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61 Msd Project Manager Jobs Hiring Near You

Patterson-UTI

Designer MSD

Houston, TX · On-site

... MSD safety standards and guidelines. The Mechanical Designer will work closely with senior ... to manage time effectively, prioritize tasks, and execute multiple projects simultaneously.

Patterson-UTI

Designer MSD

Houston, TX · On-site

... MSD safety standards and guidelines. The Mechanical Designer will work closely with senior ... to manage time effectively, prioritize tasks, and execute multiple projects simultaneously.

MSD

Scientific Content Manager

Rockville, MD · On-site

$78K - $116K/yr

... of MSD's technologies, products, and platforms. This position ensures our marketing materials ... Excellent project management and organizational skills; able to manage multiple deadlines ...

Meso Scale Discovery

Project Manager II

Rockville, MD · On-site

$101K - $154K/yr

The incumbent will manage a portfolio of projects that are typically less defined with a long ... BENEFITS SUMMARY At MSD, we offer a comprehensive benefits package to support our employees' well ...

Noblis

Project Manager (FAA required)

Washington, DC · On-site

The Project Manager will serve as a key interface between government program authorities, technical ... Overview Overview Noblis and our wholly owned subsidiaries, Noblis ESI and Noblis MSD, take on some ...

Noblis

Project Manager (FAA required)

Washington, DC · On-site

The Project Manager will serve as a key interface between government program authorities, technical ... Overview Overview Noblis and our wholly owned subsidiaries, Noblis ESI and Noblis MSD, take on some ...

MSD

Director, Scientific Affairs

Rockville, MD · On-site +1

$174K - $272K/yr

Act as MSD spokesperson at conferences to deliver key information about MSD products and services ... Minimum of 10 years of experience in pharma or biotech, leading drug development projects KNOWLEDGE ...

MSD

Director, Scientific Affairs

Rockville, MD · On-site +1

$174K - $272K/yr

Act as MSD spokesperson at conferences to deliver key information about MSD products and services ... Minimum of 10 years of experience in pharma or biotech, leading drug development projects KNOWLEDGE ...

MSD

Manager, Quality Engineering

Rockville, MD · On-site

$116K - $177K/yr

... support of MSD software, instrumentation, associated test kits, consumables and reagents ... Strong logical problem solving skills and demonstrated ability to organize and move project tasks ...

MSD

Engineer I, Systems

Gaithersburg, MD · On-site

$67K - $101K/yr

The Systems Engineer I is responsible for assisting in the development and management of ... Work within cross-functional teams to support the design and development of MSD instrumentation.

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Infographic showing various Project Manager job openings at Msd in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 91% Physical, 4% Hybrid, and 5% Remote job distribution.

Associate Project Manager or Project Manager

Smithers-Pds-

Gaithersburg, MD • On-site

$88 - $130/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 3 days ago

New

Key responsibilities

  • Serve as the client's primary point of contact and oversee the conduct of studies to ensure deliverables are met on-time, within scope, and quality standards.

  • Interpret, analyze, and report data related to validation and sample analysis of biopharmaceutical products.

  • Provide technical advice to scientific staff and ensure compliance with GLP, FDA guidelines, and industry standards.

Job description

Associate Project Manager or Project Manager

Job Category : Operations

Requisition Number : ASSOC002389

  • Posted : August 17, 2026
  • Full-Time
  • Hybrid
Locations

Showing 1 location

Gaithersburg
11 Firstfield Road
Gaithersburg, MD 20878, USA

Gaithersburg
11 Firstfield Road
Gaithersburg, MD 20878, USA

Smithers PDS LLC (Pharmaceutical Development Services) brings new drugs to market by providing pre-clinical and clinical services for all phases of drug development. PDS works with customers to develop new methods, validate existing methods, as well as performing the assays necessary to analyze samples from patients on more than 100 clinical trials currently in different phases of the FDA regulated drug approval process. Our expert scientists perform large molecule bioanalysis, assay development, validation, and sample analysis at our GLP, GCP, and CLIA compliant laboratories.

Smithers PDS is seeking an Associate Project Manager or Project Manager who will be responsible for being the client's primary point of contact and for the overall conduct of the study. The role ensures deliverables are met on-time, within scope, and within established quality standards.

This position is classified as exempt and paid on a salary basis. Exempt employees typically work 40 hours or more to adequately perform their responsibilities. Extended work hours may be necessary to support the business in meeting client deliverable commitments. Position is generally eligible for a hybrid work schedule with at least three days on-site once all training requirements have been adequately met and proficient performance is consistently demonstrated.

The annualized salary range for an Associate Project Manager or Project Manager position is $87,500 -112,500 or $105,000 - $130,000, respectively. Experience and qualifications will determine salary and job level. Smithers PDS offers a comprehensive health insurance package including a choice of 3 medical plans, dental insurance, vision insurance, 401K retirement plan and PTO.

  • Responsible for client interaction and the conduct of studies.
  • Serve as Principal Investigator for GLP studies
  • Responsible for data interpretation, analysis, and reporting of results for validation and sample analysis of biopharmaceutical products.
  • Provide technical advice to scientific staff.
  • Experience and knowledge of Ligand-binding assays (ELISA / MSD) applicable to Pharmacokinetic, Biomarker and Immunogenicity studies is required.
  • Must understand contract immunoanalytical business objectives and is expected to be familiar with regulatory, and GLP requirements, FDA guidelines and industry standards for bioanalytical method validation.
  • Knowledge of Watson LIMS a plus.
  • Additional responsibilities include forecast of revenue, preparing and revising SOPs.

Minimum Qualifications:

  • B.S. / B.A. degree in Biology or related field and a minimum of 5 years of relevant experience in the CRO industry; or, advanced degree in Biology or related field and at least 2 years of relevant experience in the CRO industry.
  • Knowledge of GLP regulations and regulatory guidelines.
  • Excellent communication skills, both oral and written.
  • Strong leadership and excellent organizational skills.
  • Proficient in the use of basic computer applications such as MS Word and Excel.

Additional Position Requirements:

  • Ability to multi-task and produce quality analysis while working under the pressure of strict deadlines.
  • Proficient in time management and resource planning.
  • Ability to initiate and implement self-development efforts.
  • Ability to effectively interact with clients and regulatory personnel.
  • Ability to make decisions and complete assignments with minimal supervision.
  • Ability to self-direct work priorities.

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