Qualification & ExperienceMS Ophthalmology / DNB / DO in Ophthalmology with a long-term fellowship in Vitreo-Retina Experience: 2+ years of post-fellowship experience in a reputed ophthalmology institutionExpertise in managing complex retinal diseases, surgical interventions, and advanced retinal imaging

Qualification & ExperienceQualifications: MS Ophthalmology / DNB / DO Ophthalmology with a long-term fellowship in Cataract SurgeryExperience: 3+ years of post-fellowship experience in a reputed ophthalmology institutionExpertise in phacoemulsification and advanced cataract surgical techniques

ResponsibilitiesOversee daily hospital operations and ensure smooth functioning Manage OPD/IPD processes, patient flow, and service delivery Lead and coordinate cross-functional teams Ensure quality standards, patient satisfaction, and compliance Drive process improvements and operational efficiency EligibilityMinimum 6–10 years of experience in hospital operations Strong leadership and team management skills Excellent communication and problem-solving abilities Healthcare/hospital background is mandatory

ResponsibilitiesOversee responsibilities in delivering service to the client including mobilization of resources required in delivering the service and managing their performance. Work closely with the client project lead and service delivery lead to manage risks, issues, and escalations and drive successful project completion with high quality Pharmacovigilance Services involve the detection, assessment, and prevention of adverse effects related to pharmaceutical products. These services ensure the safety and efficacy of medications by monitoring and analyzing data from clinical trials, healthcare providers, and patients. The goal is to identify potential risks and take appropriate actions to protect patient health. They also help pharmaceutical companies comply with regulatory requirements. Effective pharmacovigilance services are essential for maintaining public trust in medications. Create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database as per client guidelines and applicable global regulatory requirements.Qualification & ExpeirenceQualifications:Bachelor of Pharmacy/Master of Pharmacy Years of Experience:7 to 11 years

ResponsibilitiesYou will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world’s leading biopharma companies bring their vision to life – enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience. Pharmacovigilance Services involve the detection, assessment, and prevention of adverse effects related to pharmaceutical products. These services ensure the safety and efficacy of medications by monitoring and analyzing data from clinical trials, healthcare providers, and patients. The goal is to identify potential risks and take appropriate actions to protect patient health. They also help pharmaceutical companies comply with regulatory requirements. Effective pharmacovigilance services are essential for maintaining public trust in medications. Create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database as per client guidelines and applicable global regulatory requirements. Qualification & ExperienceQualifications:Bachelor of Pharmacy Years of Experience:3 to 5 years

ResponsibilitiesPrepare and review essential documentation, including GMP, GLP, and GCP manuals. Responsible and Managing of Document Management Life Cycle and Record Management Issuance, Retrieval, Archival and Control of GMP Documents/Records and DSMs (GMP documents) through Manual and Electronic systems. Secure bin management Knowledge on PDOCs, p-log and SDS Applications Ensure compliance with Enterprise Records Retention Schedule (ERRS) maintained by the enterprise records and Information Management (eRIM) group. Location mapping & tracking of documents/ records archived in Active Record Centers. Competency in MS office, Adobe Acrobat and documentation data base systems Execute tasks supporting Quality Systems functions and oversee Documentation Control and administrative functions of the DMS repository. Qualification & ExpeirenceBachelor's Degree (Chemistry/Pharmacy) with 4+ Years of Experience or Master's Degree (Chemistry/Pharmacy) with 3+ Years of Experience Proficiency in Document Management and Control Experience with Computer Software Validation Concepts Familiarity with regulatory requirements and compliance standards Effective communication skills

