Process Development Associate Job San Diego area,California USA,Research/Development

Process Development Associate

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