Formulation Scientist

3-6 years

Not Disclosed

Bangalore

10 Oct. 22, 2024

Job Description

Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Formulation Scientist

Year of Experience:

3 - 6 Years

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 integral to our operations. We prioritize safety alongside business performance, with shared responsibility and accountability in adhering to safety guidelines, procedures, and SOPs.

Mandatory Expectations:

Adhere to safe practices and procedures for oneself and aligned teams.
Contribute to the development of procedures that ensure safe operations and compliance with company integrity and quality standards.
Promote an environment, health, and safety (EHS) mindset at the workplace.
Ensure safety protocols are followed at all times.
Complete all mandatory training related to data integrity, health, and safety on time.
Comply with Syngene’s quality standards and hold self and teams accountable for achieving safety goals.
Regularly review and govern safety metrics.

Core Purpose of the Role:

Support early and late-phase drug product development (solid and liquid orals).

Role Accountabilities:

Develop oral solid/liquid formulations and processes, including pre-formulation, scale-up, technology transfer, and cGMP manufacturing of clinical supplies.
Prepare product development documents and compile and interpret data.
Demonstrate strong communication, teamwork, and presentation skills.
Document GMP batches and execute projects within committed timelines.
Troubleshoot and solve challenges within projects and interact with cross-functional teams for project execution.
Ensure compliance with Syngene quality systems.

Specific Requirements for this Role:

Experience:

3 - 8 years

Skills and Capabilities:

Execute projects related to pre-formulation, QBD-based formulation, and process development (e.g., spray drying, pellets, capsules, tablets).
Conduct literature searches and plan experiments in consultation with management.
Experience in bioequivalence studies and data interpretation, including DOE implementation.
Prepare and review Master Formula Records, Master Packing Records, Batch Manufacturing Records, and Batch Packaging Records for GMP execution.

Education:

M.Pharm or M.S. in Pharmaceutics

Equal Opportunity Employer:

Syngene is committed to providing equal employment opportunities (EEO) to all individuals, 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, public assistance status, veteran status, or any other characteristic protected by applicable legislation or local law. We also provide reasonable accommodations for qualified individuals with disabilities.

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