Job Description
Job Description
- Participate and support continuous improvement initiatives as part of the Production System (i.e., lean six sigma elements, gemba, problem solving, solution development, planning, execution and presentation).
- Collaborate with other departments or Singapore manufacturing site to execute site or global projects
- Assist or lead project tasks for continuous improvement of manufacturing process, batch review & release and site contamination controls.
- Perform update of procedures, work instruction, job aids, elogs when requires.
- Provide inventory management support for the manufacturing process.
- Provide administrative support to the IPT Operation Support Specialist/Improvement Team such as filing, archiving, elog management, datasheet, data trending etc.
Qualification & Job Requirements
- Bachelor's Degree/Diploma in a technical field, including Chemical/Biological/Mechanical Engineering, Chemistry or Pharmaceutical Sciences Proficient with Microsoft Word and Excel
- Candidate with excel coding skill will be an advantage
- Effective oral and written management communication skills
- Demonstrate self-motivation/direction skills with a continuous improvement focus.
- Demonstrated capability in application of project management skills and structured/analytical problem-solving techniques
- Able to commit full-time for a minimum of 6 months period
Learning Outcome to be gained by the intern
Intern will be able to understand cGMP requirement of a sterile biotechnology facility and the quality system from the internship experience. Intern will also be able to demonstrate their problem-solving and project management skill from the tasks assigned. Intern will experience the importance of operation support within the manufacturing environment. Additional learning outcome includes basic microbiology, aseptic behavior, good documentation practices (GDP), basic lean six sigma elements and manufacturing process of sterile products during the internship.
Brief write-up of the department
Sterile Integrated Process Team (IPT) is one of the core departments in the sterile facility. We manufacture medicines to the highest standards in full compliance with regulations and good manufacturing practices. There are strong collaborations between departments to ensure our priorities are met. You will be an active member within the IPT Improvement Team providing support, guidance and striving for excellence to ensure the success of the IPT.
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
Preferred Skills
Job Posting End Date
11/27/2025
- 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 R345486
