Worthington, MN, USA
Boehringer Ingelheim is seeking a Laboratory Technician II Quality Control candidate for an exciting opportunity at Newport Labs in Worthington, Minnesota Candidates should have: Basic computer and reading skills. Candidate must be comfortable working in a clean environment, working with animals, and be able to stand for long periods of times. recblid 0lhtx5sp6n6fpefwyh27rcxjrsjg0p
Duties: The Bio Quality Control group is responsible for performing bio-analytical methods (immunological, in vivo, microbiological, molecular biological, or virological) for various Bio QC tests on raw materials, in-process, release or stability samples in compliance with 9CFR, EU and VICH regulatory guidelines, Outlines of Production and Special Outlines.The incumbent will initiate, execute and complete assays as per validated procedures and within Quality and Compliance guidelines. The incumbent is responsible for timely communication with supervisors to inform them of testing, compliance and/or scheduling issues, adhering to company policies, maintaining a safe work environment through Site safety KPIs, living out the Lead Learn principles and following appropriate GMP documentation. Additional duties are based up the incumbents level.Skills: Microscopy, aseptic technique, microbiological testing, previous work in a GMP environment desired.Keywords:Education: Bachelor degree in...
Ridgefield, CT 06877, USA
Duties:Experienced individual with managing projects and facilitating projects as a Project Manager or Scrum Master. Work beginning now until end of December (full-time). Experienced preferred with Jira application, working/managing project teams globally and managing teams remotely. Expectations: Will facilitate as project Scrum Master for all agile related activities including: Grooming Sessions Sprint Planning Daily Sprints Sprint Reviews Retrospective Will also serve as Project Manager, including updating BIs project management tool with budget forecasting, resource planning, schedule and updates to management, and overall IT and Business stakeholder engagement.Skills:Jira application experience preferredPrior experience working/managing project teams in different work locations such as globally and remotelyAbility to work full-time 40 hour a week scheduleGood communication skillsGreat attention to detail and ability to multi-taskEducation:Bachelors Degree
Fremont, CA, USA
DutiesThis position leads all paper/electronic batch record review that is related to manufacturing of drug substance in a multi-product facility. The position performs duties under limited supervision and according to standard operating and manufacturing procedures. It contributes to process improvement of batch records and turnaround times to ensure turnaround times and QA batch disposition deadlines are met. The position performs logistical duties related to batch record review. Independently executes (paper/electronic) batch record review- Collaborates within Manufacturing to resolve batch record discrepancies or errors as it relates to Good Documentation Practices or Manufacturing Execution System (MES) inventory.Skills Demonstrated proficiency in MS Office programs and associated computer programs. Technical knowledge of manufacturing systems, methods and procedures. Must have excellent written and verbal communication skills. Awareness and understanding of Manufacturing...