Analytical Research Associate

4 months ago


Pragathinagar Hyderabad Telangana, India Pardha Constrcution Full time

**Job Title: Research Associate**

**Department : Analytical**

**Location**: Hyderabad

**Company**: Amogen Pharma Pvt Ltd

**Position Type**: Full-Time

**Job Summary**:
**Key Responsibilities**:

- **Analytical Method Development**: Develop and optimize analytical methods for pharmaceutical compounds, including method validation and troubleshooting. Techniques may include HPLC, GC, and spectroscopy.
- **Stability Analysis**: Conduct stability studies to evaluate the shelf-life, degradation, and quality of pharmaceutical products under various conditions.
- **Data Analysis and Reporting**: Analyze experimental data, prepare detailed reports, and present findings to senior researchers and project teams. Ensure accuracy and compliance with regulatory requirements.
- **R&D Support**: Contribute to R&D projects, collaborating with cross-functional teams to drive innovation and support product development initiatives.
- **Compliance and Quality Assurance**: Ensure that all research activities adhere to industry regulations and company standards, including Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP).
- **Instrument Maintenance**: Maintain and calibrate laboratory equipment, ensuring reliable performance and proper documentation.

**Qualifications**:

- **Educational Background**: Bachelor’s and Master’s degrees in Chemistry, Pharmaceutical Sciences, Biochemistry, or a closely related field.
- **Experience**: 2 to 3 years of hands-on experience in pharmaceutical R&D with a focus on analytical method development, validation, and stability analysis. Experience must include working in a pharmaceutical industry setting.
- **Technical Skills**: Proficiency in analytical techniques such as High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), and spectroscopy (UV-Vis, FTIR). Familiarity with software for data analysis (e.g., Empower, ChemStation).
- **Knowledge of Regulations**: Strong understanding of regulatory guidelines and quality assurance practices relevant to pharmaceutical R&D (e.g., GMP, GLP).
- **Problem-Solving Skills**: Excellent analytical and problem-solving skills with meticulous attention to detail.
- **Communication Skills**: Strong written and verbal communication skills, with the ability to effectively collaborate in a team environment.

**Preferred Skills**:

- Experience with complex pharmaceutical formulations and stability studies.
- Familiarity with regulatory submissions and documentation practices.

**Job Types**: Full-time, Permanent

**Benefits**:

- Food provided
- Leave encashment
- Paid sick time
- Provident Fund

Schedule:

- Day shift
- Morning shift
- Rotational shift

**Experience**:

- total work: 1 year (preferred)

Work Location: In person


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