Development Scientist

$70K — $95K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • BS in Food, Chemical, Pharmaceutical, Biological or related science with 3 years of relevant GMP lab experience
  • MS or PhD preferred in related fields
  • 2 years of experience in formulation and/or product development
  • Experience in Pharmaceutical or OTC industries
  • Practical proficiency in R&D development processes and commercial environment

Responsibilities

  • Manage or contribute to projects supporting Brand Innovation strategy
  • Execute a variety of experiments and technical studies
  • Design and implement new methods and protocols
  • Facilitate completion of outsourced support activities
  • Maintain progress communication with supervisor
  • Ensure compliance with EHS standards in all activities
  • Produce departmental quality documentation and reports

Benefits

  • Generous 401(k) plan
  • Tuition reimbursement
  • 6 months paid parental leave
  • Healthcare programs with significant company coverage
  • Eligibility for performance-based discretionary bonuses
Full Job Description

About the role

The Development Scientist supports new product development by developing formulation, combination products (IDDC) and device and/or providing analysis and evaluation of material and products at all stages of the development process, considering scientific and timing objectives. This individual would have various levels of involvement in the development of conventional and non-conventional solid, semi-solid, liquid, and other formulations and medical devices.

Role Responsibilities

This role will provide YOU the opportunity to lead key activities to progress YOUR career.

Execution Powerhouse

  • Manages or contributes to one or more projects in support of Brand Innovation strategy.
  • Execute a wide range of experiments/technical studies/scientific tasks.
  • Design & execute new methods and protocols.
  • Facilitate completion of outsourced support activity
  • Keep supervisor informed of progress and activities.
  • Ensures all work is conducted in accordance with written procedures as per EHS standards and expectations on site and within the laboratories.
  • Produces or contributes to departmental quality documentation (eg SOP’s, batch doc, validation protocols & reports).
  • Safety & quality responsibilities for department and site (eg GMP, Audits, Health & Safety).

Growth Mindset

  • Maintains awareness of scientific literature to assist work progression& understanding, and present at internal R&D meetings.
  • Trains self and others in new technology and laboratory responsibilities.
  • Develops knowledge of regulations impacting areas of work (e.g. EP/USP/ICH/MDR).

Consumer and Customer-Obsessed

  • Participate in consumer engagement research to understand the category and needs.
  • Work with Consumer Understanding and Sensory scientists to development consumer-developed innovation.

Data-Driven

  • Maintains precise experimental records; issues report at project milestones; writes invention records to protect scientific discoveries.
  • Ensures all work is always conducted following good scientific practice and Good Manufacturing Practice (where required).

Agile

  • Sets and resets priorities to remain focused on objectives in rapidly changing circumstances.
  • Takes responsibility for specific equipment in accordance with site procedures.
  • Participates in general problem solving.
  • Develop networking skills though interactions with scientist outside of primary ‘project’ role.

Why you?

Basic Qualifications:

  • BS in Food, Chemical, Pharmaceutical, Biological or related science with 3 years of relevant experience working in a GMP lab setting.
  • Ability to apply scientific principles and techniques to assigned projects.
  • An ability to organize and report study data from internal and external sources.

Preferred Qualifications:

  • MS or PhD Chemical, Pharmaceutical, Biological or related science.
  • 2 years demonstrated experience of successful formulation and/or product development
  • Experience in Pharmaceutical or OTC industries.
  • Experience in development and formulation of oral solid dosage forms (eg. tablets, caplets, softgels, granules…) and liquids (eg. suspensions, syrups and solutions).
  • Practical application and technical proficiency of the R&D development processes and associated commercial environment.
  • Clear communicator in both oral and written form with both internal departments and external organizations.
  • Demonstrated ability to take initiative, think and work independently, problem-solve, work effectively in teams and contribute to multiple projects in parallel.
  • Ability to organize and report study data from internal and external sources.
  • Flair for creativity and innovation, with a desire to learn and have meaningful impact
  • Demonstrated computer proficiency.
  • Basic understanding of statistics and its application to experimental work.
  • Ability to connect consumer needs to product development

Location: This role is based in Richmond, VA with on-site requirements of 5 times per week.

Benefits

Haleon offers a robust Total Reward package that consists of competitive pay and a comprehensive benefits program.  This includes a generous 401(k) plan, tuition reimbursement and time off programs including 6 months paid parental leave.  On day one, you are eligible for benefits, including our healthcare programs where the company pays for the majority of your medical coverage for you and your family.  We also offer the opportunity to receive a discretionary bonus based on the achievement of key business performance and other incentive/recognition programs as part of the offering.

 

 

Job Posting End Date2026-06-16

 

 

 

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