MSAT Engineer 3

Humacyte, Inc. is bringing to market a once in a generation scientific technology platform, bioengineering readily available and universally implantable product opportunities focused on improving lives of patients and transforming the practice of medicine. Located in Durham, NC, the company develops and manufactures acellular tissues for the treatment of diseases and conditions across a wide range of therapeutic areas. The company’s innovative technology supports tissue repair, reconstruction, and replacement while overcoming limitations in existing standards of care. Initially developing a portfolio of human acellular vessels (HAVs), to target multiple vascular markets including trauma, arteriovenous access for hemodialysis, peripheral arterial disease, and coronary artery bypass grafting. Humacyte is focused on the development of future markets such as pediatric heart surgery, delivery of cellular therapies, and multiple other novel cell and tissue systems.

We are looking for additional colleagues to continue to build our expanding team.  Candidates will be expected to work both independently and collaboratively as part of the Humacyte organization. Applicants must be highly self-motivated, with solid communication skills, and demonstrates the ability to work in a team environment and lead other professionals and peers.

Position Background:

The MSAT Engineer 3 will support the GMP manufacturing of Humacyte’s unique HAV and related products with limited supervision and guidance. This role will collaborate effectively with personnel in Manufacturing, Engineering, Process Development, Quality Assurance, and Quality Control utilizing strong communication, and technical expertise to maintain and improve manufacturing operations.

Remote Work Designation: Not Remote

 Major Accountabilities:

• Responsible to ensure bioprocessing equipment is ready for use when required
• Identifies technical issues on bioprocessing equipment and recommends activities to resolve the issue. Identifies and implements procedures and activities to prevent the same issue from occurring.
• Lead efforts in troubleshooting out-of-trend manufacturing processes, providing the intellectual, scientific and engineering leadership to identify and implement corrective actions
• Provides guidance and is accountable for determining the root causes of equipment related deviations in a timely and conclusive manner.
• Ensures deep understanding of standards of practice, process science and departmental policies through participation in training and development opportunities
• Provides comprehensive training and guidance to operations staff
• Partner with Process Development to ensure successful process transfer
• Assist in equipment selection and design, qualification, and start up activities. Work with Bioprocessing to ensure robust procedures are utilized for operation of equipment
• Work with the Validation team to develop and execute validation strategies
• Identify continuous improvement opportunities in terms of cost savings, process robustness, and manufacturing efficiency gains

Special Competencies:

• Possess a demonstrated proficiency working in a Process Engineering role with a clear understanding of GMP manufacturing
• Possess a demonstrated technical foundation of cell- and tissue- based products
• Experience supporting and troubleshooting single use bioprocessing technologies as well as fixed stainless steel bioprocessing equipment
• Experience with bioprocessing deviations, change control, process optimization, and technical troubleshooting,
• Experience with cell culture operations, specifically using adherent mammalian cells
• Works well in a team environment
• Strong experience working cross functionally within a BioPharma Bioprocessing organization

General Competencies:

• Able to communicate effectively in English, both verbally and in writing
• Possess a positive roll-up-the-sleeves attitude and optimistic outlook
• Represents the organization in a positive and professional manner
• Strong ability to work in a fast-paced team environment with fluctuating priorities, and collaborate effectively with others
• Excellent organizational and time management skills with ability to set own priorities in a timely manner
• High degree of flexibility and adaptability
• Basic computer skills required, such as knowledge of MS Word, Excel, PowerPoint, and Outlook
• Must be able to work as needed to meet tight deadlines and at peak periods
• Self-motivated and organized critical thinker with solid interpersonal and business communication skills
• Demonstrated ability to work in a cross functional team
• Adheres to company and facility specific policies and procedures, including SOP, training and meeting requirements
• Always observe safety precautions and regulations in all areas where duties are performed
• Responsible for reporting all safety hazards and potential unsafe working conditions
• Reports to work on time and as scheduled

Qualifications:

• BS in Engineering or other relevant discipline required
• MS in related discipline preferred
• Background in chemical engineering, biochemical engineering, biotechnology, bioprocess, cell therapy, tissue engineering, regenerative medicine, or process development required
• 5-8 years of relevant pharma or biotech industry experience, minimum 5 years GMP experience required

Perks:

• Stock Options
• 401k Plan with 4% Match and no Vesting Schedule
• Medical, Vision and Dental Plans
• Company Paid Long Term/Short Term Disability
• Company Paid Life Insurance
• 23 Days Paid Time Off (PTO)
• 10 Company Designated Holidays + 2 Floating Holidays
• Paid Parental Leave Policies

**Please note, Humacyte does not provide sponsorship at this time and does not accept unsolicited resumes from recruiters.**