Position Details :
Our client, a world-leading Pharmaceutical Company in Sanford, NC or Andover, MA or Kalamazoo, MI is currently looking for a Manufacturing Project Manager to join their expanding team.
Job Title : Manufacturing Project Manager / Pharma Industry
Duration : 12 months contract, extendable up to 36 months
Location : Sanford, NC or Andover, MA or Kalamazoo, MI
Note :
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description :
Role Responsibilities :
The Sr Technical Project Manager will manage of highly complex technical projects (implementation of strategic initiative programs across multiple clinical and or commercial manufacturing and End to End process project).
Lead cross function teams to deliver on process robustness, and customer satisfaction through innovative solutions to manufacturing site and impact to advance breakthroughs that change patients’ lives
The position requires manage full project cycle including initiation, planning and execution and closing phase make sure team member and stakeholder engagement and alignment, plan execution, re-evaluation and adjustment when needed.
This position requires effective and direct communication skills, bold leadership and facilitation, and an effortless ability to influence and integrate various colleagues from cross functional team.
Project scope include but are not limited to cold chain project initiatives , PC1 business process development and project management, sustainability and process robustness at clinical manufacturing sites
Role Responsibilities :
As a Sr Technical Project Manager, you will to lead matrix teams to realize a variety of clinical Manufacturing and or Enterprise Initiatives at multiple clinical and or commercial manufacturing sites by the following :
Project Organization
lead multiple projects of highly complex strategic initiative with cross function teams including technical, quality, supply chain, launch excellence, packaging regulatory ect.
Solve complex problem and or lead investigations that affecting multiple areas (equipment, analytical, process, material ect) where previous experience outside of own area for process robustness and cost savings.
Make decision that require developing innovative options ; Decision-making at regional / global levels, impacting multiple stakeholders
Technical responsibility
Has comprehensive understanding / knowledge of principles and concepts of project management
Has advanced knowledge / understanding of the principle and concepts of specific technical area for example, aseptic sterile injectables, biologics, vaccines, co- development and tech transfer
Applied technical skills and line knowledge to plan project that will enable the sub operation unit (specific site) to meet goals
Interprets internal and external business challenges and best practices to recommend improvement for improvement or cost saving projects
Develop business process and or project management of PC1 business
With and through others, create an environment where innovation is the standard
The appropriate risk to advance innovative process and mythologies based on comprehensive business Knowledge
Interpersonal effectiveness
Highly respected colleague; able to influence team members across the network at cross function unit, site LT and OPU for shared goals
Establish program governance structure and Use communication tools to help ensure alignment at site and OPU leadership
Create and delivers presentations to all stakeholders
Manage teams that execute directions for sub operation unit. Provide input for senior management direction that may have an impact within sub operation unit
Interfacing with and influencing diverse customers including site groups from PGS (Ops, Technical Services, Quality) and network groups such as GTE, External Supply, PharmSci and GCMC, and global supply chain
Mindset and approach
Able to identify root causes and drive to problem resolution; orientation towards action – anticipates problems and acts proactively to resolve;
demonstrated initiative, drive, and creativity in problem solving
Knows when to or escalate risks and issues to leadership and provides alternative approaches / solutions to mitigate these risks / issues and leads towards issue resolution
Use of DMAIC principals to drive resolution of issues and drive improvement of process, and supplier
Embraces Pharmaceutical Purpose : Breakthroughs that change patients’ lives through the incorporation of the Bold Moves and Values and Behavior
Comfortable with multifunctional and multi-cultural environments.
Works independently on most assignments using knowledge and work experience to achieve desired results
Qualifications :
Masters or Bachelors with minimum of 10+ years in Engineering (Mechanical, Chemical, or Pharmaceutical preferred) or Life Sciences Experience
Excellent communication and attention to details
Demonstrated ability to be lead strategic projects with large multi-discipline teams by developing strategy and leading team through project completion
Knowledge of cGMP requirements and compliance
Excellent technical writing skills
Excellent organizational skills
Excellent Program management skills
Strong background in bios formulations and filling or packaging
Demonstrated ability to lead strategic initiative
Operations or Tech services experience is a plus
Certified PMP is a plus
Physical / Mental Requirements :
Standard office work
Non-Standard Work Schedule, Travel Or Environment Requirements
Global travel may be required
Adaptation of work schedule to accommodate meetings with colleagues in different time zones
Interview :
Teams panel interview.
Minimum Education :
Masters or Bachelors with minimum of 10+ years in Engineering (Mechanical, Chemical, or Pharmaceutical preferred) or Life Sciences Experience.
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