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Senior Project Engineer

2479a996 4c61 4623 Bd61 684f50d6e2a0 19000101 000001 · Lee, MA, US, Lee, MA · Active · $97,000–$122,000 / year · ADP Workforce Now Recruiting

Job facts

FieldValue
Company2479a996 4c61 4623 Bd61 684f50d6e2a0 19000101 000001
TitleSenior Project Engineer
Normalized title-
Department / team-
LocationLee, MA, United States
Work model-
Employment typeFull Time
Salary$97,000–$122,000 / year
Statusactive
ATS providerADP Workforce Now Recruiting
Posted / first seen2026-06-04 / 2026-06-05
Changed / last seen2026-06-06 / 2026-06-06

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PageWhat it containsOpen
Company jobsActive postings from 2479a996 4c61 4623 Bd61 684f50d6e2a0 19000101 000001.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through ADP Workforce Now Recruiting.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Lee.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

Company2479a996 4c61 4623 Bd61 684f50d6e2a0 19000101 000001
Source95b4d553-a046-4c74-bcb4-9264e4e35c82
ATS providerADP Workforce Now Recruiting

Description

Position Summary The Senior Project Engineer is responsible for leading and executing capital projects with a regulated pharmaceutical manufacturing environment. This role ensures projects are delivered safely, on time, within budget, and in compliance with cGMP and regulatory requirements. The position requires strong technical expertise, cross functional leadership, and the ability to manage complex projects from concept through commissioning and qualification. Duties and Responsibilities Lead capital projects for initiation through design, procurement, construction, commissioning, qualification, and closeout. Manage project scope, schedule, budget, and resources to ensure successful delivery of projects. Develop and maintain project documentation including User Requirement Specifications (URS), Functional Specifications, Design Specifications, and validation documentation. Coordinate cross-functional teams including Engineering, Manufacturing, Quality, Validation, and Supply Chain. Oversee contractors, vendors, and external engineering firms to ensure compliance with project requirements and site standards. Identify project risks and implement mitigation strategies to minimize impact to schedule, cost, and compliance. Ensure alignment with regulatory requirements including FDA, EU GMP Annex 1, and internal quality systems. Participate in change control, deviation investigations, CAPAs, and risk assessments associated with projects. Support commissioning and qualification activities including FAT/SAT, IQ/OQ/PQ execution and documentation. Provide technical expertise in facilities, utilities, equipment, and process systems. Drive continuous improvement initiatives related to project execution, equipment performance, and operational efficiency Develop and present project updates and metrics to senior leadership Support capital planning, budgeting, and long-term site master planning activities Ensure adherence to safety standards and promote a strong safety culture throughout project execution Other duties as assigned Qualifications To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, and/or ability required. Strong knowledge of pharmaceutical manufacturing systems, utilities, and equipment In-depth understanding of cGMP, regulatory requirements, and validation practices. Project management expertise including scheduling, cost control, and risk management Ability to develop and review engineering and validation documentation Strong problem-solving and analytical skills Excellent communication and leadership abilities Ability to manage multiple projects simultaneously in a fast-paced environment Proficiency with project management tools and Microsoft Office Suite Experience with change management and quality systems (e.g., MasterControl) preferred Ability to influence stakeholders and drive decision-making Regulatory Responsibilities Maintain working knowledge of 21 CFR 210/211, EU Annex 1, and other applicable regulatory requirements Ensure all project activities comply with cGMP, data integrity, and company SOPs Support audit readiness and participate in regulatory inspections as required Ensure proper documentation, traceability, and compliance for all engineering and project activities. Supervisory Responsibilities Provide technical leadership and mentorship to junior engineers and project team members Coordinate internal and external project resources without direct supervisory authority Influence cross-functional teams to achieve project objectives and timelines Education Bachelor’s degree in Engineering (Mechanical, Chemical, Electrical, or related field) required Master’s degree or professional certification (e.g., PMP) preferred Experience Minimum ten (10) years of experience managing capital projects Minimum five (5) years of experience in pharmaceutical or regulated GMP environments Demonstrated experience managing complex facility, utility, and/or equipment projects Proven track record of delivering projects on time and within budget Experience with aseptic processing, cleanroom environments, and/or sterile manufacturing preferred Physical Requirements Ability to sit or stand for prolonged periods of time Ability to lift and carry materials weighing as much as 50lbs Ability to stand and walk in manufacturing and construction environments as required Ability to meet cleanroom gowning requirements. Ability to travel between facilities or vendor sites as needed

