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Specialist, Sample Management

Bristol-Myers Squibb

Specialist, Sample Management

Bristol-Myers Squibb

Cruiserath - IE

·

On-site

·

Full-time

·

1w ago

Benefits & Perks

Healthcare

Pension

Paid Time Off

Gym

Life Insurance

Bonus

Healthcare

Gym

Required Skills

Sample management

GMP compliance

Laboratory operations

Communication

Teamwork

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. 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.

Bristol Myers Squibb Ireland:

Bristol Myers Squibb has been in operation in Ireland since 1964, employing over 650 people across a range of activities and business units

Located in Dublin, Cruiserath Biologics Campus, a one billion Multi-Product Cell Culture Biologics Manufacturing facility plays a central role in the Global Product Development and Supply (GPS) network as the company’s first European biologics manufacturing facility. This state of the art facility will produce multiple therapies for the company’s growing biologics portfolio. Global Biologics Laboratory (GBL) responsible for the release testing of Biologics Drug product for the network, is also based on the Cruiserath Biologics Campus.

BMS Cruiserath has been awarded “Biopharma Company of the Year 2019” in the Irish Pharma Industry Awards and is certified as a Great Place to Work since 2017, including as a Great Place to Work for Women in 2020 and 2021.

For more information about Bristol Myers Squibb, visit us at BMS.com/ie

The Role​

Bristol-Myers Squibb is seeking to recruit a QC Sample Management Specialist to join the QC Materials team at its Multi-Product Cell Culture Drug Substance Facility in Cruiserath, Dublin.

Reporting to the QC Sample Management Manager, they will be responsible for supporting site activities related to the Sample Management Laboratory, in-process samples, stability samples, retains and laboratory duties in accordance with cGMP regulations.

Key Duties and Responsibilities:

  • Liaise with manufacturing to ensure all Drug Substance samples are processed and delivered to the appropriate destination in an appropriate timeframe.
  • Liaise with Engineering Stores to ensure all Drug Product samples are processed and delivered to the appropriate destination in an appropriate timeframe.
  • Liaise with Warehouse Cryogenics Logistics (WCL) to ensure all Raw Material samples are processed and delivered to the appropriate destination in an appropriate timeframe.
  • Support the QC readiness and implementation of Drug Product Stability at Cruiserath
  • Manage Temp Tales and shipping documents when receiving samples from external sites.
  • Logging of samples to LIMS/CIMS or logbooks, and label accordingly.
  • Release samples for QC testing.
  • Storage of backups and reserve samples.
  • Perform monthly reconciliation and report deviations to Sample Management Manager, if any.
  • Reconstitute and Aliquot samples for the QC activities for Global Biologics Laboratory, Global Stability and Multi Product Cell Culture (MPCC) Facility.
  • Support buffer preparation for the QC Separations lab
  • Support enrolment of bulk Drug Product Stability Study Samples
  • Support timepoint pulls of Drug Product Stability Study Samples
  • Generate and update SOPs and other relevant documents as required.
  • Maintain a high standard of GMP compliance including the completion and provision of training as required.
  • Keeps abreast of current corporate and industry requirements and compliance trends as they pertain to laboratory operations and aseptic manufacturing.
  • Support continuous improvement initiatives across the department and within the team
  • Performing any other activities as indicated by the Lab Manager.

Qualifications, Knowledge and Skills Required:

The successful candidate must demonstrate excellent written and verbal communication skills and the ability to work in a team based collaborative environment.

The ideal candidate should hold a minimum of a third level qualification (Degree) in Chemistry/Biology or related discipline along with at least 1 year of experience in a pharmaceutical / healthcare laboratory or related technical function.

Why you should apply

  • You will help patients in their fight against serious diseases
  • You will be part of a company that encourages excellence and innovation, respects diversity, develops leaders and values its employees.
  • You’ll get a competitive salary and a great benefits package including, but not only, an annual bonus, pension contribution, family health insurance, 27 days annual leave, access to BMS Cruiserath on-site gym and life assurance.

BMSBL

If you come across a role that intrigues you but doesn’t 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.

Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.

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

If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.

R1598920 : Specialist, Sample Management

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About Bristol-Myers Squibb

Bristol-Myers Squibb

Bristol-Myers Squibb engages in the discovery, development, licensing, manufacturing, marketing, distribution and sale of pharmaceuticals.

10,001+

Employees

New York

Headquarters

$150B

Valuation

Reviews

3.4

10 reviews

Work Life Balance

4.2

Compensation

4.0

Culture

2.8

Career

2.3

Management

2.5

55%

Recommend to a Friend

Pros

Great benefits and perks

Good work-life balance

Stable company

Cons

Poor management and leadership

Frequent reorganizations and layoffs

Toxic/cutthroat culture

Salary Ranges

2,116 data points

Junior/L3

Mid/L4

Senior/L5

Director

Junior/L3 · Business Analyst

0 reports

$22,000

total / year

Base

-

Stock

-

Bonus

-

$18,700

$25,300

Interview Experience

3 interviews

Difficulty

3.0

/ 5

Duration

14-28 weeks

Interview Process

1

Application Review

2

Recruiter Screen

3

Technical Phone Screen

4

Hiring Manager Interview

5

Panel Interview

6

Offer

Common Questions

Technical Knowledge

Behavioral/STAR

Past Experience

Culture Fit

Problem Solving