DSM Project Manager

Quanta Consultancy Services Ltd; Raleigh (NC); On-site; USD 60,000 - 80,000; Full time

Job summary

An established industry player in pharmaceutical manufacturing is seeking a skilled DSM Project Manager for a 6-month contract in North Carolina. This role offers a unique opportunity to contribute to the development of a new manufacturing facility while collaborating with engineering and automation teams. The ideal candidate will have direct experience with Emerson DeltaV systems and a strong understanding of cGMP regulations. This position promises to be both challenging and rewarding, providing a platform for professional growth in a dynamic environment. If you thrive in collaborative settings and have a passion for project management, this opportunity is perfect for you.

Qualifications

• Direct experience with Emerson DeltaV DCS and DeltaV MES is essential.
• Excellent organizational and communication skills are required.

Responsibilities

• Coordinate project execution with engineering design and various teams.
• Manage delivery of specification documents and test protocols.

Skills

Project Management

Communication Skills

Collaboration

Knowledge of Drug Substance Manufacturing

Problem-Solving

Tools

Emerson DeltaV DCS

DeltaV MES

Kneat Validation Software

ComplianceWire

TrackWise

Veeva

Job description

DSM Project Manager - North Carolina - 6 Months Contract

Our client, a global pharmaceutical manufacturing organization, is looking for a talented DSM Project Manager to join their expanding team. With continued organizational growth and considerable investment across their portfolio and capital programs, this is an extremely exciting opportunity to contribute towards their brand-new manufacturing facility on the East Coast of the United States.

Essential Duties and Responsibilities:

1. Coordinate project execution with engineering design firm, FDBN CAPEX team, FDBN Automation process area owners, and system integrator.
2. Manage delivery of specification documents (e.g., platform requirements specification (PRS), functional specification (FS), design qualification (DQ), etc.) and test protocols (e.g., installation qualification (IQ), operational qualification (OQ), etc.).
3. Initiate design and provide input on Automation requirements for one or multiple process areas.
4. Manage/oversee the System Integrator’s support of loop checks & commissioning activities.
5. Provide on-call support to Commissioning, Qualification, Validation, and Operations activities.
6. Coordinate with various project workstreams including FDBN Automation, FDBD Automation, CSV, CQV, Utilities, Process Engineering, Manufacturing, and others as needed.
7. Complete Safety, Project Procedure, and Project Instruction training as required.

Requirements:

1. Personal ownership and proactive collaboration with external business partners and internal stakeholders.
2. Direct experience working with Emerson DeltaV DCS & DeltaV MES.
3. Experience in a cGMP pharmaceutical facility working with FDA regulations is required.
4. Working knowledge of Kneat validation software is required.
5. Excellent organizational, oral, and written communication skills and fluency in English with the ability to effectively communicate within cross-functional teams and to management.
6. Excellent interpersonal skills and ability to work effectively and efficiently in a team-based environment with employees at all levels.
7. Ability to manage commitments while displaying an eagerness to learn and continuously improve.
8. Knowledge of Drug Substance Manufacturing (DSM) process.
9. ComplianceWire, TrackWise, and Veeva experience is a plus.

If you are interested, please apply now for immediate consideration and further information.