8d ago
$178,420 - $216,197/yr

Associate Director Process Technology Transfer - Devens MA

United StatesUnited States·Devensexecutive
Other
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Overview

ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans,

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ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post.

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.




PRINCIPAL OBJECTIVE OF THE POSITION

Lead and develop multifunctional teams to ensure effective process technology transfer of commercial and clinical products manufactured at the Devens Single Use Facility, resolve process issues, and optimize process and facility efficiency. This role is accountable for maximizing productivity, minimizing costs, and resolving process challenges through leadership, technical expertise, and cross-functional resource coordination.


MAJOR DUTIES AND RESPONSIBILITIES

Leads technology transfer and new product introduction into the manufacturing facility. Accountable for providing support to manufacturing teams to achieve production targets for clinical and commercial products.
Directs activities associated with product changeover, continuous improvement initiatives, project prioritization, and production and maintenance scheduling to meet site metrics.
Allocates department resources to support deviations, defects, and changes associated with maintaining safe and compliant production.
Champions the company's, site's, and department's mission, goals, and guidelines, taking action that advances cultural evolution, innovation, and leadership across the organization.
Promotes and demonstrates safety leadership in pursuit of an injury-free operating environment, ensuring safety investigations and CAPAs are closed promptly.
Collaborates with Manufacturing staff to identify trends, variances, and bottlenecks in the manufacturing process, and helps develop solutions to maximize productivity, quality, and process efficiency.
Recruits and develops a high-performing team with diverse backgrounds and talents; coaches and counsels team members to build their skills and fosters an environment of continuous learning, improvement, and innovation.
Maintains and communicates performance metrics to the team, setting and upholding high performance expectations.
Establishes an environment that fosters continuous improvement in cost, quality, safety, and customer service.
Builds and maintains strong relationships inside and outside the organization.
Supports health authority inspections.

     

Responsibilities

~2 min read
KNOWLEDGE AND SKILLS

B.S. in biological sciences, chemical/biochemical engineering, or a related discipline, with a minimum of 10 years of relevant experience in the biopharmaceutical industry, or equivalent experience; or
M.S. in the same disciplines, with a minimum of 6 years of relevant experience in the biopharmaceutical industry, or equivalent experience; or
Ph.D. in biological sciences, chemical/biochemical engineering, or related discipline.
Mastery of SOPs and cGMPs, with the know-how to work and manage within a regulatory environment.
Demonstrated aptitude for engineering principles and manufacturing automation systems.
Demonstrated ability to shift the thinking of, or gain acceptance from, others in sensitive situations.
Proven leadership ability to make difficult decisions in a logical, rational manner; demonstrated ability to work as a senior management team member and engage and influence team members in a matrixed environment.
Previous managerial experience demonstrating proficiency in selecting, motivating, and retaining a high-performing 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 to coordinate with support groups and obtain needed cooperation and support in a timely and effective manner.
Demonstrated strong track record of change management, including implementation of continuous improvement and OPEX strategies.

We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.

Compensation Overview:

Devens - MA - US: $178,420 - $216,197

Location & Eligibility

Where is the job
Devens, United States
On-site at the office
Who can apply
US

About this job

Pay per year
$178,420–$216,197 a year
194% above the $67,000 median for Other jobs on Jobera (144,221 salaries).
Who can apply
United States
Posted
8 days ago
Employer
has 1,873 open jobs on Jobera in 7 countries.

Listing Details

Posted
November 5, 2026
First seen
November 5, 2026
Last seen
November 12, 2026

Posting Health

Days active
6
Repost count
0
Trust Level
45%
Scored at
November 12, 2026

Signal breakdown

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Associate Director Process Technology Transfer - Devens MA$178,420 - $216,197