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Pfizer · 21 hours ago

Sr. Manager, Technical Services

Bothell, WA

Full-time

Hybrid

Mid, Senior Level

$124K/yr - $201K/yr

5+ years exp

Pfizer is a leading biopharmaceutical company focused on developing transformative cancer therapies. The Sr. Manager, Technical Services will lead the technical transfer of Antibody Drug Conjugate production processes and provide crucial support for ongoing GMP manufacturing processes, ensuring high productivity and collaboration within teams.

BiotechnologyHealth CareMedicalPharmaceuticalPrecision Medicine

No H1B

Responsibilities

Lead technical transfer of ADC processes into the North Creek facility and ensure technical responsibilities for new product introduction competed, such as process modeling, materials planning, batch record generation and SOP generation

Provide technical support and troubleshoot highly complex technical process issues

Oversight of process validation, process monitoring, continuous process validation, and database management in partnership with digital groups

Generate process and facility-related risk assessments

Provide technical expertise to lead and close investigations, non-conformances, and corrective actions

Evaluate new and PAT enabling technology for introduction

Qualification

GMP manufacturingAntibody Drug Conjugate (ADC)Project managementProcess validationProcess automationTechnical troubleshootingCuriosity for AI toolsEffective communicationTeam collaborationLeadership skills

Required

Applicant must have a bachelor's degree with at least 6 years of experience; OR a master's degree with at least 5 years of experience; OR a PhD with 1+ years of experience

In-depth knowledge of equipment, operations, and engineering principles related to antibody drug conjugation production

Effective written and verbal communication skills

Strong interpersonal skills and the ability to work collaboratively in a team environment across various business functions

Experience in project management and leading complex projects

Ability to develop and manage plans to achieve objectives

Preferred

Strong knowledge of GMP manufacture of antibody drug conjugate (ADC) and monoclonal antibody (mAb) purification production processes and associated at-scale equipment and unit operations

Knowledge of cytotoxic drug-linker handling and solubilization

Identify process and technology gaps and issues; develop solutions and implementation plans

Knowledge of cGMPs and regulatory requirements including 21 CFR Parts 210 and 211, and ICH Q7

Experience deploying single-use technologies for manufacturing processes

Intermediate level understanding of process automation (Wonderware and DeltaV) used for bioprocessing controls systems

Strong leadership and team management skills

Ability to influence and drive alignment across stakeholders

Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity

Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use