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Parenteral Formulation Jobs (NOW HIRING)

Sr Project Engineer

Melrose Park, IL

$96K - $126K/yr

Technical expertise is needed to drive innovation & development of new/alternative complex formulation and processing technologies for the improvement of current commercial projects for parenteral ...

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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.
Sr. Principal Process Engineering SME, Parenteral

Sr. Principal Process Engineering SME, Parenteral

Eli Lilly and Company

Philadelphia, PA

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 10 hours ago


Eli Lilly and Company rating

8.8

Company rating: 8.8 out of 10

Based on 63 frontline employees who took The Breakroom Quiz

8th of 74 rated pharmaceutical


Job description

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.

Overview:

At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism.

Responsibilities:

The Engineering Tech Center is responsible for providing global technical expertise in the engineering sciences related to Process Engineering and secondary/tertiary loop disciplines. This includes knowledge and stewardship of the following: First Principles, unit operations, Equipment Flow Diagrams, Capability Calculations, Material & Energy Balances, Facilities (fitness for use), Root Cause applications, Equipment and Unit Operation Changes/Improvements including new technologies, Scale-ups, Periodic Reviews, Process Safety, Maintenance/Reliability, etc. This function has a global presence. This team provides engineering support to global manufacturing sites for the customer network, Global Facilities Delivery (GFD), development sites, as well as external manufacturing organizations and alliances.

This Aseptic Process Engineering position serves as a technical resource in Aseptic Processing and Parenteral Technologies such as Equipment Preparation, Formulation, Filling, Freeze Drying, and Isolation systems, providing expert process engineering support globally. Parenteral sites supported include Indy Parenteral (IN),Fegersheim (France), Sesto (Italy), Suzhou (China), Research Triangle Park (NC), Concord (NC), Kenosha (WI), Alzey (Germany), and Lehigh Valley (PA). This position also applies technical knowledge to effectively guide and support Lilly's partner companies and contract manufacturers as well as mentor other engineers.

Key Objectives/Deliverables:

  • Technical and Discipline leadership -Partners with other technical staff to direct discipline activities, oversight of the community, new technology development and technology assessments, creation and maintenance of Engineering Standards, Master specifications and Best Practices for the discipline, and coaching and mentorship of junior engineering staff.
  • Safety and Compliance - Ensure personal and team compliance with all applicable regulatory and corporate policy requirements; ensure appropriate safety practices and procedures are in place and are followed to prevent injuries; ensures the ETC meets current Quality expectations and is a part of actively monitoring evolving Quality and other regulatory expectations related to engineering
  • Consultation - Assists sites globally with technical evaluations, master planning, technology assessments, and specific problem resolution including troubleshooting and root cause analysis
  • Knowledge sharing - Provides ongoing technical support to site engineering groups, domestic and global. Serves as a mentor to Lilly engineers with a focus on technical development and functional capability building. Interfaces with and develops site technical experts in Parenteral Engineering. Reviews and prepares protocols and technical reports.
  • External Influence - Monitors and, when appropriate, influences change in external codes and standards on Lilly's behalf. Ensures external learnings are effectively communicated within Lilly and works to ensure ongoing compliance with these learnings.
  • Major Capital Support - Provides technical consulting and leadership, both conceptual and detailed design, to Global Facilities Delivery on major capital projects. Will often lead multi-functional/multi-site project teams.
  • External Manufacturing Support - Provides technical consulting and leadership to Lilly's external manufacturing partners. Responsibilities will be range from due diligence, tech transfer, engineering batches to deviation investigation support. Will work closely with cross-functional projects teams managing the relationships with our partners
  • Platform Owner - Provides Network technical leadership, oversight, and ownership for designated equipment platforms or processes. Influences platform alignment across the Network to maximize project delivery, operational and maintenance efficiencies, and replicated cost benefits. Develops strong relationships with our Original Equipment Manufacturers (QEMs) and leverages these partnerships as we develop new designs, trouble-shoot equipment issues and maintain our equipment.
  • Innovation - Investigates, develops, and integrates emerging technology and capabilities applicable to the Parenteral manufacturing process to meet production and compliance requirements.

Basic Qualifications:

  • Bachelorsdegree in engineering or related technical field.
  • Minimum 10 plus years in cGMP manufacturing or manufacturing support experiencewith increasing technical responsibility

Additional preferences:

  • Extensive knowledge of parenteral processing equipment and operations including formulation, filling, freeze drying, and isolation equipment.
  • Demonstrated ability to solve technical problems and implement projects.
  • Deliverables include input and support of facility design, equipment layout, technical specifications, and equipment optimization, testing and qualification.
  • Familiarity with technology advances in vial, cartridge, and syringe container closure systems.
  • Strong interpersonal and communication skills to be effective in a team-based situation.
  • Ability to work across boundaries (functional, geographic, external company,etc).
  • Demonstrated learning agility.
  • Ability to work effectively with outside suppliers.

Additional information

  • Business title is subject to changebased on leveling.
  • Must be able to travel up to 35% of the time with potential for more, US and international.
  • Role would be based at an existing Lilly Site and not eligible for remote work
  • Potential for short term assignments (1-6 months) at Lilly or partner sites may be requiredincluding international.
  • Will require occasional work in a variety of manufacturing environments; some safety equipment and/or gowning may be required.
  • Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.


Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.

Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is

$117,000 - $209,000

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

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About Eli Lilly

Sourced by ZipRecruiter

Eli Lilly, based in Indianapolis, IN, US, is one of the pioneers in the pharmaceutical industry with a rich history dating back to 1876. This global pharmaceutical company focuses on discovering, developing, manufacturing and selling pharmaceutical products in approximately 120 countries. The company's product categories include endocrinology, oncology, cardiovascular, neuroscience, and immunology. Having invested over $9 billion in research and development in the past decade, Eli Lilly is also committed to creating high-quality medicines that meet real needs. As a recipient of several awards and recognitions, Eli Lilly is known for its focus on life-saving research and drug development. Their mission is to make medicines that help people live longer, healthier, and more active lives.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Indianapolis, IN, US

Year founded

1876