What are the responsibilities and job description for the Manufacturing Specialist position at Bristol-Myers Squibb?
Company Overview
Bristol-Myers Squibb is a leading pharmaceutical company dedicated to transforming patients' lives through science. With a single vision, every 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.
Salary
The starting compensation for this position ranges from $49,000 to $61,000, plus incentive cash and stock opportunities based on eligibility.
Job Description
Working with Us
Challenging. Meaningful. Life-changing. Those aren't words 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 production lines 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.
PURPOSE AND SCOPE OF POSITION:
The primary purpose of the Manufacturing Technician role is to complete production assignments with high quality and timely output in a cellular therapeutic manufacturing environment.
QUALIFICATION REQUIREMENTS:
Education: An associate or bachelor's degree in a related field is preferred. Minimum of a high school diploma and/or equivalent combination of education and experience is required.
Experience: 0-1 years of cGMP manufacturing experience is desired or equivalent in work experience or education. Proven experience working on teams where combined contribution, collaboration, and results were expected. Demonstrated proficiency in common computer tools such as word processing, spreadsheet, and web-based applications. Experience where attention to detail and personal accountability were critical to success. Demonstrates good interpersonal skills, is attentive, and approachable. Maintains a professional and productive relationship with area management and coworkers.
ROLES AND RESPONSIBILITIES:
Bristol-Myers Squibb is a leading pharmaceutical company dedicated to transforming patients' lives through science. With a single vision, every 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.
Salary
The starting compensation for this position ranges from $49,000 to $61,000, plus incentive cash and stock opportunities based on eligibility.
Job Description
Working with Us
Challenging. Meaningful. Life-changing. Those aren't words 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 production lines 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.
PURPOSE AND SCOPE OF POSITION:
The primary purpose of the Manufacturing Technician role is to complete production assignments with high quality and timely output in a cellular therapeutic manufacturing environment.
QUALIFICATION REQUIREMENTS:
Education: An associate or bachelor's degree in a related field is preferred. Minimum of a high school diploma and/or equivalent combination of education and experience is required.
Experience: 0-1 years of cGMP manufacturing experience is desired or equivalent in work experience or education. Proven experience working on teams where combined contribution, collaboration, and results were expected. Demonstrated proficiency in common computer tools such as word processing, spreadsheet, and web-based applications. Experience where attention to detail and personal accountability were critical to success. Demonstrates good interpersonal skills, is attentive, and approachable. Maintains a professional and productive relationship with area management and coworkers.
ROLES AND RESPONSIBILITIES:
- Works on routine manufacturing assignments per written procedures, where ability to recognize deviation from accepted practice is required.
- Adheres to Good Manufacturing Practices and standard operating procedures.
- Weighs and checks raw materials. Assembles, cleans, and sanitizes process equipment, monitors processes.
- Completes work instructions and maintains a clean room environment to comply with regulatory requirements.
- Trains for proficiency in the operation of primary production equipment within the assigned functional area.
- Trains for proficiency in process systems (i.e., Syncade MES and Oracle interfaces) and some supporting business systems (i.e., Oracle, ETQ, BMRAM etc.).
- Assist with the revision and creation of process documents, such as SOPs and electronic work instructions.
- Assists in maintaining material and components inventory levels.
- Supports a safe work environment.
- Works on assignments that are routine in nature where judgment is required in resolving problems and making routine recommendations.