ResponsibilitiesEvaluate, review, and approve validation master plans, protocols, and reports, ensuring compliance with company standards and regulatory requirements. Troubleshoot validation issues for equipment and performance processes, providing expertise for resolution. Conduct statistical analysis of testing results and process anomalies and provide high-level data analysis support for Quality Investigations. Guide the writing, review, and approval of validation process documents and technical reports, ensuring adherence to the latest Pfizer Quality Standards. Contribute to moderately complex projects, manage time effectively, and develop plans for short-term work activities. Manage routine Quality systems such as Change Control, Quality Agreement, Documentation, and Investigations, and coordinate testing with functional groups. Maintain the Site Validation Master Plan, support regulatory audits, and represent engineering validation on site or network teams. Support product transfers, new product development, regulatory queries, cost improvement projects, and Cleaning Validation, ensuring integration of validation schedules in production and participating in deviation investigations. Qualification & ExpeirenceHigh school diploma (or equivalent) with 8+ years of experience or associate’s degree with 6+ years of experience or BA/BS with 2+ years of experience or MBA/MS with any years of relevant experience Proven expertise in Good Manufacturing Practices Strong working knowledge of various quality systems and processes

ResponsibilitiesLead people, technology, and financial resources. Identify and develop innovative concepts for process or product improvements, taking calculated risks to achieve results. Solve complex problems, leveraging experience from various areas as needed. Recognize and address development needs, creating growth opportunities for colleagues. Oversee and manage multiple projects and ongoing work activities, ensuring compliance with approved methodologies and cGMP documentation. Provide technical expertise and support for laboratory and core applications, collaborating with business partners to identify and implement improvement areas. Qualification & ExpeirneceMSC in microbiology / biotechnology with 10+ years of experience Proven experience in leading colleagues and managing projects A deep understanding of Good Manufacturing Practices (cGMP) compliance requirements for Quality Control Laboratories Proficiency with Quality Control Microbiology instruments and methodologies The Media Lead is currently accountable for managing the entire Media Management Program, which encompasses media preparation, inventory control, and execution of Growth Promotion Testing

Responsibilities  Stability Study Execution Coordinate withdrawal of stability samples of finished products and ensure submission to QC for analysis. Prepare and review stability protocols and stability summary reports. Prepare risk assessments related to stability studies and storage conditions. Handle and document change control investigations related to stability activities.  Control Sample Management Ensure proper control sample setup, monitoring, withdrawal, destruction, and maintenance of related logbooks. Maintain control-sample inventory dashboard — RM and FP retention samples. Coordinate with QC for control-sample analysis where required.  Storage Conditions & Calibration Monitor and review storage conditions including temperature, relative humidity, and pressure differential. Ensure calibration of thermo-hygrometers and chamber sensors per defined frequency. Coordinate chamber alarm and excursion response per SOP — chamber recovery, sample-impact assessment.  Self-Inspection & Software Operations Prepare and execute self-inspection plans as per QA requirements. Ensure online documentation compliance as per GMP requirements. Perform activities in validated software systems (Quantum or equivalent) as per assigned user access rights.Qualification & ExpeirneceQualification B.Pharm / M.Pharm Experience 1 – 3 years (OSD experience preferred)

Responsibilities Investigation Management Conduct investigations related to Market Complaints, Deviations, Change Controls, Incidents, Laboratory Incidents, CAPA (Corrective and Preventive Actions), Returned Goods, and Product Recalls. Quality Management System (QMS) Documentation Supervise issuance, distribution, retrieval, and destruction of all QMS documents in accordance with company procedures. cGMP Compliance Ensure effective implementation and adherence to current Good Manufacturing Practices (cGMP) at the manufacturing site. Documentation Support Assist in preparation, review, and maintenance of Quality Assurance documentation. Audit Handling Coordinate and support internal and external quality audits. Prepare and review compliance reports following audits. Quality System Documentation Prepare and maintain key quality documents including: Self-Inspection Plan Site Master File (SMF) Validation Master Plan (VMP) Quality Manual Software System Operations Perform assigned activities in the Quantum software system as per authorized user rights. Quality Risk Management Prepare, review, and maintain Quality Risk Management (QRM) documents.