Full job record

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Org IDffbe8dfc-07e3-4259-8a85-b9f1dd382d16
Source ID95b4d553-a046-4c74-bcb4-9264e4e35c82
Board ID95b4d553-a046-4c74-bcb4-9264e4e35c82
Provideradp_workforcenow
Provider Job Key594395
TitleSenior Project Engineer
Normalized Title—
Statusactive
Activeyes
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Department—
Team—
Employment Typefull_time
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CountryUnited States
RegionMA
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Salary Raw97000.00 To 122000.00 (USD) Annually
Salary Min97,000
Salary Max122,000
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Source URLhttps://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=2479a996-4c61-4623-bd61-684f50d6e2a0&ccId=19000101_000001&lang=en_US&type=JS&jobId=594395&jwId=9201157224944_1
Apply URLhttps://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=2479a996-4c61-4623-bd61-684f50d6e2a0&ccId=19000101_000001&lang=en_US&type=JS&jobId=594395&jwId=9201157224944_1
First Seen At2026-06-05 02:58:05Z
Last Seen At2026-06-06 13:18:53Z
Last Checked At2026-06-06 13:18:53Z
Last Changed At2026-06-06 13:18:53Z
Inactive At—
Source Posted At2026-06-04 19:56:00Z
Source Updated At—
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    "requisitionDescription": "<div><table border=\"1\" cellspacing=\"0\" cellpadding=\"0\" width=\"720\" style=\"width:539.75pt;border-collapse:collapse;border:none;\" data-pasted=\"true\"><tbody><tr><td valign=\"top\" style=\"width: 20.1669%; border: 1pt solid windowtext; padding: 0in 5.4pt; height: 27.4pt; vertical-align: top;\"><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Position Summary</span></strong></p></td><td valign=\"top\" style=\"width: 79.8331%; border-width: 1pt 1pt 1pt medium; border-style: solid solid solid none; border-color: windowtext windowtext windowtext currentcolor; border-image: initial; padding: 0in 5.4pt; height: 27.4pt; vertical-align: top;\" class=\"fr-cell-handler \"><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-size:15px;font-family:\"Calibri\",sans-serif;color:#2D2D2D;'>The Senior Project Engineer is responsible for leading and executing capital projects with a regulated pharmaceutical manufacturing environment. This role ensures projects are delivered safely, on time, within budget, and in compliance with cGMP and regulatory requirements. The position requires strong technical expertise, cross functional leadership, and the ability to manage complex projects from concept through commissioning and qualification.&nbsp;</span></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><br></p></td></tr><tr><td valign=\"top\" style=\"width: 20.1669%; border-width: medium 1pt 1pt; border-style: none solid solid; border-color: currentcolor windowtext windowtext; border-image: initial; padding: 0in 5.4pt; height: 126.85pt; vertical-align: top;\"><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Duties and Responsibilities</span></strong></p></td><td valign=\"top\" style=\"width: 79.8331%; border-width: medium 1pt 1pt medium; border-style: none solid solid none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; height: 126.85pt; vertical-align: top;\"><div style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 5.050000000000001px;\"><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:\"Calibri\",sans-serif;font-size:15px;'>Lead capital projects for initiation through design, procurement, construction, commissioning, qualification, and closeout.&nbsp;</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:\"Calibri\",sans-serif;font-size:15px;'>Manage project scope, schedule, budget, and resources to ensure successful delivery of projects.&nbsp;</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:\"Calibri\",sans-serif;font-size:15px;'>Develop and maintain project documentation including User Requirement Specifications (URS), Functional Specifications, Design Specifications, and validation documentation.&nbsp;</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:\"Calibri\",sans-serif;font-size:15px;'>Coordinate cross-functional teams including Engineering, Manufacturing, Quality, Validation, and Supply Chain.&nbsp;</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:\"Calibri\",sans-serif;font-size:15px;'>Oversee contractors, vendors, and external engineering firms to ensure compliance with project requirements and site standards.&nbsp;</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:\"Calibri\",sans-serif;font-size:15px;'>Identify project risks and implement mitigation strategies to minimize impact to schedule, cost, and compliance.&nbsp;</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:\"Calibri\",sans-serif;font-size:15px;'>Ensure alignment with regulatory requirements including FDA, EU GMP Annex 1, and internal quality systems.&nbsp;</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:\"Calibri\",sans-serif;font-size:15px;'>Participate in change control, deviation investigations, CAPAs, and risk assessments associated with projects.