The Role
Responsible for ensuring quality standards in testing, monitoring, compliance, deviation management, auditing, and training personnel in quality procedures.
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 - Hyderabad
· 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 of experience in Quality Control and formulation for pharma chemicals.
- Knowledge of cGMP & regulatory standards. Strong skills in deviation investigation, RCA & CAPA. Experience in audits & documentation. Good analytical, problem-solving, and communication skills.
Other Benefits
- Corporate Uber and MMT access for travel, Sodexo food card.
- Insurance Benefits - coverage for 5 members of family up to 5 lakhs.
- Monthly outing and engagement.
- Monthly official corporate dinner and party/trips.
- Parental support - Maternity benefit, parental benefit program, Day-care support program.
- Wellness Program - Employee Assistance Program, Onsite Medical Center, Emergency Support System, online doctor consultation.
- Mobility Benefits - Relocation Benefits, Transfer Support Policy, Travel policy.
- Retirement Benefits - Employee PF contribution, Flexible PF contribution, NPS.
- Other Benefits - Car Lease, Salary Advance policy.
Official Website : https://www.scimplify.com/
Skills Required
- Experience in Quality Control and formulation for pharma chemicals
- Knowledge of cGMP & regulatory standards
- Strong skills in deviation investigation, RCA & CAPA
- Experience in audits & documentation
- Good analytical, problem-solving, and 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.
