Come join the Training team at Penumbra, a company dedicated to saving lives.

In this role as a Training Specialist, you will develop and execute training programs to support the stability and growth of our Production environments.  

Perform tasks as assigned to increase the knowledge and understanding of GMP and Production processes.  

Current programs include: New Hire Orientation, Train the Trainer and Quality System (QSR) initiatives, etc.  

Develop and maintain current programs and materials, and develop new programs as future needs are identified from cross-functional sources.  

• Develop and maintain current training materials 

• Present information using a variety of instructional techniques, tools and formats 

• Conduct and/or co-facilitate professional development, computer skills, software orientation and training programs for employees 

• Co-ordinate support, facilitate and grade written and microscope exams during company job fairs 

• Train and test personnel for proficiency in manufacturing medical devices per Penumbra’s Quality System 

• Provide training on SOPs, WIs and Quality System requirements to incoming product builders

• Co-ordinate required training with cross functional groups as outlined by ECOs for changes to SOPs, WIs and MQIs in the manufacturing area

• Complete verification of training records for completeness and accuracy 

• Respond to training record inquires via the Service Now Help Desk System 

• Collect, organize and deliver data using Microsoft Excel, PowerPoint and TurningPoint software 

• Drive resolution of process and/or documentation issues including origination and implementation of change requests  

• Maintain clean room standards, practices, and housekeeping according to standard operating procedures and the illness and injury prevention program 

• Responsible for completion of personnel training records

• Adhere to the Company’s Quality Management System (QMS) as well as domestic and global quality system regulations, standards, and procedures. 

• Ensure other members of the department follow the QMS, regulations, standards and procedures.

• Perform other work-related duties as assigned.         

• High School or GED, plus five years of manufacturing experience in the medical device, pharmaceutical or biotech industry, or an equivalent combination of education and experience   

• Two or more years of learning and development or training experience   

• Strong verbal, written and interpersonal communication skills   

• Basic math skills are required, as well as proficiency with Microsoft Word, Excel, Access and Power Point   

• Strong attention to detail, organization and teamwork skills   

• Basic knowledge of cGMP/QSR requirements    

• Ability to work day shift hours of 6 am to 2:30 pm

• General office, laboratory, and cleanroom environments.  

• Potential exposure to blood-borne pathogens.  

• Requires some lifting and moving of up to 25 pounds.  

• The employee is frequently required to stand, walk, sit, and reach with hands and arms, and to use a computer, sitting for extended periods. 

• Specific vision abilities required by this job include ability to read, close vision, distance vision, color vision, peripheral vision, and depth perception.    

We offer a competitive compensation package plus a benefits and equity program, when applicable.  

Individual total compensation will vary based on factors such as qualifications, skill level, competencies, and work location. 

•A collaborative teamwork environment where learning is constant, and performance is rewarded.

•The opportunity to be part of the team that is revolutionizing the treatment of some of the world's most devastating diseases.

•A generous benefits package for eligible employees that includes medical, dental, vision, life, AD&D, short and long-term disability insurance, 401(k) with employer match, an employee stock purchase plan, paid parental leave, eleven paid company holidays per year, a minimum of fifteen days of accrued vacation per year, which increases with tenure, and paid sick time in compliance with applicable law(s).

Penumbra, Inc., headquartered in Alameda, California, is a global healthcare company focused on innovative therapies. Penumbra designs, develops, manufactures, and markets novel products and has a broad portfolio that addresses challenging medical conditions in markets with significant unmet need. Penumbra sells its products to hospitals and healthcare providers primarily through its direct sales organization in the United States, most of Europe, Canada, and Australia, and through distributors in select international markets. The Penumbra logo is a trademark of Penumbra, Inc.