Senior Technician, QC Sample Management - Devens MA

Job Description
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. Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post.

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits.

This is work that transforms the lives of patients, and the careers of those who do it.

The QC Sample Management Technician is responsible for the movement and control of QC samples and materials, including in-process, finished drug product, characterization, retain, and stability samples processed through the QC laboratories. This includes, but is not limited to, sample collection and distribution, inventory control, chain of custody, sample tracking, and sample delivery.

SHIFT

This role works from 6AM to 6PM following a 12-hour rotating shift (36/48 hours over a 2-week period) which includes working every other weekend, holidays falling on scheduled workdays, and during adverse weather conditions in support of QC and the manufacturing facility. Flexibility to work irregular hours and short notice overtime may be required.

• Job Description:
  
  Responsible for performing routine management of in-process, final product and stability samples and QC data throughout the sample lifecycle from receipt to disposition. Performs periodic sample and data inventory maintenance activities.

Duties/Responsibilities

• Perform routine management of in-process, final product and stability samples and QC data throughout the sample lifecycle from receipt to disposition. Performs periodic sample and data inventory maintenance activities.
• Performs data compilation and review of GMP documentation in support of method trending.
• Compiles lot files for QC disposition review. Generate SOTR and manual CoA.
• Support document revision, project, CAPA and deviation/ investigation related tasks and/ or continuous improvement efforts.
• Train analysts on general job duties.
• Perform other tasks/duties as assigned.

Auto req 484170

Minimum Education Required Bachelors

Qualifications
Additional Qualifications/Responsibilities
Specific Knowledge, Skills, Abilities

• Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements.
• Knowledge of LIMS, ELN and laboratory data analysis systems preferred.
• Problem-solving ability/mentality, technically adept and logical.
• Ability to communicate effectively with peers, department management and cross-functional peers.

Experience With Writing Technical Documents Preferred.
Education/Experience/ Licenses/Certifications

Bachelor's degree or equivalent required, preferably in science.

Netherlands:
Bachelor's degree /HLO in (bioanalytical) science preferred. MLO level 4 with equivalent combination of work experience may be considered.

2+ years of relevant LIMS or QC experience or equivalent combination of education and experience, preferably in a regulated environment.

Demonstrated experience in LIMS and knowledge of Chain of Identity and Chain of Custody.

Job Safety Requirements& Essential Physical Demands

Abilitytoperform lifting tasks up to 20 lbs (9 kg) at floor and waist height. Ability to…