Search for Jobs

38 Results
Elanco
Liverpool, North West England, United Kingdom
18 days ago
Quanta'
West Midlands, United Kingdom
18 days ago
Synairgen Research Limited
UK, United Kingdom
30+ days ago
Nordic Nanovector
Nationwide, United Kingdom
30+ days ago
GSK
Brentford, Greater London, United Kingdom
30+ days ago
Medley Pharma Limited
Bootle, Merseyside, United Kingdom
1 day ago
Docs International UK Limited
Luton, Bedfordshire, United Kingdom
2 days ago
AL2S3 Ltd
United Kingdom
19 hours ago
CK GROUP
South East London, London, United Kingdom
9 days ago
AL2S3 Ltd
United Kingdom
3 days ago
CK GROUP
Hull, East Riding Of Yorkshire, United Kingdom
9 days ago
Newton Colmore Consulting Ltd
West London, London, United Kingdom
1 day ago
AL2S3 Ltd
South East London, London, United Kingdom
5 days ago
SEC Life Sciences
South East London, London, United Kingdom
4 days ago
AL2S3 Ltd
United Kingdom
3 days ago
SEC Life Sciences
South East London, London, United Kingdom
2 days ago
GE Healthcare
Chalfont Saint Giles, ENG, GB
Jobs from the Web
Barking, Havering and Redbridge University Hospitals Trust
Romford, ENG, GB
Jobs from the Web
Compass Life Sciences
Weybridge, ENG, GB
Jobs from the Web
Swansea University
Swansea, WLS, GB
Jobs from the Web
Maxxima
London, ENG, GB
Jobs from the Web
Paramount Recruitment Ltd
ENG, GB
Jobs from the Web
Hobson Prior
Welwyn Garden City, ENG, GB
Jobs from the Web
Precision Medicine Group
Edinburgh, SCT, GB
Jobs from the Web
1 - 25 Results of 38
Elanco
Liverpool, North West England, United Kingdom
18 days ago

Description

To provide the Quality Assurance Team the assurance that manufacturing is carried out in accordance with cGMP and Regulatory commitments and that production records provide full and accurate documentation of batch manufacture in accordance with SOP. The QAR is authorised, as appropriate, by the QA Team Leader to disposition materials with consideration being given to the Regulatory requirement for QP release of veterinary and medicinal products. The job holder also exercises control on the general cGMP activities for those teams he/she has QA responsibility for.

For relevant areas and products, QAR supports Feed Safety Management.

Functions, Duties, Tasks:

  • Disposition raw materials, including packaging items, water, intermediates and products according to the available data, including evaluation of any deviation reports, environmental monitoring (where appropriate), and advise on reprocessing or preventive actions in such cases.
  • Monitor trends and identify problems in quality of purchased materials, packaging, intermediates, products, water and environmental data and promote action having regard to changes in processes, facilities, equipment and procedures.
  • Write/revise/approve and give advice on quality documentation e.g. batch production records, specifications, procedures (Team and Site), PMIS sheets, Stability protocols.
  • Review and approve SOPs (Team and Site), change control documentation, validation protocols, completed validation packages, IQ/OQ/PQ protocols and any CQSA documentation.
  • Manage the Site stability program to meet Corporate and Regulatory requirements.
  • To advise on the investigation of customer complaints, approve customer complaint reports and promote corrective/preventive actions.
  • Participate in self-inspections and other audits of the manufacturing and relevant Support areas with particular reference to cGMP as defined by the various regulatory authorities.
  • Provide training, support, advice and proactive assistance in the Site Quality systems to the product and support teams.
  • Advise on and support appropriate validation of plant, processes and new projects, liaising with other disciplines appropriately to ensure that facilities are designed and commissioned to meet cGMP.
  • Provide cover for other QARs in their absence.
  • Prepare Quality Agreements as appropriate.
  • In addition to the above, if the QAR is working with a product manufactured on behalf of a customer (contract manufacturing) they should liaise with customer, as appropriate, to ensure that the specific requirements of the applicable QTA are met.
  • In addition to the above if acting as the Responsible Person for Warehousing the Responsible Person (RP) section of Job Description JD0405 applies
  • In addition to the above, if the QAR is involved in activities and processes which influence the feed safety and quality of product (Enzymes) they must ensure compliance with relevant regulatory requirements. Personnel working within the area should be appropriately trained (i.e. HACCP SOP) and should have knowledge of feed safety requirements
  • In addition to the above, if the QAR is a named Power User, they shall provide support and training for their area of expertise. Interact with Site and Global teams as required, and represent the Speke site as required at Global meetings

Minimum Qualification (education, experience and/or training, required certifications):

Degree level or significant experience (3 years +) working in a pharmaceutical company in a quality related function.

Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status



Job Information

  • Job ID: 57686600
  • Location:
    Liverpool, North West England, United Kingdom
  • Position Title: Quality Assurance Representative
  • Company Name: Elanco
  • Job Function: Quality Assurance
Jobs You May Like
Filters
Job Function
Industry
Location
Country