Larry Weiner
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Larry Weiner Email & Phone Number

Executive Leader, Biopharma Technical Operations & CMC at Sumitomo Pharma America, Inc.
Location: Cambridge, Massachusetts, United States 18 work roles 5 schools
2 work emails found @biogenidec.com 3 phones found area 617 and 781 LinkedIn matched
✓ Verified Jun 2026 4 data sources Profile completeness 100%

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Role
Executive Leader, Biopharma Technical Operations & CMC
Location
Cambridge, Massachusetts, United States

Who is Larry Weiner? Overview

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Quick answer

Larry Weiner is listed as Executive Leader, Biopharma Technical Operations & CMC at Sumitomo Pharma America, Inc., based in Cambridge, Massachusetts, United States. AeroLeads shows a work email signal at biogenidec.com, phone signal with area code 617, 781, and a matched LinkedIn profile for Larry Weiner.

Larry Weiner previously worked as Head/VP of Cell Processing at Sumitomo Pharma America, Inc. and Member Board of Directors at Sunflower Therapeutics. Larry Weiner holds Master’S Degree, Chemical & Biological Engineering from Tufts University.

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Email format at Sumitomo Pharma America, Inc.

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{first_initial}{last}@biogenidec.com
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Profile bio

About Larry Weiner

Larry Weiner is a biopharmaceutical operations leader with significant experience with Manufacturing, CMC, Program Management, Supply Chain, Project Management, Facilities and Engineering. Larry leads Manufacturing, Engineering and CMC operations at the regenerative medicine division of Sumitomo Pharma America (formerly Enzyvant Therapeutics). Larry led Technical Operations at Unum Therapeutics and Late Stage Program Management and Real Estate & Facilities operations at Indigo. As the Senior Director of Strategic Programs and Program Management at Biogen, innovation program responsibilities included leading drug substance, drug product, device, and new technology innovation initiatives that addressed significant business opportunities and/or were disruptive to the industry. Led the teams that established Biogen's gene therapy, oligonucleotide, and drug product operations strategies. Program management responsibilities included CMC, new product launches, and supply chain support for clinical and commercial therapeutic assets. Additional responsibilities included resource planning and operations portfolio management.Experience includes engineering & facilities operations, capital project management, process development, manufacturing, innovation, engineering and management positions of increasing responsibility at Amgen, Serono Laboratories, Wyeth, MassBiologics, Biogen, Indigo, Unum, and Enzyvant. Larry has a BS Ch.E. from Tufts University, MBA in Operations & Finance from Babson College, and a Masters in Bioengineering from Tufts. Executive Certificates include Operations & Value Chain Management (MIT) and Drug Development (Harvard). Professional interests include delivering results, enabling innovation, developing people, creating sustainable systems, and creating high-performance teams.

Listed skills include Biotechnology, Validation, Gmp, Manufacturing, and 16 others.

Current workplace

Larry Weiner's current company

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Sumitomo Pharma America, Inc.
Sumitomo Pharma America, Inc.
Executive Leader, Biopharma Technical Operations & CMC
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18 roles · 37 years

Larry Weiner work experience

A career timeline built from the work history available for this profile.

Head/Vp Of Cell Processing

Current

Marlborough, Massachusetts, US

  • In July 2023, Enzyvant merged into it’s parent company Sumitomo Pharma America.
  • Responsibilities at Sumitomo Pharma are the same as my Enzyvant responsibilities inclusive of CMC, Supply Chain, and Engineering oversight of internal and external manufacturing & technical operations.
Jul 2023 - Present

Strategic Consultant

Medford, MA, US

  • Supports the creation of corporate strategy including the identification of economic opportunities and threats.
  • Provides strategic guidance concerning product pricing, market placement, and services.
  • Provides technical guidance and project management oversight to equipment design and build firms developing Sunflower’s novel, fully automated, continuous, yeast-based drug manufacturing systems.
  • Acting Head of Regulatory: Ensures equipment and support systems comply with phase appropriate expectations.
Mar 2018 - Sep 2022

Senior Vice President Of Pharmaceutical Development & Manufacturing

Cambridge, Massachusetts, US

  • Primary contact for issues related to strategic operations/supply decisions
  • Leads the CMC team responsible for the supply of commercial product
  • Responsible for Manufacturing, Engineering, cGMP Facilities, MS&T, Manufacturing IT, and Process Development.
  • Responsible for establishing strategic oversight and execution of all aspects of technical operations, including development, external manufacturing, supply chain management, S&OP Planning, and product delivery.
  • Leading the effort to deliver a commercial and clinical regenerative manufacturing facility.
  • Active participate in CMC regulatory strategy development, regulatory filings, meetings with regulatory agencies, and inspection preparation.
Jun 2022 - Jul 2023

