Job Description

Responsibilities:

Ensure project is delivered in a manner compliant with project planning documents procedures and guidelines defined by the PMO

Plan monitor and control project activities for the area

Monitor and manage automation scope for the area

Communicate with global facilities delivery (GFD) PM for the area and report progress against plan

Communicate automation staffing requests needed to meet project timelines to the Program Automation Leader & Program Automation Manager

Lead and Manage Automation resources for successful project execution

Interface with other disciplines and stakeholders to ensure the project meets business needs

Collaborate with MES BMS and Data Historian project managers who will take responsibility for the delivery of the MES BMS and Data Historian in that node.

Lead preparation of requests for proposal and bid analysis for the area

Lead initiation of system integration work for the area

Provide necessary progress data to the PMO to allow preparation of monthly reports to stakeholders

Document and share lessons learned with PMO

Support preparation of cost estimates for project gate reviews

Support schedule development integration and analysis for the area

Record issues into centralized issue tracking system

Coordinate execution of project automation integrated change control for the area

Participate in Identifying and analyzing risks and planning responses

Support organization and delivery of training modules and events

Maintain compliance with training requirements

Requirements

BS Engineering (or equivalent experience)

5 years working experience in Automation Project Management in the Pharmaceutical Industry

Previous Pharmaceutical Automation Large Project/Program experience/expertise.

Preferable 5 years experience in DeltaV controlled / batchbased capital projects

Proficiency in commonly used project management tools (scheduling P6/MS Project) metrics risk management)

Exceptional teamwork abilities

Preferable solid knowledge of GMP s regulatory requirements computer system validation

Excellent written and verbal communication skills for both technical and nontechnical audiences

Formal Project Management credentials desirable

Reside is a daily commutable distance to and from Portsmouth, New Hampshire, and work on site 2-3 days per week minimum; onsite days per week may change due to projects DeltaV Proficiency: Strong expertise in DeltaV system configuration, programming, and troubleshooting, with a thorough understanding of its application within the pharmaceutical manufacturing environment. Experience: Minimum of 5 years of experience in managing automation projects within the pharmaceutical sector, with a specific focus on DeltaV systems. Experience with processes such as freezers, filling, and formulation is highly preferred. Project Management Skills: Proven track record of successfully managing complex projects, including project planning, resource allocation, risk management, and budget oversight. Regulatory Knowledge: Familiarity with regulatory guidelines and compliance requirements within the pharmaceutical industry, including FDA regulations and Good Manufacturing Practices (GMP). Strong Communication: Excellent verbal and written communication skills, with the ability to communicate technical concepts to technical and non-technical stakeholders. Leadership Abilities: Demonstrated ability to lead and motivate cross-functional project teams, fostering collaboration, and achieving project goals. Problem-Solving Skills: Strong analytical and problem-solving skills, with the ability to identify and resolve technical and operational challenges in a timely and efficient manner. Adaptability: Ability to thrive in a dynamic and fast-paced environment, managing multiple projects simultaneously and adjusting priorities as needed. Attention to Detail: Meticulous attention to detail, ensuring accuracy in project documentation, adherence to standards, and compliance with regulations. Education: Bachelor\'s degree in Engineering, Computer Science, or a related field. Advanced degrees or certifications in automation or project management are desirable. Join our team as an Automation Project Manager and play a crucial role in driving automation initiatives within the pharmaceutical sector. Apply your expertise in DeltaV systems and process automation to optimize manufacturing processes and ensure the delivery of high-quality pharmaceutical products.

Job Tags

Work experience placement, 2 days per week, 3 days per week,

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