Batch Records Jobs in USA

Working with UsChallenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the latest breakthrou...

Supervisor - Biomanufacturing Downstream/mRNAPosition Summary:Work Schedule: 2nd shift 2pm-12am Wednesday-Saturday100% on-site (Madison WI)Catalent Inc. is a leading global Contract Development and Manufacturing Organization (CDMO). Located in Madison WI this facility features advanced mammalian cel...

Work Schedule12 hr shift/daysEnvironmental ConditionsAble to lift 40 lbs. without assistance Adherence to all Good Manufacturing Practices (GMP) Safety Standards Cleanroom: no hair products jewelry makeup nail polish perfume exposed piercings facial hair etc... allowed Loud Noises (Equipment/Machine...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards OfficeJob DescriptionAs part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing...

The Production Clerk / Production Administrator is responsible for the accurate execution validation and control of all production related transactions within the ERP system (D365). This role ensures alignment between physical production activities and system data maintaining inventory accuracy supp...

The Pharmacy Weigher is responsible for weighing components in the pharmacy area in preparation for blending or manufacturing process. Responsibilities: Accurately dispense all raw materials as per batch record Record weight information on batch records Review and follow the batch records with 1...

BandLevel 2Job Description Summary-Shift Lead I -The Shift Leader is responsible for managing his team to carry out the manufacturing operations according to schedule in compliance with HSE and GMP rules. -Process Specialist / Equipment Specialist -Execute assigned manufacturing tasks and activities...

DescriptionThis position is responsible for quality oversight of the Human Cellular Therapy lab. Responsibilities include but not limited to developing and maintaining the quality management plan managing SOPS form and document approvals coordinating and participating in audits occurrence management...

Use Your Power for PurposeOur breakthroughs would not reach the hands of patients without our dedicated pharmaceutical manufacturing team. We rely on agile members who understand the critical impact of their role in Pfizers mission. Patients need colleagues like you who take pride in their work and...

Be the First to Apply DivisionPiramal Pharma SolutionsPiramal Pharma Solutions is a contract development and manufacturing organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilit...

AstraZeneca is looking for a highly motivated and experiencedDrug Product Scientist for viral vector process development. The candidate will play a critical role in forming a high-performingteamthat accelerates AstraZenecas emerging Cell Therapy modalities portfolio. Youwill design execute andoptimi...

Position OverviewMake a direct impact bringing lifesaving therapies from partner sites to GMP manufacturing. As a Manufacturing Specialist Tech Transfer you will lead and execute end-to-end drug substance tech transfers from external partners/CMOs into our site coordinating cross-functional activit...

Full-time Part-timeDescriptionManufacturing TechnicianJob Type: Non-exempt Part-time / Full-timeLocation: Onsite in Fort Wayne IN with potential travel to Auburn INCompensation: $17.00 $23.00 per hour depending on experience and qualifications.Hours: 30-40 hours per week with overtime and weekends...

At West were a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through...

Works and communicates effectively with QC personnel and members of other departments (Manufacturing Customer Support Development Maintenance and Logistics)Understands and follows documents relevant to responsibilities e.g. Work flows Work Instructions Checklists Batch Records and LogsMakes Quality...

DescriptionThis position is responsible for maintaining quality control processes testing products and recording and analyzing results gathered to ensure Sherwin products meet quality specifications. This position is responsible for testing production batches according to specific written testing me...

Responsible for supporting all aspects of the Computer Systems Validation (CSV) Lifecycle for the Validation Department to ensure all systems are in a qualified state suitable for the intended use. This will include authoring of protocols test scripts and data tables to facilitate collection expert...

Senior Associate I - Quality Assurance Operations Position Summary:Work Schedule: Mon-Fri 8am-5pm100% on-siteWorking for Catalent Biologics is an opportunity to join an entrepreneurial team. Catalent Biologics is making significant investments in people and capabilities. This is a unique opening to...

Please Note: This is a day shift opportunity that follows a 2-2-3 scheduleJob SummaryThe QA Manufacturing Specialist Senior is responsible for ensuring raw materials products processes facilities documentation and systems conform to quality standards internal procedures systems and governmental regu...

Please Note: This is a day shift opportunity that follows a 2-2-3 schedule.Job SummaryThe QA Manufacturing Specialist is responsible for ensuring raw materials products processes facilities documentation and systems conform to quality standards internal procedures systems and governmental regulation...