Pharmaceutical Systems Integration Engineer – Raleigh-Durham, NC

Pharmaceutical Systems Integration Engineer – Raleigh-Durham, NC

 

Pharmaceutical Systems Integration Engineer – Raleigh-Durham, NC

Are you a skilled engineer with a passion for integrating cutting-edge pharmaceutical manufacturing systems? We are seeking a Pharmaceutical Systems Integration Engineer to join a leading pharmaceutical solutions provider in the vibrant Raleigh-Durham, NC area. This is a unique opportunity to work on advanced system integration projects, drive process automation, and ensure seamless technology deployment in a highly regulated industry. If you have a strong background in pharmaceutical engineering and a drive for innovation, this role could be your next big career move.

Drive System Integration Excellence in the Heart of North Carolina

A top pharmaceutical solutions company based in Raleigh-Durham, NC is looking for a Pharmaceutical Systems Integration Engineer to support their growing operations. The ideal candidate will possess expertise in system integration, automation technologies, and regulatory compliance within the pharmaceutical or biotech sectors. If you are passionate about optimizing processes, delivering quality solutions, and collaborating across multidisciplinary teams, this is your chance to play a critical role in transforming pharmaceutical manufacturing.

Key Responsibilities of the Pharmaceutical Systems Integration Engineer – Raleigh-Durham, NC

System Integration & Automation: Lead the integration of cutting-edge pharmaceutical systems into manufacturing processes. Ensure seamless automation and connectivity between various systems to optimize production workflows and reduce operational inefficiencies.

Process Optimization & Improvement: Work closely with cross-functional teams to analyze and enhance existing systems, focusing on performance optimization, cost reduction, and process automation within a regulated pharmaceutical environment.

Regulatory Compliance & Quality Assurance: Ensure all system integrations comply with industry regulations, including FDA, GMP, and other relevant standards. Ensure that integration efforts maintain product quality, safety, and operational consistency.

Collaboration & Cross-Functional Leadership: Act as the bridge between IT, engineering, and operations teams. Lead the coordination of integration projects and troubleshoot issues across departments to ensure timely and efficient implementation.

Project Management: Oversee system integration projects from initiation through execution, ensuring that timelines, budgets, and quality expectations are met. Regularly report on project status and manage risks and challenges throughout the lifecycle.

Technology Deployment & Support: Provide technical expertise and support during the deployment of new systems and technologies. Train team members and stakeholders on new processes and ensure continuous support for integrated systems.

Continuous Improvement & Innovation: Stay up-to-date with industry trends and technological advancements. Proactively identify opportunities for process improvements and the integration of new technologies that align with business objectives and regulatory requirements.

Documentation & Reporting: Maintain accurate and comprehensive documentation for all system integration processes. Prepare reports for management on the status, progress, and outcomes of integration projects, highlighting key performance indicators (KPIs).

Vendor & Supplier Coordination: Manage relationships with third-party vendors and service providers involved in system integrations. Ensure that vendor solutions align with project requirements and quality standards while optimizing cost-efficiency.

Risk Management & Issue Resolution: Identify potential risks related to system integration and implement risk mitigation strategies. Lead troubleshooting efforts and resolve any technical issues promptly to minimize disruptions in operations.

What the Client is Looking for in You

As the Pharmaceutical Systems Integration Engineer, the client is seeking a highly skilled and innovative professional with a deep understanding of system integration and automation within the pharmaceutical industry. You should have a proven ability to implement cutting-edge technologies, drive continuous improvement, and ensure operational efficiency in a highly regulated environment.

Proven Experience in Pharmaceutical Systems Integration

The client is looking for someone with strong expertise in integrating complex systems and technologies in the pharmaceutical or biotech sectors. You should have hands-on experience working with automation, system integration tools, and enterprise systems that meet industry standards, particularly in regulated environments such as FDA and GMP compliance.

Strong Technical and Analytical Skills

As a key contributor to system integration projects, you should possess solid technical and analytical skills, with a focus on problem-solving and optimization. The ideal candidate will be capable of analyzing existing systems, identifying opportunities for improvement, and implementing technical solutions that optimize workflow, reduce downtime, and increase productivity.

