Independent Solutions help Pharmaceutical, Biotech and MedTech industries to address skill shortages and resource constraints.
We deliver end to end professional services such as Project Management, Validation, Regulatory Compliance, ISO Implementation, Auditing, Training, Agile Practices and Well-being & Specialized Talent to enable our clients to reach their desired outcome.
We have a continuous dynamic range of specialized opportunities available within the sector, we pride ourselves in a high success to hire rate.
Each successful candidate is an integral part of our team and has continued access to our support mechanism and shared knowledge.
Our expertise, hands on approach, inside knowledge of the processes, understanding of the client requirements delivers a successful experience for both our professionals and clients.
Project Managers work closely with the clients to determine and implement the exact needs of the client, based on knowledge of the client,
Validation is defined as a means of providing documented evidence that assures, to a high degree of confidence, that a method, system.
Regulatory compliance ensures that personnel are aware of and take steps to comply with relevant regulations. This ensures that all necessary.
Accreditation can be defined as a Procedure by which an authorisation body gives formal recognition that a body is competent to carry out.
Our team consists of full-time qualified and experienced employees that can “hit the ground running”.
All have proved experience within the Biopharmaceutical and Medical Devices Industry.
For over the last 20 years and since the foundation of Independent Solutions in 2006 we have provided consulting and placement services to the Biopharmaceutical and Medical Devices Industries.
We are approved suppliers for key Biopharmaceutical and Medical Devices Companies.
Our wide network provides us with a deep pool of talented individuals to support client contracts / permanent resource requirements at VERY competitive costs.
Our Project Leaders/Managers have excellent track records at delivering a diverse range of global projects – managing the key elements of scope, time, risk and budget without compromising on quality.
Our Validation Engineers have exceptional experience in authoring and delivering the full suite of validation lifecycle documents: Planning, Specification, Design, Testing and Release, including continuous Risk Assessment.
Our Quality Personnel are highly skilled in delivery of best practices, and have a thorough understanding of the International Regulations and Quality Standards.
We are professional, extremely organized with excellent problem solving, effective time management and communication skills.
Our industry experience is diverse within this ever changing regulatory environment.