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Quality Assurance In Pharmaceutical Jobs (NOW HIRING)

Alkermes

Product Quality Lead

Waltham, MA · On-site

... Quality Assurance in support of pharmaceutical development operations. * Ability to be main point of contact and interact effectively in relation to on-site cGMP audits by external auditors.

Manpower

Quality Assurance Associate

Windsor, CO

$19.62/hr

Quality Assurance Associate Windsor, CO Pay: $19.62/hour Are you detail-oriented, quality-focused, and looking to grow your career in pharmaceutical manufacturing? We are seeking a Quality Assurance ...

New

Sourcing HR Solutions

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Pharmaceutical Quality Assurance

Sylmar, CA · On-site

$25 - $30/hr

A pharmaceutical Quality Assurance (QA) professional ensures that drug products are safe, effective ... S.) in Chemistry, Pharmacy, Biology, or a related scientific discipline. * Experience: Typically ...

Strive Pharmaceuticals Inc.

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IPQA-In process Quality Assurance

East Brunswick, NJ · On-site

$25/hr

As the In-Line Quality Assurance you play a crucial role in ensuring the quality, safety, and ... Conduct real-time inspections of pharmaceutical products at different stages of the manufacturing ...

Vrtx

QA Manager- Finished Goods Commercial

Boston, MA · On-site

Bachelor's degree in Life Sciences, Pharmacy, or a related health field. * 4+ years of experience in pharmaceutical manufacturing (Packaging and Labelling Operations preferred), quality assurance, or ...

Strive Pharmaceuticals Inc.

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IPQA-In process Quality Assurance

East Brunswick, NJ · On-site

$25/hr

As the In-Line Quality Assurance you play a crucial role in ensuring the quality, safety, and ... Conduct real-time inspections of pharmaceutical products at different stages of the manufacturing ...

Ascend Staffing

Quality Assurance

Twin Falls, ID

$20/hr

S. or higher with experience in nutraceutical, medical device or pharmaceutical cleanroom ... Quality Assurance jobs in the Twin Falls, ID area go fast! ABOUT ASCEND STAFFING Ascend Staffing ...

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Blistex Inc

Quality Assurance Specialist

Oak Brook, IL · On-site

$69K - $78K/yr

Bachelor's degree in Chemistry, Biology, or related scientific discipline with 3-5 years of applicable Quality Assurance environment preferable in the pharmaceutical OTC industry. * Master's degree ...

Astrix Inc

QA Specialist II

Vista, CA · On-site

$35 - $52/hr

Our client a leading biotech company is looking for a skilled QA Specialist to join their team in ... regulated pharmaceutical manufacturing environment. This role ensures that drug substances ...

Alkermes

Product Quality Lead

Waltham, MA

$128K - $142K/yr

... Quality Assurance in support of pharmaceutical development operations. * Ability to be main point of contact and interact effectively in relation to on-site cGMP audits by external auditors.

AMRI

Quality Assurance Specialist III

Hopkinton, MA · On-site

$92K - $114K/yr

Quality Assurance Specialist III in Hopkinton, MA Build your future at Curia, where our work has ... work experience in pharmaceutical, biotechnology, medical device, and/or cGMP FDA-regulated ...

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How much do quality assurance in pharmaceutical jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for quality assurance in pharmaceutical in the United States is $23.19, according to ZipRecruiter salary data. Most workers in this role earn between $17.55 and $24.28 per hour, depending on experience, location, and employer.

Is quality assurance a good career in the pharmaceutical industry?

Quality assurance in the pharmaceutical industry is a stable and growing career, focusing on ensuring products meet safety and regulatory standards. It often requires knowledge of Good Manufacturing Practices (GMP), quality control processes, and relevant certifications, making it a vital role for maintaining product integrity and compliance.

What are some common challenges faced by quality assurance professionals in the pharmaceutical industry, and how can they be effectively managed?

Quality Assurance (QA) professionals in the pharmaceutical industry often face challenges such as keeping up with evolving regulatory requirements, ensuring consistent documentation, and coordinating cross-functional teams during audits. Managing these challenges requires continuous training, strong attention to detail, and effective communication skills. Collaboration with other departments, such as production and regulatory affairs, is key to identifying issues early and maintaining compliance with Good Manufacturing Practices (GMP). Establishing clear quality procedures and staying proactive with process improvements also help QA professionals maintain high standards and reduce risks.

What are the key skills and qualifications needed to thrive as a quality assurance professional in the pharmaceutical industry?

A successful Quality Assurance professional in pharmaceuticals needs a solid background in life sciences or pharmacy, understanding of GMP regulations, and relevant QA experience. Familiarity with quality management systems (QMS), documentation software, and regulatory compliance tools is typically required. Attention to detail, critical thinking, and effective communication are essential soft skills for excelling in this role. These skills ensure product safety, regulatory compliance, and the consistent delivery of high-quality pharmaceutical products.

What does quality assurance do in the pharmaceutical industry?

Quality assurance professionals in the pharmaceutical industry ensure that products meet safety, quality, and regulatory standards throughout the manufacturing process. They develop and implement procedures, conduct audits, and review documentation to prevent defects and ensure compliance with Good Manufacturing Practices (GMP).

What does a quality assurance professional do in the pharmaceutical industry?

