Title:  Formulation Scientist

JOB DESCRIPTION

Job Title:  Formulation Scientist – Pharmaceutical Development

Job Location: Bengaluru

About Syngene :  Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific  services from early discovery to commercial supply.

At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit

Mandatory expectation for all roles as per Syngene safety guidelines

• Overall adherence to safe practices and procedures of oneself and the teams aligned
• Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company’s integrity & quality standards
• Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times.
• Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace.
• Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self
• Compliance to Syngene’ s quality standards at all times
• Hold self and their teams accountable for the achievement of safety goals
• Govern and Review safety metrics from time to time

Core Purpose of the Role:

Early and late phase drug product development (Solid orals and/or liquid orals)

Role Accountabilities

• Oral solid/liquid formulation and process development, pre-formulation, scale up, technology transfer and cGMP manufacturing of clinical supplies, product development writing, data compilation and interpretation, communication skills, team player, presentation Skills, GMP batches documentation, seamless execution of projects as per committed timelines, Troubleshooting and problem solving for challenges within projects, interact with cross functional teams for execution of projects, compliance and Adherence to all Syngene quality systems.

Syngene Values

All employees will consistently demonstrate alignment with our core values

•  Excellence
•  Integrity
•  Professionalism

Specific requirements for this role

1. Experience
2. Demonstrated Capability
3. Education

Experience

4- 8 years

Skills and Capabilities

Execute projects related to pre-formulation, QBD based formulation and process development (Spray drying/pellets/capsules/tablets), scale up, technology transfer and cGMP manufacturing. Literature search and planning of experiments in discussion with manager or as required for the project, experience in bioequivalence studies and data interpretation, DOE implementation.  

Preparation and review of Master formula records, Master Packing record, Batch manufacturing records and Batch packaging records for execution of GMP batches

Education

M.pharm or M.S in pharmaceutics

Equal Opportunity Employer

It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.