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Part Time Pharmaceutical Quality Control Jobs (NOW HIRING)

Antheia

Senior Quality Control Manager

Menlo Park, CA · On-site

$160K - $195K/yr

Antheia is the advanced biosynthesis company transforming pharmaceutical manufacturing and ... Part-time ( temporary roles are not eligible for Company sponsored benefits. * Comprehensive ...

Elanco

Academic Worker - Quality (QA/QC)

Elwood, KS

This role offers a comprehensive introduction to the pharmaceutical quality environment, providing ... Understand and analyze QA/QC workflows to create visual process flows and updated Standard ...

Fastenal Company

Quality Control

Winona, MN · On-site

$15/hr

Working as Part-time Quality Control, you will help facilitate the movement of product throughout our distribution center to company owned branches. You will be responsible for auditing and ...

Fastenal Company

Quality Control

Atlanta, GA · On-site

Working as Part-time Quality Control, you will help facilitate the movement of product throughout our distribution center to company owned branches. You will be responsible for auditing and ...

Fastenal Company

Quality Control

Winona, MN · On-site

$15/hr

Working as Part-time Quality Control, you will help facilitate the movement of product throughout our distribution center to company owned branches. You will be responsible for auditing and ...

MasTec

Part-Time QC Technician

Mesquite, NV

$16.50 - $21.25/hr

We are seeking a Part-Time QC Technician with at least 5 years of experience performing aggregate and concrete testing in both field and laboratory environments for a position based in Mesquite, NV

MasTec

Part-Time QC Technician

Mesquite, NV

$16.50 - $21.25/hr

We are seeking a Part-Time QC Technician with at least 5 years of experience performing aggregate and concrete testing in both field and laboratory environments for a position based in Mesquite, NV

MasTec

Part-Time QC Technician

Mesquite, NV · On-site

$16.50 - $21.25/hr

We are seeking a Part-Time QC Technician with at least 5 years of experience performing aggregate and concrete testing in both field and laboratory environments for a position based in Mesquite, NV

Q&B Foods

QC Technician (Part-Time)

Irwindale, CA · On-site

$25 - $26/hr

... a Part-time position working a maximum of 24 hours per week. The position will mostly support weekend operations and weekdays, when weekend operations are not running. QC Technician is responsible ...

Dana Safety Supply

Quality Control Technician

Wall, NJ · On-site

$25/hr

Description Elite Vehicle Solutions is seeking a Part Time Quality Control Technician. As a Quality Control Technician, you will be responsible for ensuring every vehicle that leaves our facility ...

Garver

Quality Control (QC) - Sr. Process Engineer

AR · On-site +1

As part of Garver's WBL QC Team, you will be performing quality control reviews on designs for ... This position can be full-time with benefits or part-time on your schedule. These tasks can be ...

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Part Time Pharmaceutical Quality Control information

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How much do part time pharmaceutical quality control jobs pay per hour?

As of Jun 29, 2026, the average hourly pay for part time pharmaceutical quality control in the United States is $21.48, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $24.04 per hour, depending on experience, location, and employer.

What is the difference between Part Time Pharmaceutical Quality Control vs Part Time Pharmaceutical Quality Assurance?

AspectPart Time Pharmaceutical Quality ControlPart Time Pharmaceutical Quality Assurance
ResponsibilitiesTesting raw materials, in-process, and finished products for quality and complianceDeveloping, implementing, and maintaining quality systems and procedures
Required CredentialsDegree in pharmacy, chemistry, or related field; GMP knowledgeSimilar credentials; GMP and regulatory knowledge
Work EnvironmentLaboratory settings, quality testing labsOffice and laboratory settings, documentation review
Industry UsageCommonly used in pharmaceutical manufacturing plantsUsed alongside QC, focusing on process and system quality

Part Time Pharmaceutical Quality Control focuses on testing and analyzing products to ensure quality, while Part Time Pharmaceutical Quality Assurance emphasizes establishing and maintaining quality systems. Both roles require similar credentials and are integral to pharmaceutical manufacturing, but they differ in daily tasks and focus areas.

More about Part Time Pharmaceutical Quality Control jobs
What cities are hiring for Part Time Pharmaceutical Quality Control jobs? Cities with the most Part Time Pharmaceutical Quality Control job openings:
What are the most commonly searched types of Pharmaceutical Quality Control jobs? The most popular types of Pharmaceutical Quality Control jobs are:
What job categories do people searching Part Time Pharmaceutical Quality Control jobs look for? The top searched job categories for Part Time Pharmaceutical Quality Control jobs are:
Part Time Pharmaceutical Quality Control jobs near you
Infographic showing various Part Time Pharmaceutical Quality Control job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 72% Full Time, and 27% Part Time. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $44,668 per year, or $21.5 per hour.
Senior Quality Control Manager

