Scientist, Clinical Supply Operations
Company: Disability Solutions
Location: New Brunswick
Posted on: May 3, 2024
Job Description:
Working with UsChallenging. 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 rich in diversity. 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 .Our Clinical Supply Operations is
responsible for the supply of drug product administered to patients
in clinical studies worldwide. In Global Product Development and
Supply the team works closely with our partners to deliver quality
products safely, efficiently and on time while operationalizing the
innovative technologies that will deliver the transformative
medicines of tomorrow. As a member of our team, you will get the
chance to play a pivotal role to positively impact patients' lives
while developing professionally to achieve your own career goals.
Position Summary: The Clinical Supply Operations Scientist will
lead the manufacture of oral solid dosage products in a cGMP
environment, ensuring strict adherence to applicable regulatory,
safety, and company policies and procedures. In addition, the
Scientist will be responsible for leading a variety of engineering
projects in support of oral solid dosage manufacturing
operations.Role and Responsibilities:
- Leads the manufacture of assigned oral solid dosage product
batches and completes all required documentation
- Supports successful technical transfer and scale-up of new
products
- Participates in new technology evaluation and
implementation
- Establishes plans for managing workload with efficient resource
utilization and within designated timeframes. Effectively adjusts
plans to deal with changes and obstacles.
- Troubleshoots and resolves manufacturing related issues.
- Effectively supervises assigned pharmaceutical development
technician(s) to ensure efficient batch execution.
- Strictly adheres to departmental, Company, and Regulatory
policies, procedures, and regulations.
- Communicates effectively with management, quality unit, peers
and colleagues within and outside the department for all
manufacturing, quality and safety related issues.
- Participates in SOP writing and review.
- Participates in selected initiatives leading to the
improvements on cGMP compliance, safety compliance and
productivity. Experience & Qualifications:
- B.S. in engineering, pharmaceutical sciences, or related
discipline
- 3+ years relevant experience in pharmaceutical manufacturing
and/or formulation or related field
- The successful candidate must have excellent scientific,
analytical and troubleshooting skills.
- Strong written, verbal and interpersonal communication skills
are required to communicate effectively and contribute to
multidisciplinary project teams.
- Additional experience with cGMP requirements and process
automation systems would be beneficial. Why You Should Apply 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.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
accommodation prior to accepting a job offer. If you require
reasonable accommodation in completing this application, or 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.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 CareersWith 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 an inclusive culture, promoting
diversity 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 a diverse 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. 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. BMS cares about your well-being and the
well-being of our staff, customers, patients, and communities. As a
result, the Company strongly recommends that all employees be fully
vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
BMS will consider for employment qualified applicants with arrest
and conviction records, pursuant to applicable laws in your
area.Any data processed in connection with role applications will
be treated in accordance with applicable data privacy policies and
regulations.
Keywords: Disability Solutions, Sayreville , Scientist, Clinical Supply Operations, Healthcare , New Brunswick, New Jersey
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