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Manager Program Biotech Jobs in California (NOW HIRING)

PSC Biotech

CQV Engineer

Los Angeles, CA

$85K - $100K/yr

PSC Biotech provides the life sciences with essential services to ensure that health care products ... Experience with validation lifecycle management and risk-based approaches. Excellent analytical and ...

IQVIA

CRA 1, IQVIA Biotech

San Francisco, CA · On-site

$71K - $119K/yr

The ability to manage multiple tasks, prioritize effectively, and work independently while ... training program considered. * Basic knowledge of clinical research regulations (GCP/ICH)

IQVIA

CRA 1, IQVIA Biotech

San Francisco, CA · On-site

$71K - $119K/yr

The ability to manage multiple tasks, prioritize effectively, and work independently while ... training program considered. * Basic knowledge of clinical research regulations (GCP/ICH)

IQVIA

CRA 1, IQVIA Biotech

Carlsbad, CA · On-site

$71K - $119K/yr

The ability to manage multiple tasks, prioritize effectively, and work independently while ... training program considered. * Basic knowledge of clinical research regulations (GCP/ICH)

PSC Biotech

CQV Engineer

Los Angeles, CA

$85K - $100K/yr

PSC Biotech provides the life sciences with essential services to ensure that health care products ... Experience with validation lifecycle management and risk-based approaches. * Excellent analytical ...

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All JobsManager Program Biotech JobsManager Program Biotech Jobs in California

Manager Program Biotech information

What is the difference between Manager Program Biotech vs Project Coordinator Biotech?

AspectManager Program BiotechProject Coordinator Biotech
Required CredentialsBachelor's/Master's in Life Sciences, Project Management certification often preferredBachelor's in Life Sciences or related field, PMP or similar certification beneficial
Work EnvironmentOversees multiple projects, manages teams, strategic planningSupports project teams, coordinates activities, tracks project progress
Employer & Industry UsageBiotech companies, pharmaceutical firms, research organizationsBiotech firms, research labs, clinical trial organizations

The Manager Program Biotech typically holds a higher level of responsibility, overseeing multiple projects and managing teams, whereas the Project Coordinator Biotech focuses on supporting project execution and coordination. Both roles require similar educational backgrounds and certifications, but differ in scope and leadership responsibilities.

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

To thrive as a Manager Program Biotech, you need a strong background in life sciences, project management experience, and typically an advanced degree such as an MS or PhD in biotechnology or a related field. Familiarity with project management software, regulatory compliance systems, and knowledge of drug development processes are essential. Outstanding leadership, communication, and problem-solving skills set exceptional candidates apart in this role. These competencies ensure effective coordination of complex projects, regulatory adherence, and successful cross-functional team management in a rapidly evolving industry.

What are some typical challenges faced by a Manager Program in the biotech industry, and how can they be addressed?

A Manager Program in biotech often encounters challenges such as coordinating multidisciplinary teams, managing complex project timelines, and navigating shifting regulatory requirements. Effective communication and proactive risk management are crucial to address these issues. Building strong relationships with stakeholders and fostering a collaborative team environment can also help ensure project milestones are met while maintaining compliance with industry standards.

What does a Manager Program Biotech do?

A Manager Program Biotech oversees and coordinates biotechnology projects within an organization. They are responsible for planning, executing, and monitoring projects to ensure they meet scientific, regulatory, and business objectives. This role involves leading cross-functional teams, managing budgets and timelines, and communicating progress to stakeholders. Managers in this position often work closely with research scientists, regulatory affairs, and business development teams to bring biotech products from concept to market.
What cities in California are hiring for Manager Program Biotech jobs? Cities in California with the most Manager Program Biotech job openings:
Manager Program Biotech jobs near you
Manufacturing Associate - Biotech

Manufacturing Associate - Biotech

TekWissen LLC

Vacaville, CA • On-site

$25 - $27.50/hr

Temporary

Posted 5 days ago

Job description

Overview:  
  
TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide.   Our client is a leading biotechnology company that combines technological insight with world-class manufacturing, scientific expertise, and process excellence and helps their customers to deliver new and innovative medicines that help treat a wide range of diseases. Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom manufacturing, Biotechnology, Life science ingredients, Nutrition, Microbial Control, Agriculture, Materials Science, Personal Care, and cell and gene therapy.  
  
Job Title:     Manufacturing Associate - Biotech 
Location:     Vacaville, CA, 95688 
Duration:     12 Months    
Job Type:    Temporary Assignment 
Work Type: Onsite 
Pay Rate:     First Shift - $25 per hour
                      Night Shift: $27.50 per hour
 
Shifts Pattern
  • 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.
Responsibilities
  • 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.
Required Skills / Qualifications
  • High School Diploma or equivalent (AS/BS in a science-related discipline preferred).
  • 0–3 years’ experience (prior manufacturing experience preferred).
  • Basic understanding of cGMP compliance (to be attained during training).
  • Knowledge of good documentation practices (GDPs).
  • Ability to perform laboratory techniques (pH, conductivity, sampling).
  • Demonstrated aseptic technique in handling materials.
  • Proven logic and decision-making abilities.
  • Strong critical thinking skills.
TekWissen® Group is an equal opportunity employer supporting workforce diversity.

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Our global footprint covers six countries: United States, Canada, Australia, India, United Kingdom and the Philippines. This allows us to work in close partnership with organizations and manage everything from global talent needs with demanding resourcing strategies, to single sites with lower recruitment volumes.

TekWissen® is an equal opportunity employer supporting workplace diversity. 

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About TekWissen

Sourced by ZipRecruiter

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Industry

Recruiting and staffing services

Company size

501 - 1,000 Employees

Headquarters location

Ann Arbor, MI, US

Year founded

2009

Social media

Twitter

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