Product Quality Lead (Compliance) - 9-12 Month Fixed Term Contract ​/ Secondment 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

.: HRJOB
11800

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.

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 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.

• 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)

(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.

We will no longer be accepting applications after 5pm on Monday 31st August at 5:00pm