ALWAYS NEEDED
Our values are to understand your desired career path and to help you reach that goal. We are recognised by existing and past candidates as being a recruitment company which listens to what you are seeking in your next role, not only what you can do now. As a result we listen to your goals and seek to match you not only with a position that offers you a step in your chosen direction, but also with a company that reflects the culture you value.
BIOSTATISTICIAN
- Pharmaceutical and allied industries
- Local, regional and global centres
You will collaborate with colleagues to develop study protocols, statistical analysis plans, analyse data and prepare clinical reports. Your team will facilitate the appropriate application of statistical methodology to study design, analysis and reporting. You will also contribute to scientific presentations and publications based on clinical data and provide input into the training and education of clinical colleagues on statistical and general clinical trials methodology.
With a minimum of a Master’s degree in statistics or related discipline, ideally you will have three years experience in design, analysis and reporting of clinical trials.
You will also need to have:
- Knowledge of statistical concepts and methodologies
- Proficiency in the use of statistical analysis computer software (typically SAS)
- Knowledge of ICH guidelines and regulatory requirements
- Experience with coordination and analysis of clinical trials in one or more of the CNS, CVS, anti-infective, allergy, diabetes areas is desirable.
- Ability to work in a matrix organisation
- Ability to work effectively in a multi-cultural context
- Good communication skills
- English verbal and written communication skills are required
To be considered for a position when a role becomes available, please register with On Q Recruitment by sending your CV and cover letter as one Word document (please avoid using tables when formatting) quoting Ref # WAN-Biostatistician - Apply Now
Please note only applicants whose technical skill and experience meet essential criteria will be entered onto the On Q Recruitment database.
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CLINICAL DATA MANAGEMENT
- Leading Pharmaceutical Company
- Growing Regional Data Management Centre
Our client is in constant need of experienced Data Management Associates for their Sydney regional data management centre. These role represent a great opportunity to be involved with the facility in the second phase of their expansion.
With at least 1 - 3 years experience in managing medical data in clinical trials or hospital medical records, you are very knowledgeable in data management concepts and ICH guidelines. You will be degree qualified, ideally in a science related discipline.
An excellent communicator, you will be assigned to specific clinical studies, where you will perform edit and quality checks prior to data release.
To be considered for a similar position when a role becomes available, please register with On Q Recruitment by sending your CV and cover letter as one Word document (please avoid using tables when formatting) quoting Ref # WAN-CDM - Apply Now
Please note only applicants whose technical skill and experience meet essential criteria will be entered onto the On Q Recruitment database.
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CLINICAL RESEARCH ASSOCIATE
- Contract & Permanent
- Pharmaceutical Companies
Our clients, including global pharmaceutical companies and CRO’s, are constantly seeking Clinical Research Associates to become members of their Clinical Research Teams.
Typically, you will be responsible for all aspects of trial management, including the development of protocols, investigator selection and site monitoring.
The level of responsibility in individual roles will reflect your experience and training progress.
You will hold a Degree in Life Sciences (or equivalent) and have at least 2-3 years Clinical Trials experience with excellent computer literacy skills. Your ability to problem solve, good communication skills and high attention to detail will win you this job.
To be considered for a position when a role becomes available, please register with On Q Recruitment by sending your CV and cover letter as one Word document (please avoid using tables when formatting) quoting Ref # WAN-CRA - Apply Now
Please note only applicants whose technical skill and experience meet essential criteria will be entered onto the On Q Recruitment database.
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HPLC ANALYTICAL CHEMISTS
- Experienced with HPLC?
- Are you seeking better pay and greater opportunities?
We have on-going vacancies for entry level and experienced chemists with a selection of our valued clients. We recruit for a wide variety of both international Fortune 500 corporations and Australian owned companies in the following sectors:
- Pharmaceutical
- Animal Health
- Food
- FMCG
- Biotech
- Cosmetics/Personal Care
- Medical Devices
- Contract Manufacturing
Accordingly, we can offer you a choice of clients with permanent, contract and temporary opportunities which have the potential to match your chosen career path and desired working environment.
Typical vacancies include:
- Quality Control
- Quality Assurance
- Incoming and Raw Materials inspection
- In-Process & Production support
- Finished Goods & Stability analysis
- Method Validation, cGMP, cGLP and ongoing compliance
- Documentation support
- New product introduction support
- Formulation and Product Development
- Research & Development
- Management
We are keen to hear from you if you have tertiary science qualifications and experience in the Pharmaceutical, Animal Health, Consulting Laboratory, Biotech, Food, FMCD, Cosmetics, Personal Care, Medical Devices or Environmental sectors. Ideally you will bring a variety of technical skills to these roles including HPLC, GC, FTIR, NIR, wet chemistry and common analytical techniques. You should be familiar with cGLP or cGMP, TGA or HACCP and equipment specific software such as Waters Millennium, HP
ChemStation or Agilent.
To be considered for a similar position when a role becomes available, please register with On Q Recruitment by sending your CV and cover letter as one Word document (please avoid using tables when formatting) quoting Ref # WAN-HPLC - Apply Now
Please note only applicants whose technical skill and experience meet essential criteria will be entered onto the On Q Recruitment database.
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PHARMACISTS – CAREER CHANGE
- Capitalise on your qualifications
- Permanent or Contract Opportunities
Do you want to capitalise on the your professional qualifications and skills?
