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Planet Pharma is seeking a skilled professional to participate in the manufacture and process sustaining of oligonucleotides. You will contribute to design, development, and quality testing activities while collaborating across R&D, Manufacturing and Quality to improve existing processes and develop new ones.
The role emphasizes data-driven approaches, statistical methods, and robust documentation to ensure compliant, scalable production in a fast-paced biotech environment.
Target PR Range: 33.00–41.25/hr DOE
Participate in manufacture; process sustaining, definition and improvement; design, development and quality test activities in the making of oligonucleotides. Work cross functionally with R&D, Manufacturing and Quality to develop processes for new products and improve processes of existing products.
Work experience in the biotech or pharmaceutical industries is desirable. Experience with chemical processes (preferably organic) preferred. Experience with statistics, Statistical Process Control and DOE techniques is a plus. Experience with high volume production in a high tech, high volume consumables industry is a plus. Experience with product development processes and project management is a plus. Good interdepartmental communication skills and documentation skills are required. Listed responsibilities are an essential, but not exhaustive list, of the usual duties associated with the position. Changes to individual responsibilities may occur due to business needs.