2 Pharmaceutical Environment Jobs

As an Artwork Proofreader at Bristol Myers Squibb in Hyderabad, India, you will play a crucial role in ensuring the accuracy and quality of artwork content for various regulatory and packaging requirements. Your responsibilities will include verifying text content, conducting technical reviews, approving artwork for printing, and managing associated cGMP documents. You will collaborate closely with the Artwork Designer, Regulatory teams, packaging sites, and print vendors to deliver high-quality artwork solutions. Key Responsibilities: - Proofreading: You will meticulously proofread the Regulatory text against the provided artwork to ensure accuracy and consistency. - Technical Verification: Conduct thorough technical verification of the artwork in alignment with packaging site requirements and printer specifications. - Deployment: Deploy approved artwork to the packaging site or printer suppliers for production. - Approval: Review and approve the final artwork for printing as provided by the print vendor. - Documentation: Complete all necessary cGMP documents associated with the artwork verification process. - Collaboration: Offer support and partnership to the Artwork Designer, packaging site teams, and Regulatory market stakeholders to ensure seamless workflow. Skills and Knowledge required: Prerequisites: - Strong background in the Graphical Industry and Pharmaceutical sector. - Proficiency in artwork comparison techniques. Educational Qualifications: - Advanced professional certificate in Graphical Industry profession, such as CFC. Experience: - Minimum of 2 years of experience in artwork and labeling processes. Technical Skills: - Familiarity with Global Vision software and other Proofreading tools. - Sound understanding of cGMP standards and their application in the pharmaceutical industry. - Knowledge of packaging design principles. - Proficiency in Adobe Creative Suite and other relevant graphical design software. - Competence in using common MS Office software. Language Skills: - Fluent in English; knowledge of additional languages is advantageous. Join us at Bristol Myers Squibb and be part of a team dedicated to transforming patients" lives through innovative treatments. We value diversity, inclusion, and individual contributions in a collaborative and empowering work environment. Our commitment to employee well-being is reflected in our competitive benefits, services, and programs that support personal and professional growth. Apply now to make a meaningful impact on global healthcare.,

Our imaging services are experiencing rapid growth, and we are currently looking for a full-time, office-based Imaging Technologist specializing in MRI or Nuclear Medicine to join our team in Mumbai, India. If you are seeking an exciting career where you can utilize your existing expertise and further enhance your professional growth, this opportunity is tailored for you. As an Imaging Technologist, your responsibilities will include performing quality assurance checks on medical imaging data to ensure compliance with protocol-specific requirements. You will be tasked with executing established image processing techniques across MRI or Nuclear medicine imaging modalities using both proprietary and third-party software. Additionally, you will be responsible for compiling and maintaining project-specific status reports and timelines associated with imaging studies, as well as carrying out project-specific tasks in adherence to Good Clinical Practices (GCP), regulatory requirements (21CFR Part 11), departmental SOPs, and project protocols. To qualify for this role, you should hold a Bachelor's Degree and be a graduate of an accredited school of Radiologic Technology or echocardiography program. Preference will be given to candidates with PET/CT, CNMT (Certified Nuclear Medicine Technologist), or ARRT - R certification. Ideally, you should possess 1-3 years of experience in clinical research or imaging-related fields, with a minimum of 2 years of experience as an Imaging Technologist in a hospital or imaging center. Previous experience in clinical trials or the pharmaceutical environment is considered advantageous. Medpace is a comprehensive clinical contract research organization (CRO) that offers Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our core mission is to expedite the global development of safe and effective medical therapeutics through a scientific and disciplined approach. With headquarters in Cincinnati, Ohio, and a workforce of over 5,000 individuals spanning 40+ countries, we leverage local regulatory and therapeutic expertise across various key areas such as oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective. At Medpace, we value People, Purpose, and Passion. Joining our team means making a difference tomorrow. We have positively impacted the lives of numerous patients and families dealing with various diseases over the past 30+ years, and the work we do today will continue to enhance the lives of individuals battling illness and disease in the future. Medpace offers a range of perks, including a flexible work environment, competitive compensation and benefits packages, structured career paths with opportunities for professional advancement, company-sponsored employee appreciation events, and initiatives promoting employee health and wellness. Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023, and 2024, Medpace has also been consistently acknowledged with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility. If you are interested in this opportunity, a Medpace team member will review your qualifications and reach out with further details on the next steps. Medpace is an Equal Opportunity/Affirmative Action Employer committed to diversity in the workplace.,