Almac Group
Product Quality Lead (Compliance) - 9-12 Month Fixed Term Contract / Secondment (Craigavon or Dundalk)
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Location: Craigavon OR Dundalk
Hours: 37.5 Hours
Contract: 9-12 Months Fixed Term Contract (Secondment opportunity for internal applicants)
Salary: Competitive
Business Unit: Pharma Services
Open To: Internal & External Applicants
Ref No.: HRJOB11800
The Role
Working as part of the Pharma Services Business Unit, the Product Quality Lead (Compliance) will support the company Qualified Persons in fulfilling their responsibilities for batch certification and release.
The post holder will review third party annual Product Quality Reviews (PQR) to assess consistency of the existing process, to highlight trends and to identify any product / process improvements.
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.
Joining Almac means becoming part of a fast‑paced, growing organisation within a highly regulated industry. We offer a supportive and collaborative working environment, with excellent opportunities for learning, development and long‑term career progression across the Almac Group.
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Our approach is simple – we support, develop and reward our people, build fulfilling careers and together we advance human health. More information can be found here; Life at Almac - Almac
Further information
Further information on the essential and desirable criteria required for this role can be found in the Job Description attached to this advert.
A fantastic salary and benefits package is available, including annual bonus, generous holiday allowance, healthcare reimbursement scheme, and a rewarding role where your work contributes to the advancement of human health.
Essential Criteria
- A Bachelor’s degree (or equivalent) in a Science discipline OR significant relevant industry experience
- Previous significant experience working within an established Quality System within a Pharmaceutical Industry (e.g. GMP, ISO)
Desirable Criteria
(The following criteria may be applied if a large pool of applicants exist)
- Experience in the manufacture and / or packaging of solid oral dosage products.
- Experience of sterile fill/finish or biologic manufacture.
- Experience in customer facing role.
- Experience in a QP supporting role
- Previous experience in batch record review processes.
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How To Apply
Apply online and tailor your CV to outline how you meet the role criteria. Please upload your CV in PDF format where possible.
Internal Secondments
Prior to applying for this secondment opportunity, please discuss with your line manager to ensure that you can be released from your current location for the duration of the secondment should your application prove successful.
If you are interested in finding out more or would like to discuss the terms and conditions further, reach out directly to Diane Harshaw.
Closing Date
We will no longer be accepting applications after 5pm on Monday 31st August at 5:00pm
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 CV’s received or submitted directly to Hiring Managers will be considered unsolicited and no fee will be payable. Thank you for your cooperation.
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