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Senior Specialist Engineering, Sterile/Liquids (Onsite)

MSD
Posted 18 hours ago, valid for 12 days
Location

Upper Gwynedd, PA, US

Salary

$117,000 - $184,200 per year

Contract type

Full Time

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Sonic Summary

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  • The Senior Specialist, Engineering position at the Sterile/Liquids Pilot Plants in West Point, PA, focuses on supporting the formulation and filling of clinical supplies for various pharmaceutical products.
  • Candidates are required to have a Bachelor's degree in Chemical Engineering, Chemistry, Biology, or a related scientific field, along with a minimum of 3 years of experience in a technical or operations support role.
  • The role includes responsibilities such as providing technical input on sterile processes, project management oversight, and ensuring compliance with Good Manufacturing Practices (GMP).
  • The salary range for this position is between $117,000 and $184,200, with eligibility for annual bonuses and long-term incentives.
  • The company offers a comprehensive benefits package, including medical, dental, vision, retirement benefits, and paid time off.

Job Description

Description – Sr. Specialist, Engineering

The Sterile/Liquids Pilot Plants (SLP,) located in Bldg. 17 at West Point, is part of the Pharmaceutical Sciences organization.  The SLP supports the formulation and filling of clinical, stability, and developmental supplies for vaccines, small molecules, and therapeutic proteins.  The SLP interfaces with a large network including multiple of our Company's Research Laboratories teams, Sterile/Liquids Commercialization (SLC), commercial supply, and other pilot plants within the PharmSci network.  SLP supplies support critical program needs related to new products undergoing process development, new products undergoing scale-up, launch, and transfer to the supply network, and existing commercial products undergoing process optimization.

The Process Engineer (PE) provides technical input on sterile processes from a facility and operational standpoint, provides manufacturing project management oversight, and GMP expertise to ensure timely availability of clinical supplies and development batches to meet Clinical Development program requirements.  This person is the main interface with development scientists for the activities required for the manufacturing of sterile liquid clinical and development batches in the SLP.  Additional responsibilities include deviation management, process improvement projects, implementation of new technologies, and process design.

Qualifications:

Education Minimum Requirement:

  • Required:  Bachelor's of Science in Chemical Engineering, Chemistry, Biology or related Scientific Field    

Required Experience and Skills:

  • Minimum of 3 years in a technical or operations support role

  • Sterile process manufacturing and/or formulation development

  • Knowledge of manufacturing equipment and Good Manufacturing Practices

  • Project management 

  • Analytical problem-solving skills

  • Cross functional leadership

  • Technical writing – including batch documentation, investigations, protocols

Location:

  • West Point, PA

eligibleforERP

Required Skills:

Adaptability, Adaptability, Analytical Testing, Batch Production Records, Biologics, Chemical Engineering, Chemistry, Clinical Manufacturing, Cross-Functional Project Management, Data Analysis, Detail-Oriented, Deviation Management, Documentation Preparation, Drug Formulations, Equipment Qualification, Functional Management, Good Manufacturing Practices (GMP), Manufacturing, Manufacturing Processes, Problem Identification, Process Design, Process Development (PD), Process Engineering, Process Hazard Analysis (PHA), Process Optimization {+ 7 more}

Preferred Skills:

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.

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

The salary range for this role is

$117,000.00 - $184,200.00

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:

No Travel Required

Flexible Work Arrangements:

Not Applicable

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

n/a

Job Posting End Date:

09/5/2026

*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.




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