What You ll Do: Seamlessly manage travel - Flight & hotel bookings, visa assistance, airport transfers, and corporate travel coordination. Handle corporate contracts - Build and maintain relationships with travel agencies & hotels. Oversee insurance & payments - Manage renewals, club memberships, and official expenses. Support honorary consular duties - Assist with donations and official engagements. Be the backbone of executive operations - Provide high-level administrative support to key executives. What We re Looking For: Strong organizational & multitasking skills Experience in executive assistance or administration Ability to handle confidential tasks with discretion Location: Koramangala, Bangalore

Were Hiring: Deputy Manager/Manager, HR (Training & Development) Are you passionate about learning & development in the pharmaceutical manufacturing industry? We re looking for an experienced Deputy Manager/Manager - HR (Training & Development) to join our team in Hosur! (20 mins drive from Electronic city bangalore and 5 Mins drive from Attibele) Key Responsibilities: Identify, design, and implement training programs across QA, QC, Production, and R&D. Ensure regulatory compliance (GMP, GDP) through structured training initiatives. Develop e-learning modules and innovative training methodologies. Support talent acquisition and onboarding processes. Oversee administrative functions such as pest control and laundry management. Who We re Looking For: Experience in pharmaceutical manufacturing (training & development). Strong knowledge of regulatory training requirements. Ability to drive learning culture and enhance workforce capabilities.

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. Roles & Responsibilities: Working as a part of a team in Method Validation Research Laboratory. Setting up Laboratory Equipment and conducting tests and experiments. Recording the data. Presenting results to senior research staff. Keeping up to date with relevant scientific and technical developments. Performing Synthesis Reactions. Job Specification: Qualification : M.Sc. Organic Chemistry/M.Sc. Chemistry. Experience: 1 to 4 Years in Pharma Industry Location: Hosur, Tamil Nadu Job Role: Junior Research associate Notice Period: Minimum 1 -3 Months

Job Title: Officer - Admin (HR Department) Location: Hosur Department: Human Resources Reporting To : Deputy General Manager - HR Company: Global Calcium Pvt Ltd Job Summary: We are looking for a proactive and detail-oriented Officer - Admin to manage various administrative and employee welfare activities within the HR department. The ideal candidate will be responsible for overseeing pest control, canteen operations, laundry services, and other general administration tasks to ensure a smooth and efficient workplace environment. Additionally, the role requires maintaining and updating SOPs, GMP documents, agreements, and having strong audit-facing skills. Key Roles & Responsibilities: Pest Control Management Oversee end-to-end pest control activities across company premises. Coordinate with vendors for timely pest control services and ensure compliance with safety standards. Maintain records of pest control schedules and ensure adherence to hygiene protocols. Canteen Management Supervise canteen operations, ensuring food quality, hygiene, and timely service. Coordinate with vendors and staff to manage menu planning and food supply. Address employee feedback and concerns regarding canteen services. Employee Welfare Activities Plan and execute employee engagement and welfare programs to enhance workplace morale. Organize recreational activities, wellness programs, and awareness campaigns. Ensure smooth implementation of employee benefits related to welfare initiatives. Laundry Management Oversee laundry services for employees, ensuring efficiency and quality control. Coordinate with external vendors or in-house staff for laundry operations. Maintain records and manage inventory related to laundry services. General Administration Activities Manage day-to-day administrative operations and support HR functions. Handle vendor coordination, procurement of office supplies, and facility maintenance. Ensure compliance with company policies and regulatory requirements. Documentation & Compliance Maintain and update SOPs and GMP documents as per regulatory standards. Ensure timely updates and renewals of agreements with vendors and service providers. Possess strong audit-facing skills and the ability to present documentation and compliance records during audits. Required Skills & Qualifications: Bachelors degree in Business Administration, HR, or a related field. 2-5 years of experience in administration, facility management, or HR support. Strong organizational and multitasking abilities. Good vendor management, negotiation, and compliance skills. Proficiency in MS Office (Excel, Word, PowerPoint). Ability to handle audits

