Bristol-Myers Squibb

Senior Director, Process Unit Head Launch Operations

Boudry, Neuchatel, Switzerland

Not SpecifiedCompensation
Senior (5 to 8 years), Mid-level (3 to 4 years)Experience Level
Full TimeJob Type
UnknownVisa
Pharmaceutical ManufacturingIndustries

Requirements

Candidates should possess a Bachelor’s degree in a scientific discipline, such as Chemistry, Chemical Engineering, or a related field, and hold a minimum of 10 years of experience in pharmaceutical manufacturing, with at least 5 years in a leadership role within a cGMP environment. Strong experience with solid oral dosage form manufacturing, including aseptic processing and sterile manufacturing, is required. Demonstrated leadership skills and the ability to build and manage high-performing teams are essential.

Responsibilities

The Senior Director will oversee all drug product manufacturing activities for the P3 manufacturing facility, ensuring timely completion of technical transfers, development activities, Phase 3 clinical manufacturing, and future commercial production of oral solid dosage products. They will develop and implement manufacturing strategies, build strategic relationships with internal BMS partners, and drive initiatives to improve Process Unit performance. Additionally, the Senior Director will be responsible for creating a cohesive team, fostering a flexible and agile mindset, and partnering with site leadership to establish operational goals and culture while ensuring seamless transition from development to commercialization.

Skills

cGMP
Solid Oral Dosage Form
Aseptic Processing
Sterile Manufacturing
Manufacturing Strategy
Technical Transfer
Clinical Manufacturing
Process Unit Performance

Bristol-Myers Squibb

Develops and delivers biopharmaceutical medicines

About Bristol-Myers Squibb

Bristol Myers Squibb (BMS) develops and delivers medicines aimed at treating serious diseases, focusing on areas like cancer, autoimmune diseases, and heart conditions. The company conducts extensive research and development to create new drugs, which are sold after receiving regulatory approval. BMS also produces generic drugs, offering affordable alternatives that meet the same quality standards as their branded counterparts. What sets BMS apart from competitors is its dual focus on both innovative and generic medicines, enhancing access to healthcare. The company's goal is to improve patient outcomes while maintaining a commitment to sustainability and corporate responsibility.

Key Metrics

New York City, New YorkHeadquarters
1887Year Founded
$33,706.1MTotal Funding
IPOCompany Stage
Biotechnology, HealthcareIndustries
10,001+Employees

Benefits

Flexible Work Hours
Hybrid Work Options
Professional Development Budget

Risks

Increased competition in oncology from emerging biotech firms like ArsenalBio.
BMS's lawsuit over the 340B Drug Pricing Program may lead to regulatory challenges.
Rapid AI and digital tech evolution may pose integration challenges for BMS.

Differentiation

BMS focuses on innovative cancer treatments through collaborations like ArsenalBio for T cell therapies.
The company emphasizes digital health technologies, enhancing clinical trial management and patient engagement.
BMS offers both innovative and generic medicines, increasing affordable healthcare solutions.

Upsides

BMS's partnership with Medidata enhances clinical research processes and patient outcomes.
The collaboration with AI Proteins advances novel miniprotein-based therapeutics, expanding therapeutic modalities.
BMS's global license agreement with BioArctic expands its portfolio in neurodegenerative diseases.

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