Knowledge of Industry Standards and Regulatory Compliance

The client values professionals who are well-versed in regulatory compliance and industry standards (e.g., FDA, GMP). You should have a deep understanding of the technical aspects of pharmaceutical manufacturing processes and the regulatory requirements that must be adhered to in the integration and automation of systems.

Project Management and Cross-Functional Collaboration

You should be an effective project manager, capable of leading cross-functional teams to deliver system integration projects on time and within budget. Experience in managing multiple projects simultaneously while collaborating with various teams, including IT, engineering, and operations, is essential to success in this role.

Innovation and Process Improvement Mindset

The client is looking for someone who continuously seeks to innovate and improve systems and processes. You should have a strong focus on driving automation, identifying opportunities for efficiency gains, and staying updated on the latest technologies to improve system performance and reduce costs.

Strong Communication and Stakeholder Engagement

In this role, you will need to effectively communicate complex technical information to both technical and non-technical stakeholders. The client values clear and transparent communication, especially in collaborating with vendors, managing internal teams, and reporting on project progress to leadership.

Attention to Detail and Quality Assurance

Attention to detail is critical when working in a highly regulated pharmaceutical environment. The ideal candidate should have a keen eye for ensuring all integrations meet high-quality standards and comply with regulatory requirements, reducing the risk of errors and improving the overall quality of processes.

Commitment to Continuous Learning and Adaptability

The client seeks an engineer who is committed to continuous learning and development. The ability to adapt quickly to new technologies and industry trends, while maintaining focus on business goals and regulatory requirements, is highly valued in this role.

FAQs About the Role – Pharmaceutical Systems Integration Engineer – Raleigh-Durham, NC

1. What are the key responsibilities of the Pharmaceutical Systems Integration Engineer in this role?
As a Pharmaceutical Systems Integration Engineer, your primary responsibilities will include leading system integration projects for pharmaceutical manufacturing processes, ensuring seamless automation, optimizing workflows, and ensuring compliance with industry regulations such as FDA and GMP. You will collaborate with cross-functional teams, manage vendor relationships, and drive continuous improvement in system performance to enhance operational efficiency. You’ll also oversee project management, documentation, and support for deployed technologies.

2. What qualifications and experience are required for this position?
The ideal candidate should have a background in systems integration, automation, or engineering, with a deep understanding of the pharmaceutical or biotech industry. A degree in engineering (such as Mechanical, Electrical, or Chemical Engineering) is preferred, along with practical experience working with automated systems, integration tools, and industry standards. Familiarity with regulatory compliance requirements and experience in project management are also essential. Additional certifications or experience with specific pharmaceutical systems or software will be a plus.

3. What technical skills and knowledge are essential for this role?
The client is seeking a candidate with strong technical skills in system integration, automation, and pharmaceutical manufacturing technologies. You should have proficiency in integration software, control systems, and automation tools, as well as experience with technologies such as SCADA, PLCs, and MES. A solid understanding of regulatory standards like FDA and GMP is crucial, along with problem-solving and troubleshooting abilities to handle technical challenges that may arise during system deployment.

4. What challenges can I expect in this role?
In this role, you will face challenges related to the integration of complex systems within a regulated environment. Ensuring systems meet both functional and compliance requirements while optimizing efficiency can be demanding. You may also encounter challenges in coordinating across multiple departments, managing the complexity of different software and hardware systems, and addressing issues that arise during deployment. Staying up to date with technological advancements and adapting them to meet business needs will also be a key challenge.

5. What is the expected impact of the Pharmaceutical Systems Integration Engineer on the company’s operations?
Your contributions will significantly impact the efficiency, productivity, and regulatory compliance of the company’s manufacturing processes. By leading the integration of advanced systems and driving process automation, you will help streamline operations, reduce costs, and ensure that systems are aligned with industry regulations. Your role will be crucial in improving operational excellence, reducing downtime, and enhancing the overall quality of products.

