Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.
We are PCI.
Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
To perform the Analytical testing function in an efficient and effective manner in full compliance with relevant documented procedures and pertinent regulatory/company requirements.
Main responsibilities:
1. To perform routine laboratory procedures right first time with minimal personal OOS results and if relevant and instructed to do so, to assist others within the team.
2. To plan and prioritise own day to day workload in line with client requirements and adapt this where necessary in line with client needs and expectations.
3. To assist in preparation of technical documentation within the Department, as required.
4. To assist in training of others, as required.
5. To ensure that all work carried out complies with departmental procedures and is cGMP compliant
6. To ensure that all personal lead times are complied with, subject to the absence of attenuating circumstances.
7. To assist in the performance of project work within the team, as required.
8. To review analytical and laboratory data within the team for accuracy, completeness and compliance with documented procedures.
9. To communicate effectively with others on site and to assist with departmental problem solving as required.
10. To ensure that all health and safety procedures are adhered to with respect to personal duties and the duties of others.
11. To undertake other laboratory and business related tasks as and when required to meet department and business needs and within the scope of the job-holder’s capabilities and responsibilities.
12. To undertake such tasks and to manage specific internal or ad hoc projects as and when required to meet department and business needs and within the scope of the job-holder’s capabilities and responsibilities.
13. Self-motivated to gain additional pharmaceutical Development Knowledge.
14. Actively seeks and demonstrates to perform tasks for the department outside of set analysis activities.
Regulatory/Industry Responsibilities:
General
15. The job holder is responsible for adhering to PCI SOPs, Health & Safety, GMP and other regulatory guidelines.
GMP Requirements Hierarchy
16. GMP Skill Level 1 is essential for this role.
(further information regarding GMP Requirements Hierarchy, can be obtained at SOP-L&D-001)
Qualifications:
A degree in a scientific subject as a minimum (preferably Chemistry).
Experience:
Previous laboratory and analytical experience essential (minimum 1 year), preferably in a pharmaceutical environment.
Join us and be part of building the bridge between life changing therapies and patients.