Analytical Development Scientist

Clinical Professionals Limited; Liverpool City Region; On-site; Full time

Job summary

An established industry player is seeking an Analytical Development Scientist to join their innovative team in Liverpool. This dynamic role involves providing technical leadership in the development of cutting-edge biopharmaceutical and vaccine products. You will play a crucial part in executing laboratory studies, ensuring compliance with safety and quality standards, and driving continuous improvement through collaboration and innovation. If you are passionate about analytical science and eager to contribute to impactful projects in the healthcare sector, this opportunity is perfect for you.

Qualifications

• Degree or higher in chemistry, biochemistry, or related discipline required.
• 2+ years in analytical method development or relevant experience preferred.

Responsibilities

• Provide technical expertise for analytical projects in biopharmaceutical development.
• Plan and execute laboratory studies and ensure compliance with safety standards.

Skills

Protein Chemistry

HPLC

ELISA

UV Spectroscopy

CE-SDS

Analytical Method Development

Data Interpretation

Collaboration

Education

Degree in Chemistry

Higher Degree in Biochemistry/Biotechnology

Tools

Mass Spectrometry

Job description

Reference Number: JO-2502-547888
Analytical Development Scientist
Rate: Negotiable
Job Type: Contract
Location: Speke, Liverpool

Position Overview:

Analytical Development Scientist

Speke

12 month Contract

£18.15 – £24.21 per hour

Cpl Life Sciences are currently partnering with an animal healthcare company recruiting for an Analytical Development Scientist to join a dynamic process and analytical team responsible for the development of new biopharmaceutical and vaccine products.

Key Responsibilities:

1. Provide technical expertise and leadership for delivery of the analytical agenda within process development projects based in the development laboratories and pilot plant areas at Speke or for projects across the global network. Includes HPLC, ELISA, UV, CE-SDS techniques.
2. Plan, execute and evaluate laboratory studies through hands-on experimentation. Make sound technical judgements through data interpretation, knowledge and experience for project direction and delivery.
3. Provide regular communications for project progress to senior technical staff and key stakeholders globally. Deliver high quality peer-reviewed technical reports. Work collaboratively with other team members.
4. Responsible for ensuring and driving compliance in all safety and quality aspects for process development activities. Be accountable for spend/cost control.
5. Drive continuous improvement activities through innovation and shared technical knowledge across the global network.
6. Develop links and collaborations with external organisations for analytical development and carry out tech transfers according to project and business requirements.

Qualifications & Experience:

1. Degree or higher degree within chemistry, biochemistry, biotechnology/biologics or related discipline.
2. At least 2 years hands-on knowledge and expertise in analytical method development or other relevant experience, such as a PhD, is preferable.

Essential Skills:

1. Good knowledge and understanding of protein chemistry.
2. Expertise in the development of new analytical methods and optimisation specifically HPLC, UV, ELISA & CE-SDS.
3. Ability to lead, plan and execute method validations or fit for purpose studies.
4. Ability to work collaboratively and across sites with other team members.
5. Deep scientific curiosity, research mind-set. Ability to resolve issues for early to late phase development.
6. Experience/ability to interpret structural analytical data e.g. mass spec knowledge or cell-based assay data would be preferable.

If you are interested in this role then please apply or email [e-mail]