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Sales assistant - Kuwait City, الكويت - Al Rifai Arabia
وصف
About PSC Biotech
PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with Global operations in Ireland, India, Singapore, Australia and the US, serving 350 clients in more than 23 countries We provide cloud-based software solutions for Quality Management and Regulatory Inspections, pharmaceuticals contract manufacturing professionals, and metrology services to our Take your Career to a new Level
PSC Biotech disrupts the conventional consultancy model by aligning our EVP as one of the unique selling point which includes the opportunity to work with the most talented cohort of like-minded professionals operating in the Pharma/ Biotech We offer a permanent contract of employment giving exposure of working in Top Pharmaceutical client sites in a diverse-cultural work Employee Value Proposition
Employees are the heartbeat of PSC Biotech, we provide unparalleled empowering career development though Learning & Development in-house training mentorship through constant guidance to facilitate career We believe in creating high performing teams that can exceed our client s expectations with regards to quality of all scalable and business unit deliverables, staying under budget and ensuring timelines for our deliverables are being
Description:
Senior Project Manager Process Development
Overview:
Experience in a leadership role in a pharmaceutical or biotech manufacturing facility that engages with site SMEs and managers, and global
The ability to influence and lead cross functional teams to deliver to ensure the smooth introduction of new products and the health of existing
The ability to work independently and identify risks and mitigation pathways for new and existing
A passion for continuous improvement applied to product and program
Scope of Role:
Arrange agreement among the project team, customers, and management on the goals of the
Develops and maintains the Project schedule/plan that addresses quality, objective, scope, cost, schedule, resources, and responsibilities - to deliver the project, and measure progress against schedule and
Effectively communicate with everyone involved in the
Have a controlled scope in place, that is understood by all stakeholders and maintained throughout completion of the
Execute prudent risk and issue
Maintains Actions/Risk and Decision
Generates and owns the GMP change
Motivate, support and direct project team members to deliver on project
Leads Team meetings and cross functional
Works with resource managers from across the organisation to effectively obtain and allocate resources to complete programs and projects on
Compliance Related Tasks:
Always ensure compliance to cGMP
Ensure safety & compliance standards are maintained to the highest standards
Ensure financial compliance in line with Business & Financial guidance
Support a culture of personal responsibility within reporting structure
Skills & Knowledge:
High Energy and Commitment
Ability to work independently
Comfortable leading across multiple stakeholders & multinational teams
Strong ability to influence and affect change
Capable of resolving issues of conflict effectively
Strong communicator
A proven track record in the ability to transfer goals and objectives into measurable plans
Ability to identify gaps/risks and put appropriate remediation plans in place
Uses strong relationships to identify requirements and potential opportunities
Employs project management techniques and Problem Solving
Provides leadership, guidance, and advice in own field of project management
Requirements
Qualifications and Experience
Technical Degree and/or Masters or equivalent
5-8 years of experience (including min of 3yrs as Project Manager) in a Life Science / Pharmaceutical / Biotechnology Environment
Preferred Experience: Portfolio Management, Portfolio Resource Management, Business Case Development
Systems / Equipment:
MS Office, MS Project, MS PowerPoint and MS Visio,
Change Control & Document Management Systems
Preferred Requirements: Smartsheet
#LI-DM1
Qualifications and Experience Technical Degree and/or Masters or equivalent 5-8 years of experience (including min of 3yrs as Project Manager) in a Life Science / Pharmaceutical / Biotechnology Environment Preferred Experience: Portfolio Management, Portfolio Resource Management, Business Case Development Systems / Equipment: MS Office, MS Project, MS PowerPoint and MS Visio, Change Control & Document Management Systems Preferred Requirements: Smartsheet #LI-DM1
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