Chemist- In-process Quality Assurance
Steril Gene Life Sciences
- Posted: 1 week ago
- Openings: 10
- Applicants: 0
Job Description
- Develop and implement quality control procedures to ensure compliance with regulatory requirements.
- Conduct regular audits and inspections to identify areas for improvement in quality systems.
- Collaborate with cross-functional teams to resolve quality-related issues and improve overall product quality.
- Analyze data and trends to identify opportunities for process improvements and implement corrective actions.
- Maintain accurate records of quality control activities and results.
- Ensure adherence to Good Manufacturing Practices (GMP) and other regulatory guidelines.
Job Requirements
- Bachelor's degree in Chemistry or related field.
- Minimum 2 years of experience in quality assurance, preferably in the pharma, biologics, or medical device industry.
- Strong knowledge of quality control principles, regulations, and standards.
- Experience with analytical techniques such as HPLC, GC, and UV spectrophotometry.
- Excellent communication and problem-solving skills.
- Ability to work effectively in a fast-paced environment and meet deadlines.
Disclaimer : This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
More Info
Education
Any Graduate
Not Disclosed
Required Skills
Chemistry
uv
Pharmaceutical
quality control
Regulatory
GMP
HPLC
regulatory requirements
Contact Details
Steril Gene Life Sciences
+91 987654567
business@steril-gene.com
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