Formulation Scientist

Date: 25 Aug 2025

Location:

Bangalore, KA, IN, 560099

Custom Field 1: Development Services

Job Description
Job Title: Formulation scientist
Job Location: S18, Syngene, Bengaluru
Department: Formulation Development Centre (FDC)
About Syngene: Syngene (

) 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

• Responsible for product development for parenteral drug products, which includes pre-formulation, formulation design, process optimization & characterization, and technology transfer from R&D to different manufacturing sites.
• Lead all activities for transferring lab process to GMP manufacturing site and facilitate drug product manufacturing in GMP fill finish facility, in coordination with production and quality team.
• Responsible for optimization of manufacturing processes (right first time approach) to support drug product supply for clinical trials

Role Accountabilities

• Hold self-accountable for the achievement of client milestone.
• Meet Compliance related expectation

Leadership Capabilities

• Self-Driven
• Self-Motivated
• Communication and coordination to deal with cross functional teams

Syngene Values
All employees will consistently demonstrate alignment with our core values

• Excellence
• Integrity
• Professionalism

Experience
At least 3 years of industrial research experience in formulation development and technology transfer of parenteral drug products for small molecules & large molecules
Responsibilities

• Responsible for product development for parenteral drug products, which includes pre-formulation, formulation design, process optimization & characterization, and technology transfer from R&D to different manufacturing sites
• Lead all activities for transferring lab process to GMP manufacturing site and facilitate drug product manufacturing in GMP fill finish
• Experience of working with third party manufacturing facility
• Responsible for optimization of manufacturing processes (right first time approach) to support drug product supply for clinical trials
• Drive troubleshooting for technical batches, clinical batches, and registration batches for injectable fill finish facility
• Responsible for writing & reviewing lab development and GMP manufacturing related proposals & report for client

Skills And Capabilities

• Must have appreciable experience in parenteral drug products formulation and process development, from early to late phase including commercialization
• Expertise on selection and process/packaging development of vials, PFS, autoinjectors and its associated regulatory requirements for USA and Europe
• Extensive experience in de-formulation of reference product, comparability study and it's characterization
• Hands on experience for product and process development for both complex and conventional injectable Familiar with analytical characterization techniques for determining purity, potency and similarity assessment for biosimilars
• Good understanding of engineering principles & process controls related to equipment and processes across scales to transfer or receive processes/ injectable products
• Hands on experience on process validation and trouble shooting
• Hands on experience for working in GMP environment, ensuring data integrity and compliance to safety
• Good understanding of filter selection, filter optimization and filter validation studies
• Understanding of containment/isolator requirement for potent large molecules will be plus
• Know how knowledge for manufacturing process techniques for complex injectables such as liposome, nanoemulsions, polymer conjugates, nanoparticles, microspheres, and complex formation
• Expertise in design and optimization of lyophilization cycle for large molecules
• Handful skills for interpretation of results, drawing scientifically based conclusions, writing, and reviewing technical report
• Work closely with Manufacturing, quality, engineering, and validation teams of third-party manufacturing facility to achieve successful site technology transfer
• Knowledge of phase appropriate GMP quality system (early phase & late phase) and appreciable understanding of clinical study DP supply requirement
• Knowledge of preparing and review of GMP documents such as MFR,MPR, BMR, BPR, PPQP and PPQR
• Knowledge of QMS system, scientific methodology for handling product related deviations, OOT, OOS and CAPA, with full awareness of company's policy and procedures.
• Have a strong power of analysis, illustrated by the ability to quickly recognize the core issues, trends and risks assessment
• Earlier exposure to regulatory and client audit will be added advantage.
• Good oral communication and interpersonal skills for successfully driving programs involving multiple stakeholders
• Prior experience of contributing to regulatory filing of drug product dossier for regulated markets such as US, EU & ROW
• Work closely with both functional and project managers to identify and mitigate technical issues, manage project milestones to adhere to project timelines.
• Earlier exposure to regulatory and client audit will be added advantage

Education
Master of Pharmacy (Pharmaceutics or industrial pharmacy or process technology)

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.