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Greenlight Guru Announces the Formation of Its New Regulatory Advisory Board
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Leading medical device QMS provider establishes Regulatory Advisory Board comprised of global regulatory experts
Greenlight Guru is continuing to push the ideal of harmonization and industry best practices forward through the formation of our Regulatory Advisory Board. INDIANAPOLIS (PRWEB) May 27, 2021 Greenlight Guru, the leading medical device quality management software platform, today announced the formation of its new Regulatory Advisory Board (RAB), comprised of nine veteran medical device professionals. Members of Greenlight Guru’s RAB have prior experience with regulatory bodies, including FDA and EU notified bodies, and have significant medical device industry expertise with respect to regulations, standards, and requirements impacting the medical device industry.
Validation Engineer
We are looking for a Validation Engineer. You will be working in our newest plant where we make products for the healthcare market.
A new plant for the production of cell culture media is being built at our location in Tilburg. Cell culture media are raw materials for the biopharmaceutical industry, where they are used for the production of medicines or vaccines. For this new production facility we have a vacancy for a Validation Engineer in the department Quality Systems / Regulatory Affairs (QS/RA).
The position
Within Life Science Manufacturing (LSM), the QS/RA department is responsible for all activities relating to quality. This includes the approval of raw materials, the release of finished products and all tests on these materials, but also supplier evaluations, deviations during production and change control. Document control also falls under this department. As Validation Engineer, you are responsible for carrying out and setting up various validati
Quality Control Supervisor
We are looking for a Quality Control Supervisor. You will be working in our newest plant where we make products for the healthcare market.
A new plant for the production of cell culture media is being built at our location in Tilburg. Cell culture media are raw materials for the biopharmaceutical industry, where they are used for the production of medicines or vaccines. For this new production facility we have a vacancy for a QC Supervisor in the department Quality Systems / Regulatory Affairs (QS/RA).
The position
Within Life Science Manufacturing (LSM), the QS/RA department is responsible for all activities related to quality. This includes the approval of raw materials, the release of finished products and all tests on these materials, but also supplier evaluations, deviations during production and change control. Document control also falls under this department.
Radient Technologies Inc.: Radient Technologies Announces Strategic Licensing Agreement with HighGrade Supply Ltd.
Edmonton, Alberta (Newsfile Corp. - May 5, 2021) -
Radient Technologies Inc. (
TSXV: RTI) (OTC Pink: RDDTF) ( Radient or the Company ) is pleased to announce an exclusive licensing and extraction agreement with HighGrade Supply Ltd., ( HighGrade ) to manufacture a wide range of premium concentrates for sale into both the medicinal and rapidly growing recreational cannabis markets in Canada. The agreement grants Radient the exclusive rights to the HighGrade technology, HighGrade IP, and established cannabis culture legacy brand. The HighGrade team has been innovating and perfecting cannabis processing technology in Canada for the last decade. The team has experimented with every viable extraction technology in the market and are set to release a wide range of top quality and affordable cannabis products across the country for the recreational, medical, and wholesale