Associate Director, Technical Product Management

Rahway, NJ - USA

Monthly Salary: $ 139600 - 219700

Posted on: 30+ days ago

Vacancies: 1 Vacancy

Job Summary

Job Description

We are seeking an experienced Technical Product Manager to lead pharmaceutical process and method development data product portfolio. This unique

role combines a strong understanding of biopharma research hands-on experience withdomains of pharmaceutical process method development and tech transfer for commercial manufacturing and the ability to drive product strategy and execution. Successful candidate will be accountable for timely availability of quality reliable data to support insights needs for scientific and operational decisions helping innovation and productivity.

Key Responsibilities:

Collaborate with stakeholders to understand their business data needs for in silico research defining the core capabilities required to support these needs.

Develop and communicate a product vision strategy and roadmap for pharmaceutical process and method development data products that align with business objectives and market opportunities.

Act as the primary point of contact for stakeholders regarding product vision strategy and roadmap updates.

Apply Agile methodologies in managing the product development lifecycle including sprint planning backlog management and performance assessments.

Apply prototyping techniques to learn and evolve the product.

Create and lead cross-functional teams comprised of data scientists information architects software engineers and product designers to drive product development and execution.

Conduct regular meetings with stakeholders and product team members to provide updates on progress and motivate the team to achieve execution goals.

Ensure that the product team is aligned with the overall product vision and motivated to contribute to successful execution.

Leverage hands-on experience with data to inform product features.

Support the development of tools and methodologies that facilitate the processing and analysis of process and analytical data.

Foster a collaborative environment that encourages open communication and aligns team efforts with the product roadmap.

Advocate for the adoption of FAIR (Findable Accessible Interoperable Reusable) data principles in the development of pharmaceutical process and method development data products.

Highlight the need for and help stakeholders with creation of data capture master data standards and documentation practices to ensure the findability and accessibility of data

Take responsibility for enabling automation and monitoring solutions that enhance workflow efficiency and data integrity.

Ensure compliance with GxP and audit requirements for data usage and dashboarding.

Act as a key point of accountability for the execution and delivery timelines related to pharmaceutical process and method development data products.

Drive adoption of delivered data products through user training documentation pilots and evangelism; collect feedback and iterate.

Measure and report on adoption metrics and business outcomes (reduced cycle time fewer deviations improved batch yield).

Qualifications:

Bachelors degree in Life Sciences Biomedical Engineering Chemical Engineering Computer Science or a related field; advanced degree preferred.

5 years of experience in technical product management particularly within the biopharma or healthcare sectors.

Demonstrated understanding of Physicochemical process stability and other analytical data.

Experience with cloud storage and compute infrastructure (e.g. AWS Azure) and knowledge of automation and monitoring tools.

Familiarity with FAIR data principles and best practices related to data management and interoperability.

Strong experience with Agile methodologies and product management frameworks.

Excellent leadership communication and stakeholder management skills

Ability to simplify complex technical and scientific concepts for nontechnical stakeholders.

Proven ability to prioritize competing demands and drive cross-functional teams.

Proven ability to motivate cross-functional teams and drive product strategy from conception to execution.

Familiarity with systems like Signals PKM Pi Databricks Redshift modern data architecture tools any others

Strong understanding of data modeling governance and analytics platforms (e.g. Power BI Collibra).

Knowledge of GxP compliance and regulatory data standards.

Preferred qualifications

Prior experience in a pharma/biotech organizations process development manufacturing or automation team.

Hands-on experience with specific tools: LIMS (e.g. Labware) ELN (e.g. Benchling) MES SCADA OSIsoft PI Apache Kafka SparkDatabricks or similar.

Experience participating in tech transfer projects method validations or PAT-enabled implementation.

Familiarity with AI/ML use cases in bioprocessing (digital twins predictive control anomaly detection).

Demonstrated experience translating process/experimental requirements into data/IT solutions and shipping data products in regulated environments.

Required Skills:

Agile Methodology Asset Management Backlog Management Benefits Management Biomedical Engineering Chemical Engineering Cloud Infrastructure Cloud Storage Customer Experience Management Management System Development Motivating Teams Organizational Performance Management Product Development Product Management Product Roadmap Product Strategies Requirements Management Software Product Management Sprint Planning Stakeholder Engagement Stakeholder Relationship Management Strategic Planning System Designs

Preferred Skills:

Collaborating Data Management

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:

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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.

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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

$139600.00 - $219700.00

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:

Regular

Relocation:

No relocation

VISA Sponsorship:

Travel Requirements:

10%

Flexible Work Arrangements:

Hybrid

Shift:

1st - Day

Valid Driving License:

Hazardous Material(s):

N/a

Job Posting End Date:

12/10/2025

*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.

Required Experience:

Director

Job DescriptionWe are seeking an experienced Technical Product Manager to lead pharmaceutical process and method development data product portfolio. This uniquerole combines a strong understanding of biopharma research hands-on experience withdomains of pharmaceutical process method development and ...