&nbsp;</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:\"Calibri\",sans-serif;font-size:15px;'>Support commissioning and qualification activities including FAT/SAT, IQ/OQ/PQ execution and documentation.&nbsp;</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:\"Calibri\",sans-serif;font-size:15px;'>Provide technical expertise in facilities, utilities, equipment, and process systems.</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:\"Calibri\",sans-serif;font-size:15px;'>Drive continuous improvement initiatives related to project execution, equipment performance, and operational efficiency</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:\"Calibri\",sans-serif;font-size:15px;'>Develop and present project updates and metrics to senior leadership</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:\"Calibri\",sans-serif;font-size:15px;'>Support capital planning, budgeting, and long-term site master planning activities</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:\"Calibri\",sans-serif;font-size:15px;'>Ensure adherence to safety standards and promote a strong safety culture throughout project execution</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:\"Calibri\",sans-serif;font-size:15px;'>Other duties as assigned&nbsp;</span></li></ul></div></td></tr><tr><td valign=\"top\" style=\"width: 20.1669%; border-width: medium 1pt 1pt; border-style: none solid solid; border-color: currentcolor windowtext windowtext; border-image: initial; padding: 0in 5.4pt; height: 27.4pt; vertical-align: top;\"><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Qualifications&nbsp;</span></strong></p></td><td valign=\"top\" style=\"width: 79.8331%; border-width: medium 1pt 1pt medium; border-style: none solid solid none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; height: 27.4pt; vertical-align: top;\"><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, and/or ability required.&nbsp;</span></p><div style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: -0.25in;\"><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Strong knowledge of pharmaceutical manufacturing systems, utilities, and equipment</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>In-depth understanding of cGMP, regulatory requirements, and validation practices.</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Project management expertise including scheduling, cost control, and risk management</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Ability to develop and review engineering and validation documentation&nbsp;</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Strong problem-solving and analytical skills</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Excellent communication and leadership abilities&nbsp;</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Ability to manage multiple projects simultaneously in a fast-paced environment&nbsp;</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Proficiency with project management tools and Microsoft Office Suite</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Experience with change management and quality systems (e.g., MasterControl) preferred</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Ability to influence stakeholders and drive decision-making&nbsp;</span></li></ul></div></td></tr><tr><td valign=\"top\" style=\"width: 20.1669%; border-width: medium 1pt 1pt; border-style: none solid solid; border-color: currentcolor windowtext windowtext; border-image: initial; padding: 0in 5.4pt; height: 23.95pt; vertical-align: top;\"><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Regulatory Responsibilities</span></strong></p></td><td valign=\"top\" style=\"width: 79.8331%; border-width: medium 1pt 1pt medium; border-style: none solid solid none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; height: 23.95pt; vertical-align: top;\"><div style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 5.050000000000001px;\"><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:\"Calibri\",sans-serif;font-size:15px;'>Maintain working knowledge of 21 CFR 210/211, EU Annex 1, and other applicable regulatory requirements</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:\"Calibri\",sans-serif;font-size:15px;'>Ensure all project activities comply with cGMP, data integrity, and company SOPs</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:\"Calibri\",sans-serif;font-size:15px;'>&nbsp;Support audit readiness and participate in regulatory inspections as required</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:\"Calibri\",sans-serif;font-size:15px;'>Ensure proper documentation, traceability, and compliance for all engineering and project activities.