Bryce Eckley Email & Phone Number

Lawrence Township, Nj, Us

Écully, Auvergne-Rhône-Alpes, Fr

Cambridge, Massachusetts, Us

· Safely produce mRNA medicines and ensure plans and resources (people, facilities, supplies etc.) are efficiently utilized to manufacture mRNA medicines and deliver on time to the clinic · Oversee the hiring, training, development, retention and performance of staff for the leadership and execution of manufacturing operations. · Develop batch records, SOPs and training materials for ramp up for COVID-19 production at the Norwood Facility · Provide on the floor support with trouble shooting equipment issues, as well as trouble shooting automation issues in order to ensure that the electronic batch records run efficiently and to avoid production delays· Closely partner with QA peers for rapid disposition of Moderna medicines, as well as provide support in deviation investigations, closures and CAPA implementations · Develop comprehensive operating plans and monitors achievement of business and financial goals. · Development of effective working relationships with both internal and external partners.

Cambridge, Massachusetts, Us

· Execute manufacturing operations using disposable technologies, automation, and Manufacturing Execution Systems (MES) to produce mRNA · Strict adherence to current good manufacturing practices, standard operating procedures, and manufacturing documentation. Establish and follow written procedures for the clear and accurate documentation of equipment operation and process instructions, and of process data, as well as utilize process knowledge to improve operational efficiency. · Monitor process operations to ensure compliance with specifications. · Practice safe work habits and adhere to Moderna’s safety procedures and guidelines. · Adhere to documented waste handling procedures to respect environmental regulations.

Lawrence Township, Nj, Us

- Proficient in the use of Automated Systems i.e. Delta V and Syncade- Provide training and support to aid the on-boarding of new operators.- Provide scheduling support to accommodate manufacturing objectives.- Perform area and equipment walkdowns prior to and following the execution of batch records.- Perform Protein Purification operations including column chromatography, UFVF, UFBF and viral inactivation using Buffer solutions- Prepare buffer formulations to support downstream purification operations while adhering to cGMP and all pertinent biologics CFR’s.- Perform Steam-In-Place and Clean-In-Place preparatory procedures.- Perform raw materials weigh-and-dispense operations.- Work with Automation and Management to troubleshoot technical process issues.- Work in interdepartmental teams to facilitate Metrology, Validation, and Cleaning Initiative studies.

Paris, France, Fr

My responsibilities as a Manufacturing Associate include the following:- Provide a source of on-the-floor leadership and lead 2-3 person functional groups.- Provide quality event support by originating, investigating, and closing deviations through the Trackwise quality system.- Perform duties of area supervisor which include assignments of personnel based on the operation need, schedule breaks, ensuring safe and clean areas, reviewing production records and other process related documentation- Improve documentation by revising Standard Operating Procedures and driving their processing and approval through the Livelink Validated system.- Drive the establishment of an organized and safe work environment by performing area audits and walkthroughs.- Provide training and support to aid the on-boarding of new operators.- Provide scheduling support to accommodate manufacturing objectives.- Prepare buffer formulations to support a multi-product downstream purification operation while adhering to cGMP and all pertinent biologics CFR’s.- Perform Steam-In-Place and Clean-In-Place preparatory procedures.- Perform raw materials weigh-and-dispense operations.- Troubleshoot technical process issues.- Work in interdepartmental teams to facilitate Metrology, Validation, and Cleaning Initiative studies.

Paris, France, Fr

- Prepare buffer formulations to support a multi-product downstream purification operation while adhering to cGMP and all pertinent biologics CFR’s.- Perform Steam-In-Place and Clean-In-Place preparatory procedures.- Perform raw materials weigh-and-dispense operations.- Troubleshoot technical process issues.- Work in interdepartmental teams to facilitate Metrology, Validation, and Cleaning Initiative studies.

Pursued Assoiates, Educa

Pursued Associates, Business Administration And Management, General