Job Description
Our companycan start your journey on the career path within the Pharmaceutical industry. Not only will you learn skills both technical and professional but work on projects that will contribute towards enhancing and enhancing people’s lives across the world.
You will be part of a diverse and inclusive, multi-skilled global team of highly motivated individuals. We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the world’s most challenging healthcare needs.
So, what will you will be responsible for?
Bringing energy, knowledge, innovation and leadership to carry out the following:
- Participate in continuous improvement initiatives, including process optimisation and troubleshooting.
- Preparation of documentation associated with the projects in accordance with GDP (good documentation practice) and site procedures.
- Participate in cross-functional projects, problem solving teams for troubleshooting, and investigations across site.
- Prepare, review and approval of technical documents, procedures, CAPAs, change control, deviations, metrics, etc.
- Support of Validation execution on the shop floor
- Peer review of Validation documentation
- Participate in daily meetings and ensure effective communication of testing progress, deviations etc.
- Provide support with audit/inspection requirements to ensure department compliance/readiness.
- Collaborating with others by sharing your skill-set and expertise
This internship will be completed fully on site (Carlow)
The ideal person will have:
Working towards an Engineering/ Science qualification or relevant discipline
So, if you are ready to:
Invent solutions to meet unmet healthcare needs, Impact the future by driving one of the world’s leading healthcare companies, and inspire your team to reach their full potential and push the boundaries of science and technology, please apply today.
PQ20
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:
HybridShift:
Valid Driving License:
Hazardous Material(s):
Job Posting End Date:
09/27/2024*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.
Job Posting End Date:09/27/2024
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:R309291