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18 Job openings at Global Calcium
About Global Calcium

Global Calcium is a leading manufacturer of calcium-based products, specializing in the production and distribution of calcium carbonate, calcium phosphate, and other related chemicals.

Stores Associate/Officer

Hosur

5 - 10 years

INR 7.0 - 12.0 Lacs P.A.

Work from Office

Full Time

Roles and Responsibilities: Handling inward and outward stock movement Maintaining inventory records and physical stock Coordinating with purchase and production teams Ensuring proper documentation and labeling as per SOPs Maintaining cleanliness and order in the storage area Assisting in stock audits and compliance requirements Desired Candidate Profile: Any Graduate / Diploma Holder (B.Sc, B.Com, B.Pharm preferred but not mandatory) Freshers or candidates with up to 5 year of experience Basic computer knowledge (Excel, ERP systems preferred) Good communication skills Willingness to work in a team and learn

Executive - Solvent Recovery Plant (SRP)

Hosur

2 - 4 years

INR 4.0 - 6.0 Lacs P.A.

Work from Office

Full Time

Company Information Company Name: Global Calcium Pvt Ltd Location: Hosur Responsibilities Key Responsibilities: Operate and monitor solvent recovery systems including distillation columns, condensers, receivers, and associated utilities. Perform batch-wise solvent recovery, monitor parameters (temperature, pressure, flow rate), and make necessary adjustments to ensure optimal performance. Ensure compliance with GMP, SOPs, and safety protocols in all SRP operations. Coordinate with QA/QC for sampling and approval of recovered solvents. Maintain accurate records of solvent recovery, utility consumption, downtime, and yield reports. Support maintenance activities, troubleshoot minor issues, and escalate technical problems to the engineering team. Adhere to statutory environmental norms (CPCB/SPCB guidelines) for air and water discharge. Qualifications B.Tech in Chemical Engineering, Chemistry, or relevant field. 2-4 years of experience in Solvent Recovery in the pharmaceutical industry.

QA Executive

Hosur

4 - 6 years

INR 6.0 - 8.0 Lacs P.A.

Work from Office

Full Time

What We re Looking For: Qualification: M.Sc. Chemistry / B.E. Chemical / B.Pharmacy Experience: 4-6 years in the pharmaceutical industry Strong knowledge in: QMS, Validation (Process, Equipment, Cleaning), and Qualification (IQ/OQ/PQ) Good documentation skills and regulatory understanding: GMP, FDA, ISO

Purchase Officer

Hosur

2 - 4 years

INR 4.0 - 6.0 Lacs P.A.

Work from Office

Full Time

Company Name: Global calcium Pvt Ltd Location: Hosur Job description Roles and Responsibilities Manage procurement activities of Engineering items, CAPEX, Lan consumables and lab instruments Sending inquiries and collecting quotes from vendors upon receipt of Purchase Requisition Preparing comparative statement, Preparation of purchase orders, meeting the criteria of quality, price, timeliness, reliability, and the companys standards. Develop new vendor development plans to improve supply chain efficiency. Conduct price negotiations with vendors to optimize costs. Oversee purchase activities from initiation to execution. Ensure timely delivery of materials through effective logistics management. Desired Candidate Profile 2-4 years of experience in purchasing or procurement role. Any Graduates. Strong understanding of buying, capex, capital procurement, capital purchase, material procurement, opex, pricing strategies. Candidates are preferred from pharma/Chemical/Food industry

Assistant Manager / Senior Executive - QA

Hosur

8 - 12 years

INR 25.0 - 30.0 Lacs P.A.

Work from Office

Full Time

Job Summary: We are seeking a dedicated and detail-oriented Data Integrity (DI) Specialist to join our Quality Assurance and Compliance team. The ideal candidate will be responsible for ensuring that all data generated and maintained across the site meets regulatory, quality, and organizational standards. The DI Specialist will play a critical role in fostering a culture of data integrity by ensuring adherence to ALCOA++ principles and implementing comprehensive data governance practices. To ensure that Data Integrity is being followed across the site. Ensuring all the data are as per ALCOA++ principles. Creating and maintaining documentation on data policies. Ensure compliance with data regulations and security standards. Verifying and ensuring the companys computer system data are safely maintained. Monitoring who accesses sensitive data. Installing protective measures in terms of Data Integrity. Ensuring employees follow Data Integrity assurance standards. Allowing only authorized personnel to access protected information. Ensuring Data Integrity assurance culture across the site. Involving in remediation team to ensure Data Integrity assurance practices are followed by the employees Qualification : MSc Chemistry / B Pharma

Senior Executive - QA

Hosur

5 - 7 years

INR 7.0 - 9.0 Lacs P.A.