Vice President Of Pharmaceutical Development & Manufacturing

Cambridge, Massachusetts, US

  • Organized and led the CMC effort that successfully resolved a CRL and enabled FDA commercial approval of a novel regenerative medicine, tissue-based product
  • Leads the CMC team responsible for the supply of commercial product
  • Drives and guides strategies for process, analytical and formulation development from pre-clinical evaluation through commercial life cycle management.
  • Manages relationships with CMOs to deliver on objectives and maintain productive partnerships
  • Responsible for establishing strategic oversight and execution of all aspects of technical operations, including process development, external manufacturing, supply chain management, and manufacturing sciences.
  • Active participate in CMC regulatory strategy development, regulatory filings, meetings with regulatory agencies, and inspection preparation.
Jul 2020 - Jun 2022

Vice President Of Technical Operations

Waltham, Massachusetts, US

  • Responsible for leading Technical Operations for Unum’s autologous cell therapy drug products and virus drug substances inclusive of Manufacturing & Technical Operations.
  • Responsible for Process & Analytical Development method development and tech transfer.
  • Responsible for manufacturing coordination at contract manufacturing and analytical testing laboratories, including process controls, procedures, compliance, schedule, and budget
  • Responsible for the development and implementation of CMC strategy including development activities, CMOs, testing labs, tech transfer, regulatory submission planning & support, and clinical supply.
  • Develops and implements strategies for manufacturing, supply chain, and product development
  • Leads strategic and capital planning for manufacturing, CMC and supply chain operations
Mar 2020 - Jul 2020

Vice President Of Manufacturing & Cmc

Waltham, Massachusetts, US

  • Responsible for leading cGMP manufacturing for Unum’s autologous cell therapy drug products and virus drug substances
  • Responsible for manufacturing coordination at contract manufacturing and analytical testing laboratories, including process controls, procedures, compliance, schedule and budget
  • Responsible for the development and implementation of CMC strategy including process & analytical development, CMOs, testing labs, tech transfer, regulatory submission planning & support, and clinical supply
  • Develops and implements strategies for manufacturing, supply chain and product development
  • Leads strategic and capital planning for manufacturing, CMC and supply chain operations
  • Negotiates and owns contracts with suppliers, contract manufacturing, and contract testing organizations
May 2019 - Feb 2020

Head Of Global Real Estate & Facilities

Boston, MA, US

  • Full ownership of Indigo’s long term real estate plan and facilities organization in the United States and globally.
  • Responsibility for capital projects that deliver office, laboratory, greenhouse, manufacturing and warehouse facilities across the United States and internationally.
  • Leadership of facilities and capital project teams at three sites.
  • Partnered closely with R&D, Manufacturing, Commercial, Supply Chain, Logistics, Quality, Legal, Finance and Product Management to implement proactive world-class systems and facilities that supported Indigo’s.
Sep 2018 - Apr 2019

Senior Director Project Management

Boston, MA, US

Responsible for ensuring the execution of projects for the process development, formulation development, seed application development, and manufacturing of Indigo’s proprietary microbial products with exceptional quality, speed, and efficiency. Works closely with the Project Management, Bioprocessing, Quality Assurance, Manufacturing, Supply Chain.

Sep 2017 - Aug 2018

Senior Director, Strategic Programs & Program Management

Cambridge, MA, US

Led and focused strategic innovation in the pharmaceutical operations and technology organization. Innovation responsibilities included leading manufacturing drug substance, drug product, device and new technology game-changing initiatives that address significant business opportunities. Responsibilities also included leading disruptive innovation programs.

2015 - 2017 ~2 yrs

Senior Director, Strategic Programs

Cambridge, MA, US

Led and focused strategic innovation in the pharmaceutical operations and technology organization. Innovation responsibilities include leading manufacturing drug substance, drug product, device and new technology game-changing initiatives that address significant business opportunities. Responsibilities also include leading disruptive innovation programs.

