Associate Specialist, Process Engineer - Oral Solid Dosage, Clinical Manufacturing (Onsite)

Merck; Rahway (NJ); Vor Ort; USD 72.000 - 113.000; Vollzeit

Zusammenfassung

Merck & Co. in Rahway, NJ, is seeking an Associate Specialist – Process Engineer to lead clinical supply manufacturing in a GMP piloting facility.

You will manage on-the-floor batch production, ensure safety and quality, and draft batch records, change controls, and related documentation. The role requires experience with pilot plant manufacturing, electronic batch records, and MES systems, plus knowledge of drug product processing.

Qualifikationen

• Experience executing GxP manufacturing in pilot plant environment.
• Experience supporting electronic batch records and MES systems.
• Knowledge and experience of drug product processing.
• Willingness to learn and contribute through independent problem-solving.
• Experience leading and supporting quality investigations and change management.

Aufgaben

• Lead on-the-floor batch manufacturing to ensure safety and quality of clinical supplies.
• Draft and execute GxP documentation including batch records, equipment qualification and cleaning, change records and deviations.
• Build partnerships by developing relationships within and across work groups of formulators, engineers, safety and quality representatives.
• Foster culture of collaboration, learning and innovation.

Kenntnisse

Continuous Improvement

Engineering Standards

Equipment Qualification

GMP Compliance

GMP Validation

Lean Manufacturing

Process Control

Process Optimization

Teamwork

Ausbildung

Associate's degree in chemical engineering or related field

Bachelor's degree in chemical engineering, chemistry, pharmaceutical sciences, or related

Master's degree in chemical engineering, chemistry, pharmaceutical sciences, or related

Tools

Electronic batch records

MES systems

Jobbeschreibung

Job Description

The Formulation, Laboratory, and Experimentation (FLEx) Center is a multi-modality (small molecule, biologics, vaccine) Drug Product development and clinical manufacturing facility in Rahway, New Jersey. This team works with non-sterile formulations, typically oral solid dosage (blending, roller compaction, encapsulation, tableting) including spray dried intermediates, liquid suspension/bottle fills, and autoinjector assembly. We are part of the research division, focusing on development and clinical deliveries in a GMP piloting facility supporting our Company’s research division.

The Oral Solids Dosage (Non-Sterile) team at the FLEx Center in Rahway is looking for an Associate Specialist – Process Engineer to lead clinical supply manufacturing, scientific rigor of processes, and ultimately to enable flexibility and speed of our Company’s pipeline.

This Person Will

• Lead on-the-floor batch manufacturing to ensure safety and quality of clinical supplies to augment and accelerate our products.
• Draft and execute GxP documentation including but not limited to batch records, equipment qualification and cleaning, change records and deviations.
• Build partnerships by developing and leveraging relationships within and across work groups of formulators, engineers, safety and quality representatives.
• Foster culture of collaboration, learning and innovation.

Required Experience And Skills

• Experience executing GxP manufacturing in pilot plant environment.
• Experience of interest in supporting electronic batch records and MES systems.
• Knowledge and experience of drug product processing.
• Desire and willingness to learn and contribute through independent problem-solving.
• Experience in leading and supporting quality investigations and change management.

Education Minimum Requirements

• Associate’s degree in chemical engineering, Chemistry, Pharmaceutical Sciences or related field with a minimum of 3 years relevant experience
• Bachelor’s in chemical engineering, Chemistry, Pharmaceutical Sciences or related scientific field.
• Master’s degree in chemical engineering, Chemistry, Pharmaceutical Sciences or related scientific field

Preferred Experience And Skills

• Knowledge of Investigational drug regulatory requirements
• Understanding of Clinical Supply Chain Operations
• Experience with Commissioning, Qualification and Validation
• Experience with spray dried intermediates and/or hot melt extrusion

Required Skills

• Driving Continuous Improvement, Engineering Standards, Equipment Qualification, Estimation and Planning, GMP Compliance, GMP Validation, Lean Manufacturing, Manufacturing Quality Control, Manufacturing Scale-Up, Process Control, Process Optimization, Teamwork

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.

Requirements

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

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

Primary Location

USA - New Jersey - Rahway

Compensation

Where required by law, the compensation range for this role is provided below.

The salary range for the primary location of this role is:

$71,900.00 - $113,200.00

This range reflects the Company's reasonable expectation of the base salary applicable to this role at the time of 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.

Additional location(s)

Please note the salary range above applies to the Primary Location of the position. Where a role has other listed locations, different compensation guidelines may apply. You may find the salary ranges for additional locations below. If the salary range is not listed for the location you are applying to, our Talent Acquisition team will provide further information to you relevant to your location.

Additional location(s) Compensation Information

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

Not Indicated

Valid Driving License

No

Hazardous Material(s)

Acetone, Iso-Propyl Alcohol

Job Posting End Date

11/6/2026

• 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.

Requisition ID

R423989