Senior QC Microbiology Associate, Lab Operations

Working with Us
Challenging. Meaningful. Life-changing. Those aren’t 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 breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.

Position Summary

To perform QC testing in support of bulk drug substance manufacturing using defined methods in a GMP-compliant laboratory. Ensures test results are accurately recorded, and abnormal data or equipment/instrument malfunctions are properly reported and escalated to management

Key Responsibilities

Responsibilities include but are not limited to: 

• Execute routine Bioburden, Endotoxin, and Microbial Identification testing in accordance with SOPs, safety, and cGMP guidelines to support the release and stability of finished products, raw materials, in-process materials, and various components. 
• Perform clean utility sampling/monitoring on critical operating parameters for equipment and instrumentation to ensure standard operation. 
• Identify, report, and document deviations from established test methodologies, specifications, and alert limits.
• Maintain up to date knowledge of cGMP, job related SOPs and complete all assigned training on time. 
• Coordinate sample receipt, logging, tracking, storage, distribution and archival. 
• Work closely with subject matter experts with regards to discrepancy reporting, investigations and CAPAs associated with the process. 

Qualifications & Experience
 

• BS/BA in Biological, Chemical/Life Sciences, or its equivalent in experience. 
• Minimum 1 to 2 years of experience in a regulated microbiology laboratory preferred. 
• Excellent manual dexterity including proficiency in aseptic and pipetting techniques. 
• Experience executing Bioburden, autoclaves, micro-ID methods, and endotoxin testing. 
• Experience requiring one to work independently as well as part of a team, to complete assignments within defined time constraints. 
• Demonstrated ability to concurrently conduct multiple routine tasks, procedures, and operations effectively and consistently. 
• Attention to detail and demonstrated organizational skills.
• Demonstrated ability to be resilient and adapt quickly in a fast-paced environment is essential.
• Demonstrated ability to quickly learn and adapt to new information, technologies, and processes.
• Demonstrated ability for efficient time management.
• Knowledge of basic electronic systems including proficiency with Microsoft based platforms.

This position is Wednesday through Saturday 1st shift position. 0700 – 1700. (B-Shift)

Contacts:

Will work in teams and have continual interactions with team members as well as other sub-teams within and outside the Quality Control organization to exchange information regarding testing completion, in-process, and planned activities. Daily interaction with management and team leads. Routine contact with management for coaching and general performance management discussions. Occasional contact with other line management staff relating to specific projects may be expected.

Working Conditions:

QC Associates primarily work in GMP laboratory and follow techniques which require one to be alert, giving a high attention to detail, to properly use Personal Protective Equipment (PPE) and to handle hazardous material.

Overtime work may be required on weekdays, weekends, holidays and during adverse weather conditions in support of manufacturing facility.

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. Yo