Entry Level Pharmaceutical Consultant Jobs
New grad pharmaceutical consultant jobs welcome recent graduates and entry level candidates with zero to two years of experience, where strong internship work or a relevant academic project can carry more weight than a lengthy resume. Most openings are on-site roles across Biotechnology & Pharmaceuticals, Education, and Science & Research, with employers like Catalent Pharma Solutions, IQVIA, and Viatris hiring at this level now.
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Showing 5 of 14+ Entry Level Pharmaceutical Consultant jobs
About Site
Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses.
Position Summary
We have an opportunity for a Pharmaceutical Development Senior Associate Scientist I to join our team. In this role, you will support formulation design and development of oral solid drug products. You will train others in clinical trial manufacturing operations using sound pharmaceutical principles and ensure all work complies with regulatory requirements, good manufacturing practices, and standard operating procedures. This position offers the chance to contribute to meaningful projects that impact patients worldwide.
Shift: M-F 8am-5pm
Location: Kansas City, MO
100% Onsite
The Role
- Train others on procedures and laboratory techniques.
- Execute efficiency improvement projects with guidance.
- Apply knowledge of principles and concepts within the discipline.
- Use technical and functional knowledge to perform duties on most projects or assignments within the team.
- Conduct work in a Good Manufacturing Practice (GMP) area under minimal supervision.
- Other duties assigned.
The Candidate
Minimum Requirements
- Master’s degree in a related life science or physical science field with 0+ years of related work experience preferred, or Bachelor’s degree in a related life science or physical science field with 2+ years of related work experience preferred.
- Maintain high-quality laboratory documentation in accordance with applicable regulatory guidance and site standard operating procedures.
- Draft technical documents such as laboratory notebook writeups, protocols, and batch records.
- Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
- Perform parallel review of GMP documents and laboratory notebooks and may become qualified to conduct compliance technical reviews.
- Execute procedures, methods, and manufacturing processes with minimal complexity, high quality, and limited supervision.
- Propose deviations from established procedures and methods based on sound judgment.
- Client interactions are very limited and supervised.
- Demonstrate mathematical and scientific reasoning ability.
- Assist with process efficiency under significant supervision.
- May contribute material to publications and/or external presentations.
- Stand, walk, sit, use hands to manipulate, and reach with hands and arms for up to 8 hours per day.
- Frequent sitting, standing, walking, reading of written documents, and use of computer monitor screen.
- Able to work with respirator (P100, PAPR, etc.).
- Occasional lifting and/or moving up to 50 pounds.
Preferred Skills & Background
- Previous solids development experience preferred.
Why You Should Join Catalent
- Defined career path and annual performance review and feedback process.
- Diverse, inclusive culture.
- Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.
- Competitive paid time off plus 8 paid holidays.
- Community engagement and green initiatives.
- Medical, dental, and vision benefits effective day one of employment.
- Tuition reimbursement.
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.
Volunteer Work Disclosure: Applicants for employment in Massachusetts may include in their employment history any verified work performed on a volunteer basis.
Massachusetts Lie Detector Test Notice: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law may be subject to criminal penalties and civil liability. Consistent with Massachusetts law, Catalent does not require or administer lie detector tests as a condition of employment or continued employment.
About Site
Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses.
Position Summary
We have an opportunity for a Pharmaceutical Development Senior Associate Scientist I to join our team. In this role, you will support formulation design and development of oral solid drug products. You will train others in clinical trial manufacturing operations using sound pharmaceutical principles and ensure all work complies with regulatory requirements, good manufacturing practices, and standard operating procedures. This position offers the chance to contribute to meaningful projects that impact patients worldwide.
Shift: M-F 8am-5pm
Location: Kansas City, MO
100% Onsite
The Role
- Train others on procedures and laboratory techniques.
- Execute efficiency improvement projects with guidance.
- Apply knowledge of principles and concepts within the discipline.
- Use technical and functional knowledge to perform duties on most projects or assignments within the team.
- Conduct work in a Good Manufacturing Practice (GMP) area under minimal supervision.
