AddressCompany Description
SeerPharma's mission is to advance Quality and GMP Best-Practices to Pharmaceutical and Medical Device companies in the Asia-Pacific region. We look to achieve this by offering training, consulting, software, and contract employment services addressing the Quality and GMP compliance issues companies face. SeerPharma has assisted firms involved with and/or conducting step(s) of manufacturing pharmaceuticals and medical devices for over 35 years. We have an outstanding history of successful work with a broad client base across the APAC region and a great team of over 30 consultants and trainers assisting with a vast cross-section of the major international standards, including PIC/S, FDA, EU, WHO, and ISO.
We have a friendly and inclusive culture and testimony to this is the length of time our staff stay at SeerPharma. It is also an excellent opportunity to increase the breadth and depth of your knowledge, due to the variety of work we do.
A Full-time position has arisen for a self-motivated Validation Engineer with an HVAC/Mechanical Engineering background to join the SeerPharma team in Melbourne. This role is pivotal as SeerPharma has secured several major projects, and has a pipeline of large facility projects in the Pharmaceutical industry.
The successful candidate will have a strong understanding of HVAC design for cleanrooms and cleanroom design plus demonstrate a willingness and initiative to learn from our current team of experts.
The role will be primarily located in Melbourne, Victoria with flexibility for some remote work.
Key Responsibilities:
- Conducting validation activities in a GMP facility
- Writing GMP Qualification Protocols
- Conducting Validation Activities in a GMP facility
- Understanding and implementing HVAC design for cleanrooms and cleanroom design
- Demonstrating initiative and a willingness to learn
- Being open to travel and work on-site
Requirements:
- A background in HVAC/Mechanical Engineering
- 3-5 years of relevant experience
- Experience working in a GMP facility, preferably within the pharmaceutical industry
- Experience in writing GMP Qualification Protocols
- Understanding of HVAC design for cleanrooms, and cleanroom design
- Willingness to travel and work on-site
Please note, that previous applicants for this position on LinkedIn need not apply
