5 Gmps Jobs

At Lilly, you play a crucial role in uniting caring with discovery to enhance the lives of people worldwide. As a global healthcare leader based in Indianapolis, Indiana, our mission is to develop and deliver life-changing medicines, enhance disease management, and contribute to our communities through philanthropy and volunteerism. Our dedicated team prioritizes people and is committed to making a positive impact on a global scale. As an Engineer Serialization Lead within the Global Serialization Program (GSP), you will oversee the implementation of serialization systems on new packaging lines across existing and new sites. Your responsibilities will involve collaborating with Engineering and IT teams at both the global and site levels. Your technical expertise will be instrumental in supporting internal GSP initiatives, asset delivery, and process enhancements. Key aspects of your role include providing technical leadership to drive projects forward, supporting major capital projects, aligning with packaging site requirements, and ensuring compliance with Lilly's global serialization strategy. In addition to supporting packaging sites worldwide in process improvements and technology upgrades for serialization, you will assist in technical design for GSP solutions and participate in serialization change management governance. Your role will also involve providing core solution leadership, knowledge sharing, and offering ongoing technical support to site packaging engineering groups. Basic Qualifications: - Bachelor's degree in Engineering - 2+ years of experience in packaging, automation, or software related to packaging processes and equipment - 2+ years of experience in GMPs and computer systems validation (CSV) - Experience in serialization, track and trace, product labeling, and regulatory compliance - Experience in vendor management, including selection and qualification Additional Skills/Preferences: - Ability to work collaboratively across various boundaries - Project management experience - Strong communication skills in English - Analytical and problem-solving skills - Adaptability to a fast-paced environment - Desire for innovation and staying updated on emerging trends - Interpersonal skills to build relationships with stakeholders - Familiarity with industry standards and regulations - Knowledge of machine vision technologies and connectivity protocols Please note that this is not a remote position and may require travel up to 25% of the time, including international travel. Occasional work in manufacturing environments with safety equipment may be necessary. This requisition is part of an Ai Candidate Skills Matching Pilot. Lilly is committed to providing equal opportunities for individuals with disabilities. Our employee resource groups offer support networks for all employees, promoting diversity and inclusion within our organization. Compensation for this position will be based on education, experience, skills, and location, with an anticipated wage range of $64,500 - $167,200. Full-time employees are eligible for a company bonus, comprehensive benefits, and well-being programs. Join us at Lilly and be part of a team dedicated to making a difference in healthcare and beyond. #WeAreLilly,

As a production worker, you will be responsible for ensuring the cleanliness and hygiene of the production areas. Your duties will include checking tanks and equipment to ensure they are clean before the production process begins. It is essential to label tanks with the FG material number, description, and batch number accurately. You will be required to weigh, blend, and record raw material numbers precisely on the shop floor paper. Additionally, you must use personal protective equipment (PPE) and adhere to HACCP/GMP requirements. You may also be assigned other tasks as needed. In this role, you will operate electric and/or gas sit-down and stand-up reach trucks as necessary. Operating various types of equipment such as pumps, mixers, and fillers will also be part of your responsibilities. A good working knowledge of GMPs, HACCP, SAP, Excel, inventory control, and maintaining sanitation standards in your work area is crucial. You should be physically capable of using mechanical equipment, pushing/pulling 200 Kg drums, and lifting 25 Kg bags when required. Participation in the Cross-Training Program is mandatory, and you should be prepared to work independently and handle unexpected situations, especially during off-shifts. Flexibility in working overtime based on the production schedule is expected from you. To learn more about workplace diversity and inclusion at our company, visit IFF.com/careers/workplace-diversity-and-inclusion.,

Job Description The scope of work for this role is to provide QA Validation support to validation activities associated with of Laboratory instruments and Manufacturing equipment in pharmaceutical industry. The responsibility includes review and approval of Qualification/Validation documentation DQ,IQ,OQ,PQ including Risk assessment, specifications, executed protocols, summary reports, deviations, periodic reviews, procedures, and change controls. In addition, this role may provide support to the sites data integrity initiative. Successful candidate requires a strong working knowledge of global cGMP with an emphasis on validation lifecycle including computer system validation, 21 CFR Parts 210 and 211, and Part 11, Electronic Records and Electronic Signatures Candidate requires strong interpersonal, oral and written communication skills as there is a high degree of collaboration required between members of QA Validation/Qualification personnel. Candidate must be detail oriented as the main job responsibility is review and approval of validation documentation Should also have some experience in Mechanical Qualification Job Requirements Skills: Strong working knowledge of global GMPs with emphasis on validation, including computer validation Strong interpersonal, oral and written skills Detail oriented Education: Candidate must have at a minimum a BE or equivalent, engineering or related sciences with pharmaceutical or biopharmaceutical experience in a quality assurance and/or validation/Qualification role. Past experience working with Equipment Qualification, Quality Management system, Document, Document Management System, Track wise, and etc. Experience working with process manufacturing equipments (RMG, Sifter, Blender, compression m/c, Capsule filling m/c & etc), Utility (Water system, HVAC & etc) and other lab instruments is a plus.

Job Description REMOTE OPPORTUNITY!!!!!!!! Client: Technology GCC for Global Biotech Company 2+ years of relevant experience in leading teams in the development and support of IT systems Development in a GxP biotech or pharmaceutical environment 2+ years of process improvement experience, especially experience that leverages technology as part of the solution. 2+ years experience working in a regulated environment with knowledge of GMPs, GDPs. Exceptional Interpersonal, Verbal and Written Communication Strong Leadership Skills Including Ability to Inspire and Motivate Team Members Ability to Keep Track of Various Activities in Multiple Systems Task Delegation Strong Analytical / Problem-Solving Abilities Software Design and Development Test Script Writing and Execution Business Analysis Knowledge and Understanding of 21 CFR Part 11 and Data Integrity

Job Description The scope of work for this role is to provide QA Validation support to validation activities associated with of Laboratory instruments and Manufacturing equipment in pharmaceutical industry. The responsibility includes review and approval of Qualification/Validation documentation DQ,IQ,OQ,PQ including Risk assessment, specifications, executed protocols, summary reports, deviations, periodic reviews, procedures, and change controls. In addition, this role may provide support to the sites data integrity initiative. Successful candidate requires a strong working knowledge of global cGMP with an emphasis on validation lifecycle including computer system validation, 21 CFR Parts 210 and 211, and Part 11, Electronic Records and Electronic Signatures Candidate requires strong interpersonal, oral and written communication skills as there is a high degree of collaboration required between members of QA Validation/Qualification personnel. Candidate must be detail oriented as the main job responsibility is review and approval of validation documentation Should also have some experience in Mechanical Qualification Job Requirements Skills: Strong working knowledge of global GMPs with emphasis on validation, including computer validation Strong interpersonal, oral and written skills Detail oriented Education: Candidate must have at a minimum a BE or equivalent, engineering or related sciences with pharmaceutical or biopharmaceutical experience in a quality assurance and/or validation/Qualification role. Past experience working with Equipment Qualification, Quality Management system, Document, Document Management System, Track wise, and etc. Experience working with process manufacturing equipments (RMG, Sifter, Blender, compression m/c, Capsule filling m/c & etc), Utility (Water system, HVAC & etc) and other lab instruments is a plus.