Validation Specialist
Excellent Contract Opportunity for Validation Specialist with Method Validation & Micro/Biochemistry to join global pharmaceutical org. START ASAP
- Global Pharmaceutical Organisation
- Excellent Contract Opportunity - Start ASAP
- Melbourne Metropolitan Area
Operating as a major global Multinational pharmaceutical manufacturer with global sites worldwide, our client is well known for its growth and innovation and is an Australian iconic brand in the marketplace,
An opportunity now exists for a Validation Specialist and Microbiology or Chemistry background experience to lead, coordinate cross site activities for method development activities within a cGMP environment.
About the Position
Key Duties & Responsibilities include the following:
- Lead troubleshooting issues within QC methods to deliver solutions for implementations through quality systems. (CAPA, Change control)
- Act as a SME for in analytical testing techniques & industry practice.
- Perform validation in accordance to QMS System, Site Validation Master Plan and validation procedures.
- Development of current and new test methods validation lifecycle.
- Responsible for experimental design on key projects.
- Effectively with key and internal stakeholders.
- Tertiary qualifications in Science or Engineering.
- Microbiology/biochemistry background is essential.
- Industry experience in pharmaceutical. medica device.
- Method validation and validation procedures and documentation.
- Good understanding of cGMP practices & industry guidelines.
- Sound communication & interpersonal skills.
- Excellent attention to detail.
Immediate Start.
How To Apply
To apply for this role, please click the APPLY NOW button below. For a confidential discussion on this opportunity, please contact Sue Campbell on 0417 994 917.
PLEASE SUBMIT MS WORD DOCUMENTS ONLY
NB: Only shortlisted candidates will be contacted.
Science & Biotechnology > Pharmaceutical > Science & Biotechnology