Job Description

THE OPPORTUNITY:

Join a Global Innovative Pharmaceutical Company Great opportunity for Personal and Professional development

Our engineers support manufacturing operations remain operational, continuously improve and innovate. We work in the manufacturing plants with a "Safety First, Quality Always" mindset striving for continuous improvement to ensure supply of highest quality of raw materials, intermediates, and finished products and support our global manufacturing network. With our extensive range of facilities and environments, our Engineers have opportunities across many diverse areas including Chemical, Automation, Capital Projects, Maintenance, Safety, Environmental, Technical Services and Utilities.
WHAT YOU WILL DO

As a Process Engineer (Intern) you will provide process engineering support for manufacturing operations to support continuous improvement to drive safety, quality, process efficiency and compliance in cGMP manufacturing environment. Expected to support various initiatives leveraging quality, safety and project management platforms, engineering standards, codes, technology and supports department business goals and objectives.

Other main responsibilities include:

Work with Process Engineering team for API manufacturing plants in support of business continuity to meet Safety, Quality, environmental, continuous improvement, regulatory and compliance objectives. Support Deviation management related to the equipment, systems in response to deviations/ adverse events to investigate and identify point of occurrence, root cause and corrective/ preventative actions. Support global change management under various execution platforms to endure the equipment, facility and system changes are executed complying to design standards, safety standards and quality procedures. Support minor capex projects through evaluation of scope, feasibility, design, project proposals, sourcing plan, installation, commissioning & qualification with adherence to site change control procedures within the allotted timeline, budget, design requirements, and established quality standards. Demonstrates good project management skills (e.g. define core team and activities, project scheduling, stakeholder management and issues escalation etc), and demonstrates the ability to manage/ influence the project team. Execute portfolio projects to introduce new technology, engineering standards recommendations and new code and practices to support process & energy efficiencies, process safety and quality compliance. Provides technical Support during quality and safety external audits / internal inspections in providing technical representation and / or assessments in response to the auditing firms and other regulatory agencies. Perform gap assessment & periodic review of current engineering & business procedures, update SOPs and train the impacted personnel. Demonstrates leadership behaviors and leads personal career development with manager assistance through Performance Management and Employee Development Plan (EDP). Participates in process hazards analyses (PHA) and applicable Process Safety Management (PSM) activities related to new/inline products. Supports EHS audits and Safety incident investigations. Support energy initiatives & cost reduction projects Any other duties as assigned by the Supervisor.
WHAT YOU MUST HAVE

Bachelor's degree in chemical engineering or biochemical engineering. Knowledge of GMP systems, equipment qualification and commissioning Possess unit operations, equipment knowledge and trouble shooting skills. Perform Process hazard analysis, FMEA and Risk assessments. Application of engineering fundamentals to carry out feasibility studies and develop implementation plans. Project management skills to scope, plan, cost and implement actions in-collaboration with multi-functional teams.
WHAT YOU CAN EXPECT

Limitless opportunities across various areas in Pharmaceutical Manufacturing. A state-of-the-art facility that delivers solution to its customers world-wide Highly engaging team that aims to innovate the future Chance to work above site functions, project management exposure and be part of continuous project improvement plan.
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:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Not Applicable

Shift:

Valid Driving License:

Hazardous Material(s):

Required Skills:

Accountability, Accountability, Business Continuity, Career Development, cGMP Compliance, Change Management, Chemical Engineering, Communication, Data Analysis, Energy Efficiency, Energy Saving Programs, Engineering Standards, Failure Mode and Effects Analysis FMEA, Feasibility Studies, GMP Compliance, Hazard Analysis, Leadership, Lean Six Sigma Continuous Improvement, Maintenance Planning, Manufacturing Quality Control, Pharmaceutical Manufacturing, Process Design, Process Engineering, Project Estimations, Project Management {+ 5 more}

Preferred Skills:

Job Posting End Date:

12/31/2025

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:

R365454