VA",
      "city": "Richmond",
      "region": "VA",
      "country": "United States",
      "is_remote": false,
      "confidence": 0.9
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    "countries": [
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  },
  "remote_policy": null,
  "salary_period": "year",
  "workplace_type": "on_site",
  "salary_currency": "USD"
}
Extensions
{}
Native Structured
{
  "lists": [
    {
      "text": "Primary Responsibilities",
      "content": "<div><strong>Technical &amp; Project Execution</strong>\n\n<li>Provide engineering support for packaging equipment projects for new and existing products</li>\n<li>Design and develop packaging equipment lines and support systems integration</li>\n<li>Lead or support installation, commissioning, and verification of equipment</li>\n<li>Develop and execute equipment testing and qualification protocols</li>\n<li>Assist with vendor testing, factory acceptance testing (FAT), and site acceptance testing (SAT)</li>\n\n<strong>Project Management</strong>\n\n<li>Initiate, plan, and manage multiple projects simultaneously, including scope, schedule, and budget</li>\n<li>Perform cost estimation and track project expenses</li>\n<li>Support capital project planning, budgeting, and long-range planning initiatives</li>\n<li>Conduct project status updates and present progress to stakeholders</li>\n<li>Review and approve contractor bids, RFIs, and change requests</li>\n\n<strong>Cross-Functional Collaboration</strong>\n\n<li>Work with Operations, Quality, Regulatory Affairs, Engineering, Purchasing, and vendors to resolve challenges</li>\n<li>Coordinate multi-disciplinary teams to ensure successful project execution</li>\n<li>Ensure alignment with site standards, best practices, and regulatory requirements</li>\n\n<strong>Compliance &amp; Continuous Improvement</strong>\n\n<li>Ensure all activities comply with FDA cGMP and company policies</li>\n<li>Support change control processes for new equipment and process changes</li>\n<li>Manage or support equipment validation</li>\n<li>Identify opportunities for process improvements and standardization</li>\n<li>Promote and exemplify cGMP compliance in all activities</li>\n\n<strong>Documentation &amp; Training</strong>\n\n<li>Prepare and maintain project documentation including SOPs, job aids, and technical reports</li>\n<li>Maintain accurate project records and history files</li>\n<li>Train production staff on new equipment and processes</li>\n<li>Serve as a technical resource and mentor to junior team members</li>\n\n</div>"
    },
    {
      "text": "Qualifications",
      "content": "<div><strong>Education &amp; Experience</strong></div>\n\n<li>Bachelor’s degree in Mechanical Engineering or related field</li>\n<li>5+ years of experience in a manufacturing environment (pharmaceutical, personal care, or similar preferred)</li>\n<li>Experience with equipment design, installation, commissioning, and validation in a cGMP environment</li>\n\n<div><strong>Skills &amp; Abilities</strong></div>\n\n<li>Strong project management and organizational skills</li>\n<li>Ability to manage multiple projects independently</li>\n<li>Analytical, troubleshooting, and problem-solving skills</li>\n<li>Effective communication and technical writing abilities</li>\n<li>Working knowledge of FDA cGMP requirements</li>\n<li>Ability to read and interpret P&amp;IDs, process flow diagrams, and technical drawings</li>\n<li>Experience with CAD or similar design software preferred</li>\n<li>Ability to lead cross-functional teams and influence stakeholders</li>\n"
    },
    {
      "text": "Benefits & Compensation",
      "content": "\n<li>Competitive compensation package beginning at $105,000 annually</li>\n<li>Medical, dental, and vision insurance options</li>\n<li>Company-paid life and disability coverage</li>\n<li>401(k) retirement savings plan</li>\n<li>Additional employee benefit programs and resources</li>\n"
    }
  ],
  "country": "US",
  "createdAt": 1780026068686,
  "updatedAt": null,
  "categories": {
    "team": "Qualdoc Staffing",
    "location": "Richmond, VA",
    "commitment": "Direct Hire",
    "allLocations": [
      "Richmond, VA"
    ]
  },
  "salaryRange": null,
  "workplaceType": "onsite"
}
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