Walk-In for QC – Chemist Jobs at Global Calcium, June 14, 2025.
Are you a chemistry graduate looking to grow your pharmaceutical career? Global Calcium Pvt. Ltd., a leading API manufacturer in India, is conducting a walk-in interview in Hosur for multiple QC Chemist/Executive roles. With opportunities in ICP-MS, DMF support, analytical validation, and wet analysis, this is your chance to join an innovative pharma team focused on quality and regulatory excellence.
About the Company: Global Calcium is one of the leading API manufacturing companies situated in Bangalore, India. The company specializes in speciality API’s, benzodiazepines, ophthalmics, oncology, chelated minerals, and organic mineral salts.
Job Posting: QC – Chemist / Executive – Walk-In Interview at GLOBAL CALCIUM
Walk-in Interview Details
Details:
- Venue: Global Calcium Pvt. Ltd., Unit III, 19 & 19B, Sipcot industrial complex, Phase – 1, Dharga, Hosur
- Date: 14th June 2025
- Time: 9:30 AM to 11:00 AM
- Documents to Carry: Resume, Recent Photograph, Last 3 Months’ Payslips, Educational & Experience Certificates, ID Proof
Open Positions (Multiple Vacancies)
- QC ICP-MS Analyst (2 openings)
- Hands-on experience with ICP-MS instrumentation
- Knowledge of elemental impurity analysis and related regulatory guidelines as QC
- QC – DMF Support (2 openings)
- Exposure to DMF preparation, review & support documents
- Understanding of regulatory documentation and compliance standards
- QC – Analytical Validation Support (2 openings)
- Knowledge of method validation techniques (HPLC/GC/UV)
- Experience in handling validation protocols and reports
- QC – Wet Analysis (2 openings)
- Proficient in classical wet chemistry techniques as QC
- Experience in raw material and finished product testing
Eligibility Criteria
Requirements:
- B.Sc./M.Sc. in Chemistry or related fields
- 1 to 4 years of relevant pharmaceutical QC experience
- Good understanding of cGMP practices and regulatory compliance
- Willingness to work in a fast-paced manufacturing environment
Role Responsibilities
Responsibilities:
- Conduct routine and non-routine analyses using analytical techniques and instrumentation
- Develop and validate analytical methods and protocols as QC
- Prepare and maintain detailed documentation and reports
- Ensure compliance with regulatory guidelines and GMP standards
- Collaborate with other departments for cross-functional projects
- Participate in laboratory investigations and troubleshooting activities
Benefits and Perks
Benefits: As per industry standards
Keywords: dmf preparation, dmf, uv, regulatory documentation, elemental impurity analysis, cgmp practices, hplc, gc, classical wet chemistry techniques, quality control, icp-ms, wet analysis, method validation techniques
