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Assistant Pharmaceutical Quality Control Jobs (NOW HIRING)

QC Chemist II - DPI

Hauppauge, NY · On-site

$86K - $95K/yr

Job Title QC Chemist II Organization Name InvaGen Pharmaceuticals Location 7 Oser Ave, Hauppauge, NY 11788 Employment Type (Hourly/ Full Time) Full-Time - Salary/Exempt Benefits In addition to a ...

Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom ... Responsibilities: * Assist in managing projects and technical activities associated with method ...

The Academic Worker will assist in streamlining document management, optimizing laboratory ... This role offers a comprehensive introduction to the pharmaceutical quality environment, providing ...

QC Chemist

Baudette, MN · On-site

$48K - $52K/yr

About Us Welcome to ANI Pharmaceuticals, where we are dedicated to improving and enhancing patients ... Report discrepancies, and assist/mentor peers. 2. 25% Perform review of data collected under ...

QC Chemist

Baudette, MN · On-site

$48K - $52K/yr

About Us Welcome to ANI Pharmaceuticals, where we are dedicated to improving and enhancing patients ... Report discrepancies, and assist/mentor peers. 2. 25% Perform review of data collected under ...

Be Seen First

Company Overview Carie Boyd Pharmaceuticals is a national 503B FDA outsourcing registered facility ... Assist production to verify steps critical to quality of final product · Perform visual ...

QC Assistant

Princeton, NJ · On-site

$20 - $24/hr

Position Summary The Quality Control Assistant supports the Quality Control Lead by performing routine inspections, documenting quality results, and assisting in maintaining consistent product ...

Quality Control Analyst III

Rensselaer, NY · On-site

$23.75 - $32/hr

This role is ideal for an analytical scientist with pharmaceutical laboratory experience who enjoys ... Perform or assist with method qualifications, method transfers, and validation activities within ...

Prepare and Assist in the Writing of Procedures (Standard Operating Procedures, Equipment Operating ... Other science degrees, with experience in a pharmaceutical analytical laboratory, will be ...

Prepare and Assist in the Writing of Procedures (Standard Operating Procedures, Equipment Operating ... Other science degrees, with experience in a pharmaceutical analytical laboratory, will be ...

Quality Control Analyst

Houston, TX

$23 - $30.75/hr

Collaborating with innovative pharmacists, healthcare providers, and pharmaceutical manufacturers ... Identify and assess quality risks in processes and escalate issues as needed * Assist in trending ...

... Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following ... Quality Control Manager Summary: We are seeking a Quality Control Manager for a 6 month contract to ...

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Assistant Pharmaceutical Quality Control information

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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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QC Analyst III/IV - Environmental Monitoring

QC Analyst III/IV - Environmental Monitoring

Alkermes

Wilmington, OH • On-site

$21.50 - $28.75/hr

Full-time

Posted 14 days ago


Job description

POSITION SUMMARY

The QC Microbiology Analyst will be responsible for performing functions including environmental monitoring, utilities monitoring, and testing in a facility that manufactures sterile products and tablets in a GMP environment.

MAJOR RESPONSIBILITIES

Major Responsibilities

Percentage of time spent on each responsibility

Prepare documents such as change controls, risk assessments, SOP's,  protocols, final reports and support of discrepancies

35%

Review of risk assessments, deviations, protocols, change controls, and other technical documents from internal and external departments

20%

Perform training of manufacturing and EM personnel

15%

Perform environmental monitoring in aseptic, classified, and controlled areas (routine, batch, quarterly EM). Direct support of the manufacturing schedule will be required, which may  include over time, weekend or shift work, and holidays

10%

Perform utilities monitoring (WFI, CLST, PW, RO, CAIR, NIT, PWTR) and testing   (Endotoxin, TOC, Conductivity, Nitrates, Bioburden)

10%

Enumerate organisms for environmental monitoring and utility samples.

5%

Perform classified area walkthroughs and production observations

5%

QUALIFICATIONS

  • Technical writing skills which require minimal guidance from management

  • Ability to work hard and contribute to an enjoyable working environment

  • Ability to work safely; seek out and encourage safe practices

  • Gowning in an aseptic environment

  • Self-starter that takes initiative to perform work with minimal supervision 

  • Maintain documentation in accordance with GMP including timely recording of information

  • Pays attention to detail and ensures high quality work
  • Ability to cope with a rapidly changing work environment

  • Commitment to teamwork

  • Willingness to learn new things

  • Commitment to continuous improvement in all areas

  • Effective communication with co-workers, other departments, and management

  • Lead training on environmental monitoring, utilities, gowning, or aseptic practices 

  • Works closely with manufacturing for training, walkthroughs, and sample coordination

  • Able to come up with solutions and resolve issues 

  • Audit support as needed

  • Act as department representative in meetings 

EDUCATION:      Bachelors/Associates in Biology (or related field) or high school diploma with additional experience being substituted for a degree 

EXPERIENCE:     QC Analyst III - 6+ years of cGMP laboratory and/or Pharmaceutical Quality experience. Some college education may be substituted with additional years of relevant work experience.

QC Analyst IV - 8+ years of cGMP laboratory and/or Pharmaceutical Quality experience. Some college education may be substituted with additional years of relevant work experience.

WORKING CONDITIONS

  • The successful employee will have the ability to function in a microbiological laboratory and manufacturing environment. The employee should have no inhibitions regarding safely handling microorganisms present in the laboratory and no health conditions/allergies that would prevent them from doing so or conditions which would prevent them from aseptically gowning.
  • Aseptic gowning must be able to be maintained including an annual requalification.
  • Employee must be able to pass a vision exam prior to employment and annually thereafter.
  • The employee will be required to participate in an on call schedule for various shift, holiday, or weekend work as needed.

PHYSICAL REQUIREMENTS

  • Prolonged periods of sitting or standing.

  • Occasional periods of repetitive motion

  • Walking, lifting, pushing and pulling carts, reaching, climbing, and bending may all be required. 

  • Steel toe shoes, scrubs, safety glasses, and other PPE equipment must be worn based on job being performed. 

  • Makeup and Jewelry will not be permitted for work in classified areas or other areas as necessary

Alkermes, Inc. is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, disability, genetic information, veteran status, military status, application for military service or any other class protected by state or federal law.

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Why join Team Alkermes?

Alkermes applies its decades of deep neuroscience expertise to develop medicines designed to help people living with complex and difficult-to-treat psychiatric and neurological disorders. A global biopharmaceutical company, headquartered in Ireland with U.S. locations in Massachusetts and Ohio, we seek to make a meaningful difference in the way people manage their diseases. We have a portfolio of proprietary commercial products for the treatment of alcohol dependence, opioid dependence, schizophrenia, bipolar I disorder and narcolepsy, and a pipeline of clinical and preclinical candidates in development for various psychiatric and neurological disorders.

We are proud to have been recognized as an employer of choice by many national organizations. In 2024 and 2025, we were certified as a Great Place to Work in the U.S. and named one of Massachusetts' Top Places to Work by the Boston Globe, a Best Place to Work in Greater Cincinnati by the Cincinnati Business Courier and recognized as a Best Place to Work in BioPharma by Fortune Magazine. 

Alkermes, Inc. is an equal employment opportunity employer and does not discriminate against any qualified applicant or employee because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, gender expression and identity, disability, genetic information, veteran status, military status, application for military service or any other characteristic protected by local, state or federal law.  Alkermes also complies with all work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Alkermes is an E-Verify employer.