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Assistant Pharmaceutical Quality Control Jobs (NOW HIRING)

Antheia

Senior Quality Control Manager

Menlo Park, CA

$160K - $195K/yr

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 ...

Alexza

Lead QC Analyst, QC Operations

Fremont, CA · On-site

$121K/yr

Bachelor's Degree in science or related field * 8+ years relevant experience in a cGMP pharmaceutical QC environment or 5+ years with a Master's degree Physical Requirements * Prolonged periods of ...

Cipla

QC Chemist II - DPI

Hauppauge, NY

$86K - $95K/yr

Job Title QC Chemist II Organization Name InvaGen Pharmaceuticals Location7 Oser Ave, Hauppauge, NY 11788 Employment Type (Hourly/ Full Time) Full-Time - Salary/Exempt Benefits In addition to a ...

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How much do assistant pharmaceutical quality control jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for assistant pharmaceutical quality control in the United States is $22.84, according to ZipRecruiter salary data. Most workers in this role earn between $16.35 and $23.08 per hour, depending on experience, location, and employer.

Which is higher position, QA or QC?

In pharmaceutical quality control, QA (Quality Assurance) is a higher position than QC (Quality Control). QA oversees the entire quality management system, including audits and process improvements, while QC focuses on testing and inspecting products. QA roles typically involve more strategic responsibilities and require broader knowledge of regulations and standards.

What are some common challenges faced by Assistant Pharmaceutical Quality Control professionals, and how can they be addressed?

Assistant Pharmaceutical Quality Control professionals often encounter challenges such as staying compliant with evolving regulatory standards, managing time during multiple simultaneous testing procedures, and maintaining meticulous documentation. To address these, it's important to stay up-to-date with the latest regulatory requirements through ongoing training, develop strong organizational skills, and maintain open communication with colleagues and supervisors. Proactively seeking feedback and participating in regular team meetings can also help ensure consistency and accuracy in laboratory processes.

Is QC a hard job?

Quality Control (QC) roles in the pharmaceutical industry can be challenging due to the need for precision, attention to detail, and adherence to strict regulatory standards. The job often involves working with complex equipment, performing detailed testing, and maintaining accurate documentation, which requires technical skills and focus. While some find it rewarding, it can be demanding depending on workload and regulatory compliance requirements.

What is the difference between Assistant Pharmaceutical Quality Control vs Laboratory Technician in the pharmaceutical industry?

AspectAssistant Pharmaceutical Quality ControlLaboratory Technician
CredentialsDiploma or Bachelor's in Pharmacy, Chemistry, or related fieldDiploma or Associate degree in Laboratory Technology or related field
Work EnvironmentQuality control labs, manufacturing sitesResearch labs, quality testing labs
Employer & Industry UsagePharmaceutical companies, biotech firmsPharmaceutical, biotech, and research organizations
Common Search & ComparisonYesYes

The Assistant Pharmaceutical Quality Control and Laboratory Technician roles both work in laboratory settings within the pharmaceutical industry. While they share similar educational backgrounds and work environments, the Assistant Pharmaceutical Quality Control typically focuses more on supporting quality assurance processes, documentation, and compliance, whereas Laboratory Technicians often handle routine testing and sample analysis. Both roles are essential for ensuring product safety and quality, but their specific responsibilities and focus areas differ slightly.

What are Assistant Pharmaceutical Quality Control professionals?

Assistant Pharmaceutical Quality Control professionals support the quality assurance processes in pharmaceutical manufacturing. They help conduct tests, inspect products, and ensure that medications comply with regulatory standards and company specifications. Their work involves preparing samples, maintaining laboratory equipment, and documenting results. By assisting senior quality control staff, they play a crucial role in maintaining the safety and efficacy of pharmaceutical products before they reach patients.

What are the key skills and qualifications needed to thrive as an Assistant Pharmaceutical Quality Control, and why are they important?

To thrive as an Assistant Pharmaceutical Quality Control, you need a solid background in chemistry, biology, or pharmacy, typically supported by a relevant degree or diploma. Familiarity with laboratory instruments, Good Manufacturing Practices (GMP), and quality management systems is essential, along with experience in analytical techniques such as HPLC or GC. Attention to detail, strong organizational skills, and effective communication are vital soft skills for ensuring accuracy and compliance. These skills are crucial to maintain product safety, regulatory adherence, and overall quality in pharmaceutical manufacturing.
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Assistant Pharmaceutical Quality Control jobs near you
Lead QC Analyst, QC Operations

Lead QC Analyst, QC Operations

Alexza Pharmaceuticals

Fremont, CA • On-site

$121K/yr

Full-time

Posted 12 days ago

Job description

Job Summary

Having wide-ranging experience, uses professional concepts and company objectives to resolve complex issues in creative and effective ways. Works on complex issues where analysis of situations or data requires an in-depth evaluation of variable factors. Exercises judgment in selecting methods, techniques and evaluation criteria for obtaining results. Proactively identifies gaps, takes ownership of problems beyond the immediate scope of assigned tasks, and drives initiatives to completion with minimal direction. Demonstrates the confidence and sound judgment to make decisions independently and to lead cross-functional efforts when required.

Responsibilities

  • Provide timely analyses to support manufacturing and stability, assuring that deadlines are met, maintaining data integrity and ensuring compliance with company SOPs and specifications
  • Independently operate, maintain and troubleshoot laboratory instrumentation and equipment in a safe working Identify and implement appropriate instrumentation or techniques. Provide training to junior analysts on instrumentation, techniques, and test methods
  • Revise and create standard operating procedures (SOPs), author and review technical Implement QC protocols and SOPs with training provided to junior analysts for execution.
  • Conduct lab investigations and independently lead the development and implementation of corrective actions and improvements
  • Function as QC SME for select test methods and equipment to support method validations, serve as point of contact for service providers during routine PM/CAL and repair of equipment
  • Uphold QC compliance by supporting QC document revisions, data review, laboratory housekeeping, equipment PM/CAL review, equipment and supplier assessments, as needed
  • Take initiative to identify process gaps, propose solutions, and drive improvements proactively - without waiting to be directed - escalating risks and decisions appropriately while maintaining accountability for outcomes
  • Other duties as assigned

Skills required

  • Demonstrated ability to work independently and exercise sound judgment; self-directed, takes initiative, and is comfortable owning decisions and outcomes without close supervision
  • Well-organized, capable of multi-tasking, strong interpersonal skills in order to collaborate with individuals in a matrix environment
  • Expertise in performing relevant analytical techniques (HPLC, GC, FTIR).
  • Extensive experience with EMPOWER with excellent data analysis skills and attention to detail and interpretation of results
  • Excellent written, oral communication skills, and experience with computer software such as WORD, EXCEL,
  • Excellent knowledge of method validation, transfer requirements, and laboratory investigations
  • Proven track record of leading projects or initiatives, with the confidence to set priorities, rally stakeholders, and see work through from conception to completion

Education and experience

  • Bachelor's Degree in science or related field
  • 8+ years relevant experience in a cGMP pharmaceutical QC environment or 5+ years with a Master's degree

 Physical Requirements

  • Prolonged periods of sitting at a desk and working on a computer
  • Potentially prolonged periods standing
  • Must be able to lift up to 15 pounds at times
  • Must be willing to travel

Compensation

The base salary for this role starts at $121,000. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, and relevant education or training. Our compensation package also includes diverse health and other benefits and an annual target bonus for full-time positions.

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