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Quality Assurance In Pharmaceutical Jobs (NOW HIRING)

Cipla

QA Operations Specialist

Fall River, MA · On-site

$76K - $103K/yr

Quality Assurance Operation Specialist FLSA Classification : Professional, Exempt Work Location ... Bachelor's degree in pharmaceutical manufacturing, industrial management, or related field of study ...

Cipla

QA Operations Specialist

Fall River, MA

$76K - $103K/yr

Quality Assurance Operation Specialist FLSA Classification : Professional, Exempt Work Location ... Bachelor's degree in pharmaceutical manufacturing, industrial management, or related field of study ...

Cipla

$76K - $103K/yr

Quality Assurance Operation Specialist FLSA Classification : Professional, Exempt Work Location ... Bachelor's degree in pharmaceutical manufacturing, industrial management, or related field of study ...

Cipla

QA Inspector II - 2nd Shift

Fall River, MA · On-site

Experience in quality assurance in a cGMP pharmaceutical manufacturing operation and work environment is preferred. * Minimum of 2 years' experience in quality assurance in a cGMP pharmaceutical ...

Cipla

QA Inspector II - 2nd Shift

Fall River, MA · On-site

$26 - $33/hr

Experience in quality assurance in a cGMP pharmaceutical manufacturing operation and work environment is preferred. * Minimum of 2 years' experience in quality assurance in a cGMP pharmaceutical ...

Cipla

$26 - $33/hr

Experience in quality assurance in a cGMP pharmaceutical manufacturing operation and work environment is preferred. Minimum of 2 years' experience in quality assurance in a cGMP pharmaceutical ...

synergy

Pharmaceutical GMP QA Specialist

Dallas, TX · On-site

Pharmaceutical GMP QA Specialist Synergy is seeking a detail-oriented and experienced Pharmaceutical GMP QA Specialist to ensure compliance with Good Manufacturing Practices (GMP) in pharmaceutical ...

synergy

Pharmaceutical GMP QA Specialist

Dallas, TX · On-site

Pharmaceutical GMP QA Specialist Synergy is seeking a detail-oriented and experienced Pharmaceutical GMP QA Specialist to ensure compliance with Good Manufacturing Practices (GMP) in pharmaceutical ...

synergy

Pharmaceutical GMP QA Specialist

Dallas, TX

Pharmaceutical GMP QA Specialist Synergy is seeking a detail-oriented and experienced Pharmaceutical GMP QA Specialist to ensure compliance with Good Manufacturing Practices (GMP) in pharmaceutical ...

Cipla

Job Title: QA Operations Specialist F LSA Classification:Full-Time,Exempt/SalaryProfessional Work ... Bachelor's degree in Pharmaceutical science or Equivalent. Advanced vocational training or ...

Cipla

QA Operations Specialist

Fall River, MA · On-site

Job Title : QA Operations Specialist F LSA Classification : Full-Time, Exempt/SalaryProfessional ... Bachelor's degree in Pharmaceutical science or Equivalent. * Advanced vocational training or ...

Cipla

QA Operations Specialist

Fall River, MA

Job Title : QA Operations Specialist F LSA Classification : Full-Time, Exempt/SalaryProfessional ... Bachelor's degree in Pharmaceutical science or Equivalent. * Advanced vocational training or ...

TekWissen LLC

Quality Assurance Engineer

Tampa, FL · On-site

$25 - $35/hr

Specializing in pharmaceutical ingredients, bioscience, biopharmaceuticals, custom manufacturing ... Quality Assurance Engineer Location: Tampa, FL - 33634 Duration: 12 months Job Type: Temporary ...

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Quality Assurance In Pharmaceutical information

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

As of Jun 12, 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.

What does QA do in the pharmaceutical industry?

Quality Assurance (QA) in the pharmaceutical industry ensures that products meet safety, quality, and regulatory standards through activities like audits, documentation review, and process validation. QA professionals develop and implement quality systems, conduct inspections, and ensure compliance with Good Manufacturing Practices (GMP) to prevent defects and ensure product integrity.

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.

Is pharma QA a good career?

Pharmaceutical quality assurance (QA) is a stable and in-demand career that involves ensuring products meet safety and regulatory standards. It typically requires knowledge of Good Manufacturing Practices (GMP), attention to detail, and often certification or training in quality systems. The role offers opportunities for advancement and specialization within the pharmaceutical industry.

What are the key skills and qualifications needed to thrive as a Quality Assurance professional in the pharmaceutical industry, and why are they important?

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.

Which pays more, QA or QC?

In pharmaceutical quality assurance (QA) and quality control (QC) roles, QA positions generally offer higher salaries due to their focus on process improvement, compliance, and oversight, often requiring more experience and certifications. QC roles tend to have slightly lower pay but are essential for testing and inspection tasks. Salary differences can vary based on experience, location, and company size.

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.

What is the role of a quality assurance specialist in pharma?

