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Quality Compliance Officer
3 weeks ago
- Full time, Permanent
Almac Group is a global leader in advancing human health. We provide a range of expert services across the drug development lifecycle to pharmaceutical and biotech companies, supporting them in finding treatments for patients.
Skills and attributes- Analytical Skills
- Quality Assurance
- Validation
- Quality Compliance
- GMP Experience
Quality Compliance Officer – Analytical Services
Location : Craigavon, Northern Ireland, UK
Hours : 37.5 Hours Per Week. Flexible working pattern.
Business Unit: Almac Sciences
Open To: Internal & External applicants
Ref No.: HRJOB9689
The Team
The Quality Compliance team at Craigavon are part of a global quality team, working to ensure patient safety, regulatory compliance, and product quality in an efficient and effective manner.
The team consists of Quality Compliance and Quality Validation teams. Team members are involved in all aspects of GMP operations across the site, performing quality inspections to verify GMP activities and act as a supportive/advisory role, both in the manufacturing and analytical laboratories.
As a contract organization, Quality is at the heart of our relationship with customers, therefore involvement in customer communications, visits and site audits may also form part of the role.
The Role
Quality Compliance Officers participate in Quality Compliance activities and GMP improvement initiatives throughout Almac Sciences.
Analytical Services provides support to analytical projects and operations, including review of quality related documents. The post holder will also be responsible for performing reviews of Quality issues (unplanned deviations and OOS) and assist in the management the Quality Management System, supporting operations to ensure it is effective, efficient and compliant.
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.
· Degree level (or equivalent) qualification in a Life Science related discipline. Relevant experience may be considered in lieu of academic qualification.
· Experience working in a quality or laboratory environment operating to GMP principles or recognised quality system (e.g. ISO)
· Experience working in a Quality Assurance role, supporting the analysis of APIs or Drug products
· Experience of preparation and or reviewing analytical documents such as analytical method validations reports
· Experience performing investigation into quality issues such as Unplanned Deviations and OOS’s
· Experience of review of analytical data for example Stability data
· Experience of perform internal audits to identify GMP compliance gaps
Reward
For the successful candidate, we offer an attractive benefits package which will include a competitive salary, annual bonus, employer pension contributions, 34 days paid annual leave, healthcare benefits and much more. Please see further details on the Benefits Tab.
Closing Date: Sunday 2nd June 2024 at 17:00
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.
Paid Time-Off for Vacation and Sick Days
Almac Group is an Equal Opportunity Employer
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