Associate Manufacturing Cover Letter

Please consider me for the associate manufacturing opportunity. I am including my resume that lists my qualifications and experience.

In my previous role, I was responsible for process expertise in the area of buffer preparation, large scale protein purification drug substance manufacturing process (column chromatography, VI, UFDF/TFF, Viral filtration and bulk fill) to support the successful startup of Alexion’s BDS facility in Dublin.

I reviewed the requirements of the job opening and I believe my candidacy is an excellent fit for this position. Some of the key requirements that I have extensive experience with include:

• Able to lead a production team (min 3-5 persons) to meet production KPI/schedules and priorities with the general supervision of Supervisor
• Experience utilizing inventory management systems preferred
• Some computer knowledge preferred
• Cell culturing processing operations
• Sterile material and clinical supply management
• Works independently and follows applicable rules and procedures with minimum supervision or follow up
• High school diploma or equivalent level of education preferred
• Load parts into the machine

In response to your job posting for associate manufacturing, I am including this letter and my resume for your review.

In my previous role, I was responsible for direction for Formulation, Equipment Prep/Support, Cell Banking Activities, Cell Culture Expansion, various Purification Activities and Bulk Drug Substance Fills.

My experience is an excellent fit for the list of requirements in this job:

• Be open to learning new ways to think about production and teach others lean tools
• Knowledge of chromatography equipment (columns, skids, flow/UV/pH/conductivity/etc
• Effective hearing capabilities
• Experience with mammalian and bacterial cell culture processes
• Proficient with MS Outlook, Word, Excel and PowerPoint, and other electronic systems
• Knowledge of raw materials, production processes and quality control
• Knowledge of relevant equipment safety policies and procedures
• Basic understanding of production equipment and system integration

I am excited to be applying for the position of associate manufacturing. Please accept this letter and the attached resume as my interest in this position.

In my previous role, I was responsible for working knowledge and technical leadership in chromatography, ultrafiltration/diafiltration, final formulation, viral filtration, and automation system (DeltaV).

Please consider my experience and qualifications for this position:

• Knowledge and following SOPs and batch records preferred
• Experiences in related biotechnology/pharmaceutical industry strongly preferred
• Previous knowledge of oligonucleotide synthesis, purification, UF, conjugation, and lyophilization is advantageous
• Develop rapport with support groups and peers
• Understanding of upstream and downstream process management
• Background with inventory control or warehouse management preferred
• Can stand for long periods
• Inspect, calibrate, and test each system

Please consider me for the associate manufacturing opportunity. I am including my resume that lists my qualifications and experience.

In my previous role, I was responsible for subject matter expertise for the operation and maintenance of manufacturing and support systems/equipment such as autoclaves, washers, TFF, Chromatography Columns and skids, mixers and stainless tanks.

My experience is an excellent fit for the list of requirements in this job:

• Inspect parts for defects per SOS procedure and aesthetics
• Communicate with team members including, tooling, set up, materials, and Quality
• Package and label parts
• Rework and inspection of filter shells as assigned
• Communicate any continuous improvement ideas
• Cover OT as needed for other operators on PTO
• Strong PACE values
• Being able to keep up with the pace of the work

I submit this application to express my sincere interest in the associate manufacturing position.

In the previous role, I was responsible for process expertise in the area of solution/buffer preparation, large scale downstream drug substance manufacturing process (large scale chromatography, TFF steps, Viral filtration, final fill, pH adjustment, and process holds) to support the successful startup of Alexion’s BDS facility in Dublin.

I reviewed the requirements of the job opening and I believe my candidacy is an excellent fit for this position. Some of the key requirements that I have extensive experience with include:

• Be subjected to extreme heat for extended periods of time
• Experience with ISO 13485 or GMP Manufacturing
• Experience with batch records and documentation experience
• Experience with fabrication of microfluidic devices
• Experience working with PDMS, SU8 or similar materials
• Experience in optical imaging, microscopy, and metrology measurements
• Relevant experience in manufacturing or QC of Life Science products preferred
• Strong understanding of Media and Buffer equipment and processes