Bioassay Analytical Scientist Deeside
Job description
Summary of the Bioassay Analytical Scientist role
As the Bioassay Scientist you will report directly to the Senior Bioassay Analytical Scientist and will assist in the development and qualification of cell-based methods from antigen, internalisation, potency and ELISA/immunology-based assays for antibodies and antibody drug conjugate (ADC) products. You will also conduct routine testing of raw materials, intermediates, finished products and stability samples using the developed methods.
Our site in Deeside, North Wales is a short commute from Chester, Liverpool and Manchester and can be found lying alongside the waterways of the River Dee, presenting a quintessential glimpse of life in North Wales, with numerous nature parks, shopping centres and rural villages.
Relocation support will be offered for the right candidate.
Your responsibilities
- Developing and qualifying cell-based potency and enzyme-linked immunosorbent assay (ELISA)/immunology-based assays for antibodies and antibody drug conjugates (ADCs).
- Performing and reporting of analytical testing on all raw materials, intermediates, finished products and stability samples in cell-based potency assays, cytotoxicity testing and immunological assays such as ELISA, following customer, company and regulatory/industry requirements.
- Performing analytical testing, following the completion of training and qualification, using a variety of techniques including:
-Routine Cell culture
-Cell Banking
-MTT assay
-ADCC assay
-CDC assay
-other cytotoxicity assays
- Performing routine tasks and other non-routine activities required in support of quality control laboratory functions.
- Laboratory maintenance and housekeeping, self-inspections and stock control.
- Data trending and performing quality investigations.
- Documenting laboratory results in accordance with cGMP and company procedures.
- Maintaining and improving knowledge of analytical techniques and procedures.
- Contributing to team building, training and problem-solving initiatives internally and across sites.
- Liaising with functional groups both within and outside quality control as appropriate to ensure projects and plans are progressed.
- Preparing and executing laboratory protocols and reports, as assigned.
- Qualifying reagents, reference material, analytical techniques and relevant equipment.
- Ensuring that all laboratory activities are in compliance with all health and safety guidelines, with particular reference to Control of Substances Hazardous to Health (COSHH), biological safety regulations and the Health and Safety at Work Act 1974.
- Embodying our company values, which are: be reliable, be caring, be transparent and be willing.
Requirements for the role
- BSc or equivalent qualification in a relevant biological subject area.
- Previous experience in a cell biology laboratory and experience working in a regulated environment, pharmaceutical or medical laboratory in a related role to cGMP or within alternative quality system (UKAS/ISO 9001) such as a contract testing laboratory.
- Technical experience in aseptic techniques and cell culture is essential.
- Technical experience in cell-based bioassays (e.g. MTT, ADCC, CDC) and ELISA is preferred.
- Technical experience in techniques such as Bioburden, Endotoxin and Environmental Monitoring is an advantage.
- Good awareness of cGMP and regulatory requirements including the United States (USP) and European (Ph. Eur.) Pharmacopoeias, orange guide and current International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) guidelines applicable to the role.
- Excellent communication, interpersonal and organisational skills, demonstrating attention to detail and able to work in a team and individually.
How you will be rewarded
We offer a competitive compensation and benefits package including bonus, pension scheme, private healthcare, Engagement Hub, cycle to work scheme, death in service coverage, on-site health and wellbeing support including medical consultations and physiotherapy, 24/7 employee assistance programme, employee referral scheme, sports and social club as well as opportunity for training and further career development.
Why consider Sterling?
Sterling Pharma Solutions is a global contract development and manufacturing organisation (CDMO) with more than 50 years’ experience in developing and manufacturing Active Pharmaceutical Ingredients (APIs). This is complemented by Antibody Drug Conjugate (ADC) research and development bioconjugation services.
We are a fast growing, dynamic business with facilities in the UK, US and Europe, where we employ more than 1300 talented and passionate people who support our customers in bringing new medicines to market, improving and saving the lives of patients.
Our culture and our way of working is what really sets us apart as a business; we aim to deliver an exceptional experience to our customers and our employees. You can expect to be part of a supportive team, all working towards a shared goal: to deliver first-class science and service to our customers every day.
How to apply
If you have the necessary skills and experience to join our team, please apply online. For any queries or should you require any reasonable adjustments to support your application please contact [email protected]
Sterling Pharma Solutions is an equal opportunities employer and positively encourages applications from suitably qualified and eligible candidates regardless of sex, race, disability, age, sexual orientation, marriage or civil partnership, pregnancy or maternity, religion or belief.
Job Types: Full-time, Permanent, Graduate
Salary: From £30,000.00 per year
Benefits:
- Company pension
Schedule:
- Day shift
- Monday to Friday
Supplemental pay types:
- Bonus scheme
- Yearly bonus
Work Location: In person
Reference ID: VN742
Expected start date: 02/10/2023
