MSTG Scientist I

SUN PHARMA; New Brunswick (NJ); On-site; USD 76,000 - 86,000; Full time

Job summary

Sun Pharma seeks a MSTG Scientist I to drive process development, exhibit batch execution, and validation activities in a fast-paced pharmaceutical environment. You will collaborate with Manufacturing, Quality, and Technical Services to advance solid dosage products from development through transfer.

The role emphasizes data analysis, technical documentation, and regulatory compliance, with an office-based but manufacturing-adjacent work setting in New Jersey. Competitive compensation applies.

Qualifications

• Bachelor's degree in a relevant scientific field.
• Minimum four (4) years of pharmaceutical industry experience.
• 1-2 years experience with Solid Oral Dosage (OSD) product development and manufacturing.
• Proficiency with Microsoft Office applications (Word, Excel, Project, PowerPoint).
• Strong analytical reasoning, writing, and reporting skills.
• Good verbal and interpersonal communication; CEFR B1+ English.

Responsibilities

• Design and conduct DOE, process optimization studies, and qualification batches.
• Analyze process data using statistical tools to support development and improvement.
• Support product development from concept to process characterization and qualification.
• Participate in cleaning validation and related development activities.
• Develop and review Master Batch Records, Exhibit Protocols, and Validation Documents.
• Ensure compliance with cGMP and regulatory requirements.
• Provide technical troubleshooting to manufacturing operations and support tech transfer.
• Lead compliance investigations and CAPA activities; support Change Control.

Skills

Analytical thinking

Technical writing

Communication skills

Self-motivated

English proficiency

Education

Bachelor's degree in Pharmacy

Bachelor's degree in Pharmaceutical Sciences

Bachelor's degree in Chemical Engineering

Bachelor's degree in Chemistry

Bachelor's degree in other relevant scientific discipline

Tools

Microsoft Office (Word, Excel, Project, PowerPoint)

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.

Are you a scientist who enjoys turning data into solutions and driving products from development through validation and commercial readiness? We are seeking a MSTG Scientist I to support process development, exhibit batch execution, process qualification activities, and manufacturing support within a fast-paced pharmaceutical environment.

This role offers an excellent opportunity to work cross-functionally with Manufacturing, Quality, and Technical Services teams while contributing to the development, optimization, validation, and successful transfer of solid dosage pharmaceutical products.

Key Responsibilities:

Process Development & Optimization:

• Design and execute Design of Experiments (DOE), process optimization studies, and process qualification batches.
• Compile, analyze, and interpret process data using statistical tools to support process development and continuous improvement initiatives.
• Support product development projects from conceptual studies through process characterization and qualification activities.
• Participate in cleaning validation studies and related process development initiatives.

Technical Documentation:

• Develop and maintain comprehensive technical documentation throughout various stages of product development.
• Prepare and review:
  • Master Batch Records (MBRs)
  • Exhibit Batch Protocols
  • Pre-Validation Documentation
  • Process Validation Protocols
  • Validation Reports
  • Technical Study Reports
• Ensure all documentation meets cGMP and regulatory requirements.

Manufacturing & Quality Support:

• Provide technical troubleshooting support to manufacturing operations.
• Investigate process challenges and recommend scientifically sound solutions to improve product quality and operational efficiency.
• Support technology transfer, scale-up, and validation activities as needed.
• Collaborate with Manufacturing and Quality teams to support successful production and compliance outcomes.

Compliance & Continuous Improvement:

• Lead and support compliance-related investigations.
• Assist with Corrective and Preventive Actions (CAPA), commitments, and Change Control activities.
• Participate on cross-functional teams to address technical challenges, improve processes, and strengthen collaboration across departments.
• Support continuous improvement initiatives that enhance efficiency, compliance, and product quality.

Qualifications:

Required

• Bachelor's degree in:
• Pharmacy
• Pharmaceutical Sciences
• Chemical Engineering
• Chemistry
• Other relevant scientific discipline
• Minimum four (4) years of relevant pharmaceutical industry experience.
• 1-2 years experience with Solid Oral Dosage (OSD) product development and manufacturing.
• Proficiency with Microsoft Office applications, including:
• Word
• Excel
• Project
• PowerPoint
• Strong analytical thinking and problem-solving abilities.
• Excellent technical writing, documentation, and reporting skills.
• Strong verbal and interpersonal communication skills.
• Self-motivated individual with a hands-on approach and a proactive mindset.
• Intermediate English proficiency (CEFR B1+ or equivalent).

Preferred:

• Master's degree in a relevant scientific discipline.
• Knowledge of process validation, cleaning validation, and process characterization activities.
• Experience utilizing statistical tools for data analysis and process evaluation.

Work Environment:

This position is primarily office-based within a pharmaceutical manufacturing and production facility and requires regular interaction with manufacturing operations.

The Work Environment May Include Exposure To

• Manufacturing equipment and production noise
• Dust, odors, fumes, and gases
• Moving mechanical equipment
• Chemical processing environments
• Manufacturing-related safety hazards requiring adherence to established safety procedures and use of personal protective equipment (PPE)

Physical Requirements:

• Ability to navigate office and manufacturing environments, including standing, walking, reaching, and moving throughout production areas.
• Ability to frequently lift or move lightweight materials up to 10 pounds.
• Ability to wear required personal protective equipment (PPE), including respirators, safety glasses/goggles, and safety shoes.

Travel:

• Up to 10% travel may be required.

Why Join Us?

Join a collaborative team where science, innovation, and quality come together to bring pharmaceutical products from development to commercialization. As a MSTG Scientist I, you'll play a critical role in process development, validation, and manufacturing support while gaining valuable exposure to cross-functional technical and operational initiatives.

The presently-anticipated base compensation pay range for this position is $75,500 to $86,000. 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.