Upstream Manufacturing Associate ( Manufacturing / Engineering )
Sterling Life Sciences - Tallahassee, FL

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1) Coordinate upstream manufacturing activities to ensure projects are performed in accordance with cGMP guidelines and completed in a manner that meet or exceed client?s expectations2) Interact with other department heads to resolve process and operations issues promptly3) Write, review and approve written procedures, SOP?s, validation reports, design inputs, exception documents and other cGMP documents4) Help to lead technology transfer internally and externally as well as provide technical support for large-scale non-GMP and cGMP plant operations5) Ensure that staff members are properly trained for their job functions and that the training is documented in cGMP training records

1) University degree is required (preference will be given to those with degree in relevant field, though all candidates are welcome and encouraged to apply)2) Appropriate full-time work experience is mandatory (no students or fresh graduates please)3) Recent experience in the biotechnology industry is strongly preferred4) Preference will be given to people who have recent experience in Life Sciences / Manufacturing