2D Bioprocessing Associate 1

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 Bioprocessing Associate 1 participates in the hands-on production of Humacyte’s regenerative vessels. 

Remote Work Designation: Not Remote

Major Accountabilities:

Under close supervision of Bioprocessing leadership, performs basic processes and serves as a hands-on resource in Manufacturing Humacyte’s regenerative vessels by:

• Supports the daily activities of vessel production
• Assists with basic/routine cleaning and preparation of production equipment and cleaning/disinfecting of production rooms
• Assists with assembly, set-up, and disassembly of production equipment
• Ensures the proper execution of routine production process steps according to defined SOPs and BPRs
• Ensures proper documentation of activities in accordance with cGMPs
• Adheres to the proper handling of chemically hazardous goods
• Interfaces with process automation and electronic business systems
• Supports Qualification and Validation activities, as assigned
• Ensures that process issues are identified and communicated to Bioprocessing leadership and team
• Assists team effort in the effective and timely completion of root cause investigations and CAPA implementations
• Assists other Bioprocessing Team Members during launches
• Other duties, as assigned

Special Competencies:

• Works within clearly defined standard operating procedures (SOPs) and/or scientific methods
• Applies basic analytical skills or scientific methods or operational process to perform routine activities
• Able to troubleshoot basic mechanical issues
• Understands how the assigned duties relate to others in the team and has a basic understanding of how the team integrates with others
• Works as a team player, participating in activities that involve cooperating with others

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:

• High School Diploma or GED, required
• Associate or Bachelor’s degree, preferred
• 0-1 years of previous experience in pharmaceutical, biotechnology, and/or sterile production environments, preferred
• 0-1 years of cGMP knowledge and requirements, executing SOPs, and documenting work, preferred
• Basic mechanical aptitude or knowledge of electrical / mechanical equipment, preferred
• Previous cell culture experience, highly preferred
• Will spend time in a clean room environment for manufacturing operations and will be required to meet applicable gowning and personal protective equipment guidelines
• Will be required to regularly to sit; stand for prolonged periods of time. Also may occasionally be required to pull, lift and/or move up to 20 pounds
• Position may require working holidays, weekends and over-time

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.**