4089 Gmp Jobs - Page 17

Company Name Bigbasket Job Title Quality Executive (Staples) Job Location: Madurai Tamil Nadu Description About the company Starting our journey in 2011, today, bigbasket a Tata Enterprise is India's largest online supermarket with over 13 million customers and a presence in 60+ cities & towns. With our presence spanning the entire spectrum of consumer needs, we operate through a range of business lines bigbasket, bbnow, bbinstant, bbdaily, fresho, bbmandi, and bbsaathi. We offer convenience by making grocery shopping easy for customers while enhancing their experience. With more than 47,000 employees, we are a proud & growing bigbasket family. With our businesses scaling, we are keen on wor...

-Candidates should be from rubber or related industries Lead end to end operations -Deploy lean, 5S, Six Sigma, Kaizen and TPM -Drive digital transformation -Leverage CRM Systems to align production customer expectations -Utilize Power BI/Tableau Required Candidate profile -Lead Capital Project -Team building -15-20 years of experience in plant operations with focus on rubber/silicone/polymer

To analyze incoming ingredients, in process, finished goods, environmental samples, air monitoring samples, water samples, human swabs to ensure the product and work place conforms to microbiological speciation laid down by the organization. QUALITY CHECKS Ensure daily plating of samples. Check that all finished product that producing, comply with the company s specification. Take the necessary samples as laid out per the QC procedure. Grade all finished product as laid out by the QC sampling procedure, record information on to all relevant physical and electronic documentation Perform adequate testing s procedures on individual finished products. Performs environmental swabs of lines on a m...

Execute production as per plan & SOPs. Ensure quality, yield & safety. Maintain BMRs/logbooks. Coordinate with teams, support troubleshooting, report deviations, and uphold EHS, GMP & area cleanliness standards. Suggest process improvements.

Perform daily production as per SOPs & batch instructions. Operate reactors, filters, centrifuges. Maintain BMRs, ensure GMP/EHS compliance, proper labeling & raw material handling. Coordinate with shift in-charge for smooth operations.

Job Title: Manager - Regulatory Affairs / Quality Assurance Company: GreenSignal Bio Pharma Pvt Ltd Location: Gummidipoondi, Chennai, Tamil Nadu Experience: 10-15 years in Quality Assurance and Regulatory Affairs, specifically within the Vaccine, Injectable, and Sterile Industry Educational Qualification: Bachelors or Masters in Pharmacy M.Sc in Biotechnology, Microbiology, or a related field Additional qualifications in life sciences or pharmaceutical sciences are a plus Job Overview: As the Manager QA / Regulatory Affairs , you will play a pivotal role in ensuring that our vaccine , injectable , and sterile pharmaceutical products meet global regulatory requirements and quality assurance (...

Preferred candidate profile Diploma in Chemical Engineering / B. Sc Chemistry with minimum 1 year of experience in API Production Recruiter Mohaneswara Reddy https://www.linkedin.com/in/mohaneswarareddy

Pharmacist, Sourcing & Procurement (Medicines Division) Position Overview Selligence is seeking a highly motivated and experienced Pharmacist to join our Sourcing and Procurement team in Hyderabad, specifically focusing on raw materials for Eva Pharma s Medicines (Generics) division. This role is crucial for maintaining a robust and sustainable supply chain, supporting Eva Pharma s global product development initiatives. Key Responsibilities Lead sourcing and procurement activities for raw materials specific to Eva Pharma s Medicines (Generics) division, ensuring timely, cost-effective, and quality-compliant acquisition. Collaborate closely with Eva Pharma s internal IP (Intellectual Propert...

1. Quality System Management: Establish, implement, and maintain the Quality Management System (QMS) as per cGMP, WHO, and regulatory norms . Oversee activities related to change control, deviations, CAPA, OOS/OOT investigations, and risk assessments . Ensure all QA processes align with company policies and current regulatory requirements. 2. Documentation & Compliance: Review and approve SOPs, BMRs, BPRs, validation protocols , and analytical reports. Ensure all documentation complies with Good Documentation Practices (GDP) and data integrity requirements. Supervise document control , issuance, archival, and version management systems. 3. Batch Release & In-Process Quality Assurance: Ensure...

Experience in Vaccine/Injectable/Sterile manufacturing setup Review and evaluate facility, utility, process equipment & instrument design Prepare and review URS, DQ, FAT, SAT, IQ, OQ, PQ documents Conduct Computer System Validation (CSV) as per GAMP & 21 CFR Part 11 Coordinate with project teams to meet timelines and milestones Ensure compliance with GMP and regulatory standards Investigate deviations, failures, and non-conformances Identify root causes and implement CAPA Support audits and inspection readiness activities Job Location: Kadi, Gujarat ( Bus facility available for daily commute) Note: Immediate joiners will be preferred first

Company Description At TAPI, we're not just a companywe're a community committed to advancing health from the core. As the world's leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we're shaping the future of health worldwide. Our strength lies in our peoplea team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that t...

Job Title: Senior Automation Engineer Pharmaceutical Manufacturing Location: Remote Experience: 10+ years Industry: Pharmaceutical / Biotech Manufacturing Job Summary: The Senior Automation Engineer is responsible for driving automation initiatives across pharmaceutical manufacturing systems, ensuring compliance with GMP, and enhancing equipment reliability and process efficiency. This role involves overseeing automation design, programming, validation, and maintenance of PLC, SCADA, and related control systems used in production and utility areas. Key Responsibilities: Managed automation systems supporting production, utilities, and cleanroom environments in compliance with GMP and regulato...

