Senior Manager, Logistics

Posted Yesterday
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Harmans, MD, USA
In-Office
160K-180K Annually
Senior level
Biotech • Pharmaceutical
The Role
Leads end-to-end logistics across multiple pharmaceutical manufacturing sites, overseeing warehousing, receiving, shipping, materials control, cold-chain operations, inventory accuracy, 3PL contracts, freight, budgets, compliance, safety, and logistics systems. Manages leaders and shift coverage, supports audits and inspections, drives KPI improvements and cost savings, and partners with Planning, Manufacturing, and Quality to ensure material readiness for clinical and commercial operations.
Summary Generated by Built In

Senior Manager, Logistics

 


About Site

Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. The campus, featuring two manufacturing facilities is located 5 miles from the Baltimore Washington International (BWI) airport and 13 miles from our Baltimore location. The campus is close to Washington, DC’s I-270 Technology Corridor, top universities, and government agencies.

The Harmans/BWI-1 EMA and FDA approved facility, at approximately 200,000 sq. ft., houses 10 CGMP manufacturing suites, fill/finish, central services, testing labs, and a warehouse.

The Harmans/BWI-2 facility, at approximately 145,000 sq. ft., is under development and will house 8 CGMP manufacturing suites and cold storage warehousing.

Both facilities support Phase 3 through commercial manufacturing of advanced therapeutic products including AAV and other viral vector-based therapies and vaccines.

 


Position Summary

We have an opportunity for a Senior Manager, Logistics to join our team at the Harmans/BWI campus. In this role, you will lead the end-to-end physical flow of materials and products that support life-changing gene therapy manufacturing. You will oversee warehousing, receiving, shipping, materials control, and third-party logistics across multiple facilities. This position plays a key role in ensuring compliance, efficiency, and readiness for inspection while supporting the growth of clinical and commercial operations.



Shift: Monday - Friday, 8am-5pm
Location: Harmans, MD - BWI
100% Onsite

 

The Role

  • Lead the Logistics function across BWI, BioPark, and Cavalier, managing direct materials, shipping, receiving, and off-site operations.
  • Develop scalable operating models, staffing plans, and shift coverage to support growth and new client onboarding.
  • Manage the Logistics budget, including freight and 3PL spend, and deliver productivity and cost-saving initiatives.
  • Coach and develop leaders, build team capability through cross-training and succession planning.
  • Oversee storage, staging, and issuing of materials to manufacturing, ensuring on-time and accurate supply.
  • Manage temperature-controlled and cold-chain storage and transport, including refrigerated, frozen, ultra-cold, and liquid nitrogen materials.
  • Ensure inventory accuracy across all sites, including cycle counting and discrepancy resolution in JD Edwards (JDE).
  • Oversee inventory health, material status control, and disposition of expired or excess inventory.
  • Partner with Planning, Manufacturing, and Quality on material readiness and new product introductions.
  • Own the Cavalier Logistics contract and service levels, including KPIs and performance reviews.
  • Manage freight carriers and couriers for domestic and international shipments, ensuring compliance with import/export and dangerous goods regulations.
  • Lead logistics systems improvements, including JDE–Cavalier integration and warehouse transactions.
  • Ensure compliance with cGMP, GDP, OSHA, DOT, and site SOPs, and act as the logistics lead during audits and inspections.
  • Own logistics compliance, including SOPs, training, deviations, CAPAs, and change controls.
  • Set and report logistics KPIs such as inventory accuracy, dock-to-stock time, and shipment accuracy.
  • Lead the logistics safety program, ensuring safe operation of equipment and handling of hazardous materials.

