Microbiology Jobs at Lupin Pharmaceuticals USA
The pharmaceutical industry continues to create exciting Microbiology Jobs for professionals passionate about quality, compliance, and healthcare innovation. Lupin Pharmaceuticals Careers is offering an excellent opportunity for a Quality Assurance Associate in Coral Springs, Florida. This job in the USA provides hands-on experience in GMP compliance, pharmaceutical manufacturing quality systems, and regulatory processes. For candidates seeking a Job opportunity for life science graduates, this role offers a chance to work in a dynamic pharmaceutical environment while contributing to product quality and patient safety.
About Lupin Pharmaceuticals
Lupin Pharmaceuticals Careers offer professionals the opportunity to work with one of the leading global pharmaceutical companies. Lupin operates across manufacturing, research and development, and commercial divisions with a strong focus on generic and branded medicines. The company has a growing pipeline of pharmaceutical products and focuses on therapeutic areas including women’s health and respiratory treatments. Through its R&D facilities and manufacturing sites, Lupin continues to expand its impact on global healthcare. Professionals pursuing Microbiology Jobs at Lupin contribute to maintaining high-quality pharmaceutical standards and improving patient outcomes.
Job Details:
- Job Title: Quality Assurance Associate
- Location: Coral Springs, Florida, United States
Position Overview
The Quality Assurance Associate independently performs assigned tasks with minimal supervision to ensure compliance with LIRC Quality Assurance programs, procedures, and all applicable regulatory requirements. The role supports the maintenance of quality systems and contributes to the development of new controls and procedures as part of continuous quality improvement initiatives at the site.
The position ensures that laboratory and manufacturing functions operate in full compliance with Current Good Manufacturing Practice (cGMP), regulatory requirements, and company procedures.
This role requires flexibility to work between first and second shifts, with the schedule primarily leaning toward the second shift from 3:00 p.m. to 11:00 p.m.
Key Responsibilities of a Microbiology Job
Quality Systems and Compliance
Participate in the design and development of the company’s quality systems and support continuous improvement initiatives. Ensure laboratory and manufacturing operations remain compliant with regulatory requirements and internal quality procedures.
GMP Documentation and Inspections
Issue GMP-related documents, including logbooks, notebooks, and batch records. Inspect and release cleanrooms after cleaning activities. Inspect and release GMP areas prior to manufacturing activities. Conduct inspections of incoming materials, in-process materials, and finished products.
Documentation Review and Audits
Provide support in the review of cGMP documentation such as specifications, standard operating procedures, test methods, and batch records. Support internal and third-party audits at the LIR site.
Training and Cross-Functional Collaboration
Facilitate quality-related training and mentoring when required. Collaborate with cross-functional departments, including Operations, Product Development, Quality Control, Engineering and Facilities, Manufacturing, and Supply Chain, to ensure continuous compliance. Support employee training programs.
Quality Records and Investigations
Manage QA retain samples and maintain archival records of GMP documentation. Assist with documentation of investigations and root cause analyses. Perform additional quality assurance duties as assigned.
Education
A bachelor’s degree in Biology, Microbiology, or a related field is preferred.
Experience
- Minimum of 1–3 years of experience in a U.S. Food and Drug Administration-regulated or pharmaceutical/medical device manufacturing environment.
- Thorough knowledge of cGMP regulations applicable to drug and medical device manufacturing.
- Experience working with laboratory operations, manufacturing processes, and quality assurance systems.
Skills and Competencies for a Microbiology Job
- Ability to enforce adherence to internal quality policies, procedures, and cGMP requirements.
- Ability to collaborate effectively with diverse departments and teams.
- Strong interpersonal and teamwork skills.
- Ability to clearly communicate regulatory requirements to team members.
- Strong written and verbal communication skills in English.
- Availability to work second shift as required.
