"Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold t…
"Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold t…
"Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold t…
"Expect to grow", personnellement et professionnellement : Chez Siegfried, nous offrons des défis passionnants et de nombreuses opportunités de mettre en valeur vos talents. En tant que partenaire de confiance et respect…
Job Description Position Summary The Siegfried Advisory (“SA”) Finance Business Partner serves as the primary finance & accounting liaison between Siegfried Advisory business leaders, the Siegfried Advisory Leadership Te…
Skills: Financial Analysis, Business Partnership, FP&A, Financial Reporting, Stakeholder Management
"Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold t…
Skills: Project Management, Capital Investment Projects, EPCM Management, cGMP Compliance, FEL Methodology
"Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold t…
Skills: CapEx Procurement, Category Strategy, E-auctions, Project Management, Business Case Development
"Expect to grow", persönlich und beruflich: Bei Siegfried erwarten Sie spannende Herausforderungen und zahlreiche Möglichkeiten, Ihre Talente unter Beweis zu stellen. Als ein vertrauenswürdiger und angesehener Partner de…
Skills: HPLC, GC, UV-VIS Spectroscopy, IR Spectroscopy, Polarimetry
"Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold t…
"Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold t…
"Expect to grow", personal y profesionalmente: En Siegfried, ofrecemos desafíos emocionantes y amplias oportunidades para demostrar tu talento. Como socio de confianza y respeto en la industria farmacéutica, mantenemos l…
Skills: Material Planning, SAP, MRP, Supply Chain Management, Microsoft Excel
"Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold t…
Skills: SAP EWM, SAP WM, SAP S/4HANA, SAP R/3, Project Management
"Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold t…
Skills: SHE Policy Development, Regulatory Compliance, Risk Assessment, ATEX Zoning, Process Safety
"Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold t…
Skills: Data Analytics, Data Visualization, MS Excel, MS PowerPoint, Strategic Thinking
Director New Business Development - Northwest Region
Pennsville, New Jersey, United States · Hybrid
$158k–$197k/yr
Senior
"Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold t…
Skills: New Business Development, Pharmaceutical Sales, API Manufacturing, CDMO Industry Knowledge, Market Research
Job Description Position Summary Reporting to the Revenue Manager – Billing, the Billing Specialist is responsible for ensuring that our invoices are created and sent from our system (Workday) accurately and timely. This…
Skills: Billing, Invoicing, Workday, Microsoft Excel, Data Analysis
"Expect to grow", personnellement et professionnellement : Chez Siegfried, nous offrons des défis passionnants et de nombreuses opportunités de mettre en valeur vos talents. En tant que partenaire de confiance et respect…
Skills: Reaction Safety Studies, Organic Chemistry, Chemical Processes, RC1, DSC
"Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold t…
Skills: Chemical Production Equipment Operation, cGMP Regulations, Analytical Testing, Forklift Operation, Batch Record Documentation
"Expect to grow", personnellement et professionnellement : Chez Siegfried, nous offrons des défis passionnants et de nombreuses opportunités de mettre en valeur vos talents. En tant que partenaire de confiance et respect…
"Expect to grow", persönlich und beruflich: Bei Siegfried erwarten Sie spannende Herausforderungen und zahlreiche Möglichkeiten, Ihre Talente unter Beweis zu stellen. Als ein vertrauenswürdiger und angesehener Partner de…
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$125k–$135k/yr
Full-time
bachelor degree
Medical, Dental, Vision, Flexible Spending, HSA Options, Life Insurance
Posted 26d ago
~40 hrs/week
Responsibilities
Lead and execute capital investment projects and strategic engineering initiatives to support pharmaceutical manufacturing operations and facility expansion. Provide technical leadership throughout the full project lifecycle, from concept and design through commissioning, qualification, and validation.
Requirements
Requires a Bachelor's degree in an engineering discipline with at least 4 years of experience in highly regulated manufacturing and 2 years in CQV. Must have proven experience managing CAPEX projects and working within GMP-regulated cleanroom environments.
Full job description
"Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold the highest standards in safety, quality and sustainability, while fostering a culture that empowers you to thrive. Join a rapidly expanding global company, where diverse perspectives and experiences come together in a collaborative environment. Here, you'll find a workplace that values both collective success and your individual contributions—offering long-term opportunities to grow and make an impact.
Your Role:
The Project Engineer III is responsible for leading and executing capital investment (CAPEX) projects and strategic engineering initiatives that support manufacturing operations, facility expansion, equipment upgrades, process improvements, and new product introductions within a highly regulated pharmaceutical environment. This role provides technical leadership throughout the full project lifecycle, from concept development and design through commissioning, qualification, validation, implementation, and ongoing operational support. As a subject matter expert, Project Engineer III supports new product introductions, equipment lifecycle management, process optimization, and infrastructure expansion projects. This role requires strong technical expertise in pharmaceutical manufacturing systems, commissioning and qualification practices, project management, and engineering problem-solving, with the ability to influence cross-functional teams and deliver sustainable business results. The successful candidate will demonstrate a combination of project leadership, engineering excellence, and hands-on technical capability to enhance manufacturing performance, improve equipment reliability, maintain regulatory compliance, and support the organization's long-term growth objectives.
Your Profile:
Key Responsibilities
Project Management & Capital Execution
Lead and manage CAPEX projects from concept through completion, including facility expansions, utility upgrades, equipment installations, manufacturing process improvements, and infrastructure enhancements.
Develop project charters, business justifications, budgets, schedules, resource plans, and risk mitigation strategies.
