Chemist I

Sun Pharmaceutical Industries, Inc.; New Brunswick (NJ); On-site; USD 59,000 - 66,000; Full time

Job summary

Sun Pharmaceutical Industries, Inc. is seeking a Chemist I for its Quality Control laboratory to perform analytical testing on raw materials, in-process samples, finished products, and stability samples in a cGMP environment.

This early-career role provides hands-on experience with HPLC, GC, UV/Vis, FTIR, and dissolution instruments, in a Monday–Friday day-shift setting onsite in New Jersey, with travel up to 10%.

Qualifications

• Bachelor's degree in Chemistry or related discipline required.
• Minimum 2 years of experience in analytical chemistry laboratory.
• 2 years of pharmaceutical experience highly preferred.
• English proficiency CEFR Intermediate B1+ level.
• Strong documentation and data recording practices.

Responsibilities

• Perform routine analytical testing of pharmaceutical raw materials, in-process samples, blends, finished products and stability samples.
• Document all raw data, observations and results contemporaneously in notebooks, worksheets and electronic systems; communicate findings to supervisors.
• Maintain clean, safe laboratory environment and ensure compliance with cGMP and safety procedures.

Skills

Analytical communication

Attention to detail

Multi-tasking

Education

Bachelor's degree in Chemistry

Tools

HPLC

UPLC

Gas Chromatography

UV/VIS

FTIR

Dissolution

Karl Fischer Titrator

Particle Size Analyzer

Job description

Sun Pharma is the world’s fourth largest generics company with presence in Specialty, Generics and Consumer Healthcare products. Supported by more than 40 manufacturing facilities, we provide high-quality medicines, trusted by healthcare professionals and patients, to more than 100 countries across the globe. Over the last two decades, Sun Pharma has established itself as a leading player in the generics market in the U.S., and we are rapidly ramping up our presence in the specialty branded market with a focus on dermatology, ophthalmology and onco-dermatology.

Job Summary:

Are you passionate about analytical chemistry and eager to apply your skills in a pharmaceutical environment? We are seeking a motivatedChemist Ito join our Quality Control laboratory team. In this role, you will perform analytical testing on raw materials, in-process samples, finished products, and stability samples while supporting the delivery of safe, high-quality pharmaceutical products.

This is an excellent opportunity for an early-career chemist to gain hands-on experience with industry-leading analytical instrumentation and work in a collaborative, cGMP-regulated environment.

Monday–Friday | Day ShiftPharmaceutical Analytical Laboratory | Onsite

What You’ll Do:

Analytical Testing

• Perform routine analytical testing of pharmaceutical raw materials, in-process samples, blends, finished products, and stability samples.
• Utilize a variety of analytical instruments, including:
  • HPLC / UPLC
  • Gas Chromatography (GC)
  • UV/VIS Spectroscopy
  • FTIR
  • Dissolution Apparatus
  • Particle Size Analyzer
  • Karl Fischer Titrator
• Ensure testing is completed accurately and within established timelines.

Documentation & Data Integrity

• Document all raw data, observations, and test results contemporaneously in laboratory notebooks, worksheets, and electronic systems.
• Compile analytical results and communicate findings to supervisors in a timely manner.
• Maintain complete, accurate, and audit-ready laboratory records.

Laboratory Operations

• Perform routine maintenance of laboratory equipment as required.
• Maintain a clean, organized, and safe laboratory environment.
• Follow departmental SOPs, DEA requirements, and all applicable safety procedures.
• Support continuous compliance with cGMP and data integrity standards.

This position is based in a pharmaceutical analytical laboratory and may involve exposure to:

• Laboratory chemicals and solvents
• Fumes, odors, and airborne particles
• Standard laboratory equipment and instrumentation

Appropriate PPE and safety protocols must be followed at all times.

Physical Requirements:

• Ability to stand, sit, walk, bend, stoop, kneel, crouch, and reach as needed.
• Ability to perform repetitive laboratory tasks.
• Strong visual acuity, including close vision and depth perception.
• Ability to operate laboratory and office equipment.
• Ability to lift and carry up to 50 pounds.

Travel:Up to 10%

What You Bring:

Education

• Bachelor's degree in Chemistry or a related scientific discipline required.

Technical Skills

• Familiarity with analytical instrumentation theory and practice.
• Familiarity with wet chemistry techniques.
• Working knowledge of Microsoft Office applications, including Excel.
• Understanding of laboratory documentation and data recording practices.

Professional Skills

• Excellent written and verbal communication skills.
• Strong attention to detail and organizational abilities.
• Ability to manage multiple priorities in a fast-paced laboratory environment.
• Self-motivated with a hands-on, can-do attitude.
• English proficiency at CEFR Intermediate B1+ level.

Experience:

• Minimum 2 years of experience in analytical chemistry laboratory.
• 2 years of pharmaceutical experience highly preferred.

Why Join Us?

• Gain hands-on experience with advanced analytical instrumentation.
• Work in a collaborative, quality-driven pharmaceutical environment.
• Develop expertise in regulated laboratory operations and cGMP compliance.
• Contribute directly to the quality and safety of pharmaceutical products.
• Opportunity for professional growth and advancement within the organization.

The presently-anticipated base compensation pay range for this position is $59,000 to $66,000. Actual base compensation may vary based on a number of factors, including but not limited to geographical location and experience. In addition, this position is part of the Annual Performance Bonus Plan, and may be eligible for the Long Term Incentive Plan. Employees are eligible to participate in Company employee benefit programs which include medical, dental and vision coverage; life insurance; disability insurance; 401(k) savings plan; flexible spending accounts; and the employee assistance program. Employees also receive various paid time off benefits, including vacation time and sick time.

The compensation and benefits described above are subject to the terms and conditions of any governing plans, policies, practices, agreements, or other materials or documents as in effect from time to time, including but not limited to terms and conditions regarding eligibility.If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company, or individual department/team performance, and market factors.

The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of the incumbent(s).

We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.