DPDS BioTD AD Associate Scientist (Analytical Operations)

Job description

Job Description

Requisition ID: 1905722539W

Role: Associate Scientist – Analytical Operations
Location: Ringaskiddy Cork, Ireland
Department: Discovery , Product Development and Supply; BioTherapeutics Analytical Development – Clinical Release and Stability (DPDS, BioTD-AD)
Reports to: BioTD-AD Laboratory Management

Description

Janssen Sciences Ireland UC established its operation in Ringaskiddy in 2005 on a 100-acre site with an investment of €500 million. For more than 25 years we have been a global leader in the field of biomedicines, in particular groundbreaking monoclonal antibody technology a ground breaking approach to producing medicines that launched a new generation of products to treat immune related diseases such as rheumatoid arthritis and plaque psoriasis.
The facility in Ringaskiddy is now operational producing biomedicines for both the treatment of immune related diseases and new and creative cancer treatments.

Job Purpose

Global Clinical Release & Stability is a department of Discovery , Product Development and Supply; BioTherapeutics Analytical Development – (DPDS, BioTD-AD). The department is responsible for Tox Release testing, Clinical Release and Stability Testing for Drug Substance and Drug Product, and Stability Lifecycle management.

What you're great at:

• Daily management of the routine sample management operations/LIMS Stability Module.
• Responsible for the management of stability inventory.
• Ensure all activities follow SOP's/WI's and protocols where appropriate and are performed in compliance with regulatory guidelines.
• Perform sample management activities according to local procedures and processes in a timely and organized fashion.
• Organize stability inventory and maintain stability chambers.
• Coordinate receipt and distribution of samples throughout the laboratories.
• Perform other duties as designated by Laboratory Management.
• Develop subject matter expertise on assigned role.
• Use of laboratory software such as LIMS, SAP, SDMS, Trackwise, etc.
• Contribute to proper use, calibration and maintenance of laboratory equipment.
• Record all laboratory data in accordance with cGMP and local procedures.
• Perform data review.
• Keep up to date with existing and new SOP's and official documentation.
• Perform investigations, where required, for deviations, laboratory investigations etc.
• Independently write/revise SOP's or other official documentation and reports, when required.
• Execute independently and/or as part of a team, assigned projects/tasks.
• Train/coach other/new personnel.
• Lead/participate in lean innovation and continuous improvement projects

What we're about:

We are passionate about our work, and play vital roles across a range of professional disciplines, and care deeply about our customers and communities. At Johnson & Johnson our culture enables dynamic and impactful careers. We share a kind of DNA where we're each:

• Committed to caring
• Responsible to our communities
• Ready to apply our knowledge and know-how
• Rare in our background and experiences
• The drivers of our own success
• Passionate about doing what's right

Make a unique mark in your career

If you want to be seen for the talent you bring to your work, be the driver of your own career, and work with others who share your real passion for caring and success, then we invite you to join the Johnson & Johnson Talent Community by visiting www.careers.jnj.com
We respectively request Government Officials to identify themselves as such on application; for the purpose of the Foreign Corrupt Practices Act. If you decide to apply for the position, any personal data which you provide shall be processed by Johnson & Johnson Medical, a Johnson & Johnson company. Your personal data shall be processed for the purposes of recruitment, recruitment policy and selection.
We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

Desired profile

Qualifications

Be vital:

To be part of this high performing team you will have great attention to detail, alongside

• 3rd level qualification in a science related discipline.
• Knowledge of laboratory sample management and/or stability is preferred.
• Industry experience (GMP laboratory) is essential.
• Experience with LIMS systems is desirable.
• Good communication skills (written & verbal)
• Ability to think logically
• Ability to work well within team structures and to work on own initiative.

Primary Location
Ireland-Cork-Cork-
Organization
Janssen R&D Ireland (7566)
Job Function
Quality Assurance
Requisition ID
1905722539W