Sodexo Food Solutions India Pvt. Ltd.ces is looking for STEWARDING EXECUTIVE to join our dynamic team and embark on a rewarding career journey Supervise and manage the stewarding team, including hiring, training, scheduling, and performance management. Develop and implement standard operating procedures (SOPs) for stewarding operations to ensure efficient workflow and compliance with health and safety regulations. Maintain cleanliness and hygiene standards in the kitchen, dining areas, and other food and beverage service areas. Monitor and ensure proper handling, cleaning, and storage of all food and beverage equipment, utensils, and supplies. Coordinate with the purchasing department to ens...

Manage day-to-day office operations, including administrative tasks and employee coordination. Handle communications, both internal and external, ensuring timely responses and follow-ups. Organize meetings, prepare agendas, and take minutes for effective documentation. Maintain office supplies and ensure all equipment is in working order. Assist with budgeting, invoicing, and other financial tasks as needed.

Design Manager - HME( hot melt extrusion) / Continuous Manufacturing Division Job Summary: We are seeking a highly motivated and technically proficient Design Manager HME / Continuous Manufacturing Division to lead the design and development of Hot Melt Extrusion (HME) and continuous pharmaceutical processing systems . This role involves managing the end-to-end design function, ensuring technically sound, compliant, and innovative solutions tailored to the pharmaceutical, food and life sciences sectors. The ideal candidate will have hands-on experience in the design of advanced processing equipment, and a strong understanding of GMP and continuous manufacturing concepts. Key Responsibilities...

Job Summary: We are looking for a driven and technically competent Business Development Manager to spearhead the growth of our Containment Division across the Indian market. The ideal candidate will be responsible for promoting our advanced containment solutionssuch as isolators, glove boxes, and high-containment systemswithin the pharmaceutical and chemical sectors. The role involves direct client engagement, working with regional sales teams, and supporting projects from concept to closure. Key Responsibilities: Promote and sell containment equipment and solutions including isolators, RABS, glove boxes, sampling/dispensing booths, and other high-containment systems for HPAPI and potent com...

Looking for a skilled F&B Manager to join our team, with strong leadership skills being essential. The ideal candidate will have 7-12 years of experience in the hospitality industry. Roles and Responsibility Manage daily food and beverage operations to ensure high-quality service delivery. Develop and implement menus catering to diverse customer needs and preferences. Supervise kitchen staff to maintain efficient food preparation and presentation. Coordinate with suppliers to source fresh ingredients and materials. Maintain inventory levels and control waste to optimize resources. Ensure compliance with health and safety regulations and company policies. Job Requirements Proven experience as...

We are looking for a highly motivated and experienced Kitchen Stewarding (KST) Supervisor to join our team in the hospitality industry. The ideal candidate should have 0-2 years of experience. Roles and Responsibility Supervise kitchen steward activities to ensure efficient service delivery. Coordinate with kitchen staff to maintain high standards of food quality and presentation. Implement effective inventory management systems to minimize waste and optimize resources. Maintain a clean and organized kitchen environment, adhering to health and safety regulations. Develop and implement new menu ideas and recipes to enhance customer satisfaction. Collaborate with other departments to achieve b...

Follow up with QC/QA for Analysis of in-process and finished samples. follow GMP norms in the manufacturing area. achieve shift targeted production Handling of Reactors & all other process related Equip SHOULD HAVE KNOWLEDGE ON BMR ,BPR , GPM

QA, QC, Maintenance, Production

Role & responsibilities 1. Develop and optimize cost-effective, scalable, and robust API processes suitable for GMP manufacturing 2. Conduct lab-scale and pilot-scale experiments to evaluate process parameters and critical quality attributes (CQAs) 3. Collaborate with R&D, Analytical, QA/QC, and Production teams for successful technology transfer 4. Prepare and review technology transfer documents 5. Provide on-site support during scale-up and commercial manufacturing, troubleshooting in case of any technical issues 6. Ensure compliance with regulatory guidelines (ICH, USFDA, EMA, etc.) during development and transfer 7. Identify and implement process improvements to enhance yield, purity an...

Role & responsibilities Manufacturing of Lyophilized Drug Product Aseptic Blending & Filling Injectable Filling Lyophilization BMR Preparation cGMP Practices, Media Preparation, Vial Washing and De-pyrogenation, Validation, Labeling & Packaging, Documentation Preferred candidate profile Aseptic handling Sound knowledge of QMS Sound knowledge of cGMP, GDP

We are seeking a proactive & detail-oriented Supply Chain Manager with strong knowledge of nutraceutical ingredients and industry trends.Familiarity with GMP, quality standards, & regulatory compliance.Excellent organizational & communication skills

We are looking for a skilled Process Validation Engineer to join our team in Pune. The ideal candidate will have 3-10 years of experience in process validation and quality systems, with a strong background in regulatory compliance and hands-on experience in manufacturing activities. Roles and Responsibility Perform gap assessments and conduct remediation of documents with stakeholder inputs. Develop and maintain Manufacturing/Service Work Instructions and related documents. Create/modify process flows within the Manufacturing/Service Departments. Support the development and introduction of new products, processes, and technologies, focusing on quality systems. Monitor and drive corrective ac...

Strong skills in Core Java, J2EE, , JavaScript, JSP, and DHTML/Web Page development. Experience in Labvantage LIMS development Strong relational database knowledge and experience using either Oracle and/or SQL Server.