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Biopharmaceutical Manufacturing Associate Jobs in San Ramon, CA

Cytokinetics

Senior Scientist I

South San Francisco, CA · On-site

$162K - $189K/yr

Cytokinetics is a specialty cardiovascular biopharmaceutical company, building on its over 25 years ... Design and execute robust and scalable manufacturing routes and processes for small molecule drug ...

Trial Library

Patient Navigator

San Francisco, CA · On-site

$68K - $102K/yr

In collaboration with biopharmaceutical manufacturers, payers, and health systems, Trial Library ... Bachelor of Science in Nursing (BSN), Associate Degree in Nursing (ADN), or equivalent nursing ...

Trial Library

Patient Navigator

San Francisco, CA · Hybrid

$68K - $102K/yr

In collaboration with biopharmaceutical manufacturers, payers, and health systems, Trial Library ... Bachelor of Science in Nursing (BSN), Associate Degree in Nursing (ADN), or equivalent nursing ...

Trial Library

Patient Navigator

San Francisco, CA · On-site

$68K - $102K/yr

In collaboration with biopharmaceutical manufacturers, payers, and health systems, Trial Library ... Bachelor of Science in Nursing (BSN), Associate Degree in Nursing (ADN), or equivalent nursing ...

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Biopharmaceutical Manufacturing Associate information

See San Ramon, CA salary details

$20

$30

$44

How much do biopharmaceutical manufacturing associate jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for biopharmaceutical manufacturing associate in San Ramon, CA is $30.31, according to ZipRecruiter salary data. Most workers in this role earn between $25.77 and $35.48 per hour, depending on experience, location, and employer.

What is the difference between Biopharmaceutical Manufacturing Associate vs Quality Control Technician?

AspectBiopharmaceutical Manufacturing AssociateQuality Control Technician
Primary RoleSupports production processes, prepares materials, and ensures manufacturing runs smoothlyPerforms testing and inspection of products to ensure quality standards
Required SkillsKnowledge of GMP, aseptic techniques, and manufacturing proceduresLaboratory skills, attention to detail, knowledge of testing methods
Work EnvironmentCleanrooms, manufacturing floors, production facilitiesLaboratories, testing labs, quality control areas
CertificationsGMP training, sometimes cGMP certificationLab safety, GMP, and quality assurance training

The Biopharmaceutical Manufacturing Associate focuses on supporting the production process in manufacturing environments, while the Quality Control Technician specializes in testing and verifying product quality. Both roles require GMP knowledge and work in regulated settings, but their daily tasks and skill sets differ significantly.

What are some common challenges faced by biopharmaceutical manufacturing associates, and how can they be addressed?

Biopharmaceutical Manufacturing Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP) and troubleshooting equipment malfunctions under tight production schedules. To address these challenges, associates are trained extensively on standard operating procedures and cross-functional communication to quickly resolve issues. Teamwork and attention to detail are essential, as the role frequently involves collaborating with quality assurance, engineering, and process development teams to ensure product safety and compliance. Continuous learning and proactive problem-solving are key to success in this dynamic environment.

What is a biopharmaceutical manufacturing associate?

As a biopharmaceutical manufacturing associate, your primary responsibilities are to prepare equipment and materials for the production of biopharmaceutical products. Your duties include moving the product, supplies, and inventory to support the manufacturing process and operating devices like autoclaves and washers. You monitor the production and operations, make adjustments to increase efficiency, and ensure that you are meeting all safety regulations. You work with downstream and upstream processes to control quality. You are also in charge of preparing reports and reviewing GMP documents to ensure compliance with laws and industry regulations.

What are the key skills and qualifications needed to thrive as a biopharmaceutical manufacturing associate?

To thrive as a Biopharmaceutical Manufacturing Associate, you need a solid background in life sciences or engineering, with knowledge of GMP (Good Manufacturing Practices) and often a relevant bachelor’s degree or associate’s certification. Familiarity with bioprocessing equipment, automation systems like SCADA, and quality control tools is essential. Attention to detail, teamwork, and strong communication skills are crucial soft skills for this role. These competencies ensure the safe, accurate, and compliant production of high-quality biopharmaceutical products.

What does a biopharmaceutical manufacturing associate do?

A Biopharmaceutical Manufacturing Associate is responsible for producing biopharmaceutical products such as vaccines, antibodies, or therapeutic proteins under strict regulatory guidelines. Their tasks typically include preparing equipment, monitoring production processes, maintaining sterile environments, and ensuring that all procedures adhere to Good Manufacturing Practices (GMP). They may also be involved in quality control, documentation, and troubleshooting equipment issues. This role is crucial for ensuring the safety, efficacy, and quality of biopharmaceutical products.
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Biopharmaceutical Manufacturing Associate jobs near you
Infographic showing various Biopharmaceutical Manufacturing Associate job openings in San Ramon, CA as of August 2026, with employment types broken down into 1% As Needed, 67% Full Time, 29% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $63,041 per year, or $30.3 per hour.

