QC Chemist III

Cipla; Town of Islip (NY); On-site; USD 70,000 - 90,000; Full time

Job summary

Quality Control (QC) Chemist III at Cipla in Central Islip, NY on-site role. You will perform critical QC testing and data review to ensure GMP compliance and product integrity.

The position requires strong chromatographic skills (HPLC/UPLC/GC/IC), knowledge of GLP and GDP, and experience with Empower, LabSolutions, and LIMS/TrackWise. Collaboration with cross-functional teams and audits experience are valued.

Qualifications

• Bachelor's degree in Chemistry, Pharmaceutical Sciences, or related field required.
• Master's degree preferred.
• Minimum 5 years of experience in pharmaceutical QC testing.
• Experience with chromatographic assays, impurity profiling, degradation studies, and stability evaluation.
• Knowledge of data integrity and computerized analytical systems compliance.

Responsibilities

• Perform raw materials, finished product, and stability testing in a GMP QC lab.
• Operate and troubleshoot HPLC, UPLC, GC, IC instruments.
• Ensure GLP, GDP, data integrity, and laboratory compliance.
• Maintain chromatography data systems and software (Empower, LabSolutions, Tiamo) and LIMS/TrackWise.
• Support and participate in audits (USFDA and customer audits).
• Collaborate with cross-functional teams and communicate results effectively.

Skills

HPLC

UPLC

GC

IC

Dissolution testing

FTIR

Education

Bachelor's degree in Chemistry or related field

Master's degree preferred

Tools

Empower

LabSolutions

Tiamo

LIMS

TrackWise

Karl Fischer

Job description

NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates.

Job Title: Quality Control (QC) Chemist III

FLSA Classification: Full-Time, Exempt Professional

Work Location: Central Islip, NY (Unit 3)

Work Hours: General Shift: 8:30AM – 5:00PM (may vary based on business needs)

Reports To: Quality Control Manager

Scope:

The scope (content and statements) of this job description is designed to describe the general nature and level of work as well as provide a basic understanding of the role, responsibilities, and expectations of the person assigned to perform the job. This job description is not designed to provide an exact or exhaustive list of all job duties, tasks, skills, and qualifications. The intent is to give a general scope of the knowledge, skills, and abilities needed to satisfactorily perform the essential functions of the position and provide basic performance expectations. The scope of the job may be modified with respect to the department, group, and on an individual assigned basis to a sometimes-specific testing group. Consideration of education, relevant training, and experience or a combination of all three may also result in further modification of the role.

Duties and Responsibilities

• Hands‑on experience in Raw materials, Finished Product and Stability sample testing within a pharmaceutical Quality Control laboratory.
• Strong knowledge of chromatographic techniques, including assay testing, related substances (impurity profiling), degradation product analysis, and purity determination using HPLC, UPLC, GC, and IC systems.
• Proficient in operating and troubleshooting analytical instruments such as HPLC, GC, IC, Dissolution Testers, Karl Fischer (KF), FTIR, and XRPD.
• Sound understanding of Good Laboratory Practices (GLP), Good Documentation Practices (GDP), data integrity requirements, and laboratory compliance expectations.
• Experience with chromatography data systems and laboratory software, including Empower, LabSolutions, Tiamo, and other computerized laboratory systems.
• Working knowledge of laboratory management systems such as LIMS, and quality management software such as TrackWise.
• Familiarity with testing and analytical requirements for Oral Solid Dosage (OSD) pharmaceutical products.
• Ability to perform method execution, data review, troubleshooting, and investigation activities related to laboratory testing.
• Experience in supporting and interacting with regulatory and customer audits, including USFDA,
• Strong technical understanding of pharmaceutical analytical methodologies, laboratory investigations, and compliance‑driven laboratory operations.
• Effective communication, documentation, and problem‑solving skills with the ability to work independently and within cross‑functional teams.
• Technical clarity: Added assay, impurity, degradation product, and purity testing requirements.
  

Education and Experience

• Bachelor's degree (BS or BA),Chemistry, Pharmaceutical Sciences, Pharmacy, or a related scientific field.
• Master's degree preferred
• Chemist III - minumum of 5years' experience.
• Experience in pharmaceutical QC testing with emphasis on chromatographic assays, impurity profiling, degradation studies, and stability evaluation.
• Knowledge of data integrity principles and computerized analytical systems compliance.

Working conditions

This role works in a cGMP laboratory or manufacturing environment, where personal protective equipment is required, which may include uniforms, lab coats, safety glasses, respiratory protective equipment, hearing protection, etc. Work with or aroundsolvents, powders, or other materials commonly found in a pharmaceutical laboratory or manufacturing facility is required.

The role may be assigned on a work‑shift basis, where required (Day, Evening, Night). Weekend or Holiday work may be requested or required.

Physical requirements

• Work standing or walking unassisted for 75% or greater of an 8-hour period. Unassisted lifting up-to10 kg, may be required.
• Able to wear appropriate personal protective equipment at all times, when required.
• Sitting at a desk and/or working at a computer or other "screen" 75% or greater of an 8-hour period.

Professional and Behavioral Competencies

• Must be willing to work in a pharmaceutical packaging setting.
• 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
• No employment sponsorship or work visas.

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.

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.