Job DescriptionAbout 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 worldwide. We provide cloud-based software solutions for Quality Management and Regulatory Inspections, pharmaceuticals contract manufacturing professionals, and metrology services to our clients.
'Take your Career to a new Level'
PSC Biotech disrupts the conventional consultancy model by aligning our EVP as one of the unique selling points, which includes the opportunity to work with the most talented cohort of like-minded professionals operating in the Pharma/Biotech Industry. We offer a permanent contract of employment giving exposure to working in top pharmaceutical client sites in a diverse-cultural work setting.
Overview: The Product Lead – Process Development will report to the Sr. Manager Process Development in the Portfolio Management and Delivery group and will be responsible for leading a cross-functional product team in a matrix organization to deliver new technologies and products. The successful candidate will have at least five years of experience within the pharmaceutical or biotech industry and will have demonstrated program leadership skills.
RequirementsThe ideal candidate will have: Experience in a leadership role in a pharmaceutical or biotech manufacturing facility that engages with site SMEs and managers, and global functions.The ability to influence and lead cross-functional teams to deliver and ensure the smooth introduction of new products and the health of existing products.The ability to work independently and identify risks and mitigation pathways for new and existing products.A passion for continuous improvement applied to product and program leadership.Scope of Role: Act as the Product Health Steward and own product health for the products in their brief through product governance and effective product team leadership.Manage and develop product lifecycle management programs (multiple products).Assist in developing long-term site product vision and strategy.Serve as the main point of contact for global operations leads (GOLs) & product delivery teams (PDTs).Ensure that site's needs are presented and prioritized appropriately at site and global levels.Build and manage the relationship with the product & process knowledge SMEs at network and site level.Develop site product risks and implement plans to remediate risks.Make critical decisions and provide Process Transfer Technical Leadership on the cross-functional Tech Transfer/NPI project team and at Technology Development and Transfer Governance Forums.Engage at site product governance meetings, i.e., Product Weekly Review meeting, Site Ops meeting.Ensure changes to global product roadmap and contract books are fed back to site through Product governance and prioritized appropriately.Influence key stakeholders on site and above site and protect site strategy while meeting Network demands.Support new product/market launch.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 the reporting structure.Skills & Knowledge: Transversal working & collaborative style - must be able to work with and maintain trust at all levels of the organization.Strong understanding of development, technical, manufacturing, validation, quality, and regulatory processes and Product Lifecycle management.Strong understanding of current GMP regulations and industry practices & trends.Demonstrated project/program management skills.Excellent Communication Skills – continually communicating with peers and to stakeholders both internally and globally.Strong interpersonal skills.Strong leadership skills, especially with respect to collaboration, influencing, and coordination.Customer-focused decision-making skills.Ability to prioritize complex projects.Qualifications: Technical Degree and/or Masters' or equivalent.Experience: 5-7 years in biopharma/pharma industry.A working technical knowledge in a range of products and their associated manufacturing sciences, technologies, and analytical processes from within parenteral fill-finish, or oral dosage forms and/or packaging.Ability to identify gaps/risks and put appropriate remediation plans in place.Technical or program leadership experience.A proven track record in the ability to transfer goals and objectives into measurable plans.Strong process and manufacturing background.
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