- Other duties assigned.
The Candidate
Minimum Requirements
- Master’s degree in a related life science or physical science field with 0+ years of related work experience preferred, or Bachelor’s degree in a related life science or physical science field with 2+ years of related work experience preferred.
- Maintain high-quality laboratory documentation in accordance with applicable regulatory guidance and site standard operating procedures.
- Draft technical documents such as laboratory notebook writeups, protocols, and batch records.
- Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
- Perform parallel review of GMP documents and laboratory notebooks and may become qualified to conduct compliance technical reviews.
- Execute procedures, methods, and manufacturing processes with minimal complexity, high quality, and limited supervision.
- Propose deviations from established procedures and methods based on sound judgment.
- Client interactions are very limited and supervised.
- Demonstrate mathematical and scientific reasoning ability.
- Assist with process efficiency under significant supervision.
- May contribute material to publications and/or external presentations.
- Stand, walk, sit, use hands to manipulate, and reach with hands and arms for up to 8 hours per day.
- Frequent sitting, standing, walking, reading of written documents, and use of computer monitor screen.
- Able to work with respirator (P100, PAPR, etc.).
- Occasional lifting and/or moving up to 50 pounds.
Preferred Skills & Background
- Previous solids development experience preferred.
Why You Should Join Catalent
- Defined career path and annual performance review and feedback process.
- Diverse, inclusive culture.
- Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.
- Competitive paid time off plus 8 paid holidays.
- Community engagement and green initiatives.
- Medical, dental, and vision benefits effective day one of employment.
- Tuition reimbursement.
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.
Volunteer Work Disclosure: Applicants for employment in Massachusetts may include in their employment history any verified work performed on a volunteer basis.
Massachusetts Lie Detector Test Notice: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law may be subject to criminal penalties and civil liability. Consistent with Massachusetts law, Catalent does not require or administer lie detector tests as a condition of employment or continued employment.
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Top Industries Hiring
- Biotechnology & Pharmaceuticals
- Education
- Science & Research
- Consulting & Professional Services
Entry Level Pharmaceutical Consultant Jobs: Frequently Asked Questions
How do I get an entry level pharmaceutical consultant job?
Start by building hands-on experience through internships, co-ops, or research projects tied to drug development, regulatory affairs, or clinical operations. Employers at this level look for a relevant degree in pharmacy, life sciences, or a related field, familiarity with FDA regulatory frameworks, and strong analytical skills. Tailoring your resume to highlight coursework, lab experience, or any client-facing project work gives you a clear edge.
Which companies hire entry level pharmaceutical consultants?
Companies hiring entry level pharmaceutical consultants right now include Catalent Pharma Solutions, IQVIA, and Viatris, based on current listings on Migrate Mate as of November 2026. At this level, hiring comes from a mix of specialized life sciences consulting firms, large pharmaceutical manufacturers, and contract research organizations that bring on junior consultants to support project teams.
Are there remote entry level pharmaceutical consultant jobs?
Yes, though on-site and hybrid roles remain common at this level. About 0% of entry level pharmaceutical consultant openings are remote or hybrid as of November 2026, reflecting the hands-on and client-facing nature of much of the work. Fully remote roles do exist, often in medical affairs, market access, or regulatory consulting where collaboration happens primarily through documents and calls.
Are these new grad pharmaceutical consultant jobs?
Yes, many of these postings are new grad and junior roles that welcome candidates with zero to two years of experience, recent graduates, or those coming directly from a pharmacy or life sciences program. A new grad friendly posting typically says it welcomes entry level applicants, accepts internship or academic project experience in place of full-time work history, or lists a degree as the primary requirement.
Which industries hire the most entry level pharmaceutical consultants?
Entry Level pharmaceutical consultant roles concentrate in Biotechnology & Pharmaceuticals, Education, and Science & Research, based on current listings on Migrate Mate as of November 2026. These sectors drive junior hiring because they rely on consultants to support drug launches, regulatory submissions, and market access strategies, all areas where employers are willing to train candidates who bring strong foundational science or business knowledge.