Asst. Production Manager (Afternoon shift) 12 month contract - Immediate Start
Ensign Laboratories are seeking an experienced Assistant Production Manager on afternoon shift with a 12 month contract to commence immediately.
Summary about this job
Management
Company: Ensign Laboratories Pty Ltd
Location: Melbourne
Work type: Contract/Temp
Salary: n\a
Phone: +61-2-4222-2822
Fax: +61-8-8503-2386
E-mail: n\a
Site: n\a
Detail information about job Asst. Production Manager (Afternoon shift) 12 month contract - Immediate Start. Terms and conditions vacancy
Assistant Production Manager (Afternoon shift) 12 month contract role with an immediate start.
About Ensign:
Ensign Laboratories offers a complete range of manufacturing services. We have the capability to formulate and fill a diverse range of pharmaceutical products. Quality underpins everything we do at Ensign. We are located in Mulgrave, South-Eastern suburbs of Melbourne.
The role
An opportunity exists for an Assistant Production Manager to join the afternoon shift team at Ensign Laboratories. This is an integral and fast paced leadership role for an outstanding individual with the experience, knowledge and self-motivation to work within the pharmaceutical industry. You will be reporting directly to the Production Manager and liaise on a regular basis with key departments as required.
This role is initially commencing as a 12-month contract on afternoon shift.
Main responsibilities include but not limited to the following:
- Supervise the manufacture and packaging of therapeutic and personal care products in compliance with the Australian Code of Good Manufacturing Practice (Code of GMP).
- Ensure production of products manufactured within the facility is scheduled and executed in time to meet customer orders in terms of time, quantity, quality and delivery specification.
- Arrange appropriate training of personnel working within the GMP facility to ensure they have the necessary skills to perform their tasks.
- Ensure that Company and statutory obligations are met by all employees within the facility.
- Project leadership skills for daily production and problem solving.
- Facilitate safety measures and ensure employee accountability through all levels.
- Set goals to reach agreed KPI’s with operational plans.
- Contribute to building continuous manufacturing improvement and excellence.
- Interpret product costing for budget requirements.
- Minimise annual cost of wastage, rejects and rework.
- Maintain and provide accurate record and documentation for auditory purposes.
About You:
- A minimum 3 years manufacturing experience within a GMP facility
- Sound understanding of GMP Guidelines
- Industrial aptitude
- Excellence written and verbal communication
- Strongly developed stakeholder engagement skills
- High attention to detail
- Ability to resolve complex matters – both technical and people management
- Experience in development and implementation of business improvements within the pharmaceutical manufacturing industry
Qualifications:
- Tertiary qualifications in Engineering or related discipline are desirable.
If you believe you possess the following experience, skills and ready to take on a new challenge, please submit your current CV and Cover Letter.
For any other questions:
Please email Mary Jayme: [email protected]