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Bristol Myers Squibb Network Sr. Lab Systems Specialist in Devens, Massachusetts

At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

Bristol-Myers Squibb in searching for a remarkable Network Sr. Lab Systems Specialist to join our team in Devens, MA. As our Network Sr. Lab Systems Specialist, you will support our Quality Control Data Management Systems primarily through use of LES and LIMS. The focus of this role is LIMS Administration and maintenance.

  • Leads activities within Quality Control related to data management systems and the development of processes to maintain these systems. Collaborates with end users to maintain, processes and procedures to govern these systems.

  • Provides Quality Systems input and support to system owners on the implementation, validation, training, support, and ongoing maintenance of all the QC laboratory data management equipment.

  • Provides training and troubleshooting for all data management systems

  • Communicates issues and technical failures to direct supervisor.

  • Sustains and enhances data management systems as required to support routine testing activities, method transfers and validations and change control activities around these methods or systems.

  • Applicable methods systems include, but not limited to HPLC, spectroscopy, ELISA, Bioassay and GC methods

  • Write technical reports, SOPs and perform data analysis and trending for method transfers and process investigations.

  • Review change controls associated with these applications for impact the QC laboratories.

  • Represent QC laboratories at site, company and external system meeting.

  • Work with Automation team regarding Smart Lab program.

  • Work with CQV team, global IT team, and QC Chemistry and Microbiology teams

  • Work with automation team regarding technical issues, upgrades and updates to systems as required.

  • Work with the global IT team, QC Analytical and Microbiology teams.

  • Occasional contact with other line management staff relating to specific project responsibilities may be expected.

Role Requirements:

  • Knowledge of science generally attained through studies resulting in a B.S., in science, engineering, biochemistry, a related discipline, or its equivalent is preferred.

  • Working knowledge of databases and laboratory applications including LIMS, Smartlab, Sample Manager, Nugensis, and Empower, software desired.

  • Working knowledge of computer hardware including servers, workstations, network switches, terminal servers, and storage technologies required.

  • Knowledge of computer software and operating systems including Windows XP, Windows Server 2000, Windows 2003 Server, Oracle, SQL Server.

  • Knowledge of interfacing of the above applications and impact to each other.

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

  • Significant back room audit experience. Ability to speak to a basic SOP in the front room.

  • Minimum of 4-6 years of industry experience.

  • Work in a cGMP laboratory and manufacturing environment following techniques which require one to maintain a high attention to detail, to properly use Personal Protective Equipment (PPE) and to handle hazardous materials.

  • May work on assignments that are extremely complex in nature where independent action and a high degree of initiative are required in resolving problems and developing recommendations. Exercises judgment within broadly defined practices and policies in selecting methods and techniques and evaluation criteria for obtaining results. Makes sound decisions and applies appropriate notification to management as appropriate. Failure to obtain results or erroneous decisions or recommendations

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.

Physical presence at the BMS worksite or physical presence in the field is an essential job function of this role which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and enhances the Company culture.

To protect the safety of our workforce, customers, patients and communities, the policy of the Company requires all employees and workers in the U.S. and Puerto Rico to be fully vaccinated against COVID-19, unless they have received an exception based on an approved request for a medical or religious reasonable accommodation. Therefore, all BMS applicants seeking a role located in the U.S. and Puerto Rico must confirm that they have already received or are willing to receive the full COVID-19 vaccination by their start date as a qualification of the role and condition of employment. This requirement is subject to state and local law restrictions and may not be applicable to employees working in certain jurisdictions such as Montana. This requirement is also subject to discussions with collective bargaining representatives in the U.S.

Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an approval of accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application or if you are applying to a role based in the U.S. or Puerto Rico and you believe that you are unable to receive a COVID-19 vaccine due to a medical condition or sincerely held religious belief, during or any part of the recruitment process, please direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Company: Bristol Myers Squibb

Req Number: R1551756

Updated: 2022-01-23 01:47:12.203 UTC

Location: Devens,Massachusetts

Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.

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