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QC STAT Associate - Devens, MA

VetJobs, Harvard, Massachusetts, us, 01451

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ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is 'On-Site' at the location detailed in the job post.

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. 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.

Position: QC STAT Associate

Location: Devens, MA

Night shift (5pm-5am rotational A2 and B2 schedules), eligible for a 20% shift differential.

Key Responsibilities

Perform routine testing and data review of in-process and batch release samples of Bulk Drug Substance in a cGMP compliant environment.

Perform routine assays such as UV-VIS Spectrometry, Titer, utility testing, personnel and environmental monitoring, Total Organic Carbon testing, and more complex assays including various HPLC methodologies (e.g., sialic acid).

Perform activities to support lab operations such as housekeeping, alarm acknowledgement, reagent preparation, inventory management, material and reagent ordering, sample pickup and discarding, and execution of work orders.

Ability to understand and follow procedures while working in a fast-paced team environment, meet deadlines, and adjust to changing priorities.

May write and revise QC documents for managerial review and approval.

May train colleagues on basic and some more complex test methods.

Supports deviation investigations and laboratory investigations through data gathering or interview process. May lead no impact deviations and Lab Investigations.

Identifies and escalates challenges & barriers to execution, suggests solutions, and participates in remediation while assisting with a broad range of troubleshooting activities.

Actively and positively learns and participates in Operational Excellence (OpEx) and Continuous Improvement (CI) initiatives in the team.

Positive, supportive, and actively collaborates within the team and other sub-teams within QC or cross-functionally outside of QC.

Complete all required tasks compliantly and safely while consistently and intentionally modeling BMS values (Integrity, Accountability, Passion, Urgency, Innovation, and Inclusion).

Qualifications & Experience

High school diploma/GED or equivalent with some direct relevant experience (≥15 year).

Associate’s degree in a technical, scientific discipline with ≥9 years’ experience.

Bachelor’s Degree in a non-technical discipline with ≥5 years’ experience.

Bachelor’s degree in a Scientific relevant area with ≥1 year’s experience.

Master’s degree in a Scientific relevant area.

An equivalent combination of education and experience, preferably in a regulated environment will be considered.

Experience in analytical test methods such as UV/Vis, HPLC, TOC, and protein purification highly preferred.

Knowledge of lab software applications (e.g., LIMS, ELN (LES/SmartLab), Empower) preferred.

Excellent manual dexterity including proficiency in aseptic techniques desired.

High attention to detail with strong general laboratory and good organizational skills.

Demonstrated ability to work independently as well as part of a team, to complete assignments within defined time constraints.

Ability to interpret and apply cGMPs, USP, regulatory requirements and industry best practices.

Demonstrates problem solving and analytical thinking skills.

This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management.

If you come across a role that intrigues you but does not perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Compensation Overview Devens - MA - US: $35.82 - $43.41 per hour. The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided on the basis of demonstrated experience.

Auto req ID 458041BR

Minimum Education Required: High School/GED

Job Category: Scientific Research & Development

Affiliate Sponsor: Bristol Myers Sqibb BMS

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