Work from Office

Full Time

Job Summary : As a Quality Assurance (QA) professional with a qualification in MSc Chemistry, the primary role revolves around ensuring adherence to established quality and regulatory standards. The responsibilities cover a wide range of quality-related tasks, documentation management, and process validation activities in alignment with ISO and cGMP standards. Key Responsibilities: 1 Review and Implementation of ISO 9001 standards, Quality Management System Compliance, cGMP standards, ISO 14001, Halal & HACCP standards 2 Preparation of Certificate of Analysis, Good Receiving Note and other related documents in process QA checks. 3 Review of Purchase order coordination for dispatch activities 4 To ensure the dispatch activities and clearance 5 Coordination for finished products 6 To verify the LMR, BPR and analytical records 7 Preparation of cleaning validation protocols and reports 8 Prepartion of process validation protocols and reports 9 Preparation/revision of MFR for all new existing products based on changes 10 Review and approval of Lot Manufacturing Record and Batch Packing Record 11 Preparation of blending protocols and reports 12 Document Management Control

Executive - Onco Production

Hosur

4 - 8 years

INR 10.0 - 15.0 Lacs P.A.

Work from Office

Full Time

Job Summary Responsible for managing and overseeing the production of various products while ensuring strict adherence to cGMP, ISO, and safety standards.Leads scale-up activities, validation processes, and continuous improvement initiatives in coordination with cross-functional teams.Ensures effective documentation, audit readiness, and timely execution of production schedules through team supervision and corrective actions.Collaborates with RD for new product trials and maintains operational efficiency by liaising with quality, maintenance, and support departments. Requisition and approval of raw and packing materials, plant and utilities required for production of various products Ensuring strict compliance with cGMP standards during product manufacturing Front line management of production and scale up activity To identify and implement Continuous improvement of process and implementation of cGMP Review with Production personnel to assess production status and take corrective steps if required any to meet the schedule Carrying out inspection tests for determining the effectiveness of equipment Execution and completion of Validation Qualification activities, deviations, Out of Specification and change control procedures To Co- ordinate with RD department and facilitate trials for the new products Designing of Documentation for production activity Coordinating internal/ External audits and maintaining relevant documents Following and implementation of ISO 9001: 2015, ISO 14001: 2015, FSSC 22000/ HACCP cGMP requirements Coordinating with maintenance and utility department, Quality control and quality assurance, personnel accounts, and stores department During Execution of batches strictly follow the all "SAFETY" items should be used and safe operations to execute Education Diploma / BE - Chemical Engineering BSc / MSc Chemistry

Assistant Manager - QC

Hosur

8 - 10 years

INR 25.0 - 30.0 Lacs P.A.

Work from Office

Full Time

Job Summary : Experienced QC professional with 8-10 years in pharmaceutical quality control and compliance. Responsible for preparing specifications, test methods, and maintaining GMP, GDP, and GLP standards. Supports regulatory affairs, handles deviations, OOS, and change controls, and reviews analytical reports. Proficient in SOP creation, method updates, and team training as per cGxP and regulatory guidelines. Responsibilities: Preparation and updating specifications and test methods to ensure compliance with statutory and company standards Preparation of specification for input materials, intermediates, active pharmaceutical ingredients, finished products and stability products to ensure compliance with company standards. Maintenance of GMP, GDP & GLP in work To maintain Quality Control documents as per statutory requirements Updation and analysis of methods and analysis as per current cGCPL guidelines and regulatory requirements. Support to Regulatory affairs departments, as required Adherence to cGMP, ISO 14001, FSSC 2200 and HACCP norms and guidelines as required Preparation of SOP and related documents Initiating and involving in the incident, deviation and OOS. Initiating change control and edit form to make any changes required in the specifications, standard testing procedures, raw data sheets and SOP and closing the same Review and approval of analytical reports as required Training of concern persons related to quality documents as required Education Qualification: MSc Chemistry Years of Experience : 8 to 10 Years

QC - Chemist/Executive

Hosur

1 - 4 years

INR 3.5 - 5.0 Lacs P.A.

Work from Office

Full Time

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

QC - Chemist / Executive - Walk-In Interview

Hosur

1 - 4 years

INR 3.0 - 6.0 Lacs P.A.

Work from Office

Full Time

About Company Global calcium is one of the leading API manufacturing company situated in Bangalore, India, specialised in speciality APIs, 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

Chemist - API Production

Hosur

1 - 3 years

INR 2.0 - 3.0 Lacs P.A.

