Bioprocess Specialist

**Working with Us**

Challenging. Meaningful. Life-changing. Those arent 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. Youll 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: .

The Bioprocess Specialist uses current Good Manufacturing Practices (cGMPs) in the execution of commercial manufacturing processes for the manufacture of therapeutic proteins used in medicines that are revolutionizing the treatment of serious disease.

**This is a 2nd shift (** **2:00pm** **to** **10** **:** **0** **0** **p** **m) Mon-Fri position, therefore eligible for a 10% shift differential.**

**Key Responsibilities:**

+ Operateproduction equipment within an assigned functional area adhering to Good Manufacturing Practices and standard operating procedures

+ Revise and create process documents and assist with process related investigations

+ Train for proficiency in process automation and supporting business systems and in the operation of primary production equipment to complete process steps including buffer preparation, column packing, chromatography, and filtration in a clean room environment

+ Lead in maintaining material and components inventory level.Weigh and check raw materials?

+ Support a safe work environment and contribute to area specific initiatives associated with work safety

+ Weighs and checks raw materials.Assembles, cleans, and autoclaves process components. Assists in maintaining material and component inventory levels

+ Works on routine manufacturing assignments per written procedures that are moderately complex with minimal instructionsAssists in revising and creating process documents, i.e., SOPs and Batch Records, and assists with process-related investigations

**Qualification** **s & Experience:**

+ High school diploma is required?

+ Knowledge of science attained through completion of a certificate program or Associate degree in biotechnology or a related field is preferred

+ Prior experience successfully participating on work teams where personal accountability, attention to detail, collaboration, and results were expected

+ Demonstrated proficiency in common computer tools and web-based applications

+ Prior experience (4+ years) with Good Manufacturing Practices (GMP) regulations and prior work experience in a clean room or highly regulated environment required

+ Troubleshooting ability is required

**#LI-ONSITE #BMSBLDMA**

_If you come across a role that intrigues you but doesnt 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 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 . Visit ) 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.

**Company:** Bristol-Myers Squibb

**Req Number:** R

**Updated:** :00:57.740 UTC

**Location:** Devens-MA

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.