A Quality Assurance (QA) professional in the pharmaceutical industry is responsible for ensuring that all products meet established standards of quality, safety, and efficacy. They develop, maintain, and monitor procedures and systems that comply with regulatory requirements such as Good Manufacturing Practices (GMP). QA professionals conduct audits, review documentation, manage deviations, and support continuous improvement to ensure that medications are safe for patients. Their work is critical in preventing errors, ensuring product consistency, and maintaining the trust of regulatory agencies and consumers.

What is the difference between Quality Assurance In Pharmaceutical vs Quality Control In Pharmaceutical?

AspectQuality Assurance In PharmaceuticalQuality Control In Pharmaceutical
FocusProcesses, compliance, and preventing defectsTesting and inspecting products for defects
ResponsibilitiesDeveloping quality systems, audits, documentationSampling, testing, and analyzing products
CredentialsGMP certifications, quality management trainingLab certifications, analytical testing skills
Work EnvironmentOffice-based, quality departments, manufacturing sitesLaboratories, manufacturing facilities

Quality Assurance In Pharmaceutical focuses on establishing and maintaining quality systems to prevent issues, while Quality Control In Pharmaceutical emphasizes testing products to identify defects. Both roles are essential in ensuring pharmaceutical safety and compliance, but they differ in scope and daily tasks.

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What cities are hiring for Quality Assurance In Pharmaceutical jobs? Cities with the most Quality Assurance In Pharmaceutical job openings:
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Quality Assurance In Pharmaceutical jobs near you
Infographic showing various Quality Assurance In Pharmaceutical job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $48,237 per year, or $23.2 per hour.

Director, Quality Assurance

Aquestive Therapeutics

Portage, IN • On-site

Full-time

Re-posted 9 hours ago

Job description

Job Summary:
The Director of Quality Assurance is a leadership role, responsible for all aspects of the Quality Systems, Clinical Quality and Manufacturing Quality for Aquestive. The Director of Quality Assurance will work with their direct managerial reports, as well as Executive Leadership, to ensure a continued state of compliance while promoting a strong quality culture across the organization for all products, spanning early phase development to commercialization.
This position will be expected to work in a highly collaborative, cross functional team environment, and provide expert knowledge to risk identification/mitigation, strategy and execution.
Responsibilities:
  • Oversee all aspects of Quality Systems, Clinical Quality and Manufacturing Quality to assure compliance with FDA, EU, ANVISA, TGA and other international GMP requirements for all products manufactured at Aquestive (e.g., 21 CFR Part 210 + 211, EU GMP Volume 4 Part 1).
  • Provide strategic direction and leadership to ensure effectiveness of Quality Systems (e.g., CAPA, Change Management, Event Management, Supplier Quality, Internal Audit, Document Management, Risk Management, Record Review and Product Disposition, Training, Field Alert/Recall, etc.)
  • Lead and ensure execution of quality strategy for all development and manufacturing activities associated with all products manufactured by Aquestive, including external GMP contract manufacture operations or laboratories for drug substance and drug product.
  • Primary contact for all inspection interactions with all domestic and ex-US regulatory authorities.
  • Provide direction for escalated quality issues as they arise, determining the need for, and structuring communication for, further escalation to the Executive team and/or external parties.
  • Lead strategic quality to quality relationships with business partners, suppliers, external CMOs and third-party testing laboratories.
  • Ensure the company is upholding to Quality/Technical Agreements with business partners and suppliers.
  • Provides input to all functions to ensure clinical trial activities are conducted in compliance with GCP regulations and internal requirements.
  • Actively participate in the Site Leadership Team to drive continuous improvement activities and initiatives throughout Aquestive.
  • Analyze, report and present metrics where applicable to show health of system(s).
  • Lead GxP inspection strategies across all auditable areas to ensure the company is in an audit-ready status at all times.
  • Manage overall coaching, training, development and succession planning for the function.
  • Set, manage and monitor budget for Quality Assurance, in conjunction with finance.

Qualifications:
  • Minimum of Bachelor's degree required. Advanced degree in chemistry, engineering, biochemistry, or related science field desirable.
  • Minimum 7+ years of related work experience working in a regulated GxP industry in pharmaceutical manufacturing operation setting or service oriented laboratory.
  • Demonstrated ability to direct a function, oversee projects and teams. Minimum of 2 years overseeing direct reports.
  • Minimum of 2+ years working in a managerial role with direct reports.
  • Strong skillset in problem solving, strategic thinking, critical reasoning and decision making.
  • Strong interpersonal skills and verbal/written communication skills.
  • Excellent computer skills required (e.g., Microsoft Word, Excel, Access, PowerPoint, Visio).
  • Strong project management skills, strong organizational skills to maintain a high level of productivity, innovation, and priority-setting to complete assignments on time and on budget.
  • Strong business acumen surrounding pharmaceutical manufacturing.
  • Some travel required.

The above statements are intended to describe the general nature and level of the work being performed by colleagues assigned to this position. This is not intended to be an exhaustive list of all responsibilities, duties, and skills required. Aquestive reserves the right to make changes to the job description whenever necessary.
As part of Aquestive's employment process, final candidate will be required to complete a drug test and background check prior to employment commencing. Please Note: Aquestive is a drug-free workplace and has a drug free workplace policy in place.
Aquestive provides equal employment opportunities to all colleagues and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
The Company is required to provide a reasonable estimate of the salary range for this job in certain states and cities within the United States. Final determinations with respect to salary will take into account a number of factors, which may include, but not be limited to the primary work location and the chosen candidate's relevant skills, experience, and education.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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