Work from Office

Full Time

Maintaining Good housekeeping in workplace as per cGMP Equipment Operation and cleaning should be followed as per SOP Receipt and storage of raw material in day stock area for the batch as per Material Requisition slip Carry out the process as per manufacturing & packing record instruction All safety rules/precaution to be followed strictly in manufacturing area In process checks and documentation should be followed as per procedure Maintaining cGMP standards, ISO 9001, ISO 14001 & HACCP standards in the plan Make sure that the production facilities are clean and when appropriate disinfected Ensure that the premises and equipment are maintained and records kept in respective area Responsibility in Blending, Packing and labelling of finished goods Responsible to carry out the Food Safety activities and ensure to comply the Statutory and Regulatory requirements Any other production activity allotted by the supervisor Verification of Raw material & FG stock availability and maintenance in production facility

Officer - API Production

Hosur

2 - 5 years

INR 4.0 - 7.0 Lacs P.A.

Work from Office

Full Time

JOB DESCRIPTION: Maintaining work place-good housekeeping as per cGMP Operating and cleaning of equipment as per SOP Receipt and storage of raw material in day stock area for the batch as per request slip Carry out the process as per LMR and operation verification All safety rules/precaution to be followed strictly Execution of the production schedules for current and coming months Coordinating internal /external audits and maintaining relevant documents In process checks to be done and documented in presence of supervisor Maintaining cGMP standards, ISO 9001, ISO 14001 & HACCP standards in the plan Making sure that the premises and equipment are maintained and records kept Responsibility in Blending, packing, and labelling of finished goods .

Production Chemist

Hosur

1 - 3 years

INR 3.0 - 4.5 Lacs P.A.

Work from Office

Full Time

Roles and Responsibilities Prepare and review batch manufacturing records (BMR) and batch processing documents to ensure compliance with regulatory requirements. Monitor production processes to identify areas for improvement and implement changes to optimize efficiency and productivity. Collaborate with cross-functional teams to resolve issues related to product quality, process optimization, and equipment maintenance. Ensure adherence to cGMP guidelines throughout the production cycle.

Manager - QA

Hosur

10 - 15 years

INR 30.0 - 35.0 Lacs P.A.

Work from Office

Full Time

Job Summary: Experienced Quality Assurance professional with a strong background in the Active Pharmaceutical Ingredient (API) industry. Responsible for implementing and maintaining GMP-compliant Quality Management Systems to ensure product quality, regulatory compliance, and operational excellence. Key responsibilities include managing documentation, handling audits (regulatory and customer), overseeing batch release, deviation investigations, and ensuring adherence to global regulatory standards (cGMP, ICH, FDA, etc.). The role demands expertise in validation, change control, and continuous quality improvement within a highly regulated API manufacturing environment. Quality Planning and Scheduling Implementation of QMS, GMP, cGMP, ISO, and Food Safety Standards Compliance with Statutory and Regulatory Requirements Document Management and Control Review and Implementation of Quality System Procedures and SOPs Batch Review, Approval, and Release In-Process Control and Material Management Review of Product Stability and Test Data Handling of OOS, Deviations, and Batch Failures New Product Technology Transfer Internal, Vendor, and Customer Audit Handling Annual Product Review GMP and QMS Training Coordination Validation and Calibration Programme Control Quality Oversight and Continuous Compliance Monitoring Qualification : B Pharma or MSc Chemistry Experience : 10 to 15 Years

Assistant Manager - QC

Hosur

7 - 12 years

INR 9.0 - 14.0 Lacs P.A.

Work from Office

Full Time

Job Summary - Assistant Manager - Quality Control The Assistant/Deputy Manager - Quality Control is responsible for overseeing and managing all QC operations to ensure timely, accurate, and compliant testing of raw materials, intermediates, finished products, and stability samples. This role supports the HOD in planning, executing, and supervising laboratory functions and ensures adherence to cGMP, GLP, and applicable regulatory standards. Key Responsibilities: Supervision of day-to-day QC lab operations Acting as HOD designee in their absence Timely testing and release of raw materials, intermediates, and finished products Implementation of QMS and handling of deviations, OOS, OOT, and complaints Compliance with ISO 9001, FSSC, Halal, Kosher & cGMP standards Review and update of product and material specifications Validation and revalidation of analytical methods Training of analysts on SOPs, GLP, GDP, and lab techniques Execution and monitoring of stability studies Instrument qualification, calibration, and maintenance Review and approval of analytical reports and lab documentation Leading and supporting internal/external audits Coordination with QA and Regulatory Affairs departments Implementation of pharmacopeia updates and regulatory requirements Driving continuous improvement and supporting special projects Qualification : B Pharma / MSc Chemistry Experience : 7-12 Years

Senior Executive - QC

Hosur

4 - 8 years

INR 6.0 - 10.0 Lacs P.A.

