Gilead Sciences Inc

Senior Manager, Tech Transfer Project Management

Gilead Sciences Inc$153K — $199K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree with 8+ years experience or Master's/Ph.D. with relevant experience
  • 10+ years in pharmaceutical industry, focus on fill/finish for small molecules or biologics
  • 6+ years experience managing NPI or technology transfer projects
  • Knowledge of cGMPs and regulatory requirements in manufacturing
  • Strong leadership and cross-functional team management skills
  • Excellent communication skills with senior management experience

Responsibilities

  • Lead and manage multiple NPI projects for clinical and commercial fill/finish
  • Define product transfer scope and coordinate resources across departments
  • Ensure compliance with regulatory and quality standards
  • Develop comprehensive work plans with cross-functional teams
  • Oversee project team workflow and address potential risks
  • Represent La Verne in NPI-focused corporate meetings
  • Provide timely updates to senior management on project status

Benefits

  • Company-sponsored medical, dental, vision, and life insurance plans
  • Annual discretionary bonus opportunities
  • Stock-based long-term incentives eligibility
  • Paid time off
  • Comprehensive benefits package
Full Job Description
Job Description
Gilead's mission is to discover, develop, and deliver therapies that will improve the lives of patients with life-threatening illnesses worldwide. The Gilead Sciences La Verne Engineering Project Management Office (PMO) is seeking a Senior Manager, Tech Transfer Project Management. We seek a highly motivated and knowledgeable, individualto lead New Product Introduction (NPI) efforts for the La Verne site aseptic manufacturing of biologics or small molecule (fill/finish) and equipmentpurposed for the clinical flex fill line (Line 3) and commercial fill lines (Line 1 and Line 2), Labeling and Packaging lines.This individual will work directly with, and coordinate activities for, key stakeholders from multiple departments and cross different sites (e.g. Foster City) to ensure NPI projects, ranging from pre-pivotal to pivotal clinical phases, are executed to meet the global product technical transfer timeline, clinical demands, and commercialization to meet internal customer expectations. This position is onsite daily in La Verne, CA, relocation is not offered therefore local candidates are encouraged to apply. Key Responsibilities: Program Management: Lead and manage multiple, concurrent clinical and commercial NPI projects impacting the fill/finish or inspection, labeling and packaging areas and equipment. Define and understand product transfer scope, timelines, and demands from PNGC or PPSC endorsement through manufacturing and release, coordinating resources from the La Verne site to meet objectives. Quality and Compliance Oversight: Ensure product transfer team can deliver products to meet compliance with regulatory requirements, Current Good Manufacturing Practices (cGMPs), Good Laboratory Practices (GLPs), Safety regulations, and other relevant standards. Facilitate necessary gap assessment with the SMEs from La Verne or from the global sites. Work Plan Development: Develop comprehensive work plans for each product transfer in collaboration with cross-functional teams, including Technical Services, Packaging, Quality Assurance (QA), Quality Control (QC), Validation, Supply Chain, Regulatory/CMC, EHS, Finance, IT, and Engineering. Project Team Management: Oversee and manage daily workflow of the project team, ensuring that milestones are met and any potential risks or delays are proactively addressed. Milestones can be ranging from machine line trials, installation/debug/startup, Acceptance Testing and Commissioning (ATC), and PPQs (commercialization ready), and product runs/studies for any follow-up measures per the regulatory feedback/demands. Task Tracking and Escalation: Track the status and completion of critical tasks, such as procurement, documentation, and studies, to ensure milestones are achieved. Escalate issues when necessary to ensure timely resolution. Cross-Functional Guidance: Utilize knowledge in filling and packaging processes and equipment to provide guidance and support for global, cross-functional discussions, ensuring alignment of decisions to meet project objectives. Stakeholder Representation: Represent the La Verne cross-functional team in NPI-focused meetings with corporate stakeholders, facilitating communication and bridging any gaps in understanding between corporate and site personnel. Project Review and Leadership: Lead regular project review meetings with cross-functional representatives, ensuring projects are on track and addressing any deviations promptly. Senior Management Reporting: Provide regular and timely updates to senior management on the status of NPI projects, including upcoming, ongoing, and completed initiatives. Collaborate with senior leadership for key decision-making. Problem-Solving and Innovation: Tackle moderately complex problems by applying creative problem-solving techniques and offering innovative recommendations to drive project success. Decision-Making and Judgment: Exercise sound judgment in selecting appropriate methods, techniques, and evaluation criteria to achieve project goals while adhering to defined practices and policies. Tactical Leadership: Provide tactical guidance and management to the project team, ensuring alignment with broader Operations objectives and strategies. Procedure and Process Improvement: Contribute to the development and implementation of standardized procedures and processes to ensure consistency in Project Management. Play a key role in the creation of new concepts, techniques, and operational standards. Basic Qualifications: Bachelor's Degree and Eight Years99 Experience OR Masters' Degree and Six Years99 Experience OR Ph.D. Preferred Qualifications: 10+ years of relevant experience in pharmaceutical industry with a focus on small molecule or biologics fill/finish, inspection, labeling and packaging and a sciences BS/BA degree. 6+ years of relevant experience in pharmaceutical industry with a focus on small molecule or biologics fill/finish, inspection, packaging and a MS, MA or MBA. 5+ years successfully serving as a project manager. Proven experience in managing complex NPI or technology transfer projects. Knowledge of cGMPs, GLPs, and regulatory requirements in a manufacturing setting. Demonstrated leadership ability in cross-functional teams, including Technical Services, MSAT, Manufacturing/Packaging, QA, QC, Validation, Supply Chain, and Engineering. Excellent communication skills, with experience interfacing with senior management and cross-functional global teams. Strong problem-solving and decision-making skills, with a focus on driving project success in a fast-paced environment. Proficient in Microsoft Office applications. People Leader Accountabilities Create Inclusion - knowing the business value of diverse teams, modeling inclusion, and embedding the value of diversity in the way they manage their teams. Develop Talent - understand the skills, experience, aspirations, and potential of their employees and coach them on current performance and future potential. They ensure employees are receiving the feedback and insight needed to grow, develop, and realize their purpose. Empower Teams - connect the team to the organization by aligning goals, purpose, and organizational objectives and holding them to account. They provide the support needed to remove barriers and connect their team to the broader ecosystem. The salary range for this position is: $153,935.00 - $199,210.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*. For additional benefits information, visit: https://www.gilead.com/careers/compensation-benefits-and-wellbeing * Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.

