Quality Assurance Lead
Company
Location
Loughborough, England, United Kingdom
Posted At
12/19/2024
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Description
QA Lead (On the Floor)
Hours: 37.5 hours per week. Monday – Friday, flexible working hours.
Salary: Competitive
Ref No: HRJOB9942
Business Unit: Pharma Services
Location: Loughborough, Leicestershire
Open To: Internal & External Employees welcome to apply
The Role
The post holder will work as part of the Quality Assurance team at the Almac Pharma Services’ facility in Loughborough, providing direct quality support and oversight to cGMP manufacturing operations at the facility.
The QA Lead will utilise a broad understanding of cGMP requirements to provide direct QA support and oversight for operational activities within the Charnwood cGMP manufacturing facility, to assure that activities are undertaken in compliance with cGMP and Almac procedures, as appropriate.
As part of a busy team within a rapidly growing organisation, operating within a challenging industry you will benefit from the numerous personal and professional developmental opportunities available throughout the Almac group.
Essential Criteria
(The following criteria may be applied if a large pool of applicants exists)
Closing Date: Sunday 12th January 2025 at 1700 hours (local time)
RECRUITMENT AGENCIES PLEASE NOTE: Almac will only accept applications from agencies/business partners that have been invited to work on this role by our Talent Acquisition team. Speculative candidate CVs received or submitted directly to Hiring Managers will be considered unsolicited, and no fee will be payable. Thank you for your cooperation.
Hours: 37.5 hours per week. Monday – Friday, flexible working hours.
Salary: Competitive
Ref No: HRJOB9942
Business Unit: Pharma Services
Location: Loughborough, Leicestershire
Open To: Internal & External Employees welcome to apply
The Role
The post holder will work as part of the Quality Assurance team at the Almac Pharma Services’ facility in Loughborough, providing direct quality support and oversight to cGMP manufacturing operations at the facility.
The QA Lead will utilise a broad understanding of cGMP requirements to provide direct QA support and oversight for operational activities within the Charnwood cGMP manufacturing facility, to assure that activities are undertaken in compliance with cGMP and Almac procedures, as appropriate.
As part of a busy team within a rapidly growing organisation, operating within a challenging industry you will benefit from the numerous personal and professional developmental opportunities available throughout the Almac group.
Essential Criteria
- Bachelor’s degree (or equivalent qualification) in a scientific (Chemistry, Biology or Pharmacy) or technical (Engineering) discipline
- Significant experience in a quality role within a pharmaceutical quality system
(The following criteria may be applied if a large pool of applicants exists)
- Master’s or PhD (or equivalent qualifications)
- Direct experience in the manufacture of solid/liquid oral dosage products
- Previous QA on the Floor experience
Closing Date: Sunday 12th January 2025 at 1700 hours (local time)
RECRUITMENT AGENCIES PLEASE NOTE: Almac will only accept applications from agencies/business partners that have been invited to work on this role by our Talent Acquisition team. Speculative candidate CVs received or submitted directly to Hiring Managers will be considered unsolicited, and no fee will be payable. Thank you for your cooperation.
Advertise with us.
Please contact: hello@huntukvisasponsors.com
Please contact: hello@huntukvisasponsors.com
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