Allergan Scientist (Analytical Sciences) in Liverpool, United States

Scientist (Analytical Sciences)

Liverpool, England, United Kingdom at

May 16, 2018Post Date

179638Requisition #

The Scientist, Analytical Sciences reports into the Snr Manager of Analytical Sciences and has responsibility to perform Analytical Sciences activities within Allergan Biologics at Liverpool. The role holder is responsible for performing the analytics associated with the testing and cGMP release of products from early concept through to registration for marketing approval.

The Scientist, Analytical Sciences is responsible for performing routine and cGMP testing for new product development programmes, which may encompass fully in-house programmes, in-licensed products and products in development with partners and ensures the testing is performed by the group on time, on budget and in compliance with the established quality standards. This includes release testing of clinical drug substance.

The Scientist, Analytical Sciences is responsible for supporting optimisation/qualification and/or technical transfer of validated methods and the validation of developed assays for cGMP testing by executing experimental plans as directed by technical lead.

The Scientist, Analytical Sciences is responsible for supporting the generation of stability data through performing analytical testing, stability data collation/trending and writing stability protocols/reports.

The Scientist, Analytical Sciences is required to perform all assigned activities in accordance with regulatory requirements and HSE Policies and Procedures.

Leadership Responsibilities:

The Scientist, takes specific responsibilities for leading activities within the group, including:

Maintain exemplary standards within the laboratory.

Lead the delivery of routine analytics to support product development and cGMP production activities through all stages of bioprocessing (upstream and downstream) to meet project timelines.

To put forward and deliver ideas to overcome technical problems or introduce new efficiencies

Collaborate effectively across cross functional teams to deliver requirements of projects

Training in new analytical methods and training others in techniques/technologies.

Transfer of methods through to routine application either internally or to external partners.

Lead on the delivery of new capital equipment items to increase Analytical Sciences capabilities.

Executing method qualification and validation protocols and assist in writing the associated reports as required to support transfer of processes into the manufacturing facility, under the guidance of Snr Scientists.

Performing Analytical Sciences testing of facilities water points, raw materials, in process product release and stability and the lead the management of samples for projects assigned to them. They are responsible for interpreting and analysing experimental results and communicating them effectively via study reports and presentations to Snr Manager, Analytical Sciences

Writing procedures to the required quality for cGMP compliance for all areas of Analytical QC and ensure traceability and documentation of the development and validation of the procedures.

Performing trend analysis of routine testing and ensuring test specifications are met for raw materials, water testing and intermediate/final products and reporting out of specifications to Snr Manager, Analytical Sciences.

Initiation and investigation of OOS’s, Deviations, Change Controls and CAPAs and notifying Snr Manager, Analytical Sciences of the occurrence.

Operational Responsibilities:

Responsible for supporting the Snr Scientists, Analytical Sciences to ensure current project timelines by;

• Ensure all documents are completed and approved before execution of tasks or experiments

• Complete all laboratory documentation in a timely and compliant manner, participating in reviews of the documentation to obtain quality sign off when necessary.

• Analyse any investigation data to a high standard and ensure that protocols and procedures are delivered with a high attention to detail

• Effectively communicating with analytical technical lead to ensure data is transferred successfully.

• Writing technical reports for issue to the client or inclusion to support internal Regulatory Submissions.

Subject matter expert in areas relating to analytical method development, transfer, qualification and validation and stability testing.

Taking ownership of the installation and validation of analytical equipment by writing and executing equipment validation documentation including but not limited to URS, trace matrix, IOQ, SOP’s, protocols and reports in line with quality procedures and guidelines.

Performing housekeeping within the Analytical Sciences Laboratories, ensuring safety standards are maintained.

Ensuring equipment logbooks are kept up to date and filled in using the appropriate guidelines.

Providing training to colleagues in analytical methods, as required.

Maintaining stock levels of consumables and reagents by ordering reagents in a timely manner and ensuring COSHH assessments/MSDS are present and up to date before ordering reagents.

Proactive in personal development and maintain an up-to-date, accurate training record to meet all required operating procedures for activities and including ensuring all heath safety and environment training is complete.

Contribute to 5S as a means for continuous improvement to ensure that department goals are achieved and the incidence of non-conformances are reduced

Undertake other responsibilities as required depending upon work demands and support working shifts.

Education and Experience required:

  • BSc science graduate (or equivalent) with biopharmaceutical or pharmaceutical experience.

  • Experienced in the analysis of biomolecules.

  • Experience of current Good Manufacturing Practice (cGMP)

  • Working knowledge of analytical techniques including but not limited to:

  • Electrophoresis (SDS-PAGE, Western Blot, IEF)

  • Chromatography (SE-UPLC, RP-HPLC, AEX, HILIC)

  • Immunoassays (ELISA, Potency, HCP)

  • Experience in writing procedures, protocol and reports.

  • Clear understanding of the science and a passion for keeping abreast and implementing analytical advancements.

Personal Attributes:

  • Good analytical skills with the ability to analyse, interpret results and solve complex problems.

  • Strong organisational skills with the ability to manage/prioritise workloads for various project types in order to meet project timelines

  • High level of IT proficiency

  • Demonstrable communication and interpersonal skills to report and communicate experimental findings effectively.

  • High attention to detail, adaptable, personable and technically competent.

  • Ability to work effectively within a dynamic team.

  • Aptitude for identifying and implementing new technologies.

Behaviours – linked to the Allergan BOLD culture

We Build Bridges with each other, customers and partners

We will use excellent interpersonal skills to build relationships internally and with external partners, such as CROs and CMOs. They will collaborate closely with Analytical Sciences throughout development and with Pharmaceutical Technology during process validation.

We Power Ideas that change healthcare

We will challenge “traditional” ways and strive for innovative solutions. They will seek new ways to gain optimum process knowledge whilst minimizing the analytical burden. They will solve complex problems with simple solutions.

We Act Fast to be responsive to customers and business opportunities

We will adapt to changing demands and be action oriented to overcome challenges. They will apply strong problem solving skills to resolve issues and seek simple solutions. They will be make quality decisions on outcomes.

We Drive Results and execute our plans

We will focus on strong planning, risk mitigation strategies and delivery. They will be push themselves and others to deliver and exceed the goals

Equal Employment Opportunity Employer

Allergan is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other protected status.