 


The Candidate

Minimum Requirements

  • Bachelor’s degree in Supply Chain, Logistics, Operations, Business, or a related field; equivalent experience considered.
  • 10+ years of warehouse, logistics, or materials management experience in pharmaceutical, biotech, or other GMP-regulated manufacturing; cell and gene therapy or CDMO experience highly desirable.
  • 5+ years of people leadership, including managing managers and shift supervisors across multiple shifts or locations.
  • Experience managing 3PL contracts, service levels, freight, and logistics budgets, including cold-chain and temperature-controlled distribution.
  • Strong knowledge of cGMP, GDP, dangerous goods (IATA/DOT), and inventory control practices, with experience supporting audits and inspections.
  • Advanced knowledge of Microsoft Office and Excel, with a data-driven approach to KPIs and cost.
  • Ability to support a 24/7 operation, including off-shift escalation and on-call coverage.
  • Experience managing deviations, CAPAs, and change controls in TrackWise.
  • Ability to lift and move materials up to the site-approved weight limit.
  • Ability to operate or work around powered industrial trucks (PITs).
  • Ability to wear safety shoes and the required PPE.
  • Demonstrable leadership experience at Catalent (including but not limited to participation in Catalent‑sponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may be considered in place of external experience.

Preferred Skills & Background

  • Proficiency in ERP warehouse and inventory transactions; JD Edwards (JDE E1) strongly preferred.
  • Lean/Six Sigma experience desirable; ASCM/APICS certification (CLTD or CSCP) preferred.

 


Pay

The anticipated salary range for this position in MD is $160,000 – $180,000 Plus Bonus. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states.

 


Why You Should Join Catalent

  • Defined career path and annual performance review and feedback process.
  • Diverse, inclusive culture.
  • Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.
  • Competitive paid time off plus 8 paid holidays.
  • Community engagement and green initiatives.
  • Medical, dental, and vision benefits effective day one of employment.
  • Tuition Reimbursement.

Catalent offers rewarding opportunities to further your career!  Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. 


personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.


Catalent is an Equal Opportunity Employer, including disability and veterans.


If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to [email protected]. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

    

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.


Important Security Notice to U.S. Job Seekers:

Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to [email protected] for us to investigate with local authorities.


California Job Seekers can find our California Job Applicant Notice HERE.


Volunteer Work Disclosure: Applicants for employment in Massachusetts may include in their employment history any verified work performed on a volunteer basis.


Massachusetts Lie Detector Test Notice: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law may be subject to criminal penalties and civil liability. Consistent with Massachusetts law, Catalent does not require or administer lie detector tests as a condition of employment or continued employment.

Skills Required

  • Bachelor's degree in Supply Chain, Logistics, Operations, Business, or a related field; equivalent experience may be considered.
  • 10+ years of warehouse, logistics, or materials management experience in pharmaceutical, biotech, or other GMP-regulated manufacturing.
  • 5+ years of people leadership experience, including managing managers and shift supervisors across multiple shifts or locations.
  • Experience managing 3PL contracts, service levels, freight, logistics budgets, cold-chain, and temperature-controlled distribution.
  • Knowledge of cGMP, GDP, dangerous goods regulations including IATA and DOT, and inventory control practices.
  • Experience supporting audits and inspections.
  • Advanced knowledge of Microsoft Office and Excel, with a data-driven approach to KPIs and cost.
  • Ability to support a 24/7 operation, including off-shift escalation and on-call coverage.
  • Experience managing deviations, CAPAs, and change controls in TrackWise.
  • Ability to lift and move materials up to the site-approved weight limit.
  • Ability to operate or work around powered industrial trucks.
  • Ability to wear safety shoes and required personal protective equipment.
  • Proficiency in ERP warehouse and inventory transactions; JD Edwards E1 strongly preferred.
  • Lean/Six Sigma experience.
  • ASCM/APICS certification, such as CLTD or CSCP.

Catalent, Inc. Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Catalent, Inc. and has not been reviewed or approved by Catalent, Inc..

  • Leave & Time Off Breadth — Paid time off is commonly described as roughly 152 hours per year plus about eight paid holidays for U.S. roles. Eligibility and exact counts vary by location, but the allotment is positioned as competitive.
  • Retirement Support — A 401(k) with a company match (often described as dollar‑for‑dollar up to 6%) is part of the package. The match level is commonly referenced as a meaningful component of total rewards.
  • Inclusive Benefits Coverage — Medical, dental, vision, life/disability, HSA/FSA, EAP, tuition reimbursement, adoption assistance, commuter and dependent‑care benefits, and wellness programs are offered. Some roles indicate benefits eligibility begins on the first day for direct hires.

Catalent, Inc. Insights

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The Company
HQ: Tampa, FL
13,715 Employees
Year Founded: 2007

What We Do

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually. For more information, visit www.catalent.com.

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