Job Advert Instructions
 
 
Below are the fields required for the job adverts. Please edit in the word template prior to pasting into the Job Details field in Sage People. This ensures consistency in text and colours.
 
Instructions to convert text to match the headings and body in this template:
Note you will need to do it by heading and body.
 
Select original text and copy (Ctrl+c) then paste by Ctrl+v then immediately Ctrl then t – this will change the format of the text to match:
 
Heading text = Museo Sans 300 size 14, Colour RGB = 0/113/185
Body text = Museo Sans 300 size 11)
Footer text = Museo Sans 300 size 14, Colour RGB = 133/200/75
 
Please ensure that you read Sterling Writing Guidelines and follow the requirements for external writing.
 
All adverts must be reviewed in line with the guidelines prior to posting!
 
We reflect the Sterling brand with our job adverts, so this is important. It’s also essential for search engine optimisation (SEO) to ensure that our online content (adverts and website) is shown to our potential candidates (and customers). A study found that 88% of candidates begin their job search on Google and will visit the results which appear on the first page of Google for their chosen search. By having the right wording in our adverts, we will confidently entice candidates before they search on generic job boards (we’ll also post their too).
 
Some examples of common blunders, with corrections:

• Check use of acronyms; detail current general manufacturing practises (cGMP) instead of just cGMP
• Check for unnecessary capitalisation especially for departments
• Use and instead of &
• Use “one”, “two” for number 1-9 and numbers for 10+

 
Vacancy Name: QC Analytical Scientist Bioassay
 
Summary of Analytical Scientist Bioassay role
 
As the Bioassay Scientist you will report directly to the Team Lead (Bioassay) 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 Quality Control 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 centers and rural villages.


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 Quality Control 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
  • MTS assay
  • ADCC assay
  • CDC assay
  •  other cytotoxicity assays
  • ELISA
• 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.

Key Skills and Competencies

• 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.

 
We also require candidates to be competent with IT systems, and in particular Microsoft Office including Outlook, PowerPoint, Word and Excel.
 
You will receive
 
A competitive salary, pension scheme, private healthcare, retail discounts through reward gateway, cycle to work, 26 days annual leave and bank holidays, death in service coverage, on-site health and wellbeing support and medical consultation and physiotherapy, 24/7 employee assistance programme. Training and opportunities for further career development.
 
Optional to include
This role is a shift role to support our 24/7 operation with annual leave and rest days built into the shift plan.
 
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 complimented by Antibody Drug Conjugate (ADC) research and development bioconjugation services.
 
We are a fast growing, dynamic business with facilities in the UK, UK and Ireland, where we employ 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. 
 
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.