We are seeking a highly motivated Research Associate / Executive to join our API Research & Development (R&D) team . The role involves chemical synthesis, process optimization, and scale-up of Active Pharmaceutical Ingredients (APIs). The candidate will be responsible for designing and executing synthetic routes , improving process efficiency , and ensuring cost-effectiveness . Key responsibilities include analyzing and characterizing products using advanced analytical techniques such as HPLC, GC, while maintaining regulatory and quality compliance throughout the development process. The candidate will collaborate with cross-functional teams to facilitate smooth technology transfer and troubleshooting. Qualifications: M.Sc. in Chemistry (Organic / Analytical / Pharmaceutical) Strong proficiency in laboratory techniques, purification methods, and analytical tools Hands-on experience with HPLC, GC, and spectroscopic techniques

Job Description 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 R&D 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

Are you an experienced API (Active Pharmaceutical Ingredients) sales and marketing professional looking for an exciting opportunity? Join our team and drive business growth in the West India region ! Job Title: Manager - API Pharmaceuticals Sales & Marketing Location: West India Region (Mumbai & Ahmedabad Market) Department: Sales & Marketing - API Pharmaceuticals Key Responsibilities: Develop and implement sales strategies to achieve revenue targets and expand market share. Build and maintain strong relationships with pharmaceutical manufacturers, distributors, and key industry stakeholders. Conduct market research and competitor analysis to identify new business opportunities. Manage lead generation, follow-ups, and convert prospects into long-term clients. Negotiate contracts, pricing, and terms while ensuring compliance and profitability. Collaborate with regulatory, production, and logistics teams to ensure smooth order execution. Monitor sales performance, generate reports, and provide strategic insights. Represent the company at trade shows, exhibitions, and industry events to enhance brand visibility. What We re Looking For: Education: Bachelor s degree in Pharmacy, Chemistry, Life Sciences, or related field. (MBA in Sales/Marketing is a plus!) Experience: 5-10 years in API sales and marketing in the pharmaceutical industry , preferably in the West India region . Strong understanding of API products, regulatory requirements, and the pharmaceutical supply chain. Excellent communication, negotiation, and relationship management skills. Self-motivated, target-driven, and capable of working independently . Proficiency in MS Office and CRM tools. Willingness to travel extensively within the region. Join us and make an impact in the pharmaceutical industry! If youre ready to take on this challenge, we d love to hear from you.

Global Calcium is looking for an experienced Manager - Regulatory Affairs with expertise in DMF & CEP filings and global regulatory submissions. If you have a passion for ensuring regulatory compliance and working with global health authorities, we want to hear from you!Key Responsibilities: DMF & CEP Filings: Prepare, review, and submit Drug Master Files (DMFs) in eCTD/NeeS format for USFDA, EU, and other markets. Handle amendments, annual updates, and regulatory deficiency responses. Regulatory Submissions & Compliance: Collaborate with R&D, Quality, and Manufacturing teams to compile technical data while ensuring adherence to GDP & global regulatory guidelines. Regulatory Communication & Strategy: Act as a liaison with regulatory authorities (USFDA, EU-GMP, TGA, etc.) and provide guidance on compliance strategies. Audits & Documentation: Support regulatory inspections & audits, ensure all regulatory documents are updated, and train internal teams on submission processes.Qualifications & Skills: Education: M.Pharm / B.Pharm / M.Sc. in Pharmaceutical Sciences, Regulatory Affairs, or Chemistry. Experience: 08+ years in Regulatory Affairs, with expertise in DMF & CEP filings. Key Skills: Regulatory guidelines, documentation, stakeholder management, analytical thinking, and communication skills.Why Join Us? Work in a globally recognized organization in the pharmaceutical industry. Contribute to key regulatory approvals across international markets. Collaborate with a team of experts in a dynamic environment. Interested candidates can send their resumes to: ramakrishnar.r@globalcalciumpharma.com Know someone who might be a great fit? Share this opportunity!

Education: MCA, M.Sc. CS, B.E. CS Experience: Relevant experience in the pharmaceutical industry Key Responsibilities: Install & configure software, hardware, computers, and laptops Troubleshoot PC, laptop, and network issues Manage system policies & user accounts Backup & data recovery to ensure security & compliance Install & maintain CCTV, printers, switches, and other IT infrastructure What We re Looking For: Pharma IT experience - Understanding of regulatory & data security requirements Network & system administration skills Troubleshooting expertise for hardware & software issues Strong documentation & compliance knowledge

