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Senior Manufacturing Associate Jobs in San Ramon, CA

Senior Associate

Palo Alto, CA · On-site

$100K - $185K/yr

Senior Associate: Yamaha Motor Ventures ( YMV ) exists to catalyze innovation by supporting ... Domain expertise in manufacturing, robotics or AI * Ability to synthesize several, sometimes ...

Senior HR Generalist

Stockton, CA · On-site

$69K - $90K/yr

Description: Senior HR Generalist Full-time | Permanent Salaried | $85k - $115k *We are not ... Lead full-cycle recruitment for manufacturing associates, engineering, maintenance, supply chain ...

The Senior HV Battery Technician is a hands-on technical expert responsible for the advanced ... Associate's degree in a technical field, ASE certification, or equivalent experience. * Proficiency ...

Senior HR Generalist

Stockton, CA · On-site

$69K - $90K/yr

Description Senior HR Generalist Full-time | Permanent Salaried | $85k - $115k *We are not ... Lead full-cycle recruitment for manufacturing associates, engineering, maintenance, supply chain ...

Senior HR Generalist

Stockton, CA · On-site

$69K - $90K/yr

Job Type Full-time, Temporary Description Senior HR Generalist Full-time Temporary Salaried $85k ... Lead full-cycle recruitment for manufacturing associates, engineering, maintenance, supply chain ...

... manufacturer focusing on treatment options for diseases and conditions for which there is no ... The company is looking for a Sr. QC Associate to join the team. This is an amazing opportunity to ...

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Showing results 1-20

Senior Manufacturing Associate information

See San Ramon, CA salary details

$11

$20

$43

How much do senior manufacturing associate jobs pay per hour?

As of Jul 17, 2026, the average hourly pay for senior manufacturing associate in San Ramon, CA is $20.60, according to ZipRecruiter salary data. Most workers in this role earn between $16.11 and $19.33 per hour, depending on experience, location, and employer.

What is the difference between Senior Manufacturing Associate vs Manufacturing Associate?

AspectSenior Manufacturing AssociateManufacturing Associate
CredentialsTypically requires 2+ years of experience, relevant certifications (e.g., GMP, OSHA)Entry-level or 1+ year experience, basic certifications often sufficient
ResponsibilitiesSupervising processes, troubleshooting, quality checks, mentoringPerforming manufacturing tasks, operating equipment, following procedures
Work EnvironmentManufacturing floors, quality control labs, team leadership rolesProduction lines, assembly areas, routine manufacturing tasks
Usage in IndustryUsed for experienced roles with additional responsibilitiesEntry to mid-level manufacturing roles

The main difference between a Senior Manufacturing Associate and a Manufacturing Associate lies in experience, responsibilities, and level of supervision. Senior Manufacturing Associates typically have more experience, take on supervisory or troubleshooting roles, and may mentor junior staff, whereas Manufacturing Associates focus on executing manufacturing tasks under supervision.

What does a Senior Manufacturing Associate do?

A Senior Manufacturing Associate is responsible for overseeing and executing complex manufacturing processes in industries such as pharmaceuticals, biotechnology, or electronics. They ensure that production runs smoothly and efficiently, maintaining quality standards and troubleshooting any issues that arise. Additionally, they often provide training and guidance to junior team members and help implement process improvements. Their role may also involve documentation, compliance with safety regulations, and collaborating with other departments to meet production goals.

How does a Senior Manufacturing Associate typically collaborate with cross-functional teams during production processes?

A Senior Manufacturing Associate frequently works alongside quality assurance, engineering, and supply chain teams to ensure smooth and efficient production workflows. They are often responsible for communicating production issues, facilitating process improvements, and ensuring compliance with safety and regulatory standards. This collaboration is essential for troubleshooting equipment problems, implementing new protocols, and maintaining high product quality. The role requires strong interpersonal skills and the ability to coordinate with diverse teams to meet production goals and deadlines.

What are the key skills and qualifications needed to thrive as a Senior Manufacturing Associate, and why are they important?

