
Job Information
Merck Specialist, Mechanical Coordinator in Rahway, New Jersey
Job Description
The Enabling Facilities (EF) group within the Chemical Engineering Research & Development (CERD) Department is seeking a highly motivated individual to work in a fast-paced job that provides a high degree of practical technical, mechanical and planning responsibility. The Equipment Development and Facility Engineering (EDFE) Mechanical Coordinator position will report to the Associate Director, Engineering and will be a member of the MACS EF Team at the Rahway, NJ facility. EF is responsible for development of new technologies/capabilities, execution of capital and non-capital improvement projects, and the automation system assets spanning production, utility systems and associated infrastructure. EDFE's role within EF includes design, installation, qualification, startup, maintenance and troubleshooting of equipment and systems.
Responsibilities of the MACS EDFE Mechanical Coordinator include the following:
The Mechanical Coordinator role at the Specialist level will serve as a team member supporting the Modality Agnostic Chemistry Scaleup (MACS) Center. This is a new potent, multi-modality (small molecule, macrocyclic peptides, bioconjugates) Drug Substance development and GMP clinical manufacturing plant currently planned in Rahway, New Jersey. The Specialist will serve as a valued team member during the MACS Center Execution Phase and will support the facility’s operations after start-up.
As the facility is currently under construction, the selected candidate will contribute to equipment and facility design, system commissioning/qualification, and operational readiness planning to enable facility startup. Upon start-up, the selected candidate will lead the daily mechanical activities and be responsible for the planning and execution supervision of maintenance, improvement and yearly shutdown/turnaround efforts. It will involve learning, understanding, and applying the maintenance requirements and safe work practices in effect at the Rahway site to prepare the facility and its equipment for a multi-discipline team of internal tradesmen and 3rd party contractors to execute said maintenance and improvement activities.
Daily activities include:
Prioritization of mechanical work to meet the timelines of the business
Hazardous permits including line breaks, Class A & B hot work, elevated roof, and confined space entry.
Lockout/Tagout and Energy Control Procedure implementation and development
Emergency Repairs/Troubleshooting
Calibration/Routine Preventative Maintenance
Process Equipment set-up and re-qualifications
Design of small facility modifications
Materials sourcing and procurement
Interaction with Computerized Maintenance Management System (CMMS) applications
The candidate will liaise with operations specialists, facility engineers, compliance representatives, and other team members to ensure a safe work environment, the quality and safe delivery of clinical supplies, and an optimized work plan. A successful candidate will stay well attuned to the status of production activities in a very dynamic production environment, the readiness of maintenance work and will adjust priorities of the work on an ongoing basis, which ultimately will contribute to the flexibility and speed of the Company's pipeline.
Education Minimum Requirement:
- High School Diploma/GED plus at least four (4) years of relevant experience in Pharmaceutical, Chemical, Petrochemical or Food Processing/Manufacturing.
Required Experience and Skills
A strong mechanical aptitude,
Maintenance experience in manufacturing environments,
History interacting with skilled trades (Piping, Electrical, Millwrights, Instrumentation, 3rd party contractors and vendors),
Ability to read and understand P&IDs and technical/mechanical diagrams,
Familiarity with Change Management processes and principles,
Excellent organizational skills with an ability to multi-task,
Effective interpersonal and communication skills, both verbal and written,
A collaborative mindset,
Desire and willingness to learn, contribute and lead,
Track-record of independent problem-solving,
Fluent in Microsoft Office, use of email.
Desired Experience and Skills:
Maintenance experience in GMP pilot plants or manufacturing environments,
Familiarity with US and EU Safety and GMP compliance regulations,
Experience with Potent Compound processing and containment systems (e.g., isolators), or clean room facilities.
Experience operating/maintaining pilot scale or prep lab scale equipment.
Experience with coordinating maintenance activities around processing activities to support reliable facility operation.
Experience with GMP facility design, equipment start-up and/or qualification.
Experience with high-risk work including, but not limited to, Lockout/Tagout, Hazardous Energy Control, Elevated Work, and Confined Space Entry.
Experience with Electrical Classifications for solvent and dust (Class I and II, Div I and II).
Experience with preparing Standard Operating Procedures (SOP) and cGMP documents.
Trained in use of SAP for Plant Maintenance management.
Experience working in an environment with an Automation System (DeltaV, PLC, etc.).
#MSJR #eligibleforerp
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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.
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 (https://www.eeoc.gov/sites/default/files/2022-10/22-088_EEOC_KnowYourRights_10_20.pdf)
EEOC GINA Supplement
Pay Transparency Nondiscrimination (https://www.dol.gov/sites/dolgov/files/OFCCP/pdf/pay-transp_%20English_formattedESQA508c.pdf)
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 (https://www.msdprivacy.com/us/en/CCPA-notice/)
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:
$85,600.00 - $134,800.00
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 (https://www.benefitsatmerck.com/) .
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:
Domestic
VISA Sponsorship:
No
Travel Requirements:
10%
Flexible Work Arrangements:
Not Applicable
Shift:
1st - Day
Valid Driving License:
No
Hazardous Material(s):
chemicals and solvents
Job Posting End Date:
04/9/2025
*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: R341878
Merck
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