Key Responsibilities: Develop and implement sales strategies to achieve revenue targets and expand market share. Build and maintain strong relationships with pharmaceutical manufacturers, distributors, and key industry stakeholders. Conduct market research and competitor analysis to identify new business opportunities. Manage lead generation, follow-ups, and convert prospects into long-term clients. Negotiate contracts, pricing, and terms while ensuring compliance and profitability. Collaborate with regulatory, production, and logistics teams to ensure smooth order execution. Monitor sales performance, generate reports, and provide strategic insights. Represent the company at trade shows, exhibitions, and industry events to enhance brand visibility.What Were Looking For: Education: Bachelor’s degree in Pharmacy, Chemistry, Life Sciences, or related field. (MBA in Sales/Marketing is a plus!) Experience: 5–10 years in API sales and marketing in the pharmaceutical industry, preferably in the West India region. Strong understanding of API products, regulatory requirements, and the pharmaceutical supply chain. Excellent communication, negotiation, and relationship management skills. Self-motivated, target-driven, and capable of working independently. Proficiency in MS Office and CRM tools. Willingness to travel extensively within the region. Join us and make an impact in the pharmaceutical industry! If you're ready to take on this challenge, we’d love to hear from you. Apply now! Send your resume to ramakrishna.r@globalcalciumpharma.com

Qualification: M.Sc. Chemistry Experience: 3-6 Years About the Role: Join Global Calcium Pvt. Ltd. , a leading pharmaceutical manufacturer, and be part of our Analytical Research & Development (AR&D) Lab . If you have a passion for analytical techniques, compliance, and innovation, this is your chance to grow with us! Key Responsibilities: Conduct wet and instrumental analysis (HPLC, GC, IR, UV) for pharmaceutical raw materials, intermediates, and finished products. Perform Auto Filtration, Karl Fischer (KF) Titration, and Analytical Calibration for instruments. Develop, validate, and optimize analytical methods as per regulatory guidelines. Ensure compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) . Troubleshoot analytical instruments, conduct stability studies, and perform impurity profiling. Prepare and maintain analytical documentation, reports, and SOPs . Collaborate with cross-functional teams to support R&D and quality control . What We re Looking For: Technical Expertise - Hands-on experience with analytical instruments (HPLC, GC, UV, IR, KF Titrator). Regulatory Knowledge - Familiarity with ICH, USFDA, and other global guidelines . Problem-Solving Skills - Ability to troubleshoot instruments and analytical challenges. Attention to Detail - Strong documentation and data interpretation skills. Team Player - Ability to collaborate with R&D, QC, and regulatory teams.

We Are Hiring Senior Manager / AGM Manufacturing (Nutraceuticals/API)Are you an experienced manufacturing leader in the pharmaceutical industry looking for your next big opportunity? We are seeking a dynamic and results-driven professional with 15 to 20 years of experience in Nutraceuticals / API manufacturing to join our team at Global Calcium Pvt. Ltd.Why Join Us? Be a part of a leading pharmaceutical company driving excellence in API & Nutraceuticals. Lead large-scale manufacturing operations with a focus on efficiency, compliance, and innovation. Work in a GMP-compliant, globally recognized manufacturing environment. Collaborate with R&D, Quality, and Supply Chain teams to enhance productivity and operational excellence.What We Are Looking For: 15 to 20 years of experience in Nutraceuticals / API manufacturing. Strong expertise in GMP, regulatory compliance, and process optimization. Proven leadership in managing large-scale pharmaceutical operations. Experience in lean manufacturing, operational excellence, and continuous improvement. Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc / Chemical Engineering or equivalent. Interested candidates can share their CVs at ramakrishna.r@globalcalciumpharma.comIf you know someone who fits this role, please tag them or share this opportunity with your network! Lets connect great talent with the right opportunity.

