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Parenteral Formulation Jobs (NOW HIRING)

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Parenteral Formulation information

What jobs can I do with a pharmaceutical science degree?

A pharmaceutical science degree can lead to roles such as parenteral formulation scientist, quality control analyst, regulatory affairs specialist, or research and development scientist. These positions often require knowledge of drug development, formulation techniques, and laboratory skills, and may involve working in manufacturing, quality assurance, or regulatory compliance environments.

What is a parenteral formulation?

A parenteral formulation refers to a sterile preparation of a drug intended for injection or infusion, bypassing the digestive system. Parenteral formulation specialists ensure the product's safety, stability, and compatibility with delivery devices, often working in sterile environments and following strict regulatory standards.

What is the difference between Parenteral Formulation vs Pharmaceutical Scientist?

AspectParenteral FormulationPharmaceutical Scientist
Required CredentialsDegree in Pharmacy, Chemistry, or related field; GMP trainingDegree in Pharmacy, Chemistry, or related field; research experience
Work EnvironmentManufacturing labs, sterile environmentsResearch labs, development facilities
Employer & Industry UsagePharmaceutical manufacturing companiesResearch & development departments in pharma companies

Parenteral Formulation specialists focus on developing sterile injectable products, ensuring proper formulation and manufacturing processes. Pharmaceutical Scientists work on drug discovery, formulation, and testing across various dosage forms. While both roles require similar educational backgrounds, Parenteral Formulation roles are more specialized in sterile manufacturing, whereas Pharmaceutical Scientists have broader research responsibilities.

What is parenteral formulation?

Parenteral formulation refers to the development and preparation of medications that are administered by injection through routes such as intravenous, intramuscular, or subcutaneous, bypassing the digestive system. These formulations must be sterile, stable, and safe for direct entry into the body. The process involves choosing suitable solvents, stabilizers, and packaging to ensure the drug remains effective and free from contamination. Parenteral drugs are commonly used for patients who cannot take medications orally or when rapid onset of action is required.

What are the key skills and qualifications needed to thrive as a Parenteral Formulation Scientist, and why are they important?

To thrive as a Parenteral Formulation Scientist, you need a solid background in pharmaceutical sciences, chemistry, or a related field, often supported by a relevant advanced degree. Familiarity with aseptic processing, analytical instrumentation (such as HPLC), and regulatory standards like cGMP is crucial. Strong problem-solving skills, attention to detail, and effective collaboration are essential soft skills in this role. These competencies ensure the development of safe, stable, and effective injectable drugs while meeting strict regulatory and quality requirements.

What are some common challenges faced when developing parenteral formulations, and how can they be addressed?

Professionals working in parenteral formulation often encounter challenges such as ensuring drug stability, preventing contamination, and achieving the desired solubility and bioavailability. Managing sterility throughout the formulation and manufacturing process is critical, as parenteral products must be free from microbial contamination and particulates. Collaborating closely with analytical chemists, quality assurance teams, and regulatory experts is essential to address these challenges and ensure that formulations meet strict industry standards. Staying updated on new technologies and regulatory changes also helps in proactively solving formulation issues.

What is an example of a parenteral formulation?

A parenteral formulation is a sterile preparation of a drug intended for injection, such as an intravenous (IV) solution, intramuscular (IM) injection, or subcutaneous (SC) injection. These formulations are prepared under aseptic conditions and often require expertise in compounding and sterile techniques. Common examples include saline solutions, glucose solutions, and antibiotic suspensions used in clinical settings.

What are common pharmaceutical careers?

Common pharmaceutical careers include roles such as formulation scientist, quality control analyst, manufacturing technician, regulatory affairs specialist, and research scientist. These positions often require knowledge of drug development, laboratory skills, and adherence to Good Manufacturing Practices (GMP) and safety regulations.
More about Parenteral Formulation jobs
Infographic showing various Parenteral Formulation job openings in the United States as of July 2026, with employment types broken down into 75% Full Time, and 25% Part Time. Highlights an 100% In-person job distribution.
Scientist, Formulations

Scientist, Formulations

Alcami Corporation

Morrisville, NC • On-site

Full-time

Posted 27 days ago


Alcami rating

7.3

Company rating: 7.3 out of 10

Based on 5 frontline employees who took The Breakroom Quiz


Job description

At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record.

