Job Introduction
A Senior Scientist to produce phase-appropriate formulations and processes to support clinical studies or client needs as defined in the agreed work package.
- Vibrant and dynamic employment – we are a highly specialised, growth company operating in a critical sector of the economy – our future is strong and exciting!
- Opportunities to develop your skills and yourself – our rapid growth brings greater opportunities for you to learn and grow faster!
- A great team where we all support each other – enjoy your work – after all you spend about a third of your time here!
- Degree or equivalent and in Pharmacy, Pharmaceutical Science, or Chemistry related discipline
- At least 3 years industrial experience in formulation and clinical manufacture
- Excellent and relevant laboratory skills and analytical skills
- Familiarity with formulation and processing techniques specific to Formulation Development
- Problem solving skills, data processing and analysis skills
- Effective organizational and time management skills
- Effective written and oral communication skills, including the ability to effectively present scientific findings to colleagues
- Good interpersonal skills
- Work within and contribute to a multi-disciplined environment
- Ability to work as part of a team
- Conscientious and meticulous in laboratory and written work
- Self-motivated and capable of sound judgement in knowing when to seek input from more experienced colleagues
- Willing to get involved with new ideas and initiatives
- Commitment to self-development and learning
- Willingness to share information and help others
- Design and plan work activities to ensure that project and/or initiatives are conducted and completed efficiently in terms of time, cost and coordination with associated work programmes.
- With guidance as required, conduct work and studies within established key workflows and/ or regulations as described by SOPs, corporate policies and external regulatory guidance (e.g. GxP, ICH, etc) to ensure the manufacture of clinical supplies and stability batches are in accordance with cGMP.
- Document and report results of all experiments in a manner consistent with department practices and governing policies, as applicable. Periodically, may be required to conduct second scientist review of experimental data or documentation.
- Collate data and update reports for the purpose of presentation production, to share results and progress with key stakeholders.
- Input, propose and modify as appropriate, SOPs, risk assessments and training curricula.
- Liaise closely with matrix partners, cross functional and global teams to support the coordination of projects and assist in the development and achievement of project timelines.
- Contribute to the evaluation and development of new technologies.
- Expand knowledge base and share knowledge through the training and mentoring of colleagues.
- Ensure personal development through training, knowledge accumulation and skill development activities.
- Performs roles and duties in accordance with current Good Manufacturing Practice guidelines and principles, and Pharmaron Hoddesdon Policies, Standard Operating Procedures, and Supporting documents.
- Follow all Health, Safety and Environmental requirements that are defined on work instructions or communicated in training.
- Work efficiently and tidily such that work is carried out in a well-planned and organised way and timely manner.
- Ensure that any operating practice or instrument defect, which may affect safety at work, is brought to the attention of Management.
- Provide Customers with high Quality service and high Quality products.
- Create and encourage a transparent and trustworthy environment.
- At all times upholds the highest professional standards and acts in the interest of the patient / patient safety.
- Encourage continuous improvement through an effective Quality Management System (QMS) striving to improve processes and practices.
- Promote and contribute to a best in class Quality culture and reputation based on collaboration.
- Promote leadership collaboration and employee engagement with the same Quality goals ensuring GMP compliance.
- Promote the culture that ‘Quality is everyone’s responsibility’.
- Assist with the general running of the Formulation Development group by maintaining a good standard of laboratory housekeeping and help with routine tasks.
- Ensures both initial and continued personal training is carried out and adapted according to need. Ensure all employees are suitably trained in all processes before undertaking where appropriate.
- Responsible to maintain own training file.
- We offer a competitive salary and a progressive and comprehensive suite of employee benefits.
- We offer state of the art working environment on site.
- We offer the opportunity for growth and development and will support funding for relevant training and development programmes.
- This is an opportunity for you as a Senior Scientist professional to make a real impact in a highly scientific and regulated environment, demonstrate leadership, ambition and the desire to grow with the department.
- Build and shape your career in an environment that sets and commits to the highest standards.
- To be part of a team who support each other, embrace and solve technical challenges and put excellence at the heart of all that we do.
