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Manufacturing Biotechnologist

3 months ago

Edinburgh, Edinburgh, United Kingdom RoslinCT Full time

Manufacturing Biotechnologist

Location:
Edinburgh BioQuarter, Little France

Who are we?


We are RoslinCT, a world-leading cell and gene therapy contract development and manufacturing organisation creating cutting-edge therapies that change people's lives.


Collaborative, dedicated and talented people are the backbone of our culture, working both autonomously and in driven teams to make life-changing products utilising ground-breaking science.

Find out more about what we do here

Why join us?

  • The opportunity to join a rapidly expanding company which is changing lives, giving you the skills and experience to develop your career
  • A generous salary package we reward our people at the level they deserve
  • 31 days of annual leave, plus 4 public holidays which increases with tenure
  • A competitive company pension scheme to help you save for the future
  • Group Life Cover you are automatically covered for three times your basic salary to give you and your family peace of mind
  • Private healthcare and access to mental health/wellbeing support as your health and wellbeing means a lot to us
  • Flexible benefits such as retail discounts and access to the Cycle2Work scheme.

Your new role

  • An exciting opportunity for a
    Manufacturing Biotechnologist to join our team
  • You will work on a shift pattern (exact shifts TBC, but likely to rotate between Mon-Fri 9am5pm, Mon-Fri 7am3pm, Mon-Fri 11am7pm and weekend work)
  • You will be responsible for performing a range of activities in support of the delivery of different cell and gene therapy products, meeting all the required quality and regulatory standards
  • Perform the manufacture of cellular and gene therapies according to GMP within a controlled clean room environment
  • Complete quality related documentation to a high standard, including batch production records, change controls, incidents/deviations, and risk assessments in accordance with GMP and standard operating procedures
  • Prepare and maintain standard operating procedures, batch records, and standard forms for batch manufacture
  • Prepare formal documentation for new projects to enable developments to be introduced in a suitable controlled manner
  • Ensure confidentiality of all information relating to clients and patients is maintained at all times
  • Ensure compliance with all Health & Safety policies, embracing a Safety First culture
  • Occasional communication of procedures and results with clients, and demonstration of excellent customer service skills for both internal and external customers
  • Plan and undertake the validation of new manufacturing processes and equipment
  • Provide out of hours cover for critical equipment alarms as required on a rotational basis
  • Routine qualification, calibration, and maintenance of manufacturing equipment
  • Support daily manufacturing housekeeping activities, including but not limited to cleaning, stock control, and ordering materials.

About you

  • Ideally, you will have experience working in a GMP cleanroom manufacturing environment however this is not essential
  • Excellent communication skills in report writing/recording outputs, engaging with colleagues at all levels and professional liaison with customers
  • Excellent IT skills with experience in Microsoft Word and Excel
  • Good organisational and planning skills with the ability to multitask in a fastpaced environment
  • You will be able to create a positive environment through selfawareness and social skills Excellent attention to detail with a real desire to continually develop and improve our processes.

Qualifications

  • You will hold a HNC, HND, or BSc in a Life Science discipline, or have equivalent Manufacturing experience.
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