Chemist II

SUN PHARMA; New Brunswick (NJ); On-site; USD 69,000 - 77,000; Full time

Job summary

SUN PHARMA is seeking a detail‑driven Chemist II to join the analytical laboratory team in New Jersey. You will perform routine analytical testing of materials and products, operate key instrumentation, and ensure data integrity in a cGMP environment.

The role emphasizes method development support, regulatory compliance, and accurate reporting. You will report results to supervisors and maintain clean, compliant laboratory records in a fast‑paced setting.

Qualifications

• Bachelor’s degree in Chemistry or related field; Master’s preferred.
• Minimum 4 years in a pharmaceutical analytical lab; or 3 years with a Master’s.
• Experience with wet chemistry and USP monographs.

Responsibilities

• Perform routine analytical testing of raw materials, in-process samples, blends, finished products, and stability samples.
• Operate and maintain analytical instrumentation: HPLC/UPLC/GC, dissolution, UV/Vis, FTIR, particle size analyzer, Karl Fischer titrator.
• Maintain accurate documentation of raw data, observations, and results.
• Assist method development, transfer, and validation activities.
• Ensure compliance with cGMP, ICH, FDA requirements and internal SOPs.
• Work Monday–Friday, 8:30 AM – 5:00 PM; travel up to 10%.

Skills

Excel

GMP/ICH/FDA knowledge

Analytical thinking

Communication skills

CEFR B1+ English

Education

Bachelor's degree in Chemistry or related field

Master’s degree preferred

Tools

HPLC

UPLC

GC

Dissolution apparatus

UV/Vis

FTIR

Karl Fischer titrator

Particle size analyzer

Job description

Job Summary

We are seeking a detail‑driven and technically skilled Chemist II to join our analytical laboratory team. In this role, you will perform critical testing of drug substances and products, ensuring quality, accuracy, and compliance with regulatory standards.

This is an excellent opportunity for an experienced chemist who enjoys hands‑on laboratory work, analytical problem‑solving, and contributing to high‑quality pharmaceutical products in a cGMP‑regulated environment.

What You’ll Do:

Analytical Testing & Execution

• Perform routine analytical testing of raw materials, in‑process samples, blends, finished products, and stability samples.
• Operate and maintain analytical instrumentation, including:
• HPLC / UPLC / GC
• Dissolution apparatus
• UV/VIS, FTIR
• Particle size analyzer
• Karl Fischer titrator
• Ensure timely execution of testing and accurate reporting of results.

Data Integrity & Documentation

• Maintain concurrent and accurate documentation of raw data, observations, and test results.
• Compile and report analytical results to supervisors in a timely manner.
• Create and maintain clear, concise laboratory records (paper and electronic systems).

Method Development & Validation

• Assist with method development, method transfer, and method validation activities.
• Perform working standard qualifications and support analytical lifecycle management.

Equipment & Compliance

• Perform calibration and routine maintenance of laboratory instruments.
• Ensure compliance with cGMP, ICH, FDA, and DEA requirements, as well as internal SOPs.
• Maintain a clean, organized, and inspection‑ready laboratory environment.

Work Schedule:

• Monday–Friday, 8:30 AM – 5:00 PM
• Travel: Up to 10%

Work Environment:

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

• Moderate noise levels
• Chemical fumes, odors, gases, and airborne particles
• Laboratory equipment and hazardous materials
• Standard laboratory safety risks

Appropriate use of PPE and adherence to safety protocols is required at all times.

Physical Requirements

• Ability to stand, sit, walk, and perform repetitive motion tasks
• Use hands and fingers for handling instruments and materials
• Ability to stoop, kneel, crouch, or reach as needed
• Close vision, depth perception, and ability to focus
• Ability to operate laboratory and office equipment
• Ability to lift and carry up to 50 lbs

What You Bring:

Education & Skills

• Bachelor’s degree in Chemistry or related discipline required; Master’s preferred
• Understanding of GMP, ICH, and FDA guidelines
• Proficiency in Microsoft Office, especially Excel
• Strong analytical thinking and problem‑solving skills
• Excellent verbal and written communication skills
• A self‑starter with a hands‑on, proactive, and team‑oriented approach
• English proficiency at CEFR Intermediate B1+ level

Experience:

• Minimum 4 years of experience in a pharmaceutical analytical laboratory
• OR 3 years with a Master’s degree in Chemistry
• Hands‑on experience with analytical instrumentation and techniques
• Experience with wet chemistry and USP monograph interpretation

Why Join Us?

• Stable day‑shift schedule with consistent hours
• Hands‑on role with advanced analytical instrumentation
• Opportunity to contribute to quality and compliance of pharmaceutical products
• Collaborative laboratory environment with growth opportunities

The presently-anticipated base compensation pay range for this position is $69,000 to $77,000 annually. 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.

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.

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.

Notice To Agency And Search Firm Representatives

Sun Pharmaceuticals (Sun) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Sun employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Sun. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral.