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This is where you make a difference in our patients’ safety. As a member of the Baxter Quality team, you will play an essential part in our mission of saving and sustaining lives. Quality is important throughout the entire product lifecycle and works collaboratively with all areas of the organization. Because Quality touches everything Baxter does, a role in Quality provides many opportunities for growth, learning and a successful career that has a daily impact on people’s lives. Baxter Thetford is looking for a candidate to work in QC Chemistry Team as a Senior Analyst. You will be responsible for supervising the analytical testing required during various stages of the manufacturing of products at Thetford working as part of a team following established practices and within the required time frames. You will also be responsible for team compliance items, provide technical support, development of direct reports. Within this role you will work rotational 5am–1pm and 9am–5pm, Monday – Friday. This is a fantastic opportunity to gain wider exposure in a laboratory for a global pharmaceutical company and is the ideal role for a graduate. You will work closely with your team of QC Analysts, and work together to ensure we are releasing the highest quality products.
Job Responsibility:
Manage and develop direct reports through performance reviews (ACE Check-In) and identify training or development needs
Conduct testing, stability studies, reporting, and checking/reviewing of results in accordance with relevant local and global procedures, testing methods, protocols, and/or pharmacopeial requirements
Ensure direct reports meet safety, quality, and performance standards, and escalate any issues to the QC Manager
Initiate, conduct, and manage quality records, such as deviations, CAPAs, effectiveness checks, and laboratory investigations
Initiate and coordinate document updates, change controls, and successfully manage timelines for implementation of changes
Perform the batch release activities
Participate in internal, customer, and regulatory audits
complete any assigned action items in a timely manner
Perform if required and coordinate general laboratory support activities including housekeeping, equipment maintenance, and inventory of supplies and reagents/ standards
Perform and coordinate calibration checks in accordance with written procedures
Ensure that equipment within laboratory is operated and maintained correctly
Responsible for clear escalation and troubleshooting of technical issues and challenges relating to equipment or test methods
Check and review the test results in accordance with relevant local and global procedures, testing methods, protocols, and/or pharmacopeial requirements
Ensure accurate, timely entries are made in electronic laboratory notebook, LIMS or paper documentation
Perform and manage all aspects of sample handling e.g., collection, receipt, storage, and disposal of samples as per procedure
Participates in any required laboratory investigations as required
Follows Good Quality Control Laboratory Practices at all times and ensures the work area they are responsible for is maintained in a clean and tidy state
Provide support to the supervisor in any reasonable request relating to the laboratory operation
Requirements:
Science based degree (preferably in Chemistry, BioChemistry Biology OR Microbiology)
Experience working in a laboratory essential
Demonstrates strong leadership skills
Excellent understanding of Microsoft Office Packages
Previous experience in a GMP environment/ pharmaceutical QC laboratory