To thrive as a Senior Manufacturing Associate, you need in-depth knowledge of manufacturing processes, quality control, and production standards, usually supported by experience in a similar environment and relevant technical training. Familiarity with manufacturing software (such as ERP systems), lean manufacturing methodologies, and compliance certifications like GMP are typically expected. Leadership, problem-solving, and effective communication are vital soft skills for guiding teams and addressing production challenges. These skills and qualifications are crucial to ensuring efficient operations, maintaining high product quality, and driving continuous improvement on the production floor.
What job categories do people searching Senior Manufacturing Associate jobs in San Ramon, CA look for? The top searched job categories for Senior Manufacturing Associate jobs in San Ramon, CA are:
What cities near San Ramon, CA are hiring for Senior Manufacturing Associate jobs? Cities near San Ramon, CA with the most Senior Manufacturing Associate job openings:
Sr Associate, Outsourced Manufacturing

Sr Associate, Outsourced Manufacturing

Gilead

Foster City, CA

$117K - $152K/yr

Full-time

Medical, Dental, Vision, Life, PTO

Posted 11 days ago


Gilead Sciences rating

9.0

Company rating: 9.0 out of 10

Based on 8 frontline employees who took The Breakroom Quiz

6th of 74 rated pharmaceutical


Job description

At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.

Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact.

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.
Job Description

Senior Associate, Global External Manufacturing works to ensure uninterrupted supply of Gilead's clinical and commercial products

through execution of manufacturing campaigns within our global external contract manufacturing network, while ensuring compliance with cGMP, regulatory requirements, and environmental, health, and safety legislations.

This position is part of the Manufacturing Operations group within the larger Pharmaceutical Development and Manufacturing organization (PDM). This role requires collaboration with the Development, Quality, Regulatory, Analytical, Supply Chain, and Product & Portfolio Strategy organizations within PDM to ensure successful technology transfer, commercialization, launch, routine supply, and proactive management of changes across the product lifecycle.

This position will be based at the Gilead Foster City campus.

Responsibilities:

  • Responsible within Global External Manufacturing to execute the network strategy.
  • Responsible for tactical execution of the business with external manufacturing organizations, and management of supplier performance
  • Effectively collaborates with functions within and external to PDM to achieve corporate, cross functional, and departmental goals.
  • Responsible for coordination of inter- and intra-company technical transfers. Partners with Technical Development and internal Gilead manufacturing sites for successful technology transfer and validation of new or existing processes/products to the identified CMO(s)
  • Executes the regular, tactical management of CMOs to ensure Gilead's products are manufactured in accordance with the registered process and approved Master Production Record
  • Enables timely resolution of issues associated with manufacturing and/or compliance, including handling of deviations complaints, out-of-specification investigations, Material Review Board associated investigations, finished product trending, and change control
  • Fosters and facilitates continuous improvement of production and business processes to reduce cost, improve quality, increase efficiency, and ensure sustainability.
  • May represent manufacturing on one or more cross-functional Development or Commercial CMC teams with responsibility for proactively managing product strategy across the life cycle from clinical supply to commercial product launch and routine supply, and then to sunset or divestiture

Basic Qualifications:

  • BA or BS degree in science or engineering and 5+ years of progressively responsible experience in a pharmaceutical/biotech organization. OR MS or MBA degree may be substituted for 2 years of relevant experience
  • Experience in drug product manufacturing and supply chain execution and oversight in the pharmaceutical industry
  • Experience and/or working understanding and application of manufacturing principles governed by current Good Manufacturing Practices (cGMP).

Preferred Qualifications:

  • Working knowledge of worldwide regulatory requirements, including pharmaceutical ICH guidance
  • Knowledge of the contract manufacturing organization (CMO) landscape; knowledge of CMO capabilities and limitations for worldwide drug product manufacturing is a plus
  • Ability to travel internationally, including overnight up to 20% of the time is required
  • Exceptional verbal and written communication skills, including ability to interact effectively with senior management at Gilead and contract manufacturing organizations.


The salary range for this position is: $117,895.00 - $152,570.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.

For additional benefits information, visit:

https://www.gilead.com/careers/compensation-benefits-and-wellbeing

* Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.


For jobs in the United States:

Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability,genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact ApplicantAccommodations@gilead.comfor assistance.


For more information about equal employment opportunity protections, please view the'Know Your Rights' poster.

NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT
YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT


Gilead Sciences will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the legal duty to furnish information; or (d) otherwise protected by law.

Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.


Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.


For Current Gilead Employees and Contractors:

Please apply via the Internal Career Opportunities portal in Workday.


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