Kinetica
About the Company
For over twenty years Kinetica has been at the forefront of the global search for talent in the scientific, MedTech, and healthcare sectors. Forming partnerships with businesses developing products that are revolutionising the medical treatment that the world receives. From the development of heart valves to the production of the Covid 19 vaccine, Kinetica’s people have built the teams that created, manufactured, tested, and delivered those breakthroughs.
Knowing we play a small part in that revolution is what drives us.
Listed Jobs
- Company Name
- Kinetica
- Job Title
- Validation Specialist
- Job Description
-
Validation Specialist – Kent – Pharmaceuticals
About the Company:
We are looking for an experienced Validation Specialist to join a pharmaceutical manufacturing site in Kent (commutable from SE London). You will have the opportunity to work in a newly built GMP manufacturing facility.
This is a 1-year parental cover contract on a FTC.
Responsibilities:
• Completion of validation activities and projects for equipment and processes.
• Maintenance of relevant documentation.
• Preparation and execution of validation procedures and protocols for re-qualification, cleaning validation, and temperature mapping.
• Maintenance of the re-qualification schedule for validated equipment.
• Gathering and analysing validation data and prepare reports.
• Assisting with the compilation of and maintain the validation master plan (VMP).
• Providing advice and suggestions concerning changes and improvements.
• Providing technical expertise in terms of investigation, trouble shooting and finding solutions.
• Maintaining documentation and files.
Requirements:
• An understanding of and experience in IQ, OQ, PQ and PV.
• Experience of temperature mapping and cleaning validations.
• Experience working in a process and equipment validation position in the pharmaceutical, biopharmaceutical or biotechnology manufacturing industry.
• Ability to write and carry out validation procedures.
• An understanding of the principes of calibration.
• Excellent communication skills.
• An understanding of the requirements of GMP.
Kent, United Kingdom
On site
08-04-2025
- Company Name
- Kinetica
- Job Title
- Engineering Manager
- Job Description
-
Engineering Manager (1 Yr FTC or Contractor) – North Wales/Cheshire – Medical Device
About the Company:
We are looking for a highly experienced Engineering Leader with management experience and an excellent knowledge of process improvement and technical transfer to join a company at their established manufacturing site on a contract basis.
Responsibilities:
• Process implementation/ technical transfer.
• Process improvement.
• Root cause and CAPA.
• Communication with a wide range of stakeholders and suppliers.
• Development and management of engineering and quality-based strategies.
• Recording, analysis of and reporting on data.
• Training and mentoring.
• Budget management.
Requirements:
• Significant experience in manufacturing process development and improvement.
• People management and mentoring experience.
• Excellent knowledge of six-sigma and Lean principles.
• Experience working in a highly regulated assembly manufacturing environment.
• A good understanding of GMP and ideally ISO 13485.
• Beng in Manufacturing Engineering or related.
Wales, United Kingdom
On site
28-04-2025