The Role
Manage quality control testing and analysis for specialty chemicals using HPLC, GC, UV, IR, and dissolution techniques. Monitor quality across warehouse, packaging, and dispatch operations; maintain cGMP-compliant documentation; investigate deviations and non-conformances; conduct root cause analysis and CAPA; support audits and inspections; train teams; and improve quality procedures and operational processes.
Summary Generated by Built In
About Us
Key Responsibilities:
Qualifications & Skills:
We are a specialty chemicals manufacturing company with a full stack solution from R&D to manufacturing and doorstep delivery of innovative chemicals. Headquartered in Bengaluru, India we cater to pharmaceutical, agrochemical, personal care, and home care industries.
Our B2B fulfillment platform supports businesses globally in developing and manufacturing chemicals from lab to commercial scale. With a team of in-house R&D experts and scientists, we offer custom synthesis and route scouting services to support manufacturers in product development.
We are VC backed - here is a read. We are 400+ people strong and have offices in India, UAE and Indonesia. We are currently exporting to over 17 countries from India currently.
Read to learn more ▶️ https://lnkd.in/gd7brT8S
Location - Bangalore
·Testing & Analysis: Perform testing using HPLC, GC, UV, IR, and Dissolution techniques to ensure accuracy and reliability of test results. Maintain consistency in analytical procedures to meet quality standards.
·Quality Monitoring: Ensure quality is maintained across warehouse, dispatch, and packaging activities. Collaborate with operations teams to identify and resolve quality issues in real-time, preventing defects and ensuring compliance.
·Compliance & Documentation: Adhere to cGMP and regulatory guidelines while maintaining accurate documentation of all quality-related activities. Ensure records are up to date and comply with industry standards.
·Deviation & CAPA Management: Investigate deviations and non-conformances, conduct root cause analysis (RCA), and implement corrective and preventive actions (CAPA) to mitigate risks and enhance process efficiency.
·Audits & Inspections: Participate in internal and external audits, ensuring compliance with regulatory requirements. Assist in preparing responses to audit observations and contribute to continuous improvement initiatives.
·Training & Process Improvement: Provide training to teams on quality standards, best practices, and regulatory updates. Support the development and review of quality procedures to enhance operational efficiency and ensure adherence to the latest industry trends.
Qualifications & Skills:
- Experience: Relevant years in Quality Control for speciality industrial chemicals.
- Knowledge of cGMP & regulatory standards. Strong skills in deviation investigation, RCA & CAPA. Experience in audits & documentation. Good analytical, problem-solving, and communication skills
Official Website : https://www.scimplify.com/
Skills Required
- Relevant experience in quality control for specialty industrial chemicals
- Knowledge of cGMP and regulatory standards
- Experience with deviation investigation, root cause analysis, and CAPA
- Experience with audits and quality documentation
- Strong analytical and problem-solving skills
- Strong communication skills
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The Company
What We Do
Scimplify is a science-first company specializing in the end-to-end development and manufacturing of specialty chemicals, serving industries such as pharmaceuticals, agrochemicals, and industrial chemicals.