OverviewThe Deputy Manager - QA plays a crucial role in maintaining the quality standards of products and processes within the organization. This position requires a vigilant professional who ensures that the quality assurance processes are strictly followed to meet customer satisfaction and compliance regulations. Responsible for leading a team of QA specialists, the deputy manager will oversee testing procedures, quality audits, and corrective actions to mitigate risks. In an environment where precision and reliability are paramount, the Deputy Manager - QA will work closely with various departments to foster a culture of quality and continuous improvement. This role is critical in minimizing potential defects, enhancing product performance, and ultimately supporting the organizations goal of delivering superior value to customers. Establishing effective quality management systems and providing training for staff are essential elements of this position, making it pivotal for both product integrity and organizational efficiency.Key ResponsibilitiesLead the quality assurance team, providing guidance and support.Develop, implement, and maintain QA processes and standards.Conduct regular quality audits to ensure compliance with regulatory requirements.Analyze quality metrics and prepare reports for senior management.Identify areas for process improvement and implement corrective actions.Collaborate with cross-functional teams to resolve quality issues.Ensure effective communication of quality concerns across departments.Manage external supplier quality assessments and audits.Train and mentor QA staff to enhance their skills and knowledge.Develop and conduct internal training programs on QA principles.Maintain and update the Quality Management System (QMS).Introduce and promote best practices in quality control.Participate in product design reviews to influence quality requirements.Oversee the documentation of quality assurance processes and results.Facilitate root cause analysis for non-conformances and implement solutions.Required QualificationsB.Pharma / M.Pharma / M.Sc Chemistry or related field. At least 8+ years of experience in a quality assurance role.Proven leadership skills, with prior experience managing teams.Certification in quality management systems (e.g., ISO 9001).Familiarity with industry standards and regulations.Strong understanding of statistical process control (SPC).Experience with quality auditing and compliance assessment.Excellent analytical and problem-solving abilities.Proficiency in quality management software and tools.Capacity to manage multiple tasks and priorities efficiently.Strong written and verbal communication skills.Ability to collaborate effectively with different stakeholders.Attention to detail and a commitment to quality excellence.Experience in training and developing team members.Knowledge of risk management practices in quality.

Position: Trainee - API Quality Control Experience Required: 0-1 Year (Freshers Welcome!) Key Responsibilities: Understanding Quality Control Basics - Introduction to GMP, GLP, and Data Integrity. Sampling Handling of Raw Materials, In-Process, Finished Products. Performing Basic Wet/Chemical Analysis - Assay Titration, Loss on Drying (LOD), Sulphated Ash. Preparation of Volumetric Solutions Standardization. Basic Instrument Handling - FTIR, UV, and pH Measurement. Learning Assisting in Documentation - Lab Records Analytical Reports. Ensuring Compliance with Regulatory Requirements. Required Skills: Strong interest in analytical chemistry laboratory techniques Understanding of basic quality control parameters Eagerness to learn pharmaceutical industry standards Why Join Us Structured training mentorship programs Career growth opportunities within QC Analytical Research Competitive compensation benefits

Receiving Raw Materials from stores Preparing feed solution and transferring the feed solution into the cell where the electrolysis is planned. Operating electrolytic cells as per relevant SOP Maintaining Relevant Documents. Operating the rectifier as per relevant SOP. Operating filter press as per the relevant SOP Filtering the solution. Maintaining work place-good housekeeping as per cGMP. Making online entries in the Batch Manufacturing Records. Assist in Implementation of ISO 9001,ISO 14001,FSSC 22000,HACCP, Halal cGMP requirements. Ensuring implementation of OCP Nos : OCP/PROD/07 OCP /STR/02. Cleaning the relevant equipments, accessories which is in the work place. To comply with all requirements, All safety rules/precautions to be followed strictly. Handing over charge to the reliving production associate.

Key Responsibilities: Leadership Team Management: Lead and mentor the QC team, ensuring efficient workflow and compliance. Review Approval of Analytical Documents: Oversee Analytical Reports, COAs, Method Validations, and Instrument Calibration Records. Analytical Expertise: Extensive experience in Wet Chemical Analysis, Instrumental Techniques (HPLC, GC, FTIR, UV, Auto Titration, Particle Size Analysis, etc.). Quality System Management: Handle Out of Specification (OOS), Out of Trend (OOT), Deviation Investigations, CAPA Implementation. Regulatory Compliance: Ensure adherence to GMP, GLP, ICH, WHO, FDA, and EU-GMP guidelines. Preparation of SOPs, Specifications, and STPs: Develop and maintain robust quality control procedures. Handling QMS Documents: Oversee Change Control, Market Complaints, Incidents, and Laboratory Investigations. Audit Readiness Compliance: Provide responses and corrective actions for regulatory audits (USFDA, WHO, EU-GMP, MHRA, etc.). Cross-Functional Collaboration: Work closely with Production, RD, and Quality Assurance teams to drive continuous improvements. Required Skills: Strong leadership problem-solving skills. Expertise in API Quality Control, including chemical and instrumental analysis. Proficiency in Regulatory Compliance QMS Documentation. Excellent communication team management capabilities. Hands-on experience in CAPA, Deviation Management, and Analytical Method Validations. Exposure to handling regulatory inspections audit preparations.

