Job Description
Job Description:
The Biologics Process Research & Development organization within our Company Research Labs is responsible for developing the drug substance manufacturing processes for our Company's biologics pipeline. We work closely with colleagues in Discovery, Pre-clinical, and Early Development to rapidly develop processes for diverse biotherapeutics and efficiently produce material to supply clinical trials. We are also responsible for commercial process development, and development and implementation of new technologies. We work with our partners in our Company Manufacturing Division to commercialize and launch new products.
This role will support the Next Generation Biologics (NGB) facility, which will be a premier, state-of-the-art facility, that is a key part of our Chemistry, Manufacturing, and Controls (CMC) hub at our site headquarters in Rahway, NJ. This facility will be fully online in the next few years, both in terms of facility construction and organizational realization. The GMP facility is designed for multi-product operations with flexible operating suites, which can adjust as the clinical pipeline demands change. It is capable of meeting all historic, currently existing, and cutting-edge biologics program demands from supporting development to pilot scale, small and large scale potent material handling, and the ability to integrate new technologies and cell-line platforms.
The Master Scheduler will be a member of the NGB Facility Team. In this role, this individual will be responsible for the facility capacity planning, and scheduling and coordination of critical operational readiness tasks. Additionally, this individual will be managing both short- and long-term activities and projects, be a key contributor to determining how work is achieved, and support delivery of our company's expansive biologics portfolio and clinical supply needs.
Job Responsibilities:
Member of the NGB capital project delivery team, who is connected into all project actions and timelines, and supports engagement of business critical timelines, ensures alignment between the facility capacity plan and finite schedule.
Leader providing project management and logistical oversight of the Operational readiness plan, which will ensure teams are ready to seamlessly start operations at facility startup
Provide transparency into ongoing NGB organizational and workstream activities, and track/trend performance in key business KPI metrics
Work closely with enterprise capacity planning roles to generate capacity models, along with other longer term facility schedules
Work with end-to-end facility functions to enable continuous improvement of the underlining capacity assumptions
Ensure product demand is kept current in the site’s ERP system in line with the material planning cycle
Lead facility supply governance forums
Required Education, Experience and Skills:
Bachelor of Science, chemistry, biochemistry, biology, microbiology, or related discipline with minimum of 5 years relevant experience, or a master’s degree with minimum of 3 years of relevant experience
At least 5+ years of previous project management & planning experience.
Preferred Experience and Skills:
Track record of working effectively with team-members of diverse skill sets and backgrounds
Strong presentations and verbal/written communication skills
Experienced in the administration of GMPs, Good Documentation Practices (GDPs), and S&E regulations as it pertains to biologics development
Excellent attention to detail, highly independent with initiative
Excellent troubleshooting and problem-solving skills
Ability to challenge the status quo with a continuous improvement mindset
Strong analytical and presentation skills.
Proficient in ERP systems (COMET/SAP in particular), planning software and system interfaces.
PRD
Required Skills:
Adaptability, Adaptability, Analytical Testing, Biochemistry, Bioprocess Engineering, Clinical Trials, Data Analysis, Detail-Oriented, Deviation Management, Dispatching, Equipment Qualification, Good Manufacturing Practices (GMP), Immunochemistry, Manufacturing, Manufacturing Processes, Microbiology, Molecular Microbiology, Physiology, Planning Process, Process Design, Process Hazard Analysis (PHA), Process Manufacturing, Process Optimization, Root Cause Analysis (RCA), SAP Enterprise Resource Planning (ERP) {+ 4 more}Preferred Skills:
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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 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
$114,700.00 - $180,500.00This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An 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:
RegularRelocation:
DomesticVISA Sponsorship:
NoTravel Requirements:
10%Flexible Work Arrangements:
Not ApplicableShift:
Not IndicatedValid Driving License:
NoHazardous Material(s):
n/aJob Posting End Date:
01/16/2026*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.