6. What is the company’s culture and work environment like?
The company fosters a collaborative and innovation-driven culture, with a strong emphasis on teamwork and continuous improvement. As a part of the team, you will work in a dynamic environment that values technical expertise, creativity, and problem-solving skills. The work culture encourages professional development, supports work-life balance, and strives to maintain high standards of quality and compliance. You will have the opportunity to contribute to shaping the company’s culture while working on cutting-edge projects in the pharmaceutical sector.

What Remuneration Can You Expect from This Job?

As the Pharmaceutical Systems Integration Engineer based in Raleigh-Durham, NC, you can expect a highly competitive compensation package designed to reward your expertise and experience in pharmaceutical system integration. The remuneration for this role typically includes:

1. Base Salary
The base salary for a Pharmaceutical Systems Integration Engineer typically ranges between $80,000 and $130,000 per year, depending on your level of experience, technical skills, and the specific demands of the role. Professionals with specialized knowledge in pharmaceutical system integration and automation may command higher salaries.

2. Performance-Based Bonuses
In addition to a base salary, you may be eligible for performance-based bonuses. These bonuses are typically tied to key project milestones, such as the successful deployment of integrated systems, achieving cost-efficiency targets, and ensuring compliance with regulatory requirements. Performance bonuses can range from 10% to 20% of your base salary, depending on company and individual performance.

3. Stock Options or Profit-Sharing
Some companies may offer stock options or profit-sharing plans as part of their compensation package. These incentives allow you to share in the company’s long-term growth and success. The value of stock options or profit-sharing will depend on the company’s performance and can be a significant part of your overall compensation.

4. Health & Wellness Benefits
The company provides comprehensive health benefits, including medical, dental, and vision coverage. You will also have access to a range of wellness programs designed to promote your health and well-being, including gym memberships and mental health support.

5. Retirement Plans & Financial Security
You will have access to a robust 401(k) plan with company contributions to help you build a secure financial future. Additional retirement benefits, such as pension plans or executive retirement accounts, may also be offered, depending on company policies.

6. Signing Bonuses & Relocation Assistance
For candidates with significant expertise, the company may offer signing bonuses or relocation assistance to help with moving costs. These one-time incentives can range from $5,000 to $25,000, depending on the candidate’s qualifications and the needs of the company.

7. Professional Development & Training
The company supports continuous professional growth and may provide funding for certifications, advanced courses, and industry conferences. This ensures that you stay at the forefront of technological advancements in pharmaceutical system integration and automation.

Total Compensation Potential

When factoring in base salary, bonuses, stock options, benefits, and incentives, total compensation for this role can range from $100,000 to $160,000 annually, with the potential for higher earnings in larger companies or those offering extensive benefits and equity incentives.

How to Apply

If you are an experienced Pharmaceutical Systems Integration Engineer with a passion for driving system optimization and automation in the pharmaceutical industry, we invite you to apply for this exciting opportunity in Raleigh-Durham, NC. This role offers you the chance to play a pivotal role in enhancing operational efficiency, ensuring regulatory compliance, and driving innovation within a highly dynamic industry.

To apply, please submit your resume and a cover letter detailing your experience in system integration, automation, and pharmaceutical manufacturing. Highlight your expertise in regulatory compliance (FDA, GMP), your hands-on experience with integration tools and technologies, and your ability to lead cross-functional teams to successful project completions. Be sure to emphasize your technical skills, problem-solving capabilities, and experience in driving continuous improvement.

This position offers an exciting opportunity to contribute to cutting-edge pharmaceutical projects and work with a highly innovative team. If you’re ready to take the next step in your career and make an impact on the future of pharmaceutical technology, we encourage you to apply today!

For more information or to explore other similar opportunities, visit our Pharmaceutical Systems Integration Careers Page.

Tags:
Pharmaceutical Systems Integration | Pharmaceutical Engineering Jobs | Automation & Integration | FDA Compliance | GMP Compliance | Pharmaceutical Manufacturing | Regulatory Compliance | System Optimization | Process Improvement | Technology Innovation

Job Category: Medical Device
Job Type: Full Time
Job Location: Raleigh-Durham

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