Associate Consultant (Commercial)

Red Nucleus

San Francisco, CA • On-site

Full-time

Retirement, PTO

Re-posted 9 days ago

Job description

Red Nucleus is hiring an Associate Consultant/ Consultant to join our global Commercial team! This is a hybrid role based out of one of our SF Bay area location.
Our purpose is advancing knowledge to improve lives. We succeed by being the premier provider of strategic learning and development, scientific advisory services (commercial, market access, medical affairs), and medical communications solutions for the life sciences industry. Our global team is composed of nearly 1,000 full-time employees whose commitment to creativity, quality, and on-time delivery is unrivaled in our space.
At Red Nucleus, we believe in providing a rich working environment that pushes us to innovate in ways that engages our employees to be their best selves. Our culture is about meaningful work, a true sense of community, and fun. We love to celebrate our people and we are proud to have been Internationally recognized as a "Great Place to Work".
How you will contribute
In this position, you will be working with our Commercial Consulting team. For more information about our commercial team, please visit Commercial | Red Nucleus.
As a Commercial Consultant (Senior Analyst, Associate Consultant, Consultant, and Senior Consultant roles also available, depending on experience and fit) at Red Nucleus, you will be at the center of a successful global consulting organization, assisting clients including biopharmaceutical and generic manufacturers, device and diagnostic companies, and financial, legal and investment firms - to maximize commercial success through advanced strategic problem solving, market research, analytics, project planning, and client interactions.
Key Responsibilities include:
  • Manage project capabilities and proposal development by working with the project team to provide relevant secondary and primary research; identify gaps in information
  • Bring structure to vaguely defined problems, pragmatically scope problem solving approach, and manage execution and effectively delegate
  • Manage up and down to secure timely and appropriate input
  • Structure and review deliverables
  • Ensure excellent internal team communication
  • Directly apply senior feedback in creation of materials and deliverables
  • Capture key takeaways from client and internal discussions, external stakeholder discussions
  • Conduct primary research interviews and extract insights for team discussion strategic recommendations
  • Prepare project deliverables for senior review in timely manner and in accordance with highest quality standards

About You
  • 2-3 years of direct and relevant experience in the pharmaceutical or biotech arena (Industry or life sciences consulting). Progressively more experience required for Consultant and Senior Consultant
  • Ability to work in a highly fluid, interactive, demanding, matrixed client environment and build strong, successful business partnerships
  • Depending on role fit (Senior Analyst, Associate Consultant, Consultant or Senior Consultant), progressively broader and deeper understanding of, and direct experience with, relevant healthcare market dynamics across a range of therapy areas
  • Strong critical thinking skills
  • Solid knowledge of healthcare market dynamics in major markets (US, EU5, Japan) as well as familiarity with patient, physician, and payer relationships
  • Experience working with commercial leaders in New Product Planning (NPP), marketing, commercial analytics, and/or sales functions
  • Illustrative project types may include: commercial opportunity assessment and forecasting, go-to-market strategy, indication prioritization, product launch strategy, launch planning, franchise / brand / tactical planning, lifecycle strategy, HCP / patient segmentation, stakeholder engagement strategy
  • Solid understanding of relevant disease background and product dynamics
  • Candidates may have emerging areas of specific expertise (content or project type)
  • Demonstrated ability to think and plan strategically, identify strategic options and trade-offs, effectively communicate business impact and strategic recommendations
  • Proficient at Microsoft Office applications, e.g., PowerPoint, Word, Excel

What You Will Enjoy at Red Nucleus
  • Competitive pay, incentives, retirement, and income security programs
  • Comprehensive benefits and wellness programs focused on healthy lifestyles
  • Generous paid time off, employee assistance programs and flexible work arrangements
  • Performance driven environment including professional development and transfer opportunities
  • People first culture fostering self expression, diversity, and a growth mindset
  • Celebrations! We love to celebrate service anniversaries, holidays, diversity and inclusion events, project milestones and anything else that is meaningful to our employees
  • Support of the community organizations you are passionate about
  • Ongoing programs and events designed to bring our global team together

Diversity, equity and inclusion are valued at Red Nucleus and we believe we have a shared responsibility to provide equal opportunity and foster an inclusive spirit. We do not discriminate on the basis of race, color, national origin, religion, caste, sexual orientation, gender, age, marital status, veteran status, or disability status.
To learn more about working at Red Nucleus, please visit Careers | Red Nucleus.
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