Manufacturing Biotech Associate
- Dublin
- Contract
- Life Sciences
Do you want to be part of one of the top 10 best companies to work for in Ireland? We have a superb opportunity for Manufacturing Biotech Associate to join our client, a global pharmaceutical organisation in their new multifunctional facility. This is a truly exciting, €400 million project that will contribute to the manufacturing of life changing treatment, offering an abundance of opportunities to work with and learn about cutting-edge technologies.
Responsibilities:
- Provide immediate feedback to others at any time to reinforce good safety and improvement behaviors and acts.
- Execute commercial manufacturing processes according to established work instructions and
- Standard Operating Procedures (SOPs).
- Ensures that all assigned task related to manufacturing documentation support is in accordance with good manufacturing practices.
- Routinely talk about any safety issues you are concerned about.
- Work as part of a dedicated process team where flexibility and teamwork are a key requirement.
- Generate SOPs/ Work Instructions (WIs) to ensure compliance with regulatory standards.
- Adhere to Right First-Time principles.
- Provide assistance and/or support maintenance, engineering, quality, or other colleagues as requested.
- Escalate issues as appropriate to manager/designee.
- Maintain a high level of personal expertise and working knowledge of all aspects of the
- manufacturing process and process equipment through continuous training and development.
- Liaise with other groups and individuals to ensure planning of tasks is effective and linked into the manufacturing process plan and site schedule.
- Challenge and identify improvements to the safety and environmental programmes on site.
- Celebrate with use of proactive recognition tools that inspire teams and individuals you collaborate with.
Requirements:
- Level 7 qualification in a science or engineering discipline, or level 6 with a minimum of 1 - 3 years’ experience in a GMP Manufacturing environment.
- The minimum education/ experience (3 years) plus:
- Experience of Upstream/ Downstream Processing.
- Experience in a highly regulated pharmaceutical manufacturing environment.
- This role will involve working shifts, on a 24/7 basis.
- Excellent communication skills and the ability to work in a cross functional collaborative environment.
If this role is of interest to you, please apply now!
#LI-DH1
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
I have always received a highly professional & personable service from the team at Quanta. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
We have worked together with Quanta for seven years now and have always received a professional service. Quanta’s speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of Quanta’s people and their ability to deliver.
Global Pharmaceutical firm
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Dawn
I manage this role.