[Hiring] Associate Director, External Manufacturing @MSD

Role Description

Our Small Molecule Technical Operations Unit is seeking a highly motivated individual to fill an open Associate Director Technical Operations, to support drug substance manufacture within our External Manufacturing Network. This is an exciting opportunity to work with key strategic external partners, contribute and enhance technical experience in drug substance manufacturing, and work on high visibility network initiatives. Our team strives to provide technical excellence in our work and be strong partners, collaborators, and leaders within the small molecule line of business at our company.

Our team of chemists and engineers help ensure that external manufacturing operations remain operational, continuously improve and innovate. With our extensive range of facilities and environments, our Engineers have opportunities across many diverse areas including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development, Technical Services, Utilities and Validation.

• Lead and act as the primary interface on technical issues between technical operations and the external partner.
• Provide technical leadership within the technical operations group for the commercialization and manufacture of drug substance.
• Provide technical guidance to the external partner, assess viability of technology in proposed process configurations, verify adherence to required standards, and ensure deliverables are technically sound.
• Collaborate with external manufacturing operations, external quality, regulatory, and others to evaluate external partner(s) performance, fostering pro-active risk management mindset and continuous improvement.
• Execute technical due diligence assessments at external partner(s).
• Ensure tech transfers are positioned for successful business outcomes. Execute technical transfers and receiving site readiness activities.
• Execute validation strategies for new and existing products.
• Provide manufacturing process support to external partner(s) to resolve production issues and to provide guidance on process and capacity optimization.
• Support/coordinate/manage complex investigations, with appropriate interface with other impacted manufacturing sites.
• Provide a technical review of external partner process change requests, deviations, and master batch record changes. Minimize duplication of efforts between external partner and our systems.
• Drive and support continuous process verification and process performance monitoring program for all products under his/her responsibility.
• Understand the true regulatory requirements and partner with operations, quality, and the external partner to develop more efficient ways to meet these requirements.

Qualifications

• Bachelor’s degree in engineering, chemistry sciences or related discipline.
• Minimum of 7 years of relevant work experience in manufacturing, in the areas of process start up, routine manufacturing and/or technical transfer.

Requirements

• Minimum of 5 years of experience in drug substance with experience in leading Drug Substance new product introduction, technical transfers, commercial manufacturing.
• Demonstrated knowledge and experience in process development, scale up and process robustness, including shop floor (person in plant) support.
• Strong problem-solving skills, root cause analysis and risk assessment/mitigation.
• Ability to work effectively across boundaries to build strong collaborative relations with internal and external teams, to drive alignment and results.
• A high level of effectiveness in professional and interpersonal communication skills, including stakeholder management.
• Authentic and inclusive people leadership, able to provide examples of your ability to engage and create a psychologically safe and collaborative culture.
• Must be able to work under own initiative, prioritize appropriately based on business need and work within tight deadlines.
• Flexibility and the ability to work independently as well as excellent organizational skills.
• Strong knowledge of quality systems, drug substance manufacturing and validation.
• Excellent command of English (both written and oral).
• Travel will be a requirement of this position at approximately 25%.

Preferred Experience and Skills

• Knowledge and experience of flow chemistry, enzyme manufacture and bio-catalysis are desirable but not essential.
• Lean Manufacturing / Six Sigma Experience.
• Project management experience.
• Knowledge of worldwide regulatory requirements, experience supporting regulatory inspections.