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Biotech Procurement Jobs in Silver Spring, MD (NOW HIRING)

Amentum

Innovation Strategist

Chantilly, VA · On-site

$124K - $160K/yr

... biotech). • 5-8+ years of experience in government contracting, business development, strategy consulting, or innovation roles, with direct exposure to federal procurement. • Proven track record ...

Pae

Innovation Strategist

Chantilly, VA · On-site

$124K - $160K/yr

... biotech). 5-8+ years of experience in government contracting, business development, strategy consulting, or innovation roles, with direct exposure to federal procurement. Proven track record of ...

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All JobsBiotech Procurement JobsBiotech Procurement Jobs in Silver Spring, MD

Biotech Procurement information

See Silver Spring, MD salary details

$16

$32

$55

How much do biotech procurement jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for biotech procurement in Silver Spring, MD is $32.77, according to ZipRecruiter salary data. Most workers in this role earn between $24.86 and $37.79 per hour, depending on experience, location, and employer.

What is biotech procurement?

Biotech procurement refers to the process of sourcing, purchasing, and managing the supplies, equipment, and services required for biotechnology research, development, and manufacturing. Professionals in this field ensure that laboratories, production facilities, and research teams have timely access to high-quality materials such as reagents, lab equipment, and specialized instruments. They also negotiate with vendors, manage supplier relationships, and ensure compliance with industry regulations and quality standards. Effective biotech procurement is critical for maintaining smooth operations and supporting scientific innovation within biotech organizations.

What are the key skills and qualifications needed to thrive as a biotech procurement specialist?

To thrive as a Biotech Procurement Specialist, you need expertise in supply chain management, negotiation, and knowledge of biotech materials and compliance regulations, often supported by a degree in business, life sciences, or supply chain management. Familiarity with procurement systems such as SAP or Oracle, and certifications like Certified Professional in Supply Management (CPSM), are typically required. Strong analytical thinking, attention to detail, and effective communication skills set high performers apart in this role. These skills ensure cost-effective sourcing, regulatory compliance, and smooth operations in the fast-paced, highly regulated biotech industry.

What are some common challenges faced in a biotech procurement role, and how can they be addressed?

Professionals in Biotech Procurement often face challenges such as sourcing specialized scientific equipment and reagents with limited suppliers, managing strict regulatory and quality requirements, and adapting to rapidly changing project needs. Building strong relationships with vendors, staying updated on industry regulations, and collaborating closely with research and development teams can help address these challenges. Additionally, developing negotiation skills and maintaining a proactive approach to risk management are key to ensuring timely and cost-effective procurement in a dynamic biotech environment.

What is the difference between Biotech Procurement vs Biotech Purchasing?

AspectBiotech ProcurementBiotech Purchasing
ResponsibilitiesStrategic sourcing, supplier negotiations, contract managementOrder placement, vendor communication, transaction processing
Required SkillsNegotiation, supply chain knowledge, vendor managementOrder management, attention to detail, communication skills
Work EnvironmentCollaborative, cross-departmental, strategic focusAdministrative, transactional, operational focus
Common CertificationsSupply Chain certifications, procurement trainingPurchasing certifications, procurement courses

Biotech Procurement involves strategic sourcing and supplier negotiations, focusing on long-term supply chain management. In contrast, Biotech Purchasing handles day-to-day order processing and vendor communication. While both roles require knowledge of procurement processes, procurement emphasizes strategy and supplier relationships, whereas purchasing centers on transaction execution.

What job categories do people searching Biotech Procurement jobs in Silver Spring, MD look for?

The top searched job categories for Biotech Procurement jobs in Silver Spring, MD are:

What cities near Silver Spring, MD are hiring for Biotech Procurement jobs?

Cities near Silver Spring, MD with the most Biotech Procurement job openings:

Biotech Procurement jobs near you
Infographic showing various Biotech Procurement job openings in Silver Spring, MD as of September 2026, with employment types broken down into 97% Full Time, and 3% Contract. Highlights an 94% In-person, 3% Hybrid, and 3% Remote job distribution, with an average salary of $68,163 per year, or $32.8 per hour.

PHARMACEUTICAL - MECHANICAL UTILITIES ENGINEER

Washington, DC

MMR Consulting
51 - 200 employees
Learn more about MMR Consultingexternal

Full-time

Re-posted 4 days ago

Job description

Previous Pharmaceutical/Biotech experience is mandatory for this role.

MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical /biotechnology and highly regulated industries. Its services include Engineering, Project Management, and Validation.

MMR Consulting has offices across North America and Asia.

This is an outstanding opportunity to join our growing team, where the successful candidate will work with a group of engineers involved in the design, commissioning & qualification, start-up and project management of various processes, systems and facilities. The work may require working out of client's facilities, in Raleigh North Carolina.

Responsibilities

  • Provide technical guidance into the design, installation commissioning, qualification, start-up and operations of various pharmaceutical / biopharmaceutical facilities and utilities such as Purified Water (PW), Water For Injection (WFI), Clean Steam (CS), Heating, Ventilation & Air Conditioning (HVAC), Process Compressed Air (CA) & Gases
  • Lead the development of key design, technology selections, engineering and commissioning / qualification deliverables such as PFDs, P&IDs, specifications, equipment and distribution loop layouts, DQ, FAT, Commissioning Test Plans & checklists, IQ, OQ, PQ during the project lifecycle
  • Able to support detailed design development, field installation and perform field execution of commission & qualification test cases and protocols
  • Serve as technical SME on the design and operation aspects of clean utilities. Possess knowledge of regulatory requirements, mechanical specifications and industry best practices and guidelines for clean utilities.
  • Lead the design, procurement, field installation, commissioning and qualification processes throughout the project lifecycle to ensure timely completion and to ensure all quality and engineering specifications are met.
  • Support development of Project Validation Plans (PVPs) to ensure the action plan to test the system is applicable and relevant.
  • Coordinate meetings with cross-functional departments, to drive design reviews, project progress, facilitate decisions, and provide updates.
  • Travel may be occasionally required for meetings with equipment fabrication vendors or Factory Acceptance Testing (FATs).
  • Work may require occasional support over shutdowns or extended hours, specifically during installation, construction, commissioning, qualification and validation phases.
  • Visit construction and installation sites, wearing necessary safety PPE.
  • You may be involved with other aspects such as client-management (maintain key Client relationships in support of business development and pursuit of new work), project scheduling/budgeting, coordination of client and MMR resources for effective project delivery, supporting business development (providing technical support to the sales as required for proposals/opportunities), presenting at industry conferences/publishing papers etc.
  • Supervise contractors during critical testing of system and equipment.
  • Other duties assigned by client, and/or MMR, based on workload and project requirements.
  • As this position requires working on client sites, you will need to comply with the client's safety rules including mandatory vaccination policies for COVID-19, where applicable


Qualifications

  • 5+ years of experience in commissioning, qualification or validation of various clean utility systems within the pharmaceutical/biotech industry.
  • Previous experience in the pharmaceutical / biotech industry, with knowledge of requirements for cGMP operations.
  • Expertise in generation, storage and distribution of pharmaceutical-grade water systems
  • Hands-on experience with industrial utilities, including:
    • Compressed air generation and distribution
    • Ammonia chillers
    • Electro boilers
    • Chilled water generation and distribution
    • Cooling water generation and distribution
    • Chilled glycol generation and distribution
    • Cooling towers
  • Hands-on experience with clean utilities, including:
    • Purified Water (PW) generation
    • Water For Injection (WFI) generation
    • Clean Steam (CS) generation
  • Hands-on experience with HVAC systems, including:
    • Air handling units (AHUs)
    • Dedicated outdoor air systems (DOAS)
    • Blower coil units
    • Air curtains
    • Computer room air conditioning (CRAC) units
    • DX cooling units
  • Experience with developing and executing validation projects to Risk-Based Commissioning & Qualification approaches, such as ASTM E-2500 or ISPE ICQ, is considered an asset.
  • Experience with commissioning and qualifications of process control systems are considered an asset.
  • Lead teams of staff, manage staff priorities, provide mentorship/oversight, help staff resolve issues. Leadership is considered an asset but not required.
  • Possess leadership skills, and be able to take initiative to lead projects, involving multiple stakeholders, departments, and varying complexities.
  • Possess mentorship skills, to coach and develop junior and intermediate employees.
  • Engineering degree, preferably in Mechanical, Electrical or Chemical.
  • Travel may be required on occasion.
  • Ability to handle multiple projects and work in a fast-paced environment.
  • Strong multi-tasking skills

Equal Employment Opportunity and Reasonable Accommodations

MMR Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Our hiring decisions are based on merit, qualifications, and business needs. We are committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please let us know the nature of your request.

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