
Documentation Officer
1 week ago
Bioproperties Pty Ltd is an Australian owned animal vaccine manufacturing company located at Glenorie in Sydney's North-West. The company is significantly increasing its production capacity to continue the supply of existing and new live vaccines to the global market. As we use chickens in our production process, we are looking to expand our team with enthusiastic people.
**Clean Glassware and Production Technicians**
**Computer Systems Validation**
**Documentation Officer**
**General Hand - Poultry**
**IT Support Officer**
**Maintenance Fitter**
**Production Operator**
**Production Supervisor**
**Quality Officer (goods inwards)**
**Quality Officer (labels)**
**Site Electrician**
**Validation Engineer**
**Clean Glassware and Production Technicians (multiple roles available) (location: Glenorie, NSW)**:
We have an exciting opportunity for technicians with drive and an interest to join our Clean Glassware and Production teams.
**Responsibilities for clean glassware include**:
- Cleaning and decontaminating glassware
- Sterilizing equipment (using autoclaves)
- Assembly of consumable equipment, such as tubing rigs
- Filling in GMP paperwork
**Responsibilities for production include**:
- Operating the sterile filling line
- Product labelling
- Product packaging
- Clean room/ corridor cleaning
- Filling in GMP paperwork
**Requirements**:
- Willingness to learn Good Manufacturing (GMP) skills
- Ability to follow Standard Operating Procedures
- High attention to detail
- Flexibility in work hours (when needed, planned)
- High motivation and physical work rate
- Team player with the ability to work autonomously
- Own transport
**What you get in return**
- Secure job in an Australian company
- Great team environment
- Working towards a better world
**How to Apply**
Angie Parkinson
Bioproperties Pty Ltd
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**Computer System Validation (CSV) (location: Glenorie, NSW)**:
Due to site / team expansion an opportunity exists for a full time Validation Engineer. Excellent opportunity for validation engineer to write protocols & reports, execute & analyse validation studies.
**The Role**
As a CSV Engineer reporting to the Validation Manager you will:
- Prepare and execute CSV validation protocols and reports
- Maintain the validated state of the computerised systems
- Provide support in computer-based improvements and changes
- Perform risk assessments
**Skills & Experience**
To be successful in this role you will need to be results driven, energetic and a practical self-starter with the following attributes:
- Tertiary qualified in either Science, Engineering or equivalent
- Excellent verbal and written communication skills in English
- Good working knowledge of GMP
- Strong computer skills
- Understanding of industry guidelines related to computerised systems like GAMP 5
- Ability to work both independently and as part of a dynamic team in a rapidly changing work environment
- Ability to drive and co-ordinate activities
- Good interpersonal skills
- Can-do attitude
- Attention to detail and ability to think logically
- Current driver's license and own transport
- Resident of Australia or current working visa for Australia
**An Advantage**
- Previous experience in validation (Pharmaceutical / Veterinary industry experience)
- Experience in writing, reviewing and executing CSV qualification documents (IQ/OQ/PQ)
- Knowledge of APVMA, TGA or EU regulations
**What's on offer**
- Bioproperties is a stable privately owned Australian company which offers a flexible and friendly working environment
- We are proud of our employees and our multiculturalism
- We are located in a picturesque rural area with stress free driving against the traffic
- The Company offers a Share of Success program for employees
**How to Apply**
Angie Parkinson
Bioproperties Pty Ltd
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**Documentation Officer (location: Glenorie, NSW)**:
Bioproperties supplies live veterinary vaccines to Australia and many other countries throughout the world and must therefore adhere to multiple regulators, like APVMA and TGA, and their guidelines (cGMP).
We are currently seeking a highly motivated, Documentation Officer to join our Eimeria production team in Glenorie reporting to the Eimeria Product Manager.
We are looking for someone with high attention to detail with experience in administration, data entry, documentation, and MS Office. Good communication and customer service are important as the role involves interacting with multiple internal stakeholders. Prior experience working in a Quality role or in a GMP/sterile manufacturing environment would be advantageous and a tertiary qualification would be highly regarded.
On completion of your in-house training, you will be able to review and prepare batch documentation in line with set deadlines, update and maintain our internal systems and databases, liaise with our Eimeria Production areas and the Quality Department, and have sound knowledge of our processes and p
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