QA Associate III

Sun Pharmaceutical Industries Limited; New Brunswick (NJ); On-site; USD 80,000 - 120,000; Full time

Job summary

An established industry player is seeking a Quality Assurance professional to oversee critical QA processes. In this pivotal role, you will manage Trackwise records, ensure compliance with audit standards, and provide essential training to staff. With a commitment to making healthcare accessible, this role offers the chance to contribute to a company that values integrity, innovation, and community health. Join a dynamic team dedicated to excellence in the pharmaceutical industry and make a tangible impact on global health initiatives.

Benefits

Medical Benefits

Dental Benefits

Vision Benefits

Health Savings Account (HSA)

Flexible Spending Account (FSA)

Prescription Drug Coverage

Telehealth Services

Short and Long Term Disability Benefits

401k Company Match

Wellness Programs

Qualifications

• Minimum 10 years of experience in QA within the pharmaceutical industry.
• Intermediate English language proficiency required.

Responsibilities

• Manage Trackwise related records and internal audit program.
• Ensure site is audit ready for inspections at all times.

Skills

Verbal Communication Skills

Written Communication Skills

Self-starter Attitude

Hands-on Approach

Education

B.S. or equivalent degree

Tools

Microsoft Office Applications

Job description

COME WORK FOR US - INVESTING IN YOU AS A SUN PHARMA EMPLOYEE!

• Medical, Dental, Vision Benefits
• Health Savings Account (HSA), Flexible Spending Account (FSA)
• Prescription Drug Coverage
• Telehealth and Behavior Health Services
• Income Protection – Short Term and Long Term Disability Benefits
• Retirement Benefits - 401k Company Match on Day One (100% vesting immediately)
• Group Life Insurance
• Wellness Programs
• Corporate Discounts on personal services: Cellular phones, Entertainment, and Consumer Goods!

Sun Pharma Vision: Reaching People And Touching Lives Globally As A Leading Provider Of Valued Medicines

Sun Pharmaceutical Industries Ltd. (Sun Pharma) is the fourth largest specialty generic pharmaceutical company in the world with global revenues of over $4.5 billion US Dollars. Supported by more than 40 manufacturing facilities, we provide high-quality, affordable medicines, trusted by healthcare professionals and patients, to more than 100 countries across the globe including the United States. Sunology is a combination of Sun Values and Ideology and is the way of life at Sun Pharma. Sunology is Humility. Integrity. Passion. Innovation. It represents our promise to all stakeholders including patients, physicians, and employees.

Our Code of Conduct

Our Global Code of Conduct governs every aspect of our operations. Sun Pharma is a family of thousands of people, working across many countries, speaking multiple languages, and all united with one common purpose: to make good health accessible and affordable to local communities and society at large. Through active fieldwork, dedicated research teams, and in recognition of the efforts who work behind the scenes to combat illness and disease, the Sun Pharmaceutical Group helps as many people as possible to secure their right to good health. The way we work every day is important to us.

DOWNLOAD OUR CODE OF CONDUCT

Under the supervision of Manager, the following activities will be performed:

• Manage Trackwise related records.
• Review and evaluate change controls related to facility, manufacturing, and laboratory.
• Manage internal audit program/module.
• Review all manufacturing and facility related investigations and deviations.
• Ensure site is audit ready at all times for inspections.
• Provide training to manufacturing and quality employees.
• Timely closure of all TrackWise records and follow up with the responsible department.

Qualifications

• B.S. or equivalent degree.
• Minimum 10 years of experience in QA within the pharmaceutical industry.
• Working knowledge of Microsoft Office Applications.
• Demonstrated excellent verbal and written communication skills.
• A self-starter with a hands-on approach and a can-do attitude.
• The requirement for English language proficiency for this job role is Intermediate-B1+ (comparable to Global CEFR Independent B1) level based on the Common European Framework of Reference for Languages (CEFR).