This role is an 11 Month Contract with a view to extension.
Documentation specialist supporting the downstream operations team. The successful candidate will be part of a day support team providing logistical and operational support to process shift teams.
• Responsibility for the timely, accurate, and efficient management of documents including access and revision control.
• Manage “Live” Documentation updates from the Operations floor
• Turnaround and issue documentation as per Operations Schedule
• Manage and implement the floor documentation control system
• Drive the Documentation Life Cycle System to ensure documents are approved in as per Scheduling requirements.
• Work with various Subject Matter Experts to approve technical documentation updates.
• Creation and revision of Standard operating Procedures (SOPs) and Work Instructions (WIs) as required
• Work closely with QA, Supply chain, and Operations core functions
• Ensure compliance with all regulatory GMP, Safety, and Environmental requirements.
• At minimum level 6 in a relevant Qualification.
• Self-motivated with excellent organizational skills.
• Experience Working in a Pharmaceutical GMP regulated industry is desirable.
• Excellent verbal and written communication skills.
• Ability to work independently and as part of a team in a cross-functional collaborative environment.
• High level of attention to detail.
• Experience working with GMP Documentation Management Systems.
• Proficient in Microsoft Office Tools (word/excel/PowerPoint ).
• Good interpersonal skills.
This role is on a 10 month contract with a view to extension. Purpose Reporting to Our Clients project manager...
Apply For This JobThis role is on an 11 Month contract with a view to extension. Purpose This role will be responsible for...
Apply For This JobTo apply for this job email your details to sarah.fennell@theaphexgroup.com.
To apply for this job email your details to sarah.fennell@theaphexgroup.com.