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Job Description

Are you looking for an exciting opportunity with a rapidly growing pharmaceutical manufacturer? If so, then this is the opportunity for you!

Large Molecule Science and Technology (LMS&T) Measles, Mumps, Rubella, Varicella and Sterile Diluent (MMRV+SD) Vaccine Technical Product Leadership (TPL) is seeking a highly motivated person for the role of Specialist, Vaccine Technical Product Leadership. This role will provide manufacturing science and technology support across the MMRV+SD vaccine sites with a focus on drug substance. The manufacturing sites include West Point, PA and Durham, NC.

MMRV+SD Technical Product Leadership is a customer-focused Above-Site technical support group with the primary focus to partner with key business units and customers to identify and implement innovative technical solutions and operational improvements that promote both process and supply chain robustness across the lifecycle of the product. The Specialist, Vaccine Technical Product Leadership will partner with groups across the Company, including Technical Operations, Operations, Quality, commercialization, process development, Regulatory-CMC, Supply Chain, and Value Chain.

Key functions:

+ Work Independently and as a Team member with Integrity | Precision | Accomplishment | Motivational Ambition | Respect | Inclusion

+ Coordinate technical teams across the network to achieve MMRV+SD Vaccine strategic goals. Participate as a technical expert and/or as a project leader in various projects.

+ Ensure process robustness for the MMRV+SD network through Process Monitoring, engaging with site technical teams to identify potential issues and drive rapid resolution.

+ Apply vaccine product/manufacturing process Subject Matter Expertise to plan and lead complex multi-site investigations and drive proactive process improvement projects.

+ Provide on-site support for critical MMRV+SD vaccine site investigations and specialized technical requests.

+ Collaborate and engage with key functional leads within LMS&T, site manufacturing, commercialization, our Research & Development Division and process development/support laboratories to identify and implement opportunities for process improvement and enhanced process robustness

+ Build and maintain strong and trusting relationships with site counterparts, functional management, and other stakeholders to ensure effective communication of plans and issues

Education Minimum Requirement:

+ M.S in Engineering or Biology/Chemistry Sciences, or related life sciences/engineering degree.

+ B.S. in Chemical Engineering, Biochemical Engineering, Bioengineering, Pharmaceuticals, Biochemistry, Microbiology, or related field with two (2) years of relevant experience; or M.S. in the same fields.

Required Experience and Skills:

+ Demonstrated problem solving, effective verbal and written communication, and strong interpersonal skills

+ Strong scientific understanding of vaccine products and processes, and their effective integration with relevant regulatory/GMP requirements

+ Collaborate effectively, across functional boundaries, to align stakeholders and sponsors on technical solutions

+ Demonstrated leadership and ability to drive results

+ Ability to work independently to drive projects to completion

Preferred Experience and Skills:

+ Minimum 2 years direct experience in vaccine drug substance process development, commercialization, or manufacturing

+ Experience in data analytics through building cross-site process monitoring tools, analyzing performance metrics to ensure processes are operating within defined thresholds, and ensuring continuous reliability improvement.

+ Experience authoring technical documentation

+ Experience managing project teams

+ Ability to travel up to 10% depending upon critical site needs

Required Skills:

Adaptability, Adaptability, Biochemistry, Change Control Management, Data Analysis, Equipment Troubleshooting, Functional Management, Good Manufacturing Practices (GMP), Immunochemistry, Lean Manufacturing, Microbiology, MUMPS Programming, Oral Communications, Personal Initiative, Process Improvement Projects, Process Improvements, Process Optimization, Product Management Leadership, Professional Integrity, Project Management, Root Cause Analysis (RCA), Stakeholder Management, Technical Writing, Technology Transfer, Vaccine Manufacturing {+ 2 more}

Preferred Skills:

Current Employees apply HERE (https://wd5.myworkday.com/msd/d/task/1422$6687.htmld)

Current Contingent Workers apply HERE (https://wd5.myworkday.com/msd/d/task/1422$4020.htmld)

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 (https://survey.sogosurvey.com/r/aCdfqL) 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 characteristics. As 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 (https://www.eeoc.gov/sites/default/files/2022-10/22-088\_EEOC\_KnowYourRights\_10\_20.pdf)

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 another’s thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts (https://www.msdprivacy.com/us/en/CCPA-notice/)

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 salary range for this role is

$85,600.00 - $134,800.00

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 employee’s 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 https://jobs.merck.com/us/en/compensation-and-benefits .

You can apply for this role through https://jobs.merck.com/us/en (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:

No

Travel Requirements:

10%

Flexible Work Arrangements:

Hybrid

Shift:

1st - Day

Valid Driving License:

No

Hazardous Material(s):

n/a

Job Posting End Date:

11/28/2025

*A job posting is effective until 11:59:59PM on the day** **BEFORE** **the 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:** R373423