Validation Scheduler

Location
Berkshire
Salary
£33000 to £40000 per annum
Posted
03 Apr 2017
Closes
01 May 2017
Ref
J3760
Contact
Matthew Langdon
Contract Type
Permanent
Hours
Full Time
An exciting opportunity has just opened up for a Validation Scheduler to join a global life sciences company based in the Berkshire area. As the Validation Scheduler you will be responsible for scheduling of Validation tasks including; routine maintenance of the Site Validation Master Plan, support for capital projects and implementation of new equipment, maintenance of policies and procedures, and technical support for GMP manufacturing and support areas.

KEY DUTIES AND RESPONSIBILITIES:

Your duties as the Validation Scheduler will be varied however the key duties and responsibilities are as follows:

1. As Validation Scheduler, you will be accountable for maintaining the validation schedule including routine, project and ad hoc work as well as allocating work packages to individuals.

2. You will be responsible for reporting progress and closure of work packages and assigning due dates for next routine test and reviews.

3. As Validation Scheduler, you will attend meetings with internal customers and key stake holders (Engineering, Operations, QA and QC) to ensure validation work is coordinated with business objectives, plans and production schedules and that support functions are aligned to support validation projects.

4. You will also be responsible for the periodic review and update of scheduling and administration procedures and policies.

ROLE REQUIREMENTS:

To be successful in your application to this exciting opportunity as the Validation Scheduler we are looking to identify the following on your profile and past history:

1. Relevant degree in a Scientific or Engineering discipline or equivalent qualification and extensive experience within a highly regulated Pharmaceutical or Biopharmaceutical environment.

2. Proven industry experience of dynamic project scheduling and delivery of work programs within a highly regulated GMP environment.

3. A working knowledge and practical experience performing validation or engineering activities is desirable.

Key Words: Validation | Planner | Scheduler | Engineering | Projects | Compliance | Quality | Quality Assurance | Facility | Equipment | Utility | CSV | Process | Packaging | GMP | IQ | OQ | PQ | Biopharmaceutical | Pharmaceutical

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer that is happy to welcome applications for any applicant who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors and is made up of a collaboration of scientists supporting science. We look forward to helping you with your next career moves.