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    Senior MSAT/Process Engineer - Durham, United States - HUMACYTE GLOBAL INC

    HUMACYTE GLOBAL INC
    HUMACYTE GLOBAL INC Durham, United States

    2 weeks ago

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    Description
    Job Description

    Job Description

    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 Senior MSAT/Process Engineer 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, technical expertise and influencing skills to maintain and improve manufacturing operations.


    Remote Work Designation :
    Not Remote

    Major Accountabilities:
    Serves as a process expert in HAV production systems; able to fully understand the manufacturing process
    Primary responsible person to ensure bioprocessing equipment is ready for use when required
    Identifies technical issues on bioprocessing equipment and initiates activities to resolve the issue quickly. 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
    Develop and execute test protocols, vendor site visits, FAT/SAT, etc.
    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
    Strong Scientific and Engineering technical experience performing and supporting cell culture based bioprocessing activities, using adherent mammalian cells preferred
    Experience supporting and troubleshooting single use bioprocessing technologies as well as fixed stainless steel bioprocessing equipment
    Experience leading projects related to bioprocessing deviations, change control, process optimization, technical troubleshooting, and bioprocessing process changes
    Works and leads 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 degree in relevant discipline, required.
    Master's degree or above in related discipline, preferred.
    Background in chemical engineering, biochemical engineering, biotechnology, bioprocess, cell technology, biomedical engineering, cell therapy, tissue engineering, regenerative medicine, or process development required
    10 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.
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