Performs pharmaceutical procedures for medications and Durable Medical Equipment, Prosthetics, Orthotics and Supplies (DMEPOs) preparation and distribution of pharmaceuticals
Prepares, compounds, packages, labels, and dispenses medication, nutritional products, IV admixture and solutions, and Durable Medical Equipment (DME) according to policies, USP 797 and 800 guidelines, state/federal regulations, and accreditation organization standards
Assists with medicine and supplies inventory management and control, including maintaining adequate stock levels, checking accuracy of pricing, and completing required regulatory documentation
Adheres to all standards, procedures, cleaning protocols, and infection control policies to maintain a safe and sterile medication area, clean rooms, and laminar flow hoods
Requirements
Graduate from an accredited Pharmacy Technician program
Lead Quality oversight for visual inspection and particulate control in pharmaceutical manufacturing.
Compensation
The estimated base salary for this position is $136,000 - $187,000 annually. The estimated salary is meant to reflect an anticipated salary range for the position. This position may also be eligible for discretionary bonuses.
Responsibilities
Lead Quality oversight for manual, semi-automated, and automated visual inspection programs
Develop and maintain risk-based particulate control strategies
Provide technical leadership for qualification and validation activities related to visual inspection systems
Direct complex investigations involving visible particulate matter, inspection trends, and product quality events
Partner with Operations, Engineering, Laboratory, and Quality teams to identify opportunities for process improvement
Requirements
Bachelor's degree in Pharmacy, Chemistry, Biology, Microbiology, Engineering, Pharmaceutical Sciences, or a related scientific or technical discipline
Nice to have: advanced degree in Pharmaceutical Sciences, Chemistry, Microbiology, Engineering
Nice to have: sterile manufacturing operations
Nice to have: particulate characterization techniques
Lead and manage quality control operations in Chemistry and Microbiology laboratories, ensuring compliance with regulatory standards and internal quality metrics.
Responsibilities
Oversee daily QC operations in Chemistry and Microbiology laboratories
Collaborate with other departments to resolve quality-related matters
Author, edit, review, and approve documents such as SOPs, CAPAs, and protocols
Manage QC administration, scheduling, and budgeting
Ensure compliance with regulatory standards and industry best practices (GxP)
Requirements
Bachelor's in life sciences, biology, chemistry or related field
Nice to have: BS/BA in life sciences, biology, chemistry or related field
Performs medication order processing responsibilities within established policies, procedures and guidelines and provides drug information while applying a thorough understanding and knowledge of drug and medical therapy.
Compensation
The disclosed salary range includes the minimum and maximum rates within which Children’s National believes an individual’s base pay rate will fall for this position. It is not typical for an individual to be hired at or near the maximum of the pay range. The exact pay rate for this position will be based on a variety of factors in alignment with the Children’s National compensation philosophy.
Responsibilities
Interpret medication orders, profile orders and oversee the packaging, labeling and distribution of medications
Perform drug therapy monitoring and intervene as necessary on drug dosing, drug administration, drug interactions, side-effects and monitoring issues
Provide accurate and timely drug information to physicians, nurses and other health professionals
Interpret research medication orders, ensure accurate preparation of investigational drugs and maintain complete and accurate records
Maintain proficiencies in medication handling (including hazardous medications), compounding sterile/non-sterile preparation(s) and completing quality assurance checks per standard operating procedures and policies in compliance with USP and guidelines
Requirements
Completion of a five-year pharmacy program in an accredited college of pharmacy
Support environmental control activities, executing environmental routine testing for viable and non-viable particles for air and product contact surfaces follow quality system and in compliance with Good manufacturing practices.
Responsibilities
Perform investigation process for out of tolerance equipment
Include new equipment at the calibration and maintenance system
Review and approve cleanroom intrusion plans
Get involved in various stages of equipment and processes validations: run or write protocols and reports for IQ, OQ, PQ and TMV; as well as any other document relating to validation
Performs or coordinate microbiology testing as offered by the Microbiology Lab, including LAL, Bioburden, Environmental monitoring
Requirements
Microbiology or Quality Technician
Biotechnology, Microbiology and Biology Bachelor degree
Lonza is seeking Bioprocess Engineers with a relevant background in Life Sciences and a passion for Biotechnology for Upstream Processing, Downstream Processing or BioConjugate Manufacturing.
Responsibilities
Ensure operational activities for clinical and/ commercial manufacturing are performed on-time and within given safety and quality standards
Act as the functional lead for preparation, manufacturing execution, cleaning and changeover in the assigned area
Lead one or more defined USP areas (e.g. seed train, main cultivation or harvest) for the production of therapeutic proteins with either mammalian or microbial expressions systems
In charge of one or more defined DSP areas (e.g. capture, polishing or filling) for the purification of therapeutic proteins from either mammalian or microbial cells
Responsible for entire processes or process units for clinical and commercial manufacturing projects regarding therapeutic BioConjugates like Antibody Drug Conjugates (ADC)
Lead the Investigational Drug Section at a clinical research site, overseeing medication preparation, dispensing, and compliance with regulatory standards.
Compensation
The annual base salary range for this role is $180,000 - $200,000 plus a significant annual bonus. Base pay may vary depending on multiple individualized factors including relevant and overall experience, job-related knowledge and skills.
Responsibilities
Partner with Director of Nursing and study operations leader to ensure efficient, high quality patient care
Collaborate with site leadership team, shared services leaders and integration team members to promote alignment in workflows and processes
Ensure adherence to all local/federal expectations for IDS space, ensuring compliance with all applicable internal SOPs
Verify medication orders including accuracy of dosages and calculations, review of basic patient eligibility criteria
Oversee the preparation and dispensing of all medications from the IDS, supervising certified pharmacy technicians
Requirements
Graduate of an ACPE accredited School of Pharmacy
Nice to have: specialty residency in oncology
Nice to have: BPS Board Certified Oncology Pharmacist (BCOP)
Atuar como referência técnica, prestando suporte, orientação e treinamento a analistas júnior e pleno na execução de métodos analíticos e na interpretação de resultados.
Locations (3)
Valinhos, São Paulo, Brazil
Campinas, São Paulo, Brazil
Vinhedo, São Paulo, Brazil
Responsibilities
Realizar o preparo, padronização e qualificação de soluções, reagentes e padrões de referência
Garantir a organização, limpeza e conformidade das áreas de trabalho do laboratório analítico
Elaborar, revisar e controlar a documentação técnica do laboratório
Conduzir e/ou apoiar atividades de desenvolvimento, otimização e transferência de métodos analíticos
Planejar e executar estudos de degradação forçada, validação de métodos analíticos e estudos de estabilidade
Specialist Scientist - Analytical Development
Syngene International Limited · Posted Nov 3, 2026
Seeking a skilled analytical scientist with hands‑on expertise in LC and CE techniques to support biologics development in a CDMO environment. The role focuses on method lifecycle management, analytical development, qualification and transfer.
Supports the Quality Management System (QMS) and Document Management System (DMS) in a GMP regulated environment, ensuring compliance with SOPs, GMP/GLP standards and client requirements.
Compensation
The hiring range in Colorado for this position is $93,750/year - $108,750/year and is eligible for a 4% annual target bonus.
Responsibilities
Perform independent quality evaluation and release of support documentation, materials, products, equipment, and/or facilities
Ensure testing/manufacturing performed per approved SOPs/methods/protocols and comply with specifications
Participate in internal, client and/or regulatory audits
Support quality events and root cause analysis
Develop, implement, and maintain procedures and policies to comply with FDA, EU, and ICH requirements
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