Job Description

Job Summary

• 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.
• Apply basic scientific knowledge to perform analysis and to solve simple analytical problems.
• 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
• Demonstrates technical proficiency and self-assuredness in applying cGMP standards.
• 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 QualificationsBachelor's degree in chemistry with experience or a Masters degree in inorganic chemistry will be preferable or ; certificates in quality assurance available for specializationJob Type: Full-timeSalary: ?12,000.00 - ?25,000.00 per monthSchedule:

• Flexible shift
• Morning shift
• Night shift
• Rotational shift

Supplemental pay types:

• Overtime pay

Ability to commute/relocate:

• Badlapur, Maharashtra: Reliably commute or planning to relocate before starting work (Required)

Experience:

• total work: 2 years (Required)