Job Summary: We are looking for a Officer / Executive - Industrial Relations (IR) to manage end-to-end industrial relations functions in our pharmaceutical company. The ideal candidate should have a basic understanding of labor laws, employee relations, and compliance management. They will be responsible for ensuring a smooth and legally compliant work environment by handling grievances, disciplinary actions, and union relations. Key Responsibilities: Industrial Relations Compliance: Handle end-to-end IR activities in line with labor laws and company policies. Ensure compliance with Factories Act, Industrial Disputes Act, Trade Union Act, and other labor laws applicable to the pharmaceutical industry. Maintain and update statutory records, licenses, and registers as per regulatory requirements. Coordinate with government labor departments and ensure timely submission of reports and returns. Employee Relations Grievance Handling: Act as a point of contact for grievance redressal and resolve employee issues proactively. Assist in conducting disciplinary proceedings and issuing notices when required. Support in handling employee disputes, legal cases, and negotiations with union representatives. Union Workforce Management: Maintain a professional relationship with union representatives and workers to ensure a peaceful work environment. Participate in union negotiations and support in drafting agreements in consultation with senior management. Monitor workplace issues and ensure compliance with company policies to prevent industrial disputes. Audits Reports: Assist in conducting internal and external labor audits and ensure corrective actions are taken. Prepare and maintain IR reports, labor compliance reports, and dispute resolution documentation. Required Qualifications Skills: Education : Bachelor s/Master s degree in Human Resources, Industrial Relations, or Labor Law. Experience: 1-3 years of experience in handling Industrial Relations (IR) in a manufacturing or pharmaceutical company. Basic understanding of labor laws, statutory compliance, and union management. Strong communication and negotiation skills. Ability to handle conflict resolution and grievance handling efficiently. Proficiency in MS Office (Excel, Word, PowerPoint). Preferred Qualifications: Experience in a pharmaceutical or manufacturing setup will be an added advantage. Knowledge of wage settlements, labor contracts, and employee welfare programs

Key Responsibilities: Perform Routine Wet Chemical Analysis - Assay Titration, Loss on Drying (LOD), Sulphated Ash, pH Measurement, Solubility Testing. Instrumental Analysis - Hands-on experience with FTIR, UV, HPLC, GC, and Auto Titration. Sampling Testing of Raw Materials, In-Process, and Finished Products. Preparation Standardization of Volumetric Solutions. Review Maintenance of Analytical Documentation - Analytical Reports, Logbooks, and COAs. Conduct Stability Studies Method Validations. Basic Troubleshooting Calibration of Analytical Instruments. Ensure Compliance with GMP, GLP, and Regulatory Requirements. Required Skills: Strong understanding of wet instrumental analysis. Hands-on experience in Analytical Techniques - FTIR, UV, HPLC, GC, Auto Titration. Knowledge of Regulatory Guidelines - ICH, WHO, FDA, EU-GMP. Understanding of Quality Management Systems (QMS) Data Integrity. Ability to handle Out of Specification (OOS) Out of Trend (OOT) investigations. Good communication documentation skills.

To execute works as per procedure and compliance with ISO 9001 standards, Quality Management System Compliance, cGMP standards, ISO 14001 & Halal, HACCP standards. Candidate should read and understand SLD Following and executing works as per related SOPs & OCP of the concerned department. Attending the Preventive Maintenance & Break down maintenance of Machineries like Chilling plant, RO Plant, GLR, SSR, Filter Press, Centrifuge, RCVD, Blender, Sifter, Water Pumps and Cooling towers, electric systems Supervising of Plant operations. Reporting the day-to-day activities to Manager- Maintenance. Coordinating with the AMC of Machineries. Check and verify the maintenance log books of each and every equipment. Entering of all works regarding preventive maintenance in records as per SOP/OCP. Candidate should have knowledge in MTBF & MTTR Candidate should have knowledge in HVAC system Candidate should have operation and maintenance of utility Equipment s Candidate should have knowledge in engineering Quality management system Candidate should have knowledge in Equipment Qualifications Candidate should have safety knowledge and adequate PPE s to be use in API industry. Qualifications [B.E, B. Tech, Diploma- Electrical/Mechanical ] Proffered Experience: Pharma, Food/chemical industry Experience. Example: Excellent verbal and written communication skills