Lant Co-ordinator

**Title**:
LANT Co-ordinator

**Company**:
Ipsen Biopharm Ltd

Ipsen is a growing and dynamic specialty-driven biopharmaceutical company focussed on innovation and specialty care.

The patient is at the heart of everything we do, and we also care for our employees because they are the ambassadors who truly make a difference. We attract and develop bold, agile and entrepreneurial individuals who take full ownership of their decisions, leaders drawn by a purpose to make a direct impact through their work in people’s lives, all of which is underpinned by our _Ipsen Way of Being._

The **LANT Coordinator** will be responsible for organising and driving activities that support the technical transfer of LANT (Long Acting Neuro Toxin) from BPD (R&D) into TechOps (Manufacturing).

This will include transfer of Production activities, such as media and reagent preparation, upstream and downstream processing and activities that support the cleaning and maintenance of the Bioprocess Suite 2 (BPS2) facility.

Working with the Tech Transfer team, the LANT Coordinator will utilise prior experience in a GMP role to ensure full compliance of product manufacturing in BPS2 with cGMP and regulatory standards for drug substance manufacturing. Manufacturing operations must be compliant with all EHS regulations and local EHS procedures and policies.

**What does the role entail**
- Generate training packages (TRM’s) and be trained in all technical aspects of the LANT manufacturing process.
- Evaluating each process step to identify, lead and drive improvements in all key strategic areas (Cost, Quality, Delivery, Process) as part of the development, transfer and GMP manufacturing phases.
- Develop documentation to support manufacture of LANT in a GMP environment
- Lead problem solving initiatives and investigations, ensuring meaningful corrective/preventative actions are assigned and completed
- Participate in process development, monitoring and data gathering to drive analysis and improvements.
- Coordinate and train BAS team members in the LANT process to ensure GMP batches can be made in a safe and compliant manner
- Review, edit and prepare SOP’s for LANT processes.

**What are we looking for**
- Manufacturing/technical experience and competency associated with cGMP manufacturing operations.
- Competent in GDP
- Experience with Trackwise, Change controls
- Proficient in writing GMP documentation
- An agile and dynamic mindset with the ability to adjust priorities in line with demands
- Comfortable in training/mentoring others
- Willingness to learn and develop drug substance manufacturing knowledge

**What’s in it for you**
- High level exposure to a growing and developing site where you can make key contributions
- An opportunity to be highly influential and have significant input to a project in its early phases
- An exciting and vastly experienced team
- The opportunity to nurture and grow your career in a business that embraces and encourages its employees to be the best they can be
- Competitive salary and enhanced benefits package including annual bonus, generous pension scheme and hybrid working, amongst others.
- Develop your career in a company that has been awarded ‘Best Workplaces’ and ‘Best Workplaces for Wellbeing’ status in the Large Organisations category for 2023
- Own your growth with structured development plans to help you achieve your career goals and aspirations
- The pride of working for a company that directly impacts and changes lives for the better