Job Description

Responsibilities:

•Generation, review and approval of process documentation. 
• Execution of development and qualification studies across commercial and non-commercial product. 
• Representing Technical Operations department at cross functional meetings. 
• Development and qualification of new processes.  
• Support investigations and troubleshooting of process studies as required. 
• Technical support for commercial manufacturing. 
• Technical support for new product introduction. 
• Ensure compliance with the QMS, industry/company specific standards and regulations. 
• Demonstrate effective communication and interpersonal skills.

• Proactively act to consistently improve personal knowledge and capability. 
• Demonstrate an awareness of own capabilities and development needs. 
• Application of technical knowledge to enable authoring of technical documents and technical decision making. 
• Support audit readiness, including preparation of story boards, ensuring GMP compliant documents are available, presentation to auditors as required. 
• Work collaboratively to drive a safe and compliant culture
• Participate in driving a high performing & inclusive culture, stimulating personal growth & development. 
• May be required to perform other duties as assigned.

Qualifications

Required

• Currently pursuing a Bachelor’s Degree or higher in a related, Science, Engineering, or other technical discipline.

• Interest in gaining experience in a related field, ideally in a manufacturing setting adhering to GMP standards.

PQ20

Required Skills:

Analytical Problem Solving, Analytical Problem Solving, Business Process Creation, Clinical Research, Data Analytics, Database Management, Data Entry, Data Visualization, Documentation Preparation, Documentation Review, Document Management, Engineering Document Management, Engineering Support, Functional Management, Health Economics, Influencing Skills, New Product Introduction (NPI), Office Applications, Proactive Thinking, Process Analytics, Process Definition, Process Implementations, Process Improvements, Product Compliance, Product Support {+ 10 more}

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

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:

Intern/Co-op (Fixed Term)

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:

09/16/2026

*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.