Abdul Muneeb Email & Phone Number

Kairana, Uttar Pradesh, India

Medical Representative Trainee:- Gain in-depth knowledge of the company's products and the competitive landscape.- Build professional relationships with healthcare professionals and deliver product presentations.- Manage a designated territory, plan visits, and organize appointments for maximum coverage.- Gather market intelligence, including competitor activities and market trends.- Participate in comprehensive training programs to enhance product knowledge and selling skills.- Adhere to laws, regulations, and ethical guidelines when interacting with healthcare professionals.- Track and analyze sales performance, customer feedback, and market dynamics.- A bachelor's degree in a relevant field is preferred.- Strong communication and presentation skills.- Self-motivated and results-oriented with a drive to achieve sales targets.- Ability to work independently and manage time effectively.- Strong ethical mindset and commitment to compliance.- Willingness to travel within the assigned territory.

Kala Amb Himachal

Responsibilities:1. Quality Management System: Develop and maintain a robust Quality Management System (QMS) that aligns with industry best practices and regulatory requirements. Establish quality policies, procedures, and guidelines to ensure compliance and continuous improvement.2. Regulatory Compliance: Stay updated on relevant regulatory requirements, such as those from regulatory bodies like the FDA or local authorities. Ensure adherence to these regulations throughout the product lifecycle, from formulation to packaging and distribution.3. Product Development: Collaborate with cross-functional teams, including R&D, manufacturing, and packaging, to ensure quality standards are integrated into the product development process. Provide input on formulation development, stability testing, and compatibility assessments.4. Quality Control: Establish and oversee robust quality control processes to verify the quality and consistency of raw materials, intermediates, and finished aerosol perfumes. Define and implement appropriate sampling plans, testing methodologies, and acceptance criteria.5. Supplier Management: Collaborate with the procurement team to establish quality agreements with suppliers and conduct supplier audits as needed. Evaluate and qualify suppliers based on their ability to meet quality and compliance requirements.6. Quality Audits and Inspections: Plan and conduct internal audits to ensure compliance with quality standards, regulations, and the QMS. Prepare for and support external audits and inspections by regulatory authorities or third-party certifying bodies.7. Corrective and Preventive Actions (CAPA): Lead and participate in CAPA investigations to address non-conformities, deviations, and customer complaints. Analyze root causes, develop corrective action plans, and track their implementation to prevent recurrence.

Baddi, Himachal Pradesh, India

Rohtak, Haryana, India

Responsibilities:1. Document Control: Implement and maintain an efficient document control system to manage all QA documentation, including standard operating procedures (SOPs), batch records, change controls, deviations, and CAPAs.2. Compliance: Ensure all QA documentation is in compliance with applicable regulatory standards, such as Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and company-specific quality standards.3. Documentation Creation and Revision: Collaborate with subject matter experts (SMEs) to develop, review, and revise QA-related documents, ensuring clarity, accuracy, and adherence to established guidelines. This includes creating and updating SOPs, batch records, and other relevant documents.4. Review and Approval: Perform thorough reviews of QA documentation to verify completeness, accuracy, and compliance with regulatory requirements.5. Change Control: Manage the change control process for QA documentation, including initiation, review, and implementation of changes. Ensure that all changes are properly documented, reviewed, and approved in accordance with established procedures.6. Training and Communication: Coordinate training activities related to QA documentation to ensure employees are aware of and understand the requirements and procedures. Conduct training sessions and provide guidance to employees on document control processes and compliance expectations.7. Audits and Inspections: Assist in internal and external audits and inspections by providing necessary documentation, addressing queries, and ensuring compliance with regulatory standards. Participate in identifying and implementing corrective actions as needed.8. Continuous Improvement: Identify areas for process improvement within the QA documentation system and propose solutions to enhance efficiency, accuracy, and compliance. Actively contribute to the development and implementation of best practices.

Rohtak, Haryana, India

Trainee Production Officer in a pharmaceutical company manufacturing ointments, creams, and ophthalmic ointments:- Provide support to the production team in day-to-day operations- Assist with equipment setup, operation, and troubleshooting- Participate in batch manufacturing activities for ointments, creams, and ophthalmic ointments- Follow established procedures, recipes, and formulations for accurate and consistent production- Learn to weigh and measure raw materials and mix and blend ingredients- Monitor critical parameters such as temperature and time during the manufacturing process- Work with specialized equipment such as mixers, homogenizers, and filling machines- Adhere to Good Manufacturing Practices (GMP) and standard operating procedures (SOPs)- Conduct in-process checks, inspections, and tests to ensure quality assurance- Perform visual inspections, pH testing, viscosity measurements, and other quality control procedures- Identify deviations, record them accurately, and report any potential quality issues- Maintain accurate and up-to-date production records, batch records, and logbooks- Understand the importance of proper documentation and data integrity- Monitor equipment during production to identify deviations or malfunctions- Report equipment issues promptly and assist in troubleshooting activities- Adhere to safety protocols and maintain a clean and organized work environment- Prioritize safety and follow personal protective equipment (PPE) requirements- Learn about equipment maintenance and its importance in uninterrupted production.

Dehradun, Uttarakhand, India

TOPIC- PHARMACOGNOSTICAL STUDY OF ASHWAGANDHA (Withania somnifera Linn)- Ashwagandha (Withania somnifera Linn) is a medicinal plant widely used in traditional medicine.- Pharmacognostical study involves evaluating the identity, quality, and therapeutic properties of medicinal plants.- Macroscopic evaluation includes observing the visible features of Ashwagandha, such as leaves, stems, and roots.- Microscopic analysis examines the cellular structures and anatomical features of Ashwagandha plant parts.- Phytochemical analysis identifies and quantifies the chemical constituents of Ashwagandha.- Ashwagandha contains bioactive compounds like alkaloids, withanolides, flavonoids, sterols, and saponins.- Thin-layer chromatography (TLC) separates and analyzes the chemical constituents of Ashwagandha.- HPTLC (High-Performance Thin-Layer Chromatography) offers improved resolution and accuracy in separating and quantifying compounds.- HPLC (High-Performance Liquid Chromatography) provides precise measurement and standardization of active constituents.- Pharmacognostical studies contribute to understanding Ashwagandha's botanical, chemical, and therapeutic characteristics.

M.Sc Pharmaceutical Chemistry, Pharmacy, Pharmaceutical Sciences, And Administration

Activities and Societies: Kabaddi player NSS (NATIONAL SERVICE SCHEMES) C CERTIFICATE HOLDER DROPOUT

Bachelor Of Pharmacy - Bpharm, Pharmaceutical Sciences, 2Nd

Intermediate, Physics Chemistry Biology, 69%