Manufacturing Process Engineer
Cork, County Cork, Ireland · عقد
كن أول من يتقدم بطلب
- خبرة
- أي
- مرتب
- —
- الوظائف الشاغرة
- 1
- تم النشر
- • 6 نجوم
- Work mode
- في المكتب
- تعليم
- Level 8 degree or higher in Biotechnology, Biochemistry, Microbiology, Science or Engineering
- Eligibility
- Recent graduates with relevant placement experience and candidates with industry experience can both be considered.
- Resume
- Required to apply
Where you'll work
المسمى الوظيفي
Role overview
This contract role in Cork is for a Manufacturing Readiness Specialist focused on supporting everyday production activities and the flow of materials through manufacturing. The position begins fully onsite for five days per week and later moves to a hybrid arrangement with three onsite days each week. It is suitable for recent graduates who have relevant placement experience as well as professionals with prior industry exposure.
Key responsibilities
- Assist with investigations and troubleshooting linked to material supply within manufacturing operations.
- Maintain records and manage change-control activities related to materials and manufacturing processes.
- Review requests for shelf-life extension of single-use consumables and support related qualification work.
- Work with Quality, Engineering, Logistics, Technical Operations and outside suppliers to address issues and put improvements in place.
- Take the lead on, and contribute to, investigations involving material-related concerns and continuous improvement efforts.
- Make sure all work follows cGMP, EHS requirements and site procedures.
- Draft, update and retain documents in accordance with Good Documentation Practices.
- Join cross-functional teams and provide guidance or training to colleagues when needed.
Candidate profile
The ideal applicant holds a Level 8 degree or above in Biotechnology, Biochemistry, Microbiology, Science or Engineering. You should be highly detail-focused, confident at solving problems and able to communicate clearly with others. Strong interpersonal skills, the ability to balance several priorities at once, and a positive, proactive attitude are important. A commitment to high standards is essential.
Desirable background
Previous experience in a GMP-regulated manufacturing setting would be an advantage. Exposure to project work or continuous improvement initiatives is also helpful. Familiarity with SAP, electronic document management tools and Microsoft Office is desirable, along with knowledge of Lean, Six Sigma or other structured problem-solving methods.
Additional information
This opportunity involves close collaboration with teams across the business and offers the chance to contribute to the production of high-quality biopharmaceutical products in a fast-moving and cooperative environment.