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Senior Reagent Manufacturing Engineer
Vizgen Waltham, MA
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$104k-123k (estimate)
Full Time 1 Week Ago
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Vizgen is Hiring a Senior Reagent Manufacturing Engineer Near Waltham, MA

Vizgen, Inc. - Cambridge, MA
Vizgen is a rapidly growing company developing the next generation of spatially resolved genomic profiling tools that enable researchers to gain new insight into the biological systems that underlie human health and disease. The company's groundbreaking MERFISH spatial transcriptomics technology images RNA molecules with high accuracy and unrivaled detection efficiency at subcellular resolution. MERFISH provides transformative insight into a wide range of tissue-scale basic research and translational medicine in oncology, immunology, neuroscience, infectious disease, developmental biology, and regenerative medicine. For more information, go to www.vizgen.com
Position Summary:
The Senior Reagent Manufacturing Engineer will play a crucial role in supporting Reagent and Consumable manufacturing for Vizgen's MERFISH spatial transcriptomics technology. Working closely with the cross functional operations and development teams, the Senior Engineer will provide advanced technical support for reagent manufacturing processes, characterize and develop manufacturing processes, conduct process verification/validation, and support new product transfers across Vizgen's portfolio of reagents and consumables.
Responsibilities:
  • Lead continuous improvement projects and programs focused on improving reagent quality, characterization, and cost reductions targets.
  • Strong technical expertise in process design, equipment selection, and process optimization for reagent product manufacturing.
  • Define and develop validation/qualification processes (IQ, OQ, TMV, CSV, PQ) and protocols, coordinate the execution of the validation/qualification protocols and write validation/qualification final reports.
  • Ensure compliance with quality systems, including material dispositions, change order implementation, nonconforming evaluations, and CAPAs.
  • Identify and implement Lean manufacturing improvements in workflows, processes, and production.
  • Support and maintain custom tools developed in house with system integrations and improvements to hardware and software.
  • Conduct root cause analysis during investigations for deviations and nonconformities.
  • Drive efforts at establishing an equipment management program.
  • Own Operations technical support during product launches and transfer of projects from development to manufacturing. Support and drive completion of reagent BOMs, routings, work instructions, batch records, standard production costs, and packaging improvements
Requirements and Qualifications:
  • Bachelor's degree in Chemical Engineering, Biochemical Engineering, or Biochemistry background 6 years of industry experience in a biotechnology or life sciences company or MS 4 years. Equivalent combination of education and experience may be accepted in lieu of any required degree.
  • Strong technical expertise in process design, equipment selection, and process optimization for reagent product manufacturing.
  • Demonstrated strong leadership, development, interpersonal, influencing and communication skills, and ability in leading, developing and managing cross-functional teams.
  • Experience working with genomics platforms and regent consumable products.
  • Excellent communication and collaboration skills to work cross-functionally with internal and external colleagues and customers from various disciplines.
  • Experience setting up business processes or programs desired but not required. This could include SPC, Equipment Management, calibration programs, etc.
  • Team player that can work with all levels of the organization.
  • Strong preference for experience in regulated environments (FDA, IVD, LDT, ISO, etc.) and owning and driving NCRs, CAPAs, and other QMS deliverables.
  • Experience working NGS reagents or consumables production facilities or chemistries.
If you aren't sure you meet every requirement but are excited about what you read here, please consider applying! We believe diversity drives innovation. Above all, we're looking for the right person with skills and talent to grow the company together all while enriching your professional and scientific experience.
We offer a competitive salary, meaningful stock ownership, 401K, health benefits, a great work environment and the opportunity to enter a high-growth startup company. We are recruiting candidates who have demonstrated leadership and excellence throughout their careers and are excited by the prospect of tackling challenging technical problems.
This position may be subject to pre-employment checks, including driving history check, drug screening and a background check for any convictions directly related to its duties and responsibilities. All pre-employment checks will comply with all applicable federal, state, and local laws.
WE ARE AN EQUAL OPPORTUNITY/AFFIRMATIVE ACTION EMPLOYER
Vizgen affords equal employment opportunity to all qualified persons regardless of race, color, religious creed, national origin, age, military status, sexual orientation, disability, genetic information, gender identity, gender expression or gender unless based upon a bona fide occupational qualification.

Job Summary

JOB TYPE

Full Time

SALARY

$104k-123k (estimate)

POST DATE

06/27/2024

EXPIRATION DATE

07/15/2024

WEBSITE

vizgen.com

HEADQUARTERS

CAMBRIDGE, MA

SIZE

<25

FOUNDED

2019

TYPE

Private

CEO

JEFFREY MOFFITT

REVENUE

<$5M

INDUSTRY

Business Services

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About Vizgen

Vizgen is a Massachusetts-based single-cell transcriptomics platform developer that offers DNA genotyping, sequencing and microarray solutions to the pharmaceutical sector.

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