Quality Assurance Jobs at Lupin Pharmaceuticals | Apply Now
Step into a rewarding pathway in the pharmaceutical industry with one of the most sought-after quality assurance jobs in the U.S. Lupin Pharmaceuticals is expanding its team, offering life science graduates the opportunity to contribute to innovation, compliance, and global patient impact. This role is ideal for professionals seeking growth, stability, and a mission-driven environment within the life sciences sector.
About the Company
Lupin Pharmaceuticals is a global pharmaceutical leader with cutting-edge R&D, advanced manufacturing, and a strong commitment to patient care. With operations across the U.S., including Coral Springs and Somerset, Lupin drives innovation in generics, branded products, and women’s health while fostering a collaborative and people-centric work culture.
Job Details:
- Job Title: Quality Assurance Associate
- Location: Coral Springs, FL
Role Summary
The Quality Assurance Associate performs QA tasks with minimal supervision, ensuring compliance with LIRC Quality Assurance programs, procedures, and all applicable regulations. The role supports the maintenance and continual improvement of Quality Systems and ensures that Laboratory and Manufacturing operations comply with cGMPs, regulatory standards, internal procedures, and continuous improvement initiatives.
Essential Duties and Responsibilities
- Participate in the design, development, and continuous improvement of Lupin’s Quality Systems.
- Issue GMP documents (logbooks, notebooks, batch records, etc.).
- Release cleanrooms following cleaning activities.
- Inspect and release GMP areas prior to manufacturing activities.
- Inspect incoming materials, in-process materials, and finished products.
- Support review of cGMP documentation (specifications, SOPs/test methods, batch records).
- Support internal audits and third-party audits at the LIR site.
- Facilitate quality-related training and mentoring as needed.
- Partner with Operations, Product Development, QC, Engineering & Facilities, Manufacturing, and Supply Chain to ensure ongoing site compliance.
- Support training program activities.
- Manage QA retain samples and GMP document archival.
- Support documentation of investigations and root-cause analyses.
- Perform additional QA duties as assigned.
Qualifications for Quality Assurance Jobs
Education & Experience
- Bachelor’s degree in Biology, Microbiology, or related field preferred.
- 1–3 years of experience in an FDA-regulated or pharmaceutical/medical device manufacturing environment.
- Thorough knowledge of cGMP regulations for drugs and medical devices required.
- Experience supporting laboratory, manufacturing, and GMP QA functions required.
Skills & Competencies
- Ability to enforce adherence to quality policies, procedures, and cGMP.
- Strong ability to collaborate with diverse departments and personnel.
- Team-oriented with excellent interpersonal skills.
- Clear and effective communication of regulatory requirements.
- Strong written and verbal communication skills.
- Ability to work second shift.
Physical Requirements for Quality Assurance Jobs
- Standing, walking, sitting, using hands/fingers, reaching, talking, and hearing.
- Occasional bending, kneeling, crouching, stooping, or crawling.
- Ability to lift up to 15 pounds occasionally.
- Work is generally performed in an office environment.
