University Intern - Quality - 5 Opportunities Available

1 x Quality Control - Restricted Area Support the Quality Control Department in the testing and release of Foot & Mouth disease antigen and vaccine batches. To perform routine testing related to active ingredient and finished product as well as utilities and environmental testing as required to maintain compliance on a GMP manufacturing site.

• Final product and in process sample testing including infectivity assays, serological assays and sterility testing.
• Performing microbial identifications & assisting in contamination investigations
• Read and process data, including generating material for trend analysis from site environmental monitoring.
• Preparation of test materials and reagents including cell culture.
• Participation and use of Quality Management Systems.
• Participation in department continuous improvement activities
• Sample reception & reconciliation.
• Assist in the maintenance of the Quality Control area in accordance with GMP, EHS & Bio-safety regulations.
1 x Quality Control - Controlled Area Support the Quality department in the development and implementation of quality systems.
• Participation and use of GxP Quality Management Systems including but not limited to cGdP, cGMP and cGLP focused practices.
• Ownership and partial co-management in the development and implementation of controlled document management, GdP and electronic ELARPA archiving systems for a restricted Quality Controlled Laboratory area
• Participation in department continuous improvement projects
• Support in standard cGLP activities such as sample reception & reconciliation
• Raw material sampling and testing.
• Assist in the maintenance of the Quality Control area in accordance with GMP & EHS regulations.
1 x Quality Assurance - Batch Review Assist the Product Quality Assurance team in delivery of strategic veterinary products. Our team's main priorities are batch record review and providing quality assurance support to production and quality control departments. You will be supporting batch record reviewers in the following activities:
• Collation and review of batch manufacturing records
• Preparation of batch certificates
• Document archiving
• Assistance with QA review of batch manufacturing records
• Checks of products for transfer from quarantine and dispatch
• Involvement in housekeeping audits in production departments
1 x Quality Assurance - Validation Execution The main purpose of this role is as a member of the Quality Team to support validation and quality assurance activities for the Pirbright Site. As part of this role you will be:
• Executing validation tests/protocols.
• Creating documentation and reports across the entire validation life cycle.
• Working together with other members of the Validation Team and Quality Assurance to ensure compliance with internal and external regulations.
• Supporting maintenance of the revalidation schedule
• Document management
1 x Quality Management - Quality Systems To provide support to the Quality Systems Team in maintaining and developing the quality system to support the manufacturing sites production activities.
• Support the Change Control Committee
• Support the CAPA Committee
• Support quality continuous improvement projects
• Support QA representatives in production areas
• Analyse quality metrics to identify quality trends
• Work on projects as required
  
  Applicants will be studying for a BSc Biology, Chemistry, Biochemistry or other Biological Sciences degree.
• 3 A levels at grade BBC (minimum) with at least one grade coming from a science subject.
• Applicants must have the ability for independent travel to work and other sites.
• Applicants must be able to comply with bio-safety regulations that apply to working in a SAPO4 facility.
• Applicants must have the right to work in the UK., You will gain experience & transferable skills from working in a dynamic and progressive Quality Control GMP environment.
• You will be trained in Quality Management Systems and Local Quality Management Structure across local, divisional and global organizations
• You will have have exposure to a continuous improvement culture.
• Working in a team but will also develop ability to work on own initiative
QA Batch Review
• You will gain experience in Good Manufacturing Practice
• You will become familiar with batch manufacturing records (BMR)
• You will become familiar with vaccine production process, from active ingredient production to vaccine formulation
• You will have a direct impact on timely delivery of strategic medicinal products
  
  As a family-owned company, Boehringer Ingelheim knows that being dedicated at work means balancing your private life with all its challenges.
• Working for a well-recognised pharmaceutical company will set a good initial exposure to Good Manufacturing Practices (Eudralex Requirements).
• Working for BIAH Pirbright, a biopharmaceutical company, will give you the opportunity to recognise the standards and regulations for Biologicals
• Working for a site that manufactures vaccines will give you the opportunity to recognise the standards and regulations for Aseptic Manufacturing.
Quality Systems
• Understand the process for manufacturing a medical vaccine
• Understand the quality and regulatory requirements in the manufacture of a pharmaceutical product
• Analysis and reporting of data
• Understand the dynamics of the working environment and improve collaboration and influencing skills
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