Monitor project progress, spending, and milestones to ensure projects are delivered safely, on schedule, and within budget.
Coordinate internal stakeholders, contractors, OEMs, consultants, and suppliers throughout the project lifecycle.
Develop detailed project plans and oversee implementation of equipment, process, and facility upgrades.
Lead and coordinate equipment commissioning, qualification, and validation activities in accordance with GMP and validation lifecycle requirements.
Develop and review User Requirement Specifications (URS), Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols and reports.
Support Computer System Validation (CSV) and Data Integrity initiatives where applicable.
Coordinate and execute Factory Acceptance Testing (FAT) and Site Acceptance Testing (SAT) activities for new equipment and systems.
Ensure qualification documentation is complete, accurate, and audit ready.
Engineering Support & Continuous Improvement
Conduct engineering investigations and provide technical leadership in the resolution of deviations, non-conformances, quality events, and CAPAs.
Perform root cause analysis and implement sustainable corrective and preventive actions.
Evaluate process performance, equipment reliability, and operational metrics to identify improvement opportunities.
Develop and implement engineering solutions that improve process robustness, product quality, safety, and manufacturing efficiency.
Analyze equipment and process performance trends to proactively identify and address operational risks.
Technical Documentation & Compliance
Develop, review, approve, and maintain engineering documentation including SOPs, maintenance procedures, calibration procedures, specifications, drawings, P&IDs, equipment files, and technical reports.
Ensure engineering activities comply with GMP, FDA, EU, ISO, and internal quality system requirements.
Maintain accurate project documentation, change control records, validation files, engineering drawings, and asset documentation.
Support internal and external audits and regulatory inspections as a subject matter expert.
Cross-Functional Collaboration & Leadership
Collaborate with Manufacturing, Quality Assurance, Validation, Maintenance, Supply Chain, EHS, and Regulatory Affairs to support business objectives.
Facilitate communication among project teams and functional stakeholders to ensure alignment and successful project execution.
Lead project meetings and present project status, risks, budgets, timelines, and technical recommendations to management.
Mentor and train operators, technicians, and inspectors on equipment operation, troubleshooting, process controls, and inspection techniques.
Provide technical support and engineering expertise to maintenance, operations, and project management teams.
Participate in strategic planning activities related to facility capacity, manufacturing expansion, and technology implementation.
Required Education and Experience
Bachelor's degree in Mechanical Engineering, Chemical Engineering, Industrial Engineering, Pharmaceutical Engineering, or a related engineering discipline.
Minimum 4 years of engineering experience within the pharmaceutical, biotechnology, medical device, or other highly regulated manufacturing industries.
Minimum 2 years of direct experience in equipment commissioning, qualification, and validation (CQV).
Proven experience managing CAPEX projects involving manufacturing equipment, cleanroom facilities, utility systems, and process improvements.
Demonstrated experience supporting GMP-regulated manufacturing environments. Hands-on experience with equipment installation, startup, troubleshooting, and qualification activities.
Experience working in classified cleanroom environments.
Strong understanding of pharmaceutical manufacturing processes and quality systems.
Experience interacting with external vendors, contractors, and regulatory auditors preferred.
Target Salary Range: $125,000 - 135,000
Individual compensation packages are based on various factors unique to each candidate, including skill set, experience, qualifications and other job-related reasons.
Your Benefits:
Medical, Dental, Vision
Flexible Spending & HSA Options
Life Insurance, Short & Long Term Disability
Pet Insurance
401K
Founded in 1873 in Zofingen, Switzerland, Siegfried has grown into a global network of 16 sites across three continents. With a team of more than 4,200 highly skilled professionals, we take the innovations of our pharmaceutical customers to industrial scale and manufacture safe drugs for patients worldwide. As a fully integrated CDMO, Siegfried is one of the few organizations today that can carry out the development and manufacturing of APIs and finished dosage forms under one roof. This unique combination of know-how and experience makes us the most trusted partner in the pharmaceutical industry.
Siegfried is a leading CDMO with 16 production sites on four continents. With our longstanding pharmaceutical and chemical experience, we are taking your innovations to industrial scale.
Siegfried is active in manufacturing pharmaceutical APIs (and their intermediates) as well as drug products (tablets, capsules, sterile vials, ampoules, cartridges and ointments) for the pharmaceutical industry and provides development services.
Offices: Untere Brühlstrasse 4, Zofingen, Aargau 4800, CH · Langes Feld 13, Hameln, Lower Saxony 31789, DE · Parc Industriel de la Plaine de l‘Ain, Saint Vulbas, Ain 01150, FR · Route du Simplon 1,36, Evionnaz, Valais 1902 , CH · Karlstrasse 15, Minden, North Rhine-Westphalia 32423 , DE
Siegfried is a leading CDMO with 16 production sites on four continents. With our longstanding pharmaceutical and chemical experience, we are taking your innovations to industrial scale.
Siegfried is active in manufacturing pharmaceutical APIs (and their intermediates) as well as drug products (tablets, capsules, sterile vials, ampoules, cartridges and ointments) for the pharmaceutical industry and provides development services.
Offices: Untere Brühlstrasse 4, Zofingen, Aargau 4800, CH · Langes Feld 13, Hameln, Lower Saxony 31789, DE · Parc Industriel de la Plaine de l‘Ain, Saint Vulbas, Ain 01150, FR · Route du Simplon 1,36, Evionnaz, Valais 1902 , CH · Karlstrasse 15, Minden, North Rhine-Westphalia 32423 , DE