All Of Our Groups

Healthcare

AssociateDirectorTS/MSCentralTeam

$123–180k Indianapolis, Indiana, United States FULL TIME
The Brief

“Associate Director – TS/MS Central Team at All Of Our Groups. Skills: TS/MS support, Manufacturing, Quality assurance, Team leadership. Maintain a safe work environment. Lead safety initiatives”

Industry & Context.

Healthcare
Problems you'll solve

Problem solving; Independent decision-making

Eligibility Requirements

Flexible in providing support, Occasional extended hour work, Occasional off-hour work

What They're Looking For.

Must Have

Bachelor's Degree in scientific disciplines, 5+ years pharmaceutical manufacturing experience, 3+ years experience leading teams, Authorized to work in the United States

Nice to Have

Technical aptitude, Ability to train and mentor, Proven Teamwork and interpersonal skills, Problem solving and independent decision-making skills, Oral and written communication skills, Ability to influence diverse groups, Experience with deviation and change management systems, Experience interacting with external vendors, Understanding of GMP supplier qualification processes

What You'll Do.

Maintain a safe work environment

Lead safety initiatives

Support HSE Corporate and Site Goals

Drive safety and quality culture

Understand scientific principles for manufacturing

Provide technical guidance

Understand manufacturing control strategy

Influence manufacturing control strategy

Drive control for the process

Drive capability for the process

Drive productivity for the process

Drive continuous improvement for the process

Review GMP documentation

Approve GMP documentation

Work cross-functionally with process teams

Provide oversight for supplier interactions

Engage with Procurement and Materials Management QA

Support GMP supplier qualification activities

Influence the technical agenda

Implement the technical agenda

Influence site business plan objectives

Implement site business plan objectives

Influence GMP Quality Plan objectives

Implement GMP Quality Plan objectives

Network with global parenteral sites

Collaborate with global parenteral sites

Understand best practices

Participate in tactical business planning

Participate in strategic business planning

Support site inspection readiness

Support site inspection execution

Interact with Regulatory Agencies

Performance management of staff

How You'll Work.

Team & Collaboration

Cross-functional teams; Global parenteral sites; Procurement and Materials Management QA

Communication Scope

Oral communication; Written communication

Free ATS check

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