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Downstream Bioprocess Associate II
| Reference: | JSC00016994 | Location: |
Dublin |
| Qualification: | Degree | Experience: | See description |
| Job Type: | Fixed Term Contract | Salary: | Not Disclosed |
We’re currently recruiting for an exciting opportunity with an award-winning Biopharmaceutical organization based in Dublin. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.
This role is a site-based position and will involve working shift, on a 24/7 basis.
This role is a site based position.
24/7 - 4-Cycle shift 33.33% shift premium
Shift Pattern - 2days - 2nights - 4 rest
Responsibilities.
Work with the manufacturing operations group, project design team, the CQV team, the Automation/CSV reps to facilitate the development and validation of the Biotech facility manufacturing facility.
• Support Equipment Design/ HAZOP and Room programming reviews as per requirements.
• 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 Page 2 of 2 Proprietary Role Functions (Functions include, but are not limited to, the following)
• Generate SOPS/Electronic Batch Records for start-up.
• Adhere to Right First-Time principals
• Provide assistance and/or support maintenance, engineering, quality or other colleagues as requested.
• Escalate issues as appropriate to Process Lead
• 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.
Required Knowledge and Experience:
• Demonstrated successes in a team environment, such as project teams, Lean Six Sigma team, etc.
• Demonstrated problem solving capabilities.
• Knowledge of applying Lean Six Sigma and Lean methodologies in a workplace environment Technical
• Experience in a highly regulated pharmaceutical manufacturing environment is desirable.
• Start-up experience in a large-scale commercial drug substance facility desirable but not essential.
• Good understanding of Upstream/Downstream Processing and experience an advantage. People
• Ability to interact with multiple stakeholders across numerous departments
• Excellent communication skills and the ability to work in a cross functional collaborative environment.
• Good interpersonal skills, attentiveness, and an approachable manner for interactions with inter departmental colleagues.
• High degree of problem-solving ability and adherence to scheduled timelines Qualifications & Education
• Minimum of a Level 7 qualification in a science or engineering discipline.
• A level 6 with a minimum of 3 years’ experience in a GMP Manufacturing requirement shall be deemed equivalent.
If interested in this posting please feel free to contact Jack Caffrey on +353 (0)87 3854921or [email protected] forfurther information.
Life Science Recruitment | Tel:+353 1 685 4848 | Fax: +353 (0)1 443 05 24 | Email: [email protected] | Copyright © 2021 Life Science Recruitment Ltd
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