Senior Scientist - Drug Product Formulation

at  Pharmaron

Job Introduction We are looking for:
A Senior Scientist to produce phase-appropriate formulations and processes to support clinical studies or client needs as defined in the agreed work package.

At Pharmaron we offer:

• 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!

REQUIREMENTS:

• 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

Key roles and responsibilities:

• 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.

Our Company: “We are a dynamic, fast-growing company, with an enviable reputation for leading edge science, offering contract research services to some of the world’s leading pharmaceutical companies, solving what were believed to be unsolvable scientific challenges”.We believe in our ability to relentlessly push forward the boundaries of scientific excellence, delivering solutions for our clients, always operating ethically and with integrity. We take pride in our professionalism and commitment to always deliver our very best work.Pharmaron acquired the Hoddesdon campus, consisting of several purpose built scientific and administrative buildings together with a purpose built conference area in February 2017. The research building has more than 5,000m2 of premier R&D space and houses an established Process Chemistry, Analytical Chemistry and Drug Discovery teams. In addition, a Formulation Development team was also recently established. The Hoddesdon site has state-of-the-art Good Manufacturing Practice (GMP) standard facilities for the development of Active Pharmaceutical Ingredients (API), Formulation Development (FD) and Process Chemistry (PC).

• 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.

Why Should You Apply?

• 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.

Pharmaron is a premier R&D service company supporting the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities having established diverse drug R&D service capabilities, ranging from synthetic, medicinal, and analytical chemistry, biology, DMPK, pharmacology, drug safety assessment, radiochemistry and isotopically labelled metabolism, chemical & pharmaceutical development to clinical development. With operations in China, US and UK staffed by over 19,000 employees, Pharmaron has an excellent track record in the delivery of R&D solutions to its partners in North America, Europe, Japan, and China

Key roles and responsibilities:

• 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

Our Company: “We are a dynamic, fast-growing company, with an enviable reputation for leading edge science, offering contract research services to some of the world’s leading pharmaceutical companies, solving what were believed to be unsolvable scientific challenges”.We believe in our ability to relentlessly push forward the boundaries of scientific excellence, delivering solutions for our clients, always operating ethically and with integrity. We take pride in our professionalism and commitment to always deliver our very best work.Pharmaron acquired the Hoddesdon campus, consisting of several purpose built scientific and administrative buildings together with a purpose built conference area in February 2017. The research building has more than 5,000m2 of premier R&D space and houses an established Process Chemistry, Analytical Chemistry and Drug Discovery teams. In addition, a Formulation Development team was also recently established. The Hoddesdon site has state-of-the-art Good Manufacturing Practice (GMP) standard facilities for the development of Active Pharmaceutical Ingredients (API), Formulation Development (FD) and Process Chemistry (PC).

• 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