Associate Director, Engineering

Job Description

General Summary:

Due to continued growth and investment our company is hiringan Associate Director Engineering within Biologics External Manufacturing Technology.

The Associate Director willbe the key technical leader interface between our company and External Partnersfor the Biologics External Manufacturing(ExM)organization.

This individual will create lead and execute technical transfers to and commercial supply from External Partner(s).The candidate will be based in the US on the west coast and report to the Director BiologicsExternal ManufacturingTechnology.

Theidealcandidate will be someone who can navigate a complex network of drug substance nodes across biologics modalities and tech support needs to collaborate across multiple technical functions to ensure the success technical transfer and commercial manufacture with theExternalPartner(s).This individual will be capable of leading several high-impact complex cross-functional divisional teams and will provide significant leadership to the role is critical to the organizations ability to support new and in-line commercial product technology transfers toExternalPartnerships and support of our in-line products with sharp oversight and technical risk management focus on the rapidly expanding biologics third party network.

Position Profile:

TheAssociate Director Engineering within Biologics External Manufacturing Technologyis accountable for achieving excellence in Compliance Supply Continuous Improvement & Cost Reduction in partnership with our internal technical partners andExternal Partner (EP)leadership supporting the Vaccines and Biologics businesses. This individual works in collaboration with theFocus Factory Operations leadmodality specificTechnologyLeads Large Molecule External Quality Assurance and Associate Director must have biologics manufacturing experience with broad process sciences and analytics strong leadership skills business acumen and interpersonal skills.

Job Details:

The primary focus of the Associate Director is to provide technical and project leadership to Biologics External Manufacturing business for:

• Providesa single point of technical contact to assigned External Partners impacted Company Manufacturing Division sitesand Commercialization.

• Providestechnical oversight management and planning support for complex partnership models. Functions independently and provides coordination communication and oversight of assigned External Partner technical issues

• Accountable to External Manufacturing for overall tech transfer delivery (on-time within budget) working closely with the Operations Unit leadership to assure resourcing for each activity.

• Providestechnical guidanceto theExternalPartner assess viability of technology in proposed process configurations verify adherence to required standards and ensure deliverables are technically sound.

• Collaborates with Procurement External Manufacturing Operations External Quality Regulatory and others to evaluateExternalPartner(s)for inclusion in theCompanyNetwork. Executes technical due diligence assessments atExternalPartner(s).

• Ensurestech transfers are positioned for successful business outcomes. Executes technical transfersandreceiving site readiness activities.

• Leads team for identification and assessment of partnerrisks and develops mitigations plans.

• Develops and executes validation strategies for new and existing products.

• Providesmanufacturing process support toExternalPartner(s)to resolve production issues and to provide guidance on process and capacity optimization.

• Ensurestargeted communications and alignment across technical functions. Guides and coaches others in change leadership.

• Support/Coordinate/Manage complex investigations with appropriate interface with other impacted manufacturing sites

• Determinesresource plans across all relevant technical functions.

• Provides a technical review of External Partner process change requests deviations and Master Batch Record of efforts between External Partner and Companysystems.

• Drive and support Continuous process verification and process performance monitoring program for all products under his/her responsibility

• In concert with Commercialization Quality and Regulatory ensures thatExternalPartner(s)are inspection ready for all new product introductions and transfers.

• Understands the true regulatory requirements and partners with Operations Quality and the External Partner to develop more efficient ways to meet these requirements.

• Collaborates with External Partners to achieve business goals and to establish a common culture that benefits both Our Companyand EP.

Education Requirements:

• A Bachelors degree in Engineering orapplicableScience is required. An advanced degree in Engineering Science or Business is preferred.

• Minimum of8 (eight) years post-bachelors degree experience in Drug Substance and/or Drug Product vaccines and/or biologics manufacturingengineeringand/or technical support of operations is required

Skill Requirements:

• Expertise and demonstrated accomplishments leading technical transfers is required

• Experience in leading cross-functional teams in support of manufacturing operations at internal sites orExternalPartner(s)is preferred

• Expertise and demonstrated accomplishments with Lean Manufacturing applications to ensure year on year productivity improvements is preferred

• Advanced problem-solving skills and experience leading teams to resolve complex business or technical issues is required

• Excellent leadership collaboration change management interpersonal analytical skills collaborationand engagement as a team player with dependable interpersonal and communication skills (bothverbal and written) is required.

• Ability to motivate a team around a common vision and deliver expected results is preferred.

• Creative innovative thinks outside of the box self-motivated applies problem-solving skills and solid base in engineering fundamentals and process troubleshootingis preferred

• Experience in complex international environment with matrix organization structures is preferred

• Experience in Large Molecule unit operation design startup and/or operation is preferred.

Travel Requirements:>30% for partner assignments outside of primary location(primarily traveling within designated EU region). Travel and flexibility in partner assignment location is required; assignments may require short term travel assignments.

Location:Location US is flexible. Position may be based in Northern California or our companys Sites in the US

Reporting Structure:This role will report to the Director Biologics External Manufacturing Technology

Required Skills:

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

US and Puerto Rico Residents Only:

Our company is committed to inclusion ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

As an Equal Employment Opportunity Employer we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race color age religion sex sexual orientation gender identity national origin protected veteran status disability status or other applicable legally protected a federal contractor we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws visit:

EEOC Know Your Rights

EEOC GINA Supplement

We are proud to be a company that embraces the value of bringing together talented and committed people with diverse experiences perspectives skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas broad experiences backgrounds and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one anothers thinking and approach problems collectively.

Learn more about your rights including under California Colorado and other US State Acts

The salary range for this role is

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employees position within the salary range will be based on several factors including but not limited to relevant education qualifications certifications experience skills geographic location government requirements and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive if applicable.

We offer a comprehensive package of benefits. Available benefits include medical dental vision healthcare and other insurance benefits (for employee and family) retirement benefits including 401(k) paid holidays vacation and compassionate and sick days. More information about benefits is available at can apply for this role through (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.

San Francisco Residents Only:We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only:We will consider for employment all qualified applicants including those with criminal histories in a manner consistent with the requirements of applicable state and local laws including the City of Los Angeles Fair Chance Initiative for Hiring Ordinance

Search Firm Representatives Please Read Carefully
Merck & Co. Inc. Rahway NJ USA also known as Merck Sharp & Dohme LLC Rahway NJ USA does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place introductions are position specific. Please no phone calls or emails.

Employee Status:

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.