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Program Biotech Jobs in Davis, CA (NOW HIRING)

TekWissen LLC

Strategic Projects Manager

Vacaville, CA · On-site

$45 - $50/hr

Our client is a leading biotechnology company that combines technological insight with world-class ... The Program Manager acts as the single point of contact for the customer, driving results through ...

TekWissen LLC

QC Analyst I

Vacaville, CA · On-site

$20 - $25/hr

Our client is a leading biotechnology company that combines technological expertise with world ... Onsite Summary The QC Stability Study Coordinator I is responsible for overseeing stability program ...

Orca Bio

Manager, Facilities

Sacramento, CA · On-site

$80K - $120K/yr

... biotechnology or pharmaceutical manufacturing facility. Skills : * Strong knowledge of building systems (HVAC, electrical, plumbing), maintenance and calibration programs, GMP regulatory standards ...

Orca Bio

Manager, Facilities

Sacramento, CA

$80K - $120K/yr

... biotechnology or pharmaceutical manufacturing facility. Skills : * Strong knowledge of building systems (HVAC, electrical, plumbing), maintenance and calibration programs, GMP regulatory standards ...

Orca Bio

Manager, Facilities

Sacramento, CA · On-site

... biotechnology or pharmaceutical manufacturing facility. Skills : * Strong knowledge of building systems (HVAC, electrical, plumbing), maintenance and calibration programs, GMP regulatory standards ...

Lonza

Senior Validation Engineer - CSV (OT)

Vacaville, CA · On-site

$93K - $155K/yr

Employee assistance programs * Paid Time Off The Senior Validation Engineer (Computer System ... Minimum of 5-8 years of experience in validation within the pharmaceutical, biotechnology, or ...

TAI

Project Manager

Sacramento, CA

$125K - $180K/yr

... and safety in a dynamic biotech environment. About TAI: TAI brings together engineering ... programs, manufacturing equipment, facilities, laboratories, and office buildings. * Ensures that ...

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All JobsProgram Biotech JobsProgram Biotech Jobs in Davis, CA

Program Biotech information

See Davis, CA salary details

$27K

$56.6K

$97.8K

How much do program biotech jobs pay per year?

As of Jun 10, 2026, the average yearly pay for program biotech in Davis, CA is $56,595.00, according to ZipRecruiter salary data. Most workers in this role earn between $43,200.00 and $64,300.00 per year, depending on experience, location, and employer.

What is a Program Biotech?

A Program Biotech is a professional who manages and coordinates biotechnology projects or programs within an organization. They oversee research and development activities, ensure compliance with regulations, manage budgets, and facilitate collaboration between scientists, engineers, and other stakeholders. Their role is crucial in bringing biotech innovations from concept to market by ensuring projects stay on schedule and meet organizational goals.

What is the difference between Program Biotech vs Laboratory Technician?

AspectProgram BiotechLaboratory Technician
Required CredentialsBiotech degree or certification, specialized trainingAssociate degree or certification in laboratory sciences
Work EnvironmentResearch labs, biotech companies, pharmaceutical firmsClinical, research, or industrial labs
Employer & Industry UsageBiotech firms, research institutions, pharma companiesHospitals, research labs, manufacturing plants
Common Search & ComparisonYesNo

Program Biotech professionals focus on research, development, and overseeing biotech projects, often requiring advanced degrees and specialized training. Laboratory Technicians perform routine lab tests and support research or manufacturing processes, typically with an associate degree. While both roles work in lab environments within the biotech and healthcare industries, Program Biotech roles are more research-oriented, whereas Laboratory Technicians handle day-to-day testing and sample analysis.

What are some common challenges faced by Program Biotech professionals when managing cross-functional teams?

Program Biotech professionals often coordinate projects that involve diverse teams, including research scientists, regulatory specialists, and business development staff. One key challenge is ensuring clear communication and alignment among team members with varying backgrounds and priorities. Additionally, balancing project timelines with regulatory requirements and scientific uncertainties can require strong problem-solving skills. Being proactive in facilitating collaboration and adapting to shifting project goals are essential for success in this role.

What are the key skills and qualifications needed to thrive as a Program Biotech professional, and why are they important?

To excel as a Program Biotech professional, you need a solid background in life sciences, project management, and regulatory knowledge, often supported by an advanced degree in biotechnology or a related field. Familiarity with laboratory information management systems (LIMS), project management software, and compliance frameworks like GLP or GMP is common. Strong leadership, problem-solving abilities, and effective communication are crucial soft skills for coordinating multidisciplinary teams. These skills and qualifications are essential to drive innovation, ensure regulatory compliance, and achieve successful outcomes in complex biotech projects.
What job categories do people searching Program Biotech jobs in Davis, CA look for? The top searched job categories for Program Biotech jobs in Davis, CA are:
What cities near Davis, CA are hiring for Program Biotech jobs? Cities near Davis, CA with the most Program Biotech job openings:
Program Biotech jobs near you
Manufacturing Associate - Biotech - Vacaville, CA

Manufacturing Associate - Biotech - Vacaville, CA

Unicon Pharma Inc.

Vacaville, CA • On-site

Contractor

Posted 6 days ago

Job description

Description:
Shifts and Hours schedule:
Upstream Day Shift: 6am - 7pm
Upstream Night Shift: 6pm - 7am
Downstream Day Shift: 6:30am - 7:30pm
Downstream Night Shift: 6:30pm - 7:30am

  • These roles follow a 3-4-3 shift pattern

Role Purpose:

  • The Manufacturing Associate is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions.
  • Level I associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment.
  • They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials.
  • 40% Set up, operate equipment, and monitor production processes, including clean-in-place (CIP) and steam-in-place (SIP) operations and report production in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs), review documentation as appropriate
  • 20% Attain qualification for all assigned tasks and maintain individual training plan
  • 10% Perform basic laboratory tasks, such as monitor pH, conductivity, test product samples, etc.
  • 10% Perform material movements, transfer raw materials, chemicals into, out of, across the production areas.
  • 10% Maintain facility and equipment through routine cleaning and sanitization, support 6S programs
  • 10% Administrative tasks – attending shift exchange, meetings, sending/receiving emails, participating in projects, perform other duties as assigned.
  • High School Diploma or Equivalent minimum; AS/BS preferred
  • Preferred area of study: Science related discipline
  • 0-3 years’ experience; some prior experience in a manufacturing setting preferred.
  • Proven logic and decision making abilities, critical thinking skills