2D Process Development Associate 1
Quick Apply Full-time 3 hours ago Full 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 Process Development Associate 1 will be a hands-on position, performing experimental protocols within the Process Development lab for Humacyte's regenerative vessels.
This position is critical to the support of the company's development effort.
This position reports to Supervisor, Process Development Operations Remote Work Designation:
Not Remote Major Accountabilities:
Assist with performing and documenting process development experiments Support aseptic sample collection and analysis using cell counters, dissolved gas analyzers, and metabolite analyzers Ensure accurate data is acquired for continuous process monitoring Ensure unexpected findings and observations during bioprocessing are reported to other PD Associates and management Troubleshooting of basic/routine processes/equipment Assist in the setup, daily monitoring, and breakdown, of bioreactor experiments Support the aseptic compounding and aliquoting of cellular growth medium and buffers Assist with the construction and packaging of bioprocessing tubing manifolds Report process alarms to Leads or Manager Other duties, as assigned Special Competencies:
Knowledge of GMP quality systems Knowledge and experience with standard bioprocessing skills as well as use and maintenance of common laboratory procedures and equipment Familiarity and understanding of foundational cGMP compliance in the biotech/bioprocessing manufacturing environment Knowledge of Code of Federal Regulations 21 CFR 1271, a plus Detail-oriented, self-motivated and scientifically driven Excellent communication and interpersonal skills Demonstrated ability to work in a cross functional team 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 is required, Bachelor's Degree in Biology, Chemistry or other related field is preferred At least 1 years of experience with cell culture, cell therapy, bioprocessing, tissue engineering, or regenerative medicine, biotech/pharma, required Previous cell culture experience, required Previous experience in Process Development, preferred Strong background/technique in aseptic processing, preferred Bioreactor experience, 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, etc.
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.
Quick Apply.
Estimated Salary: $20 to $28 per hour based on qualifications.
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 Process Development Associate 1 will be a hands-on position, performing experimental protocols within the Process Development lab for Humacyte's regenerative vessels.
This position is critical to the support of the company's development effort.
This position reports to Supervisor, Process Development Operations Remote Work Designation:
Not Remote Major Accountabilities:
Assist with performing and documenting process development experiments Support aseptic sample collection and analysis using cell counters, dissolved gas analyzers, and metabolite analyzers Ensure accurate data is acquired for continuous process monitoring Ensure unexpected findings and observations during bioprocessing are reported to other PD Associates and management Troubleshooting of basic/routine processes/equipment Assist in the setup, daily monitoring, and breakdown, of bioreactor experiments Support the aseptic compounding and aliquoting of cellular growth medium and buffers Assist with the construction and packaging of bioprocessing tubing manifolds Report process alarms to Leads or Manager Other duties, as assigned Special Competencies:
Knowledge of GMP quality systems Knowledge and experience with standard bioprocessing skills as well as use and maintenance of common laboratory procedures and equipment Familiarity and understanding of foundational cGMP compliance in the biotech/bioprocessing manufacturing environment Knowledge of Code of Federal Regulations 21 CFR 1271, a plus Detail-oriented, self-motivated and scientifically driven Excellent communication and interpersonal skills Demonstrated ability to work in a cross functional team 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 is required, Bachelor's Degree in Biology, Chemistry or other related field is preferred At least 1 years of experience with cell culture, cell therapy, bioprocessing, tissue engineering, or regenerative medicine, biotech/pharma, required Previous cell culture experience, required Previous experience in Process Development, preferred Strong background/technique in aseptic processing, preferred Bioreactor experience, 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, etc.
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.
Quick Apply.
Estimated Salary: $20 to $28 per hour based on qualifications.
|
|
 | |