A quality assurance specialist in pharma is responsible for ensuring that pharmaceutical products meet quality standards and regulatory requirements. They develop and implement quality systems, conduct audits, review documentation, and collaborate with production teams to prevent defects and ensure compliance throughout the manufacturing process.
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Quality Assurance In Pharmaceutical jobs near you

QA Operations Specialist

Cipla

Fall River, MA • On-site

$76K - $103K/yr

Full-time

Posted 22 days ago

Job description

Job Title: Quality Assurance Operation Specialist
FLSA Classification: Professional, Exempt
Work Location: Fall River, MA
Work Hours: General: 8:30AM - 5:00PM (may vary based on business needs)
Reports To: Quality Assurance Manager
Salary Range: $76,000 - $103,000
Purpose:
The QA operation specialist (MDI) position is an individual contributor role and a member of the InvaGen Pharmaceuticals Plant Quality Team.
The QA operation specialist (MDI) monitors and ensures validation and qualification of facility, utilities, equipment's, processes and ensure product quality is maintained throughout all phases of the manufacturing process in compliance with established specifications and standard operating procedures (SOPs) and provide guidance to QA associates.
Duties and Responsibilities:
The job duties for this position include but are not limited to the following:
  • Review of batch manufacturing/packaging record.
  • Review of engineering records such as temperature and humidity data calibration and PM records, pest control records and contractor related functions.
  • Review and approval of manufacturing/engineering non-conformances.
  • Review and approval of manufacturing/engineering change control, deviation investigation and CAPAs.
  • Review and approval of manufacturing/engineering validation and qualification documents.
  • Provide daily/weekly updates to shop floor and management regarding the quality highlights/concerns.
  • Create lessons learned for training as communication mechanism to shop floor personnel.
  • Perform applicable testing and prepare reports for customer complaints.
  • Identify and report any non-conformances and/or discrepancies to management if applicable.
  • Verify functionality of all the equipment and associated controls during the batch run.
  • Act as quality lead for all shop floor questions / concerns.
  • Backup for shop floor QA Associates.
  • Complete other duties or participate in project work as assigned by management.

Education and Experience
  • Advanced vocational training or education in pharmaceutical manufacturing, industrial management, or related field of study from an accredited college/university.
  • Bachelor's degree in pharmaceutical manufacturing, industrial management, or related field of study from an accredited college/university is preferred.
  • Minimum of five (5) years' experience in quality assurance in a cGMP pharmaceutical manufacturing operation and work environment.
  • Experience in MDI or combination products is preferred.
  • Minimum of five (5) years' experience in quality assurance in a cGMP pharmaceutical manufacturing operation environment.
  • Current, working knowledge of quality assurance (QA).
  • Strong knowledge and experience with analytical laboratory activities in areas such as active pharmaceutical ingredients (API), drug products, analytical development, Quality Control (QC), Good Laboratory Practices (GLP)/Good Manufacturing Practices (GMP)/Good Distribution Practices (GDP), etc.

Technical Knowledge and Computer Systems Skills
  • Understanding of machines used in pharmaceutical manufacturing.
  • Must be able to influence decision making and facilitate completion of work towards the achievement of the business plan and goals.
  • Effective interpersonal relationship skills and the ability to work in a team environment.
  • Capable of conducting troubleshooting, investigations and root cause identification and analysis.
  • Capable of handling and participating in compliance and regulatory audits at the local and federal levels.
  • Must be proficient in computer skills and software applications such as Microsoft Office tools.
  • Experience using SAP business system and applications is a plus.
  • Experience in Inhalation products (MDI) or Combination products is a plus.
  • Ability to work in a fast-paced, dynamic environment within a manufacturing operation setting.
  • Must be able to communicate clearly and concisely across all levels of the organization and possess a solid command of English language communication skills verbally, written, and interpersonally.
  • Must possess strong documentation and technical writing skills, and able to apply relevant scientific principles and practices.
  • Must be able to work under minimal supervision and able to work independently and in a team environment.
  • Must be able to exercise appropriate professional judgment on matters of significance.

Professional and Behavioral Competencies
  • Proficient user of personal computer hardware and software applications such as Microsoft Office tools, SAP, and other business applications.
  • Must be able to influence decision-making and facilitate completion of work toward the achievement of the business plan and goals.
  • Effective interpersonal relationship skills and the ability to work in a team environment.
  • Proficiency in the English language to include usage, spelling, grammar, and punctuation.
  • Must have current Good Manufacturing Practices (cGMP) knowledge.
  • Must be a self-starter and demonstrate initiative with seeking additional training or direction as needed.
  • Must have strong organization and leadership skills (written, verbal, and presentation).
  • Must be detail-oriented with the ability to multitask and prioritize tasks with strict deadlines.

Work Schedule and Other Position Information:
  • Work standing or walking unassisted for 75% or greater of an 8-hour period. Unassisted lifting up-to 10 kg, may be required.
  • Able to always wear appropriate personal protective equipment, when required.
  • Sitting at a desk and/or working at a computer or other "screen" 75% or greater of an 8-hour period.
  • Must be willing to work in pharmaceutical manufacturing and packaging quality assurance.
  • Must be willing and able to work any assigned shift ranging from first or second shift. Work schedule may be Monday to Friday.
  • Must be willing to work some weekends based on business needs as required by management.
  • No remote work available.

GLOBAL COMPANY
Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world.
Cipla employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world.
CIPLA NEW YORK (INVAGEN PHARMACEUTICALS, INC.)
About InvaGen Pharmaceuticals, a Cipla subsidiary InvaGen Pharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. As of February 18, 2016, InvaGen Pharmaceuticals, Inc. operates as a subsidiary of Cipla (EU) Limited.
EEO Statement
Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, genetic information, disability, or protected veteran status.

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