Do you enjoy providing pharmacological information to consumers and other healthcare professionals?
Whether you want to work for a small or large sized pharmaceutical company, across broad therapeutic areas or within a niche area, we can help you make the move.
A variety of roles are available within the pharmaceutical industry, including Medical Information and Drug Safety (Pharmacovigilance).
Drug Safety Associates are responsible for the processing and monitoring of adverse event reports for investigational and marketed products following company Standard Operating Procedures to ensure compliance with worldwide safety regulations, corporate and regulatory guidance documents and corporate policies. Associates process adverse event reports from clinical trials and from marketing activities to maintain regulatory compliance.
Medical Information Associates provide technical and medical information to healthcare professionals, consumers and internal staff on a wide range of new & existing products and in a variety of therapeutic areas. They liaise with patients/consumers to ensure the optimal use of company products, provide technical advice and information within the company on new and existing products. They develop and maintain a current knowledge of products and disease states
Your personal attributes will include strong attention to detail, empathy, excellent team work and sound communication skills – both written and verbal.
Academically you will hold a minimum bachelors degree in pharmacy and have Australian Hospital or Community Pharmacy working experience.
To be considered for a similar position when a role becomes available, please register with On Q Recruitment by sending your CV and cover letter as one Word document (please avoid using tables when formatting) quoting Ref # WAN-PHARM - Apply Now
Please note only applicants whose technical skill and experience meet essential criteria will be entered onto the On Q Recruitment database.
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REGULATORY AFFAIRS ASSOCIATE
Time for a change? The choice is yours…
We enjoy strong client relationships with a variety of Global and Australian pharmaceutical companies who are always interested in experienced Regulatory Affairs candidates. Tell On Q Recruitment what your job wish-list is and we will endeavour to match you with your new emplolyer!
Typically you will be responsible for:
- Preparing and submitting products for listing and registration with the TGA and for export
- Reviewing evidence to support new indications for products
- Reviewing product labelling to comply with TGA requirements
- Maintaining regular contact with key internal contacts and regulatory bodies
- Update existing product registrations
With tertiary qualifications in Pharmaceutical Science, Pharmacy or Life Sciences, you have at least 2 years experience in pharmaceutical drug registration. You will also be familiar with regulatory compliance and code requirements in various countries. Superior communication, attention to detail and organisation are your strengths.
To be considered for a similar position when a role becomes available, please register with On Q Recruitment by sending your CV and cover letter as one Word document (please avoid using tables when formatting) quoting Ref # WAN-Reg Affairs - Apply Now
Please note only applicants whose technical skill and experience meet criteria will be entered onto the On Q Recruitment database.
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SAS PROGRAMMER
- Australian and Global Pharmaceutical Companies
Your minimum of 2 years SAS development and strong background in statistics will prove crucial to your success of your new team. You will be using the latest SAS technologies as a member of a high performing team.
We are keen to receive applications from highly motivated and proactive professionals with a strong team orientation. Candidates without pharmaceutical experience may be considered for some opportunities.
To be considered for a similar position when a role becomes available, please register with On Q Recruitment by sending your CV and cover letter as one Word document (please avoid using tables when formatting) quoting Ref # WAN-SAS - Apply Now
Please note only applicants whose technical skill and experience meet essential criteria will be entered onto the On Q Recruitment database.
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SUPPLY CHAIN
On Q Recruitment enjoys strong relationships with clients in a variety of industries including:
- Pharmaceutcial
- Animal Health
- FMCG
- Food
- Biotechnology
- Medical Devices
- Environmental
- Chemicals
- Research Institutes
- Government
If your current or future position title has any of the following words
- Procurement
- Planning
- Forecasting
- Supply
- Inventory
- Logistics
- Demand
- Warehouse
And you know what these letters mean and what to do with them!
- ERP
- MRP
- MRPII
- JD Edwards
- SAP
- BPCS
- Oracle
- MFGPro
- Mapics
- AS400
- GEAC
- MAPICS
then we’d like you to register with us for upcoming opportunities.
Please register with On Q Recruitment by sending your CV and cover letter as one Word document (please avoid using tables when formatting) quoting Ref # WAN-Supply - Apply Now
Please note only applicants whose technical skill and experience meet essential criteria will be entered onto the On Q Recruitment database.
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VALIDATION ENGINEER
- Global & Australian Pharmaceutical Companies
We enjoy strong client relationships with a variety of Global and Australian pharmaceutical companies who are always interested in experienced Validation Engineers. Tell On Q Recruitment what your job wish-list is and we will endeavour to match you with your new employer!
Typical responsibilities include:
- Validation of processes, computer systems and equipment
- Preparing validation protocols and reports
- Supporting related departments throughout the validation process
Pharmaceutical experience in a validation role coupled with a strong understanding of manufacturing applications and cGMP is essential.
You must have previous experience in the development of validation protocols, execution of IQ/OQ/PQ and documentation of qualifications
Your high attention to detail, excellent communication skills and the ability to work well within a team to develop productive relationships will secure you this role.
To be considered for a similar position when a role becomes available, please register with On Q Recruitment by sending your CV and cover letter as one Word document (please avoid using tables when formatting) quoting Ref # WAN-VALIDATION - Apply Now
Please note only applicants whose technical skill and experience meet essential criteria will be entered onto the On Q Recruitment database.
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