About Client:
It is a large Indian multinational pharmaceutical company headquartered in Hyderabad Telangana India. It manufactures generic medicines and active pharmaceutical ingredients (APIs) and supplies medicines worldwide.
Role & Responsibilities:
- Conduct routine and non-routine analysis of raw materials in-process samples and finished formulations.
- Perform analytical testing using techniques such as HPLC GC UV-Vis spectroscopy FTIR dissolution and titration.
- Prepare and maintain accurate test records analytical reports and certificates of analysis.
- Ensure compliance with cGMP GLP and regulatory guidelines (FDA WHO ICH etc.).
- Support method validation transfer and stability studies for formulations.
- Investigate and document out-of-specification (OOS) and out-of-trend (OOT) results.
Required Skills & Competencies
- Strong knowledge of analytical chemistry and pharmaceutical testing methods.
- Hands-on experience with analytical instruments (HPLC GC UV Dissolution Apparatus etc.).
- Familiarity with regulatory requirements and documentation practices.
- Attention to detail accuracy and ability to work under strict timelines.
- Good communication and teamwork skills.
About Client:It is a large Indian multinational pharmaceutical company headquartered in Hyderabad Telangana India. It manufactures generic medicines and active pharmaceutical ingredients (APIs) and supplies medicines worldwide.Role & Responsibilities: Conduct routine and non-routine analysis of raw ...
About Client:
It is a large Indian multinational pharmaceutical company headquartered in Hyderabad Telangana India. It manufactures generic medicines and active pharmaceutical ingredients (APIs) and supplies medicines worldwide.
Role & Responsibilities:
- Conduct routine and non-routine analysis of raw materials in-process samples and finished formulations.
- Perform analytical testing using techniques such as HPLC GC UV-Vis spectroscopy FTIR dissolution and titration.
- Prepare and maintain accurate test records analytical reports and certificates of analysis.
- Ensure compliance with cGMP GLP and regulatory guidelines (FDA WHO ICH etc.).
- Support method validation transfer and stability studies for formulations.
- Investigate and document out-of-specification (OOS) and out-of-trend (OOT) results.
Required Skills & Competencies
- Strong knowledge of analytical chemistry and pharmaceutical testing methods.
- Hands-on experience with analytical instruments (HPLC GC UV Dissolution Apparatus etc.).
- Familiarity with regulatory requirements and documentation practices.
- Attention to detail accuracy and ability to work under strict timelines.
- Good communication and teamwork skills.
View more
View less