About Gilead Sciences Inc

Gilead Sciences is a research-based biopharmaceutical company that discovers, develops, and commercializes innovative medicines in areas of unmet need. With each new discovery and experimental drug candidate, they seek to improve the care of patients suffering from life-threatening diseases. Gilead's primary areas of focus include HIV/AIDS, liver disease, and serious cardiovascular and respiratory conditions.

Gilead Sciences Inc Careers

Join the vibrant team at Gilead Sciences Inc, a leader in the biopharmaceutical industry known for its innovative approach to healthcare. At Gilead, we are committed to advancing the care of patients around the globe through rigorous science and research.

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Start your career with Gilead through our internship programs, which offer hands-on experience in biopharmaceutical development and business operations. For seasoned professionals, our employment opportunities span across various disciplines, inviting you to bring your valuable skills to our team.

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We emphasize the importance of networking and professional development within the company. Regular workshops, seminars, and training sessions are held to enhance your skills and knowledge. Additionally, Gilead’s strong emphasis on internal networking allows for cross-departmental collaboration and innovation.

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Learn more about Gilead Sciences Inc
Size
14,400 employees
Market Cap
$107.2 billion
Industry
Net Income
$123 million
Founded
1987
5 Year Trend
-2.1%
Revenue
$24.6 billion
NASDAQ

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