About Company

Global calcium is one of the leading API manufacturing company situated in Bangalore, India, specialised in speciality API's, benzodiazepines, ophthalmics, oncology, chelated minerals and organic mineral salts of aspartate, citrate, gluconate, lactate, lactobionate, levulinate, orotate, pidolate , etc.

We are hiring for multiple roles in the QC Department!

Join us at Global Calcium Pvt. Ltd., a leading pharmaceutical manufacturer, and be part of a growing team committed to quality and innovation.

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
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
Experience in raw material and finished product testing

Eligibility Criteria

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

Walk-in Interview 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

Note: Only candidates with relevant experience in the pharmaceutical QC domain will be considered. Role & responsibilities

Role Responsibilities

Conduct routine and non-routine analyses using analytical techniques and instrumentation.
Develop and validate analytical methods and protocols.
Prepare and maintain detailed documentation and reports.
Ensure compliance with regulatory guidelines and GMP standards.
Collaborate with other departments for cross-functional projects.
Actively participate in laboratory investigations and troubleshooting activities.

Benefits and Perks

As per industry standards

Skills: 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,aas

QC - Chemist / Executive - Walk-In Interview