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Sovpharm

Formulation Scientist I

fort worth, TX

Check who can apply and the requirements below before continuing.

About this opportunity

Sovpharm lists this Formulation Scientist I opportunity in fort worth, Texas. Review the employer’s description below for duties, qualifications and application requirements.

Job description

summary/objective

Support Sovereign's Formulation development activities to achieve successful design, filing, transfer, and launch of 505(b)2, ANDA, ANADA, and OTC products.

essential functions

Monitoring their project activities to ensure timely completion.

Reviewing their protocols, manufacturing processes, and reports for accuracy

Designing protocols, developing plans, and pre-formulations and formulation activities.

Developing process, manufacturing instructions, and technology packages.

Writing project updates.

Work with process/manufacturing personnel for successful and effective transfer of technology.

Author technical documents such as protocols and reports

Performs characterization of the physical characteristics of drug products and raw materials.

Peer review laboratory notebooks, data, protocols, and reports

Identifies non-routine technical problems & recommends solutions

Provide leadership in technical transfers between companies and internally

Understand applicable cGMP, DEA regulations, and Quality Procedures

Recommends new technology & science to meet department goals

Required education and experience

Advanced degree with pharmaceutical sciences background.

2-4 years of experience in solid and liquid dosage forms development

Adhere to all laboratory requirements in accordance with SOPs and regulatory practices such as GMPs, GDPs, GLPs, and OSHA regulations.

Knowledge of pharmaceutical research and development

Statistical experimental design techniques

Bench/Pilot scale operations (granulation, compression, coating, etc.)

Preferred education and experience

Advanced degree with a pharmaceutical sciences background, PhD preferred.

2-4 years of experience in a cGMP environment, preferably in pharmaceuticals

Required skills/competencies

Effective communication skills, written and verbal

Organizational and interpersonal skills

Ability to innovate new ideas

Demonstrate project management skills

Professional Self-Starter

Organized and detail-oriented

Reliable and Dependable

Ability to handle multiple projects

Abstract problem-solving skills

Confidentiality

Highly efficient and accurate

position type/ expected hours of work

This is a full-time position. Days and hours of work are Monday through Friday, but extended (earlier or later) work times or weekend work may be required.

physical demands

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. The employee must regularly lift and/ or move up to 50 pounds. Specific vision abilities required by this position include close vision, color vision, and the ability to adjust focus. While performing the duties of this job, the employee is regularly required to stand, walk, sit, and talk or hear. The employee is occasionally required to climb, balance, stoop, kneel, crouch, crawl, and smell.

Work environment

This job operates in a professional office and laboratory environment. This role routinely uses standard office equipment such as computers, phones, and copiers. The employee is occasionally exposed to toxic and/ or caustic chemicals such as Sodium Hydroxide, Hydrochloric Acid, and other chemical solutions necessary in formulation development. The employee may also be required to wear personal protective equipment to provide adequate protection from raw materials.

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Worksite address

fort worth, TX, 76102, US

Who can apply

Review the original listing for work authorization, qualifications and employer requirements.

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