Associate Director, LSCC Downstream Manufacturing Operations (R1549019-en-us)
At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.
To plan and direct the execution of downstream commercial manufacturing process according to established electronic work instructions and production records for the manufacture of therapeutic proteins in accordance with current Good Manufacturing Practices (cGMPs).
Duties and Responsibilities:
Embraces and effectively communicates the company, site and department mission, goals and guidelines, undertaking supportive actions which contribute to the fulfillment of these values and objectives while contributing to cultural evolution, innovation and leadership within the organization.
Manages downstream functional area and provides direction and guidance to 24x7 operational staff in their daily contributions to the manufacturing process.
Allocates departmental resources (equipment, labor and inventories) to match production schedules and maximize productivity, reduce costs and increase efficiencies.
In collaboration with Engineering and Manufacturing staff, identifies trends, variances and bottlenecks in the manufacturing process and assists in the development of solutions to maximize productivity, quality and process efficiency.
Coordinates resources from the supporting organizations (e.g. QA/QC, Supply Chain, Human Resources, Site Engineering) as needed to support the core manufacturing process.
Recruits and develops a high performing team with diverse backgrounds and talents.
Coaches and counsels team members to develop their skill sets and create an environment of continuous learning, improvement, and innovation.
Maintains and communicates performance metrics to her/his team, setting and maintaining high expectations for team performance.
Maximizes the use of existing capital committed to the manufacturing process by eliminating waste, improving productivity and controlling work-in-progress levels.
Establishes an environment which fosters continuous improvement in cost, quality, safety and customer service.
Builds and maintains strong relationships inside and outside the organization
Knowledge and Skills Required:
Knowledge of science generally attained through studies resulting in a B.S., in science, engineering, biochemistry or related discipline, or its equivalent; a Masters Degree in related disciplines is desired.
A minimum of 10 years of biopharmaceutical manufacturing experience with minimum of 6 years of increasing management responsibility
Mastery of SOPs, cGMPs and know–how to work and manage within a regulatory environment.
Extensive knowledge of pharmaceutical and biopharmaceutical manufacturing process with a proven record in pharmaceutical technology, technology transfer, process development, manufacturing support.
Demonstrated aptitude for engineering principles and manufacturing automation systems.
Demonstrated ability to change the thinking of or gain acceptance of others in sensitive situations.
Previous managerial experience which demonstrates proficiency in selection, motivating and retaining a superior team, effectively managing personnel issues and planning and administering financial resources.
Adaptable to a fast paced, complex and ever changing business environment.
Effective communication skills with support groups in the coordinating system to obtain needed cooperation and support as required in a timely and effectively manner.
Knowledge of statistical process control and continuous improvement methodologies to effectively identify and implement process improvement.
Demonstrated leadership, interpersonal, communication, and motivation skills.
Knowledge of applicable business systems including: SAP, LIMS, Maximo, and Trackwise.
Knowledge of manufacturing executions systems including: Syncade, SmartLab, and distributive control systems such as DeltaV.
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.
Physical presence at the BMS worksite or physical presence in the field is an essential job function of this role which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and enhances the Company culture.
To protect the safety of our workforce, customers, patients and communities, the policy of the Company requires all employees and workers in the U.S. and Puerto Rico to be fully vaccinated against COVID-19, unless they have received an exception based on an approved request for a medical or religious reasonable accommodation. Therefore, all BMS applicants seeking a role located in the U.S. and Puerto Rico must confirm that they have already received or are willing to receive the full COVID-19 vaccination by their start date as a qualification of the role and condition of employment. This requirement is subject to state and local law restrictions and may not be applicable to employees working in certain jurisdictions such as Montana. This requirement is also subject to discussions with collective bargaining representatives in the U.S.
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 approval of accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application or if you are applying to a role based in the U.S. or Puerto Rico and you believe that you are unable to receive a COVID-19 vaccine due to a medical condition or sincerely held religious belief, during or any part of the recruitment process, please direct your inquiries to . Visit[Register to View] target="_blank"> [Register to View] to access our complete Equal Employment Opportunity statement.
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