Are you interested in joining our team?


The Scientist - Formulations is accountable for driving results in a fast-paced environment and leading formulation development studies for the design and identification of safe, stable, robust and manufactural pharmaceutical dosage forms. The Scientist - Formulations independently designs, plans, performs, interprets and reports results of scientific experiments for the preparation and timely delivery of drug products (DP), processes and procedures needed for technology transfer and manufacture of the product. The position requires superior leadership behaviors as well as expertise in functional competencies including scientific principles, laboratory practices, cGMPs and regulatory requirements for pharmaceuticals and biologicals.


  • 100% on-site position.
  • 1st Shift: Monday - Friday, 8:00am - 5:00pm.

For Liquid and Sterile Formulation:

  • Creates formulation development plans and executes well-designed experiments to define the qualitative and quantitative formulation composition.
  • Conducts design of experiments (DoE) studies to identify and investigate key and critical quality attributes to confirm formulation robustness as per ICH Q8.
  • Writes and executes protocols to prepare formulations for testing and characterization, methods development and technology transfer.
  • Records and reports study results in compliance with good scientific policy and procedures.
  • Evaluates new scientific technologies/equipment to enhance capability, capacity, and efficiency.
  • Reports and presents scientific/technical results internally and to external clients.
  • Utilizes complex tools/equipment, lab automation tools, and specialized facilities.
  • Maintains and operates equipment according to safety standards and operating procedures.
  • Reviews own work and conduct peer review.
  • Participates in scientific conferences and contributes to scientific journals.
  • Provides coaching and mentoring to junior colleagues and newcomers.
  • Ensures timely completion and compliance with SOPs and all other relevant company training requirements.
  • Other duties as assigned.

  • Bachelor’s degree in Pharmaceutical Sciences, Chemistry, or equivalent with 6-8 years of experience or Master’s degree with 2+ years of experience.
  • Strong customer service focus and excellent customer contact skills.

  • Thorough fundamental knowledge and understanding of solubility and stability theory and practice.
  • A solid understanding of drug solubilization and stabilization techniques in liquid dosage forms.
  • Hands on expertise in aseptic techniques for liquid formulation, compounding, and manufacturing.
  • Experience in aseptic filtration, terminal sterilization and lyophilization process techniques.
  • Knowledge of raw material selection strategy and criteria for parenteral and liquid dosage forms.
  • Basic understanding of physical characterization tools such as DSC, particle size and different viscometers.
  • Hands-on experience in analytical techniques such as UV-Vis and HPLC.
  • Basic understanding of quality attributes and regulatory requirements for parenteral and liquid dosage forms.
  • Basic understanding of quality attributes for biologics formulations.
  • Knowledge of methods for characterization and testing of liquid and parenteral dosage forms.
  • Ability to plan and manage multiple tasks for timely achievement of results.
  • Ability to efficiently organize work with little or no supervision.

  • Up to 5% travel required.

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. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this Job, the employee is regularly required to use hands to finger, handle, or feel; reach with hands and arms; talk or hear and smell. The employee is frequently required to sit. The employee is occasionally required to stand; walk and stoop, kneel, crouch, or crawl. The employee must regularly lift and/or move up to 10 pounds, frequently lift and/or move up to 25 pounds and occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. While performing the duties of this job, the employee is occasionally exposed to moving mechanical parts and vibration. The noise level in the work environment is usually very quiet.

While performing the duties of this job, the employee is frequently exposed to moving mechanical parts, fumes or airborne particles and toxic or caustic chemicals. The employee is occasionally exposed to wet and/or humid conditions; high, precarious places; risk of electrical shock and vibration. The noise level in the work environment is usually moderate. The employee will be required to wear the appropriate personal protective equipment for specific job duties to be performed. Such personal protective equipment may include, but not limited to safety eyewear, hearing protection, various types of respirators/breathing apparatus, lab coats, full protective body coverings, various types of gloves, etc. Other tasks involving elevated work may require the use of a body harness and lanyard. Additionally, the employee may be required to operate an industrial vehicle.


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