Cameron Albert Email & Phone Number

Boston, Ma, Us

New York, New York, Us

- Led and supported new product variant technology transfer activities including submission of master data request, MBR/SOP creation/revision, BOM submission requests, risk assessment evaluation. - Led technology transfer of a new manufacturing process from at-scale development through process validation campaign. - Supported network project across partnered sites/companies to ensure successful harmonization and completion of process validation campaigns. - Served as the main point of contact for manufacturing department internal audit which included writing audit responses and owning audit observation action items. - Facilitated and supported Permanent, Temporary, and Emergency Change Controls (CC’S) to ensure continuous manufacturing as well as for various process improvement projects.

New York, New York, Us

- Provided on floor production support for COVID mRNA vaccine ensuring product quality and regulatory standards are met - Represented Biopharmaceutical Manufacturing Operations on the cross-functional team responsible for multi-variant production of the COVID-19 vaccine drug substance. - Led and supported new product technology transfer activities including submission of master data request, MBR/SOP creation/revision, BOM submission requests, risk assessment evaluation - Coordinated, scheduled, and planned daily/weekly standard work operational tasks to ensure successful batches as well as product changeover. - Facilitated and supported Permanent, Temporary, and Emergency Change Controls (CC’S) to ensure continuous manufacturing as well as for various process improvement projects. - Authored, reviewed, and approved SOP and MBR updates as an SME driven by CAPAs, change controls, and continuous process improvement projects that led to a 67% reduction of process step related investigations, and a 56% reduction in documentation related investigations for the functional area. - Served as an SME for In Vitro Transcription (IVT) process as well as various other processing activities. - Served as a qualified trainer and trained operators on aseptic technique, major process steps as well as various contributing process activities and administrative tasks. - Served as a primary team member for both internal and external audits including the EAEU, representing manufacturing operations team. - Proposed, drove, and implemented continuous improvement and process optimization projects resulting in ~10-15 hours/month. - Coordinated functional area safety plan including defining area safety metric as well as drove suite safety improvement projects and Job Hazard Assessments.

New York, New York, Us

- Supported new product development of COVID-19 mRNA Vaccine as an SME through tech transfer to develop GMP Documentation (SOP’s and MBR’s), sample plans, process scale-up tasks.-Supported execution of various process steps (In Vitro Transcription, UFDF, Final Filtration) following GMP practices for 2 process validation campaigns.- Authored, reviewed, and approved standard operating procedures (SOP’s) and manufacturing batch records (MBR’s).- Acted as the responsible person and SME for triaging/writing up investigation reports using Six Sigma methodology. - Proposed, developed, and implemented CAPA’s in response to incidents as well as continuous improvement projects.- Supported FDA audits as well as internal regulatory audits as an SME.

Somerville, Ma, Us

• Deliver quality patient care in accordance with clinical policies, statewide protocol, and standards of care• Attend to patients in a courteous, professional manner• Complete and submit all documentation/paperwork requirements daily• Communicate effectively with EMS agencies, physicians, procedures and guidelines

Woonsocket, Ri, Us

•Assist with patients picking-up and dropping off prescriptions •Responsible for calculating and counting out medications based on days supply and amount prescribed •Effectively and efficiently dealt with problems that arose between the patient and insurances/doctor’s