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You will be updated with latest job alerts via email$ 126500 - 199100
1 Vacancy
Job Description
Reporting into the Director Packaging Platform Technical Leadership the Associate Director Medical Device and Combination Product (MDCP) Platform Packaging and Assembly Technical Leadership will be responsible and accountable for technical leadership strategic planning and portfolio execution of key packaging and assembly platforms with a focus on combination drug products such as prefilled syringes and autoinjectors.
The Packaging Technical Operations organization aims to be an industry leader in problem-solving delivering robust and pragmatic technical solutions to accelerate the commercialization of new products and ensuring an uninterrupted compliant supply of commercialized products for the benefit of patients. The Associate Director of MDCP Platform Packaging and Assembly Technical Leadership is integral to this mission. The successful candidate will possess deep technical expertise in assembly and packaging of MDCP a strong track record in problem-solving strategic acumen and execution along with exceptional leadership skills to shape the technical capabilities and strategic direction for a global cross-modality technical team.
As an individual contributor the associate director will lead cross functional teams. The leader will be responsible for executing the organizations priorities and ensuring the successful completion of projects. This includes the development and execution of robust technical plans across device assembly packaging and/or distribution and logistics of finished goods images encompassing proactive risk management strategies platform standards for standard finished goods images and packaging and assembly equipment standards technical lifecycle management and continuous improvement initiatives to guarantee the robustness and compliance of our companys product portfolio across the internal and external networks
The candidate is expected to build inclusive collaborative partnerships with internal and external stakeholders such as packaging and manufacturing sites device development and technology teams supply chain operations quality analytical regulatory and project leaders. The successful candidate will demonstrate ownership and make informed cost/benefit decisions based on the analysis of inputs outcomes risks and company-wide prioritization.
Essential Responsibilities:
Provide subject matter expertise and ensure scientific rigor technical problem solving and execution excellence across the MDCP assembly and packaging platform portfolio including interrogation of the data/ science through technical reviews and exploring alternative ways to view and solve problems to achieve results.
Drive proactive risk management activities including risk assessment risk mitigation and risk communication strategies.
Collaborate with cross-functional teams to ensure that all platforms (e.g. syringes auto injectors kits) meet safety efficacy quality and robust supply standards.
Develop and maintain strong relationships with internal stakeholders including packaging commercialization quality analytical regulatory manufacturing Device Development and Technology Technical Product Leaders and Value Chain to facilitate effective technical support and platform stewardship. This includes above site support for significant investigations complaints monitoring and rapid response activities.
Manage the portfolio of work in the platform holding the cross functional team accountable to deliver on priorities
Provide strategic leadership and direction for technical support and MDCP packaging & assembly platform stewardship including managing ongoing changes and tech transfers for the components equipment and processes. Develop maintain and refine technical platform lifecycle management plans setting and managing and optimizing platform standards.
Oversee lifecycle changes for MDCP packaging platforms ensuring internal technical requirements are achieved and ensure filings with regulatory bodies to ensure compliance with relevant regulations and standards. Ensure thorough engineering medical device and packaging science is applied to deliverables for new product introductions and tech transfers across the network inclusive of aligning the control and validation strategies.
Minimum Education Requirements and Experience:
Bachelor of Science (BS) in packaging/ mechanical/ chemical/ biochemical engineering pharmaceutical science or chemistry or related fields with twelve (12) years relevant experience pharmaceutical packaging combination product assembly and packaging or related technical fields; OR
Master of Science (MS) in packaging/ mechanical/ chemical/ biochemical engineering pharmaceutical science or chemistry or related fields with ten (10) years relevant experience pharmaceutical packaging combination product assembly and packaging or related technical fields; OR
PhD in packaging/ mechanical/ chemical/ biochemical engineering pharmaceutical science or chemistry or related fields with eight (8) years relevant experience pharmaceutical packaging combination product assembly and packaging or related technical fields
Required Skills and Experience:
Subject matter expertise in medical device and combination product commercialization and tech transfer assembly and packaging process improvement and support from early stage through launch and supply including components process and equipment as well as qualification and validation medical device design controls and device risk management and design verification/ validation.
Demonstrated experience in a leadership role; managing cross functional teams supporting medical device and/or combination product assembly and packaging.
Strong problem-solving and decision-making skills with an ability to determine interrogate the science identify true requirements and detect critical flaws including the ability to determine areas of potential risk generate gap analysis and mitigation strategies
In-depth knowledge of global regulatory requirements for medical devices and combination products and packaging.
Strong understanding of risk management principles including ISO 14971 and other relevant standards.
Strong strategic and analytical thinking with a focus on driving continuous improvement and implementing best practices in technical support and product stewardship.
Excellent communication and interpersonal skills with the ability to effectively engage with internal and external stakeholders.
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US and Puerto Rico Residents Only:
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U.S. Hybrid Work Model
Effective September 5 2023 employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week Monday - Thursday although the specific days may vary by site or organization with Friday designated as a remote-working day unless business critical tasks require an on-site Hybrid work model does not apply to and daily in-person attendance is required for field-based positions; facility-based manufacturing-based or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note this Hybrid work model guidance also does not apply to roles that have been designated as remote.
The salary range for this role is
$126500.00 - $199100.00This 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:
RegularRelocation:
DomesticVISA Sponsorship:
NoTravel Requirements:
10%Flexible Work Arrangements:
HybridShift:
1st - DayValid Driving License:
NoHazardous Material(s):
n/aRequired Skills:
Applied Engineering Change Management Combination Products Compliance Packaging Cross-Functional Teamwork Detail-Oriented Deviation Management Engineering Standards Good Manufacturing Practices (GMP) Management Process Manufacturing Scale-Up Mentorship Packaging Engineering Process Optimization Risk Management Root Cause Analysis (RCA) Social Collaboration Technical LeadershipPreferred Skills:
Job Posting End Date:
10/11/2025*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.
Full-Time