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Quality and Regulatory Affairs Administrator

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Job ID:

1705787

Location:

Cambridgeshire 

Salary:

per annum
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Job Views:

3

Employment Type:

Seasonal

Posted:

11/09/2020

Closing Date:

09/10/2020
col-wide 

Job Description:

We are looking for a skilled candidate to join our client's team on a temporary basis for 3-4 months however for the right person this could lead to a longer-term opportunity in the future. This role will be responsible for assisting in the day to day activities of the Quality department. You will be undertaking tasks that include change control tracking, quality record review, SOP development, process validation, CAPA management and report creation therefore experience within this highly regulated environment is essential.


Start: ASAP - Urgent Requirement
Duration: 3 - 4 months with review
Location: Outskirts of Cambridges, Cambridgeshire
Hours: Monday - Friday 9am - 5pm with 30-minute lunchbreak (37.5 hours per week)
Salary: £Negotiable


You will ideally have experience of using QPulse alongside relevant experience that demonstrates your ability to perform in this role. You will hold excellent organisational skills and can work under pressure.


Duties:


  • Assisting in the day to day activities that ensure the Quality department is effective and efficient
  • Change control tracking
  • Quality record review
  • SOP development & Process validation
  • CAPA management and report creation
  • Maintain all Quality modules within the QPulse database
  • Assist in regulatory affair tasks as assigned by the manager
  • Contribute to the creation and reviewal of QMS documentation and records
  • Ensure consistent application and execution of key quality processes
  • Create reports relating to quality metrics and key performance indicators
  • Support internal and external audit activities
  • Coordinate and document the calibration activities of equipment as necessary


Essential Skills/Experience/Education:


  • Experience of working within a highly regulated industry (Pharma or Scientific)
  • Superior organisational skills
  • Ability to work independently under his/her own initiative
  • Excellent aural and written communication skills
  • Ability to work under pressure and to deadlines
  • Experience of QPulse and MSOffice applications
  • Ideally a university degree OR Equivalent experience


If you have not received a response within 3-5 working days, unfortunately your application has been unsuccessful. Busy Bee Recruitment Ltd is acting as an Employment Business for this Temporary vacancy...... click apply for full job details

Company Info
Busybee Recruitment

Company Profile



Company Info

Busybee Recruitment

Phone:
Web Site:

Quality and Regulatory Affairs Administrator

col-narrow-left 

Job ID:

1705787

Location:

Cambridgeshire 

Salary:

per annum
col-narrow-right 

Job Views:

3

Employment Type:

Seasonal

Posted:

11/09/2020

Closing Date:

09/10/2020
col-wide 

Job Description:

We are looking for a skilled candidate to join our client's team on a temporary basis for 3-4 months however for the right person this could lead to a longer-term opportunity in the future. This role will be responsible for assisting in the day to day activities of the Quality department. You will be undertaking tasks that include change control tracking, quality record review, SOP development, process validation, CAPA management and report creation therefore experience within this highly regulated environment is essential.


Start: ASAP - Urgent Requirement
Duration: 3 - 4 months with review
Location: Outskirts of Cambridges, Cambridgeshire
Hours: Monday - Friday 9am - 5pm with 30-minute lunchbreak (37.5 hours per week)
Salary: £Negotiable


You will ideally have experience of using QPulse alongside relevant experience that demonstrates your ability to perform in this role. You will hold excellent organisational skills and can work under pressure.


Duties:


  • Assisting in the day to day activities that ensure the Quality department is effective and efficient
  • Change control tracking
  • Quality record review
  • SOP development & Process validation
  • CAPA management and report creation
  • Maintain all Quality modules within the QPulse database
  • Assist in regulatory affair tasks as assigned by the manager
  • Contribute to the creation and reviewal of QMS documentation and records
  • Ensure consistent application and execution of key quality processes
  • Create reports relating to quality metrics and key performance indicators
  • Support internal and external audit activities
  • Coordinate and document the calibration activities of equipment as necessary


Essential Skills/Experience/Education:


  • Experience of working within a highly regulated industry (Pharma or Scientific)
  • Superior organisational skills
  • Ability to work independently under his/her own initiative
  • Excellent aural and written communication skills
  • Ability to work under pressure and to deadlines
  • Experience of QPulse and MSOffice applications
  • Ideally a university degree OR Equivalent experience


If you have not received a response within 3-5 working days, unfortunately your application has been unsuccessful. Busy Bee Recruitment Ltd is acting as an Employment Business for this Temporary vacancy...... click apply for full job details