We are seeking a highly skilled and experienced Senior Automation Consultant to join our dynamic team in the pharmaceutics industry. As a Senior Automation Consultant, you will play a critical role in driving automation initiatives, ensuring compliance with GMP regulations, and optimizing processes within the pharmaceutical manufacturing environment. Expertise with DeltaV and extensive knowledge of GMP regulations are essential for this role.
Responsibilities:
Automation Strategy: Develop and implement automation strategies aligned with business objectives, focusing on improving operational efficiency, reducing costs, and ensuring compliance with GMP regulations.
System Design and Implementation: Lead automation projects from conceptualization to successful implementation. Collaborate with cross-functional teams to define system requirements, develop functional specifications, and oversee the design, configuration, testing, and commissioning of DeltaV automation systems.
Compliance and Validation: Ensure adherence to GMP regulations, industry standards, and company policies throughout the automation lifecycle. Develop and execute validation plans, protocols, and documentation for automated systems, ensuring regulatory compliance and data integrity.
Process Optimization: Identify opportunities for process improvements, automation enhancements, and optimization of manufacturing operations. Conduct thorough analyses, propose innovative solutions, and implement best practices to maximize efficiency, productivity, and quality in the pharmaceutical manufacturing environment.
Stakeholder Collaboration: Collaborate with internal teams, including engineering, manufacturing, quality assurance, and regulatory affairs, to ensure seamless integration of automation systems and processes. Provide technical guidance and support to stakeholders, fostering strong relationships and effective communication channels.
Training and Knowledge Transfer: Provide training and mentorship to junior automation team members and end-users, ensuring their understanding of automation systems, GMP compliance, and proper usage of DeltaV software. Foster a culture of continuous learning and knowledge transfer within the organization.
Vendor Management: Collaborate with automation vendors and suppliers to evaluate, select, and procure appropriate hardware, software, and equipment. Maintain strong relationships with vendors, ensuring timely support, and staying up to date with industry trends and technological advancements.
Requirements:
- Bachelor's degree in engineering, computer science, or a related field. Advanced degree preferred.
- Extensive experience (X+ years) in automation consulting or engineering roles within the pharmaceutics industry.
- Strong expertise with DeltaV automation system and associated software.
- Deep knowledge of GMP regulations, FDA guidelines, and industry standards.
- Proven track record in leading automation projects from concept to successful implementation.
- Experience in validation and qualification of automated systems in accordance with regulatory requirements.
- Strong analytical and problem-solving skills, with the ability to identify areas for improvement and propose innovative solutions.
- Excellent communication and interpersonal skills to collaborate effectively with cross-functional teams and stakeholders.
- Ability to manage multiple projects simultaneously, prioritize tasks, and meet deadlines.
- Willingness to travel occasionally to client sites as required.
Join our team of experts and make a significant impact on the pharmaceutics industry by driving automation excellence, ensuring regulatory compliance, and optimizing processes. If you have a passion for innovation, GMP regulations, and leveraging automation technologies like DeltaV, we invite you to apply for the position of Senior Automation Consultant. Together, let's shape the future of pharmaceutical manufacturing.
To apply, please submit your CV highlighting your relevant experience and why you are interested in this role.