2014 - 2015 ~1 yr

Senior Director, Engineering & Facilities

Cambridge, MA, US

Responsible for engineering and maintenance support of Cambridge Manufacturing, R&D, and office facilities. Operational accountability for 1.4 million square feet of space including Biogen Idec’s Corporate Headquarters.Led a five department, 90 employee function with an annual operating budget of $80M. Responsible for process engineering, automation, label.

2010 - 2014 ~4 yrs

Director, Manufacturing Engineering & Validation

Cambridge, MA, US

Led a three department, 40 employee group with an annual operating budget of $12M responsible for supporting Cambridge cGMP manufacturing operations. Supported multiple regulatory inspections including EMA, PMDA, and FDA.

2008 - 2010 ~2 yrs

Associate Director, Global Project Engineering

Cambridge, MA, US

Responsible for capital projects on the Cambridge Campus.Established a customer-centric project delivery model that earned the group a reputation for excellence, openness, and teamwork. Emphasized the function's focus on goal alignment and strong interpersonal skills. Defined, tracked and reported performance to Executive Management. Provided coaching and.

2006 - 2008 ~2 yrs

Director Engineering & Validation

Responsible for the Engineering, Metrology, Preventive Maintenance and Validation functions. Built, managed, and coached a 50 person department located at two sites. Created and maintained a high performance, results oriented culture with low turnover. Built and established cGMP policies, procedures, and systems related to engineering, validation and.

1999 - 2006 ~7 yrs

Project Manager

New York, New York, US

Responsible for the management of capital projects for the manufacturing and development functions. Provided technical leadership and fostered teamwork among team members. Delivered a fast-tracked commercial manufacturing facility on schedule and budget.

1998 - 1999 ~1 yr

Manager Mfg. Sciences & Engineering

Boston, Massachusetts, US

Manager of Manufacturing Science and Engineering 1994 - 1998 Lead process engineer for U.S. operations. Responsible for equipment design, procurement and performance. Supervisory responsibility of four process engineers.Working within a matrix reporting structure, provided technical and interpersonal leadership to approximately 25 team members during the.

1992 - 1998 ~6 yrs

Process Development Engineer

Thousand Oaks, CA, US

Process Development Engineer Planned, ran, analyzed and reported on protein purification process development scale-up and scale-down experiments for several fermentation and cell culture processes. Performed GLP runs prior to transfer into the manufacturing. Designed, scheduled, prepared, operated and maintained pilot plant equipment. Associate Process.

1989 - 1992 ~3 yrs
5 education records

Larry Weiner education

Master’S Degree, Chemical & Biological Engineering

Tufts University

Executive Certificate In Drug Development

Harvard University

Executive Certificate, Technology, Operations & Value Chain Management

Mit Sloan School Of Management

Mba, Management & Finance

Babson F.W. Olin Graduate School Of Business

B.S. Ch.E., Chemical Engineering

Tufts University
FAQ

Frequently asked questions about Larry Weiner

Quick answers generated from the profile data available on this page.

What company does Larry Weiner work for?

Larry Weiner works for Sumitomo Pharma America, Inc..

What is Larry Weiner's role at Sumitomo Pharma America, Inc.?

Larry Weiner is listed as Executive Leader, Biopharma Technical Operations & CMC at Sumitomo Pharma America, Inc..

What is Larry Weiner's email address?

AeroLeads has found 2 work email signals at @biogenidec.com for Larry Weiner at Sumitomo Pharma America, Inc..

What is Larry Weiner's phone number?

AeroLeads has found 3 phone signal(s) with area code 617, 781 for Larry Weiner at Sumitomo Pharma America, Inc..

Where is Larry Weiner based?

Larry Weiner is based in Cambridge, Massachusetts, United States while working with Sumitomo Pharma America, Inc..

What companies has Larry Weiner worked for?

Larry Weiner has worked for Sumitomo Pharma America, Inc., Sunflower Therapeutics, Enzyvant, Unum Therapeutics, and Indigo.

How can I contact Larry Weiner?

You can use AeroLeads to view verified contact signals for Larry Weiner at Sumitomo Pharma America, Inc., including work email, phone, and LinkedIn data when available.

What schools did Larry Weiner attend?

Larry Weiner holds Master’S Degree, Chemical & Biological Engineering from Tufts University.

What skills is Larry Weiner known for?

Larry Weiner is listed with skills including Biotechnology, Validation, Gmp, Manufacturing, Biopharmaceuticals, Pharmaceutical Industry, Technology Transfer, and Fda.

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