Job Description
An amazing opportunity has arisen foraLead Bioprocess Associateat Dublin Biologics, our new state of Manufacture of Commercial Large-Scale Drug Substance Biotech facility.
The Lead Bioprocess Associate will be a leader with strong interpersonal, communication and collaboration skills responsible for supporting the manufacturing process, whilst creating an inclusive culture that energizes a safety first, quality always, with a continuous improvement mindset.
What you will do:
Bring energy, knowledge, innovation, and leadership to carry out the following:
- Work with the manufacturing operations group, the Automation/CSV reps to facilitate proficient operations of the Biotech facility manufacturing facility.
- Support Operations team to consistently deliver on specific area Key Performance Indicators (KPIs), e.g. EHS metrics, Production Plan, OEE, compliance and team training.
- Execute commercial manufacturing processes according to established work instructions and Standard Operating Procedures.
- Work as part of a dedicated process team where flexibility and teamwork are a key requirement.
- Provide assistanceand/or support maintenance, engineering, quality or other colleagues as requested.
- 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.
- Generate and update SOPs/Electronic Batch Records.
- Adhere to Right First-Time principles.
- Escalate issues as appropriate to manager/designee.
- Be an advocate for continuous improvement.
- Maintain/ support a high standard of safety /GMP compliance at all times.
- Determine solutions by referencing relevant past experiences as part of problem-solving activities.
- Participate in internal audit programs and risk assessment compliance activity.
- Lead by example through coaching & mentoring on MPS systems skill transfer.
Qualifications
In order to excel in this role, you will more than likely have:
- Degreequalification (Science/Quality/Technical).
- 6 years’ experience
- Preference Lean Six Sigma
- Experience in a highly regulated drug substance manufacturing environment is essential.
- Start-up experiencein a large scale commercial drug substancefacility desirable but not essential.
- Excellent understanding ofDownstream Processing
- Ability to work as part of a team and on own initiative in a constructive manner.
Please feel free to speak to us about what flexibility means to you during your application or click on the link to find out more about our
So, if you are ready to:
Invent solutions to meet unmet healthcare needs,please apply today.
Current Contingent Workers apply
Not Applicable
*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.