Quality Compliance Officer – Analytical Services

Job title:

Quality Compliance Officer – Analytical Services

Company

Almac Group

Job description

Quality Compliance Officer – Analytical ServicesLocation: Craigavon, Northern Ireland, UKHours: 37.5 Hours Per Week. Flexible working pattern.Business Unit: Almac SciencesOpen To: Internal & External applicantsRef No.: HRJOB9689/1The TeamThe 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 RoleQuality 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.Essential Candidate Criteria· Degree level (or equivalent) qualification in a Life Science related discipline· Minimum 2 years’ experience working in a quality or laboratory environment operating to GMP principles or recognised quality system (e.g. ISO)

· Strong understanding of analytical documentation, including but not limited to analytical method validation reports and certificates of analysis.Desirable Candidate Criteria· 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 performing internal audits to identify GMP compliance gapsRewardFor 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 15th September 2024 at 17:00Please note: This is a readvertisement. If you have applied for this role within the past 6 months, we cannot consider your application. Sorry for any inconvenience caused.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.

Expected salary

Location

Craigavon, Co Armagh

Job date

Sat, 31 Aug 2024 22:42:02 GMT

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