Merck
Associate Director, Comparator Management - Hybrid
Rahway, NJ
Dec 4, 2024
Full-time
Full Job Description

Job Description

The Associate Director, Comparator Management is responsible for the sourcing and product management (assessment, order, delivery, release and applicable product blinding) of Non-Company commercial (comparator) products for all clinical trials. The incumbent will collaborate closely with internal customers including the Clinical Supply Project Managers (CSPM) and function as an independent expert in supply planning, product management and buyer of non-Company commercial products. Candidates should have proven strong expertise in Good Manufacturing Practice (GMP), Good Distribution Practice (GDP), commercial medicinal products and buying from external drug wholesalers specialized in comparator sourcing.

Primary activities include, but are not limited to:

  • Sourcing and product management for comparator products.

  • Sourcing and procuring comparator samples and documentation for comparator label and packaging component evaluation.

  • Creating and maintaining Material Masters and provide SAP Process Orders for de-packaging, pre-packaging, manipulation, and placebo manufacturing & packaging according to the routing.

  • Managing comparator blinding including but not limited to de-printing and over-encapsulation.

  • Effective communication with internal and external stakeholders.

  • Forecasting comparator pricing information to enable accurate consolidated budget planning, expense forecasting and management.

  • Maintaining oversight of shipping activities, monitoring target delivery dates and supporting release activities.

  • Creating and maintaining Purchase Requests as well as requesting Purchase Orders in SAP.

  • Utilizing systems to document/execute GxP activities.

  • Promoting continual creative improvement and actively contribute to a culture of innovation, excellence and accountability.

  • Providing mentoring and coaching to team members.

  • Champion and drive identified business process improvement initiatives, as needed.

Education:

  • Bachelor's degree in the supply chain, scientific or business discipline.

Required Experience & Skills:

  • Minimum 5 years experience in clinical supplies or procurement with knowledge of comparator sourcing markets and processes

  • Knowledge of current Good Manufacturing and Distribution Practices (cGMP/GDP) and Standard Operating Procedure execution

  • Excellent verbal and written communication skills, and effective interactive skills to partner with various stakeholders

  • Ability to work effectively across boundaries to build strong collaborative relations with other internal and external partners.

  • Competence in process optimization, including design and execution.

  • Strong project management skills and ability to organize and manage multiple tasks at one time and meet deadlines

  • High proficiency in Microsoft applications (Word, Excel, PowerPoint, Teams)

  • Experience with SAP

Preferred Skills:

  • Project management certification (e.g. PMP, CAPM)

  • Knowledge of Operational Excellence methodology such as Six Sigma and Lean methods principles and tools.

GCSCareer

#eligibleforERP

VETJOBS

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.

We are an Equal Opportunity Employer, committed to fostering an inclusive and diverse workplace. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status, or other applicable legally protected characteristics. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:

EEOC Know Your Rights

EEOC GINA Supplement

Pay Transparency Nondiscrimination

We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively.

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

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 presence.This 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 Company is required to provide a reasonable estimate of the salary range for this job in certain states and cities within the United States. Final determinations with respect to salary will take into account a number of factors, which may include, but not be limited to the primary work location and the chosen candidate's relevant skills, experience, and education.

Expected US salary range:

$135,500.00 - $213,400.00

Available benefits include bonus eligibility, long term incentive if applicable, health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and sick days. A summary of benefits is listed here.

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:

No

Travel Requirements:

10%

Flexible Work Arrangements:

Hybrid

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

n/a

Job Posting End Date:

12/17/2024

*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.


Requisition ID:R325129

PDN-9da41a5d-e922-41e1-9063-972627f7867f
Job Information
Job Category:
Science
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Associate Director, Comparator Management - Hybrid
Merck
Rahway, NJ
Dec 4, 2024
Full-time
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