Home » Jobs » Analytical Scientist – Biotech GMP Facility
Analytical Scientist – Biotech GMP Facility (The position has been filled)
Australia, Victoria
Full Time
09/01/2018
Innovative Pharmaceutical Company
Modern facilities with well equipped laboratory
Permanent Role with Competitve Salary, Friendly Work Environment & Excellent Career Opportunities
CLIENT
Our client is a well known, successful biotechnology company based in Melbourne’s CBD. Boasting modern facilities and state of the art laboratories, our client offers a friendly, supportive work environment and access to parking as well as public transport.
ROLE
As a Scientist in the Analytical Development team, you will play a critical role in supporting the analytical method development and validation of test methods including characterisation of drug substance, raw materials, and drug products.
Should you secure this position, your responsibilities will include:
Develop and validate tests methods with HPLC and GC
QC testing of raw materials, in-process samples, components and finished products
Perform stability testing for investigative samples
Test and maintain appropriate standards
Conduct Root Cause Analysis and close out investigation reports including change control mechanism within a NATA laboratory context
Train and mentor staff in the analytical team to obtain a high level of proficiency and ensure consistency
Ensure compliance with cGMP, GLP, quality systems and regulatory requirements
Create reports and documentation (methods/specifications etc)
REQUIREMENTS
You will hold a scientific degree, Masters or PhD in a releavnt discipline
You will have significant laboratory experience with and an in-depth knowledge of conventional laboratory characterisation techniques such as HPLC, GC, UV, IR and Mass Spectrometry
Must have proven ability to write sound reports and protocols including validation documentation
You will have extensive analytical and experimental design abilities
Proven problem solving skills and solid understanding of GMP
Previous experience in developing pharmaceutical generic and innovative drug products
Experience in NMRi will be highly regarded
Able to use, troubleshoot, maintain and validate HPLC and GC
Excellent organisational, proven people and time management skills
Strong verbal and written counication skills are essential, as the ability to present scientific approaches, data and interpretations across the company will be important
Attention to detail and strong ability to multi-task.
The key to this role will be your flexible “can do” attitude and excellent work ethic.
Demonstrated ability to display initiative whilst working autonomously or as part of a team.
Our client offers a dynamic environment that fosters a work culture emphasising Innovation, Urgency, Integrity, and Results with a commitment to attract and retain highly motivated and qualified people.
The working environment is one that embodies vision and values, celebrates diversity of background and thought, and supports a balance of professional and personal needs.
APPLICATIONS
To have a confidential discussion about this role, please call our team on 03 9516 0100 during office hours, or after hours Helen on 0438 620 434.
To apply, please click the “Apply Now” button below and send your resume with a covering letter addressing the above criteria to CS Executive Group.
THANK YOU
We would like to thank you for taking the time to apply for this role. Unfortunately, due to the large volume of applications we receive daily, we cannot contact all candidates. Please note, if you are not successful on this occasion, your resume will remain on our database and you may be contacted for other similar roles in the future.