Process Development Associate

Position type: Onsite
Salary Range: $55,000 to $65,000

Tempo Therapeutics is a privately held, clinical-stage technology company pioneering the future of tissue engineering. The Company is leveraging its patented Microporous Annealed Particle (MAP) technology platform with a mission to harness the power of immunomodulation and material science to transform the landscape of medical technology by developing new synthetic biomaterials for use in a variety of surgical reconstruction and therapeutic regenerative applications.

To achieve this mission, we are recruiting the best talent and building a dynamic, fast paced, and collaborative environment that enables our team to do their best work and make a real impact on society.

Tempo is seeking a driven and enthusiastic individual to fill the role of Process Development Associate. This position will heavily support the company’s Product Development and Science & Innovation teams. The ideal candidate will be responsible for performing various laboratory duties including sampling, testing, and analyzing data on raw materials, in-process and final products. The successful candidate will also develop and validate analytical methods.

Key Responsibilities – Process Development Associate:

Will include but are not limited to:

  • Create, implement, and optimize production procedures, aligning with current Good Manufacturing Practices and regulatory requirements.
  • Work with the development team to scale manufacturing processes for improved yield and reduced costs.
  • Assist with maintenance and calibration of production equipment.
  • Research and implement new methods and technologies to enhance business and manufacturing operations.
  • Work closely with R&D to develop processes for new products or formulation candidates.
  • Support technology transfer and required validation activities at contract manufacturing organizations.
  • Present data and reports on project status during group meetings
  • Interface with various departments and vendors to ensure processes and designs are compatible for new product technology transfer and to establish future process and equipment automation technology.
  • Work effectively within a team environment while satisfying individual responsibilities and objectives.

Preferred Skills and Experience:

  • General chemistry and biology
  • Data analysis using Excel; able to apply relevant statistical techniques when performing data analysis
  • cGMP experience
  • Aseptic techniques (working in a BSC or ISO-5 hood)
  • Knowledge of Tangential Flow Filtration (TFF)
  • Experience with biochemical purification systems
  • General lab bench / wet lab
  • Knowledge of biomaterials / tissue engineering
  • Excellent oral and written communication skills
  • Working within a Quality Management System (QMS)

Basic Qualifications:

  • Bachelor’s degree in biomedical engineering/bioengineering, chemical engineering, chemistry, biology or equivalent
  • 0-2 years of relevant laboratory or industry experience
  • Self-motivated, detail-oriented and willingness to take on different work assignments

Interested? Please fill out the form below.

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