HRjob8815 Production Supervisor - Craigavon, United Kingdom - Almac Group

Almac Group

Verified Company

Craigavon, United Kingdom

3 weeks ago

Posted by:

Tom O´Connor

beBee Recruiter

Description

Production Supervisor (Manufacturing Operations)

Location:
Craigavon

Hours:
40 hours per week

Salary:

Competitive, relevant shift premiums will apply

Business Unit:

Pharma Services

Open To:

Internal and External Applicants

Ref No
:

HRJOB8815

The Role

With a wealth of knowledge and experience, Almac Pharma Services have been manufacturing medicines in tablet, capsule and powder form for over 50 years.

We also pack commercial drug products into bottles, blisters and sachets and provide specialised packaging solutions for medical kits, vials and syringes.

The expert services we provide supports the provision of medicines and treatments to patients around the world.

We're currently seeking a
Production Supervisor to join our Manufacturing Operations department.

The production supervisor is responsible for a team of Production Technicians and Senior Operators and reports to the Manufacturing Team Leader.

A fantastic salary and benefits package is available, including annual bonus for all, generous holiday allowance, healthcare reimbursement scheme, and a rewarding role where the work you do will ultimately be contributing to the advancement of human health.

All applicants must be eligible to work in the UK, or hold a valid visa/work permit that allows you to work in the UK on a full time permanent basis with no restrictions

What we are looking for

If you have a Degree level (or equivalent qualification) or significant relevant experience as a production supervisor combined with experience of leading tasks and people within a technical environment, then we want to hear from you.

Whilst not essential it would be advantageous if you had a degree level (or equivalent) qualification in a Scientific, Engineering or Technical discipline, previous experience in a supervisory role within a pharmaceutical or regulated environment and previous experience within GMP manufacturing processes for solid oral dosage forms.

To be successful in this role you will need excellent communication skills, attention to detail and proficiency in the use of Microsoft office packages.

Please see attached job description for further information.

**Closing Date