Qc Chemist with Exp in Lab Autoclave

**Job Summary**
- Must have experience with GC handling & operation

Perform chemical testing of raw materials, intermediates, and Finished goods.
- Carrying out R&D work with respect to process optimisation, yield improvement and new product development.
- Responsible for utilizing common analytical techniques such as**:QUALITATIVE & QUANTITATIVE INORGANIC** analysis, titrations, gravimetric analysis and wet chemical methods.
- Execute Batch monitoring, routine analysis, with direction on more complicated analysis, method development, and project management.
- ensuring all the **GMP & GLP SOPS** are followed and support for audit requirements.
- Knowledge of **CATALYST** testing like **raney nickel catalyst, precious metal catalyst testing** will be highly preffered.
- Regulatory knowledge with respect to **SOPs, GMP** will be preferable

**Responsibilities and Duties**
- Quality control chemists prepare and test samples from all phases of a manufacturing or other handling process, with the goal of determining if the substance meets the standards or requirements of the project.
- employ a variety of methods that can vary from industry to industry but generally require basic lab-work skills and thorough understanding of chemical testing equipment and processes.
- prepare documents that report the results of their lab work. They may also be responsible for minor equipment troubleshooting and repair. QC chemists have a role in preserving workplace safety and safe materials handling as appropriate, since they sometimes work with hazardous materials.
- Learn and follow all Standard Operating Procedures (SOPs) and Good Manufacturing Practices. (GMPs)
- Revise SOPs, test methods, and GMP documents with guidance.
- Conduct analysis and interpret results.
- Review all data regarding raw materials, intermediates, and finished goods
- Performs testing for the qualification of reference standards.
- Perform cleaning validations and verifications.
- Calibrate instruments and contribute to laboratory organization and compliance.
- Other duties as assigned.
- **QUALITY/REGULATORY RESPONSIBILITIES**:

- Applies cGMP concepts in association with department specific responsibilities.
- Ensures all documentation produced is in compliance with cGMP standards.
- Responsible for contributing to audit readiness and for participating in quality audits with ISO other Regulatory Agencies, and customers, as needed.**Required Experience, Skills and Qualifications**

Bachelor's degree in chemistry with experience or a Masters degree in inorganic chemistry will be preferable or ; certificates in quality assurance available for specialization

Schedule:

- Morning shift

Ability to commute/relocate:

- Badlapur, Maharashtra: Reliably commute or planning to relocate before starting work (preferred)

**Experience**:

- GC: 2 years (required)
- total work: 3 years (required)

**Location**:

- Badlapur, Maharashtra (required)

Work Location: In person