Supervisory Pharmaceutical Scientist

Benefits

Parental leave

Not verified

Non-birth-parent leave

Not verified

Family-building benefits

• Fertility benefits: Not verified
• Adoption assistance: Not verified
• Surrogacy assistance: Not verified

Mental health support

Not verified

Relocation assistance

Not verified

Childcare support

Not verified

Learning budget

Not verified

Verification

Not verified

Salary

$169K-$232K From the posting source

401(k) match

Not verified

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Market context

U.S. role benchmark (BLS OEWS)

$111,944 U.S. median for this role

Projected growth (BLS Employment Projections)

+13.7% - Much faster than average

79% above the BLS role benchmark for data and ml aggregate.

Matched to SOC 15-1252 - Data and ML aggregate by role bucket.

Source: U.S. Bureau of Labor Statistics, OEWS, May 2024 and Employment Projections, 2024-2034.

Role

Role function

Data From the posting source

Seniority

Mid From the posting source

Schedule

Shift type

Not verified

Weekend work

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Application

Cover letter

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Assessment

Not verified

Deadline

Not stated

Where they hire

Hires in: MD From the posting source

About this role

Supervisory Pharmaceutical Scientist Beltsville, Maryland Summary This position is being filled under a stream-lined hiring authority, Title 21 of the United States Code (21 US Code 379d-3a) as amended by the 21st Century Cures Act of 2016, section 3072 and the Consolidated Appropriations Act of 2023, Section 3624. The candidate selected for this position will serve under a career or career-conditional appointment and be paid under the provisions of this authority. This position is being recruited based on the Title 21 Pay Table 1, Band E. Duties Serves as a senior advisor to the Division Director and plans, manages, organizes, and directs all laboratory functions, surveillance testing, and laboratory based investigational activities as carried out by a highly trained and skilled staff of scientific professionals. Leads scientists who conduct experiments to understand the impact of changes in specification of drug substance and ingredients, formulation, packaging, manufacturing equipment, and processes on product quality attributes. Provides input to the Division Director to formulate and develop short term and long range new drug quality assessment goals, policies, and standards. Assigns and manages projects based upon the degree of risk to product quality and public health impact. Supports a lifecycle approach to drug application approval by providing relevant expertise and laboratory data to aid quality assessment of drug applications. Manages and participates in an active research program and/or supervises research scientists engaged in a broad range of pharmaceutical quality research designed to ensure drug quality, safety, and efficacy. Manages the functional discipline and provides

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