Work from Office

Full Time

Job Summary: We re looking for an experienced and detail-oriented professional to manage and oversee all QC lab activities. This role demands strong leadership, in-depth technical knowledge, and a commitment to regulatory excellence. The selected candidate will support the HOD, lead lab teams, and drive compliance with GMP, ISO, and global quality standards. Key Responsibilities: Supervise daily QC lab operations and testing activities Act as HOD designee during their absence Ensure timely testing and release of RM, intermediates, and finished products Investigate and document deviations, OOS, OOT, and lab incidents Implement and maintain QMS in alignment with cGMP, ISO, FSSC, Halal & Kosher Review and update specifications and pharmacopeial methods Oversee validation and revalidation of analytical methods Train analysts on lab techniques, SOPs, GLP & GDP Monitor stability studies and ensure protocol adherence Manage instrument calibration, qualification, and maintenance Review analytical reports, calibration records, and lab documentation Lead/support internal and external audits Coordinate with Regulatory Affairs and QA teams Implement pharmacopeia updates and support regulatory readiness Contribute to continuous improvement and special quality initiatives Qualification : MSc Chemistry Experience : 4-8 Years

Officer - QC

Hosur

1 - 4 years

INR 3.0 - 6.0 Lacs P.A.

Work from Office

Full Time

Job Summary: We are seeking a dedicated and detail-oriented Quality Control professional to perform wet lab testing, maintain lab compliance, and ensure the accuracy and integrity of analytical data. The role involves hands-on testing, documentation, and adherence to GLP, cGMP, and internal quality standards under the supervision of senior QC personnel. Key Responsibilities: Implement SOPs, STPs, and follow department procedures accurately Analyze samples assigned by HOD/seniors and record results in prescribed formats Prepare and maintain reagents, working standards, and reference standards Store and manage control samples with proper documentation Maintain testing documentation and ensure adherence to GLP in the QC lab Calibrate laboratory instruments as per schedule and maintain records Operate and maintain wet lab instruments (e.g., pH meter, Fluoride meter, Polarimeter, IR, UV, etc.) Assist in the investigation of deviations, OOS, complaints, and CAPA Supervise cleaning and upkeep of glassware and ensure lab hygiene Perform product sampling and analysis for intermediates, semi-finished, and finished products Support in the preparation of specifications and STPs under senior guidance Review QC documents and records for completeness and accuracy Execute all other tasks assigned by seniors or departmental heads Qualification : MSc Chemistry Experience : 1-4 Years

Packing - Officer

Hosur

2 - 4 years

INR 4.0 - 6.0 Lacs P.A.

Work from Office

Full Time

Industry & Sector: Growing pharmaceutical and nutraceutical manufacturing group serving global regulated markets, specialising in active pharmaceutical ingredients (APIs) and finished dosage forms. With state-of-the-art facilities certified by WHO-GMP, US-FDA and EU authorities, the company integrates advanced automation, lean production, and rigorous quality systems to deliver high-purity calcium salts and allied products worldwide. Position: Packaging Officer (On-Site, Tamil Nadu) Role & Responsibilities Supervise end-to-end primary and secondary packaging operations for bulk powders, ensuring target output, efficiency, and cGMP compliance. Execute line clearance, batch reconciliation, and in-process quality checks; escalate deviations and implement immediate corrective actions. Prepare and review SOPs, BMRs, and logbooks; maintain accurate electronic and paper records for regulatory audits. Coordinate with Production, QA, Engineering, and Warehouse to plan material availability, changeovers, and preventive maintenance. Lead 5S, KAIZEN, and safety initiatives on the shop floor; train operators on machine settings, hygiene, and EHS protocols. Support validation, qualification, and continuous improvement projects to reduce wastage and improve OEE. Skills & Qualifications Must-Have B.Sc./B.Pharm/Diploma in chemistry / Chemical or equivalent with 2-4 years in pharma/nutraceutical packaging. Hands-on experience with blister, strip, bottle, and sachet lines (CAM, IMA, ACG, or similar). Thorough knowledge of cGMP, GDP, CFR 21 Part 11, and data integrity guidelines. Proficiency in SAP or other ERP for material posting and batch tracking. Ability to read mechanical drawings and troubleshoot minor equipment issues. Preferred Exposure to US-FDA/EU regulatory audits and documentation. Green Belt or certification in Lean Six Sigma. Working knowledge of Track & Trace / serialization systems. Experience implementing digital MES or SCADA interfaces. Benefits & Culture Highlights Transparent merit-based growth paths and technical cross-training programs. Subsidised meals, on-site medical facilities, and safe accommodation assistance. Inclusive, safety-first culture that rewards innovation and continuous improvement.

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Global Calcium

Global Calcium

Global Calcium

Manufacturing

Mineral City

200 Employees

18 Jobs

cta

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