Senior Specialist, QA Technical Operations

Responsibilities

• Supports and provides quality oversight to technical transfer sub-teams and the review and approval of technology transfer documentation
• Maintains operating procedures for the site Quality Assurance programs to ensure consistent, high-quality materials are produced.
• Provides floor support to the manufacturing process as needed in a person-in-plant function.
• Performs review and approval of Quality, Manufacturing, and Material Specifications SOPs, documents, and batch records.
• Provides oversight to Quality walkthroughs for shutdown and inspections readiness activities and ensures program management is in compliance with site and corporate procedures.
• Provide Quality review and approval of investigation records, CAPA records, change management, automation changes, and applicable document updates/creations.
• Provides strategic foresight to identify and implement changes to enhance long term goals of the department and drive continuous improvement.
• Qualifications & Experience
• Knowledge of science generally attained through studies resulting in a B.S. in science, engineering, biochemistry or related discipline, or its equivalent is preferred.
• A minimum of 5 years of relevant experience in a regulated environment with at least 3 years focused on product quality.
• Knowledge of biotech bulk and finished product manufacturing is highly desirable.
• Extensive knowledge of US and EU cGMP regulations and guidance.
• Knowledge of Quality Risk Management principles preferred.
• Knowledge of electronic systems including any of the following: SAP, LIMS, Infinity (Veeva Vault), LES, Maximo, Vault and Syncade desirable.
• Experience working in a team-based environment with a diverse group of people.
• 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.
• Compensation Overview:
• Devens - MA - US: $81,160 - $98,344
• Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.
• Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:
• Health Coverage: Medical, pharmacy, dental, and vision care.
• Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living

Benefits

Additional Information

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 . Position Summary: Support Devens site through review and approval of investigations and change controls. Provide Quality oversight and support for Technology Transfer, Automation, Cell Bank Disposition, Validation, Manufacturing Science and Technology, Master Data and Site Engineering programs. Assure the quality of manufactured products are in compliance with all applicable regulations and guidelines. May assist in preparing for and hosting of regulatory audits.

Your Match

How well this role fits your profile.

Company Intel

What employees say

Worked at Bristol-Myers Squibb? Share your experience