B

Bristol Myers Squibb

Makes drugs for cancer, blood and immune diseases

Associate Director, Process Scale-Up & Manufacturing Readiness

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeHyderabad, Telangana, IndiaNo salary listed

About the Job

Requirements

  • A Ph.D. in Chemical Engineering with 8 or more years of industrial experience, or an M.S. with 12 or more years of relevant experience, or a B.S. with 15 or more years of relevant experience.
  • Extensive experience scaling small-molecule manufacturing processes from laboratory through pilot plant and commercial production, including strong process safety and troubleshooting skills.
  • Knowledge of current Good Manufacturing Practice (cGMP) manufacturing and quality systems.
  • Demonstrated success influencing in a matrixed management environment without direct reporting relationships.
  • The position requires working within facilities handling hazardous chemical agents that, if improperly handled, may potentially affect employee health, including reproductive function and/or embryo/fetal development.

Responsibilities

  • Influence manufacturing strategies across a large portfolio of projects while mentoring US- and European-based scientists and engineers to build organizational capabilities in scale-up and cGMP manufacturing.
  • Lead technology transfer and on-site support at multiple external sites, proactively assessing and mitigating potential risks and rapidly resolving realized manufacturing issues.
  • Identify and improve company-CDMO ways of working regarding technical transfer and manufacturing readiness.
  • Lead manufacturing readiness assessments, evaluating process scalability and de-risking scale-up from laboratory through pilot plant and commercial production.
  • Serve as a subject matter expert for chemical manufacturing operations and unit operations, partnering with process chemistry, engineering, and manufacturing to define executable processes.
  • Apply process safety and risk management principles to lead readiness reviews before manufacturing campaigns.
  • Represent CPD Engineering in cross-functional and enterprise forums, contributing to broader strategic alignment.
  • Assess whether manufacturing processes fit available equipment and identify likely scale-up risks when visiting manufacturing plants.
  • Assess whether environmental health and safety and cGMP quality risks are adequately addressed, raise unresolved risks to internal and external stakeholders and leadership, and drive their resolution.
  • Assess whether the process, equipment, or operations strategy requires modification to maximize the probability of manufacturing success.

Desired Qualifications

  • Experience beyond small molecules, including antibody-drug conjugates, oligonucleotides, peptides, or radiopharmaceuticals.
  • Experience spanning clinical to commercial manufacturing.

About the Company

Bristol Myers Squibb

Makes drugs for cancer, blood and immune diseases

Bristol Myers Squibb discovers, develops and sells prescription medicines for serious illnesses, including cancer, blood disorders, immune diseases and heart disease, for patients treated by doctors and hospitals around the world. Its best-known drug is Opdivo, an immunotherapy that helps the body's own immune system find and attack many kinds of cancer. Researchers develop drug candidates in its labs or bring them in through acquisitions and partnerships, then test them in clinical trials to win regulatory approval. The company makes and markets the approved medicines and earns its revenue from sales of patent-protected drugs. Its roots go back to a business founded in 1887, and it is based in Lawrence Township, New Jersey.

Company size
10,001+
Company stage
IPO
Headquarters
Lawrence Township, NJ
Founded
1887

Recently Posted Jobs

Explore more opportunities at Bristol Myers Squibb

See more jobs