Goa, Goa
INR Not disclosed
On-site
Full Time
SR# Responsibilities 1, User Management. (ID Creation, deactivation, Unlocking, Modification, Password Reset.) 2, Data backup and Restoration. 3, Backup validation. 4 Responsible for data archival as per requirements 5 Maintain the logbooks as per requirement. 6 Desktop policy implementation and review. (Privileges, Roles and Group) 7 Date and Time verification 8 To provide support to QA department for audit trail review and periodic user management review 9 Compliance & support during internal, customer and regulatory audits. 10 Support and coordination with Vendor for troubleshooting of manufacturing equipment’s / systems. 11 Assistance to user department in equipment qualification / software validation. 12 Preparation and execution of all documentation activities as per respective SOPs 13 Ensure required documentation and validation of IT systems as per procedures 14 Preparation and execution of all documentation activity like workstation qualification / requalification, Preventive Maintenance, Schedule, Preventive Maintenan Exp: 2yrs to 3yrs in Pharma Industry / IT Job Type: Full-time Pay: ₹20,000.00 - ₹28,000.00 per month Schedule: Rotational shift Ability to commute/relocate: South Goa, Goa: Reliably commute or planning to relocate before starting work (Required) Experience: total work: 1 year (Preferred) Work Location: In person
Verna, Goa
INR Not disclosed
On-site
Full Time
We are seeking an experienced Team Leader for IT Project Management in Goa. Job Description as below: - Develop detailed project plans, timelines, and resource allocation. Lead cross-functional teams in project execution. Ensure project milestones and objectives are met within the specified timeframe. Conduct regular project status meetings, updating stakeholders on progress, risks, and changes. Work closely with business leaders, IT teams, regulatory authorities, and external vendors. Communicate effectively with stakeholders to align on project goals and expectations. Manage expectations and ensure transparent reporting on project health, issues, and risks. Ensure all IT projects comply with pharmaceutical regulatory standards such as GxP, 21 CFR Part 11, and other relevant industry guidelines. Collaborate with quality assurance and regulatory teams to ensure proper documentation and validation processes are followed. Identify potential project risks and develop mitigation strategies. Track and resolve project issues in a timely manner. Escalate significant risks and issues to senior management when necessary. Oversee the implementation of IT systems, including ERP, CRM, LIMS, and other specialized pharma systems. Collaborate with technical teams to ensure seamless integration and compliance with pharma operations. Lead and motivate a team of IT professionals, business analysts, and technical specialists. Foster a collaborative environment, ensuring cross-functional communication and teamwork. Provide guidance and mentoring to team members to support their professional growth. Eligibility: Bachelor’s degree in computer science, Information Technology, Business Administration, or related field. Master’s degree is a plus. 3+ years of experience in IT project management, preferably in the pharmaceutical industry. Strong knowledge of pharmaceutical regulations (e.g., GxP, 21 CFR Part 11). Experience managing ERP, CRM, LIMS, or other pharma-specific IT systems. Strong leadership, communication, and organizational skills. Ability to manage multiple projects and stakeholders simultaneously. Ability to work in a fast-paced, regulated environment with strict compliance requirements. Job Type: Full-time Pay: ₹30,000.00 - ₹45,000.00 per month Schedule: Rotational shift Experience: total work: 8 years (Preferred) Work Location: In person
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