CTDO LIMS Specialist
- Employer
- Bristol Myers Squibb Company
- Location
- Summit West, NJ, United States
- Start date
- Sep 29, 2020
View more
- Discipline
- Engineering, Software Engineer, Information Technology
- Required Education
- Bachelors Degree
- Position Type
- Full time
- Hotbed
- Pharm Country, Best Places to Work
Job Details
Position
LIMS Specialist
Division
CTDO Quality Control
Direct Reports
Yes
Location
Summit, NJ
Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis.
Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.
PURPOSE AND SCOPE OF POSITION:
This position is responsible for the harmonization, life-cycle management and continuous improvement of all GMP quality system elements within the Laboratory Systems technology platform including but not limited to LabWare. In this role, the incumbent will serve as the primary representative for Master Data deployment related activities and cross-functional partnerships and collaborations. This is a highly visible role with Cellular Therapy Global responsibility and crossfunctional influence that has a high degree of impact on departmental performance, broad quality initiatives, Quality Control, Quality Operations and the Business.
REQUIRED COMPETENCIES: Knowledge, Skills, and Abilities
- Must have expert GMP, Quality, and in-depth risk management knowledge.
- Must be able to effectively prepare communications with interpretation of data analysis and potential problems to management and the group with clarity and a high level of accuracy.
- Must be able to note technical/scientific attributes in potential situations or issues and process science-based solutions across a majority of the job function.
- Must provide guidance to other employees in the interpretation of Master Data within the system across a majority of the job function and manage development of Master Data initiatives and activities by interdisciplinary teams.
- Most have strong authorship and be able to critically review Master Data lists.
- Must be action-oriented and customer-focused and skilled in decision-making, building relationships, problem solving, conflict management, planning and organizing, resource allocation, coaching others, and analytical thinking. Must possess an independent mindset and tenacity.
DUTIES AND RESPONSIBILITIES
- LIMS Specialist will work within the LIMS system, and independently create, update and maintains high quality Master Data within LIMS, and translate specifications within the LIMS system by utilizing current business processes.
- The LIMS Specialist takes ownership by completing any incoming requests in a timely manner. They will escalate any issues and understand the impact towards other sites when changing / updating existing Master Data.
- In order to maintain high quality data, they collaborate with CTDO QC Laboratory SMEs to fully understand the Master Data requirements and will review all configurations for accuracy and completeness.
- The LIMS Specialist is able to mentor, lead, and train team members. The Specialist collaborates with more than 1 SME from the different S12 function groups to fully understand the Master Data requirements and will review all configurations for accuracy and completeness. The LIMS Specialist is able to lead small projects within the S12 LIMS Team, e.g. Harmonization / standardization of processes.
- Integrates instruments and applications within LIMS, performs user acceptance testing
- Creates, updates, reviews & approves Master Data (release and stability) including worksheet templates, ELN templates and sample plans.
- Management of Master Data. Examples include: - create/ modify tests, products, sample groups templates, specifications, methods, materials, etc
- Special permissions to support site business users (edit of locked data, moving data to non-routine phases, folder creation, etc)
- Work with site admins on complex issues as required Stability-specific specialty expected to support:
- Stability data management: create/modify stability protocol, stability specification, intervals, conditions, locations, etc. ELN-specific specialty expected to support:
- Site-specific ELN templates and master data (yet to be defined) Quality Control experience required.
EDUCATION AND EXPERIENCE
- Relevant college or university degree preferred. Equivalent combination of education and experience acceptable.
WORKING CONDITIONS:
Work is performed in a typical office environment and remotely, with standard office equipment available and used. Work is generally performed seated but may require standing and walking for up to 10%of the time. Lighting and temperature are adequate and there are no abnormal conditions caused by noise, dust, etc.
If you want to challenge yourself, accelerate your career, and give new hope to patients, there's no better place than here with our Cell Therapy team. Full of incredible and dedicated team members, those working on CAR-T and other forms of Cell Therapy are transforming patients' lives through science. From studying individualized cell lines to making brand new discoveries, this bold and personal discipline allows you to grow your career while making a lasting impact on the field of medicine. Join us today.
BMSCART
Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
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.
Company
Bristol Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.
At Bristol Myers Squibb, we believe in the power of science to address some of the most challenging diseases of our time. Our focus on these unmet needs comes during a remarkable time, when unprecedented scientific breakthroughs are advancing the treatment of disease as never before in human history.
We work every day to transform patients’ lives through science. Each day, our employees around the world work together for patients – they are at the center of everything we do. They inspire us. They are the reason we come to work each day.
We combine the agility of a biotech with the reach and resources of an established pharmaceutical company to create a global leading biopharma company powered by talented individuals who drive scientific innovation.
- Website
- http://www.bms.com/
- Phone
- +1-800-332-2056
- Location
-
430 E. 29th St
14th Floor
New York
New York
10016
United States
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