Upstream Manager, Manufacturing
Job Location:
Bothell, WA - USA
Yearly Salary:
Posted:
Application Deadline:
Vacancies:
Job Summary
Join Us in Bringing Hope to Life
Our purpose is to bring hope to life by enabling lifechanging therapies for patients around the globe creating a healthier and happier tomorrow. To advance this purpose we rely on team members who value excellence collaboration and meaningful work. If this resonates with you we invite you to explore the role further and apply.
Job Summary
We are looking for an Upstream Manufacturing Manager to lead GMP upstream manufacturing operations across mammalian and microbial production platforms. This role is responsible for overseeing daily manufacturing activities ensuring compliance with established processes and standards and delivering safe reliable and efficient execution of clinical and commercial production campaigns.
The Upstream Manufacturing Manager provides leadership and direction to manufacturing teams ensuring operational readiness schedule adherence and continuous improvement while supporting technology transfer process implementation and commercial manufacturing activities.
About the Manufacturing Team
Youll join a Manufacturing organization responsible for the production of biologics across multiple modalities and stages of development. The team partners closely with Quality MSAT Engineering Supply Chain and other operational functions to ensure safe compliant and efficient manufacturing operations that support both clinical and commercial programs.
Key Responsibilities
Lead upstream manufacturing operations across mammalian and microbial processes.
Monitor and improve compliance with quality systems safety procedures and company policies.
Determine production priorities staffing requirements and shift schedules to support manufacturing objectives.
Ensure effective communication and operational alignment across shifts through the Daily Management System (DMS).
Monitor manufacturing operations to ensure compliance with SOPs batch records and GMP requirements.
Identify address and prevent operational issues that may impact safety quality reliability identity or purity (SQRIP).
Train coach and mentor manufacturing associates and supervisors.
Review and approve manufacturing documentation.
Manage team performance goal setting development planning and performance reviews.
Coordinate resources and activities across manufacturing areas to meet production goals and timelines.
Ensure equipment personnel materials and manufacturing suites are prepared for scheduled operations.
Support technology transfer process implementation PPQ clinical manufacturing and commercial manufacturing activities.
Monitor production performance equipment availability schedule adherence and operational risks.
Drive continuous improvement initiatives focused on safety quality productivity reliability and cost.
Establish and maintain manufacturing KPIs and performance metrics.
Skills
Demonstrated knowledge of upstream biologics manufacturing including mammalian cell culture and/or microbial fermentation.
Experience supporting stainless steel and/or single-use bioreactor systems harvest operations aseptic processing and CIP/SIP systems.
Ability to lead manufacturing operations across multiple production areas shifts and modalities.
Strong leadership coaching and employee development skills.
Effective communication problem-solving and decision-making abilities.
Ability to build cross-functional partnerships and drive operational results.
Qualifications & Experience
Required:
Bachelors degree with 8 years of industry experience or Masters degree with 6 years of industry experience. Equivalent education and experience may be considered.
Experience leading upstream biologics manufacturing operations in a GMP environment.
Experience with mammalian cell culture and/or microbial fermentation manufacturing processes.
Prior experience managing teams in a regulated manufacturing environment.
Formalities
Location: Bothell WA
Schedule: Full-time
Compensation: $108080 - $148610
We offer a comprehensive Total Rewards package that may include annual bonus opportunities paid time off medical dental and vision coverage parental leave education assistance employee referral and recognition programs and additional wellbeing benefits. Eligibility and benefits may vary based on role location and employment status.
Who We Are
AGC Biologics is a global Contract Development and Manufacturing Organization with a strong presence in the United States. From our headquarters in Bothell Washington we develop and manufacture lifechanging advanced biologics for some of the worlds most innovative pharmaceutical companies. Together with our team members across Europe the U.S. and Japan we deliver development and manufacturing of mammalian and microbial-based therapeutic proteins plasmid DNA (pDNA) messenger RNA (mRNA) viral vectors and genetically engineered cells therapies. Across our global network we are united by one mission: To work side by side with our customers in order to improve patients lives by bringing new biopharmaceuticals to market.
We are a collaborative inclusive and equalopportunity organization where team members are valued for their expertise teamwork and ingenuity.
Required Experience:
Manager