</span></li></ul></div></td></tr><tr><td valign=\"top\" style=\"width: 20.1669%; border-width: medium 1pt 1pt; border-style: none solid solid; border-color: currentcolor windowtext windowtext; border-image: initial; padding: 0in 5.4pt; height: 23.15pt; vertical-align: top;\"><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Supervisory Responsibilities</span></strong></p></td><td valign=\"top\" style=\"width: 79.8331%; border-width: medium 1pt 1pt medium; border-style: none solid solid none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; height: 23.15pt; vertical-align: top;\"><div style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 5.050000000000001px;\"><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:\"Calibri\",sans-serif;font-size:15px;'>Provide technical leadership and mentorship to junior engineers and project team members</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:\"Calibri\",sans-serif;font-size:15px;'>Coordinate internal and external project resources without direct supervisory authority&nbsp;</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:\"Calibri\",sans-serif;font-size:15px;'>Influence cross-functional teams to achieve project objectives and timelines&nbsp;</span></li></ul></div></td></tr><tr><td valign=\"top\" style=\"width: 20.1669%; border-width: medium 1pt 1pt; border-style: none solid solid; border-color: currentcolor windowtext windowtext; border-image: initial; padding: 0in 5.4pt; height: 19.75pt; vertical-align: top;\"><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Education</span></strong></p></td><td valign=\"top\" style=\"width: 79.8331%; border-width: medium 1pt 1pt medium; border-style: none solid solid none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; height: 19.75pt; vertical-align: top;\"><div style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 5.050000000000001px;\"><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:\"Calibri\",sans-serif;font-size:15px;'>Bachelor&rsquo;s degree in Engineering (Mechanical, Chemical, Electrical, or related field) required</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:\"Calibri\",sans-serif;font-size:15px;'>Master&rsquo;s degree or professional certification (e.g., PMP) preferred</span></li></ul></div></td></tr><tr><td valign=\"top\" style=\"width: 20.1669%; border-width: medium 1pt 1pt; border-style: none solid solid; border-color: currentcolor windowtext windowtext; border-image: initial; padding: 0in 5.4pt; height: 56.65pt; vertical-align: top;\"><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Experience</span></strong></p></td><td valign=\"top\" style=\"width: 79.8331%; border-width: medium 1pt 1pt medium; border-style: none solid solid none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; height: 56.65pt; vertical-align: top;\"><div style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 5.050000000000001px;\"><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Minimum ten (10) years of experience managing capital projects</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Minimum five (5) years of experience in pharmaceutical or regulated GMP environments</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Demonstrated experience managing complex facility, utility, and/or equipment projects</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Proven track record of delivering projects on time and within budget</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:  \"Calibri\",sans-serif;font-size:15px;'>Experience with aseptic processing, cleanroom environments, and/or sterile manufacturing preferred&nbsp;</span></li></ul></div></td></tr><tr><td valign=\"top\" style=\"width: 20.1669%; border-width: medium 1pt 1pt; border-style: none solid solid; border-color: currentcolor windowtext windowtext; border-image: initial; padding: 0in 5.4pt; height: 30.1pt; vertical-align: top;\"><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Physical Requirements</span></strong><strong>&nbsp;</strong></p><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p></td><td valign=\"top\" style=\"width: 79.8331%; border-width: medium 1pt 1pt medium; border-style: none solid solid none; border-color: currentcolor windowtext windowtext currentcolor; padding: 0in 5.4pt; height: 30.1pt; vertical-align: top;\" class=\"fr-cell-fixed \"><div style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 5.050000000000001px;\"><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:#0F0F0F;'>Ability to sit or stand for prolonged periods of time</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:#0F0F0F;'>Ability to lift and carry materials weighing as much as 50lbs</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:#0F0F0F;'>Ability to stand and walk in manufacturing and construction environments as required</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:#0F0F0F;'>Ability to meet cleanroom gowning requirements.&nbsp;</span></li><li style=\"margin:0in;font-size:13px;font-family: initial;\"><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:#0F0F0F;'>Ability to travel between facilities or vendor sites as needed&nbsp;</span></li></ul></div></td></tr></tbody></table></div>\n",
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