Senior Quality Control Manager

Antheia

Menlo Park, CA • On-site

$160K - $195K/yr

Full-time, Part-time

Medical, Dental, Vision, Retirement, PTO

Posted 23 days ago

Job description

About Antheia:
Antheia is the advanced biosynthesis company transforming pharmaceutical manufacturing and innovation for the 21st century. Antheia's commercially proven technology platform produces high-value pharmaceutical ingredients in a fraction of the time compared to legacy approaches while significantly reducing supply chain risk. The company provides its global pharmaceutical customers with a resilient, efficient supply of critical ingredients at scale, while expanding the innovation frontier for new therapeutic development. Backed by leading investors and recognized by the U.S. government as a priority technology for public health and national and economic security, Antheia is manufacturing the medicines the world needs today while enabling tomorrow's breakthrough therapeutics.
Working at Antheia:
Our cross-functional team shares a vision for the future: improved pharmaceutical supply chains that can end drug shortages and drive equitable access to essential medicines. As a team, we aim to embody a culture that celebrates diversity, prioritizes knowledge sharing, encourages exploration and ideation, challenges constructively, and supports individuals in their professional and personal journeys. At Antheia, you can expect to be inspired by the science, by your teammates, and by the opportunity we have to bring about change in the pharmaceutical industry.
We're looking for a Senior QC Manager to own quality control across our GMP and non-GMP environments, from R&D through commercial manufacturing. You'd lead a team of QC Analysts and Specialists, serve as the primary interface with our CDMO and contract lab partners, and build the systems and processes that scale with us as we grow.
What You'll Own
Team & Operations
  • Lead and develop a team of QC Analysts and Specialists: hiring, mentoring, performance, day-to-day priorities
  • Build and improve lab operations infrastructure (scheduling, resource planning, data review workflows)
  • Ensure compliance with GMP, ICH, USP/EP, and FDA/EMA standards across all applicable testing

External Partnerships
  • Serve as the primary QC point of contact for CDMOs, CROs, and contract testing labs
  • Review and approve analytical packages, protocols, and reports from third parties for regulatory compliance and data integrity
  • Drive resolution when external partners hit analytical issues or timeline delays

Technical Leadership
  • Lead method development, transfer, and validation aligned with ICH Q2(R2) and Q14
  • Own complex investigations (OOS, OOT) through root cause analysis and CAPA, with a bias toward speed and continuous improvement
  • Ensure data integrity across workflows (ALCOA+ principles, LIMS, Empower, ELNs)

Strategy
    • Develop QC strategies that align with product lifecycle and multi-site growth
    • Contribute to vendor selection, lab qualification, and capital planning
    • Support regulatory filings with accurate, complete analytical documentation

Qualifications
  • Bachelor's or Master's degree in Chemistry, Biology, or related field. Advanced degree preferred.
  • 10+ years of progressive experience in pharmaceutical QC under GMP regulations, with 5+ years in a leadership or managerial role.
  • Demonstrated experience managing QC laboratories, supervising analytical staff, and coordinating external testing activities.
  • Deep knowledge of chromatographic (HPLC, GC), spectroscopic (UV/Vis, FTIR), and wet chemistry techniques; bioanalytical familiarity is a plus.
  • Strong background in method development, validation, and lifecycle management (ICH Q2, Q14).
  • Solid experience in OOS/OOT investigations, deviation handling, and CAPA implementation.
  • In-depth understanding of FDA, EMA, and ICH regulatory expectations; prior audit experience highly desirable.
  • Familiarity with laboratory systems such as LIMS, Empower, and ELNs.
  • Excellent written and verbal communication skills with ability to lead cross-functional teams and interface with regulatory agencies and partners.

Additional Information:
  • Base salary: $160,000 - $195,000 + annual bonus + equity in a high-growth company

[1] This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities and activities may change or new ones may be assigned at any time with or without notice.
Please note that Antheia doesn't discriminate based on age, race, ethnicity, national origin, religion, gender, sexual orientation, disability, medical history, and other non-merit characteristics.
For full-time employees, Antheia offers a comprehensive total rewards package. Part-time (<30 hours per week) and temporary roles are not eligible for Company sponsored benefits.
  • Comprehensive compensation package, which includes annual bonus potential and equity opportunities
  • Paid time off, in addition to company-observed holidays
  • Excellent medical, dental, and vision insurance
  • 401(k) retirement savings plan
  • Free access to the Menlo Park Labs Gym
  • Menlo Park Labs free shuttle service to CalTrain, BART Station, and SF

Antheia is an equal opportunity employer and does not discriminate based on race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical conditions, veteran status, sexual orientation, gender (including gender identity and gender expression), taking or requesting statutorily protected leave, or any other basis protected by law. In addition, Antheia prohibits the harassment of any individual on any of the bases listed above or any other characteristics protected under federal, state, or local laws.
Legal authorization to work in the United States is required. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire..

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