Bristol-Myers Squibb

Sr. Manager, Manufacturing Records and Procedures

Bristol-Myers Squibb

Summit, NJ, USA
Full-TimeDepends on ExperienceSenior LevelMasters
Job Description

Are you a detail-oriented and organized leader with a strong background in manufacturing and quality control? Do you have a passion for creating and implementing efficient processes and procedures? Bristol-Myers Squibb is seeking a highly experienced Sr. Manager for our Manufacturing Records and Procedures team. In this role, you will be responsible for overseeing and maintaining accurate records and procedures in our manufacturing facilities. If you possess a combination of technical expertise, leadership skills, and a commitment to quality, we encourage you to apply for this exciting opportunity.

  1. Develop and implement efficient and effective processes and procedures for the manufacturing records and procedures team.
  2. Oversee and manage a team of employees responsible for maintaining accurate records and procedures in the manufacturing facilities.
  3. Ensure compliance with all company and industry standards, regulations, and guidelines.
  4. Continuously monitor and improve the quality and accuracy of manufacturing records and procedures.
  5. Collaborate with cross-functional teams to identify and address any issues or discrepancies in records and procedures.
  6. Train and mentor team members on proper record-keeping and procedure documentation techniques.
  7. Conduct regular audits and reviews to ensure compliance and identify areas for improvement.
  8. Stay up-to-date with industry advancements and best practices for record-keeping and procedures.
  9. Manage and maintain all relevant documentation and records in accordance with company policies and guidelines.
  10. Communicate effectively with other departments and senior management regarding any updates or changes to processes and procedures.
Where is this job?
This job is located at Summit, NJ, USA
Job Qualifications
  • Bachelor's Degree In A Related Field Such As Pharmaceutical Science, Engineering, Or Quality Management.

  • Minimum Of 8 Years Of Experience In A Manufacturing Or Quality Role Within The Pharmaceutical Industry.

  • Strong Understanding Of Fda Regulations And Cgmp Requirements.

  • Proven Track Record Of Developing And Implementing Procedures And Systems To Ensure Compliance And Efficiency In Manufacturing Operations.

  • Excellent Leadership And Communication Skills, With The Ability To Oversee A Team And Effectively Communicate With Cross-Functional Departments.

Required Skills
  • Documentation

  • Quality Assurance

  • Process Improvement

  • Project Management

  • Data Analysis

  • Auditing

  • Continuous Improvement

  • Team Leadership

  • Regulatory compliance

  • Training and Development

  • SOP Development

  • Recordkeeping

Soft Skills
  • Communication

  • Conflict Resolution

  • Leadership

  • Time management

  • Interpersonal Skills

  • creativity

  • Critical thinking

  • Teamwork

  • Adaptability

  • Problem-Solving

Compensation

According to JobzMall, the average salary range for a Sr. Manager, Manufacturing Records and Procedures in Summit, NJ, USA is between $120,000 and $150,000 per year. However, this can vary based on factors such as years of experience, specific job responsibilities, and the company's industry and size.

Additional Information
Bristol-Myers Squibb is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Required LanguagesEnglish
Job PostedDecember 20th, 2023
Apply BeforeJune 21st, 2025
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About Bristol-Myers Squibb

Bristol-Myers Squibb Co. operates as a biopharmaceutical company, which engages in the discovery, development, licensing, manufacturing, marketing, distribution, and sale of biopharmaceutical products. It includes chemically-synthesized drugs or small molecules and products produced from biological processes called biologics.

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