Product Quality Lead (Compliance) - 9-12 Month Fixed Term Contract / Secondment (Craigavon or Dundalk)

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.: HRJOB11800/1

*Please note that if you have already applied for this position in the past 6 months, you do not need to repply as your exisiting application will remain valid*

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.

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.

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 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.

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 Tuesday 20th October 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.