Assoc. Scientist, Engineering
USA - Pennsylvania - West Point
Job Description
The Pharmaceutical Commercialization Technology (PCT) department is seeking an entry-level engineer based in West Point, PA or Rahway, NJ. The group sits within the Manufacturing Division and is responsible for pharmaceutical process development and supply for small molecule solid dosage drug products, delivering new and novel medicines to patients worldwide. PCT leads process and technology development as products enter Phase 2b through regulatory filings and process validation and supports supply for several years beyond commercial launch. Products are commercialized at a network of internal manufacturing sites, located in Ireland and Singapore, as well as contract manufacturing organizations around the world. Coupled with development centers in Rahway, NJ and West Point, PA, these sites are the foundation for our extensive small molecule solid dosage capabilities.
Success in this role requires communication and collaboration within teams, a growth and innovative mindset and eagerness for continuous learning, a passion for science and solving technical problems, and hands-on development and manufacturing from pilot to commercial scale. Partners include research and development, analytical, regulatory, quality, packaging, and operations at our commercialization and commercial supply sites. We recognize that the diversity in our team is our strength and are dedicated to creating an inclusive environment for all employees.
Key Responsibilities:
Plan, conduct, and interpret pharmaceutical process development studies with manager and team support, such as scale up, technology transfer, design space development, clinical and stability batch manufacture, and process validation.
Apply problem-solving skills and aspects of Quality by Design, including risk-based approaches to development, design of experiments, and process modeling.
Author technical documents, such as experimental protocols and reports in support of regulatory filings.
Demonstrate oral and written communication skills and effective collaboration within teams.
Evaluate new and innovative technologies and equipment, perform physical testing and data analysis, and comply with applicable safety and current good manufacturing practices.
Contribute to publications and presentations within the scientific community as appropriate.
Support digital and data analytics initiatives and contribute to an innovative environment.
Education Minimum Requirement:
Bachelor’s or master’s degree (no prior experience required) in Chemical/Biochemical Engineering, Materials Science/Engineering, Pharmaceutical Sciences, or related discipline.
Required Experience and Skills:
Proven ability to work both independently and as part of a team and execute against commitments.
Strong written and oral communication skills and an interest in solving technical problems.
Preferred Experience and Skills:
Hands-on experience in a laboratory, pilot plant, or manufacturing facility.
Demonstrated ability to design and execute experiments.
Experience with data analytics, process modeling, and/or statistical process control.
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.
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:
Pay Transparency Nondiscrimination
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
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:
$68,400.00 - $107,700.00Available 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.
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:
25%Flexible Work Arrangements:
Not ApplicableShift:
1st - DayValid Driving License:
NoHazardous Material(s):
n/Job Posting End Date:
01/7/2025*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.
ApplyJob Profile
Hybrid Hybrid work Hybrid work model On-site Puerto Rico residents only US and Puerto Rico residents only
Benefits/PerksBonus eligibility Collaboration Collaboration opportunities Continuous learning Diverse workplace Equal opportunity employer Flexible work Flexible work arrangements Hands-on experience Health Care Hybrid work Hybrid work model Inclusion Inclusive environment Innovative environment Insurance Paid holidays Retirement benefits Sick Days Vacation
Tasks- Apply problem-solving
- Author technical documents
- Collaboration
- Communication
- Compliance
- Conduct pharmaceutical process development studies
- Contribute to publications
- Data Analysis
- Design and execute experiments
- Design of experiments
- Evaluate new technologies
- Execute experiments
- Innovation
- Process development
- Regulatory filings
- Support digital initiatives
- Technology Transfer
- Validation
Analysis Analytical Analytics Biochemical engineering Chemical Engineering Clinical Collaboration Commercial Commercialization Communication Compliance Continuous Learning Contract Manufacturing Current good manufacturing practices Data Data analysis Data & Analytics Design Design of experiments Development Digital Diversity Drug Products Education Engineering Equipment Experimental Good Manufacturing Practices Inclusion Innovation Laboratory Learning Manufacturing Manufacturing Practices Materials science Modeling Operations Oral communication Organization Packaging Pharmaceutical Pharmaceutical Sciences Problem-solving Process Control Process Development Process modeling Process Validation Publications Quality Quality by design Regulatory Regulatory filings Research Research and development Safety Science Statistical Process Control Teams Technical Technical Writing Technology Technology development Technology Transfer Testing Validation Written communication
Experience0 years
EducationAS Bachelor Bachelor's Biochemical engineering Business Data Analytics Degree Engineering Health Care Master Master's Pharmaceutical Sciences Related discipline Science Technology
TimezonesAmerica/Anchorage America/Chicago America/Denver America/Los_Angeles America/New_York Pacific/Honolulu UTC-10 UTC-5 UTC-6 UTC-7 UTC-8 UTC-9