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Development Scientist Ii Jobs (NOW HIRING)

Catalent, Inc.

Development Scientist I

Greenville, NC · On-site

Development Scientist I Position Summary: * Work Schedule: Monday-Friday, 8:00am-5:00pm EST * This ... Master's degree in pharmaceutical science or chemistry or related science with at least two years ...

X Energy LLC

Fuel Development Scientist

Oak Ridge, TN · On-site

... development of robust products and processes. * Provide scientific input or leverage network of ... Level II: Support team members with the execution of the core tasks and responsibilities, listed in ...

Danaher

Senior Development Scientist

Chaska, MN

$105K - $115K/yr

The Senior Development Scientist for Beckman Coulter Diagnostics is responsible for completing ... It would be a plus if you also possess previous experience in: * 2+ years of experience in ...

Danaher

Senior Development Scientist

Chaska, MN · On-site

$105K - $115K/yr

The Senior Development Scientist for Beckman Coulter Diagnostics is responsible for completing ... It would be a plus if you also possess previous experience in: * 2+ years of experience in ...

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How much do development scientist ii jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for development scientist ii in the United States is $38.66, according to ZipRecruiter salary data. Most workers in this role earn between $28.37 and $46.15 per hour, depending on experience, location, and employer.

How much does a scientist 2 make at Thermo Fisher?

A Development Scientist II at Thermo Fisher typically earns between $70,000 and $90,000 annually, depending on experience, location, and education. The role often requires proficiency with laboratory tools and scientific methods, with salary ranges reflecting industry standards for mid-level scientific positions.

What is the difference between Development Scientist Ii vs Development Scientist I?

CriteriaDevelopment Scientist IiDevelopment Scientist I
Required CredentialsBachelor's degree in life sciences or related field; some roles may prefer a master'sBachelor's degree in life sciences or related field
Work EnvironmentLaboratories, R&D departments, collaborative team settingsLaboratories, R&D departments, entry-level team settings
Employer & Industry UsagePharmaceutical, biotech, or consumer goods companiesPharmaceutical, biotech, or consumer goods companies
Common Search & Comparison IntentUnderstanding role progression and responsibilitiesEntry-level responsibilities and qualifications

The Development Scientist II typically has more experience and may handle more complex projects compared to the Development Scientist I. Both roles work in similar environments within the pharmaceutical or biotech industries, but the II level often involves greater independence and technical expertise. Understanding these differences helps candidates and employers align expectations and career development paths.

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

To thrive as a Development Scientist II, you typically need an advanced degree in a scientific discipline, strong analytical skills, and experience in experimental design and data interpretation. Familiarity with laboratory instrumentation, techniques such as HPLC or PCR, and knowledge of regulatory standards like GLP or GMP are often required. Excellent problem-solving, project management, and communication skills help you collaborate across teams and adapt to evolving project needs. These competencies are crucial for developing robust scientific solutions, ensuring compliance, and driving successful product development in research and industry settings.

What are Development Scientist II roles and responsibilities?

A Development Scientist II is a mid-level research professional who designs, develops, and optimizes products, processes, or technologies, often in the pharmaceutical, biotech, or chemical industries. Responsibilities typically include planning and conducting experiments, analyzing data, troubleshooting technical issues, and documenting results. They also collaborate with cross-functional teams to ensure projects meet regulatory and quality standards, and may contribute to process scale-up and technology transfer. This role requires strong analytical, communication, and problem-solving skills, as well as knowledge of relevant industry regulations.

How does a Development Scientist II typically collaborate with cross-functional teams during product development?

As a Development Scientist II, you will frequently work with multidisciplinary teams including engineers, quality assurance, regulatory affairs, and manufacturing. Your role often involves communicating experimental data, sharing insights from laboratory findings, and ensuring that product specifications meet both scientific and regulatory standards. Effective collaboration is crucial for troubleshooting challenges, optimizing processes, and accelerating project timelines. Being proactive in cross-team meetings and open to feedback helps ensure that products are developed efficiently and with high quality.
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Development Scientist Ii jobs near you
Development Scientist I

Development Scientist I

Catalent, Inc.

Greenville, NC • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 16 days ago

Catalent rating

7.7

Company rating: 7.7 out of 10

Based on 50 frontline employees who took The Breakroom Quiz

45th of 71 rated pharmaceutical

Job description

Development Scientist I
Position Summary:
  • Work Schedule: Monday-Friday, 8:00am-5:00pm EST
  • This position is 100% on-site at the Greenville site.

Catalent's Greenville, N.C. facility specializes in end-to-end turn-key solutions for oral solid dosage forms, including integrated formulation development, analytical services, commercial manufacturing, and packaging. This state-of-the-art facility has had over $100M of investments in recent years and features fit-for-scale capacity with potent handling capabilities, ideal for orphan or targeted drug development.
The Development Scientist I will serve as the primary point of contact with the client regarding pharmaceutical development and clinical manufacturing project related activities. The Development Scientist I is responsible for supporting these activities in the areas of supervision, process development, clinical trial batch manufacturing, packing and documentation.
The Role
  • Independently design and execute experiments.
  • Solve formulation and process problems.
  • Author SOP's, IQ/OQ/PQ documents, development and technical reports, and CMC sections for regulatory submissions.
  • Maintain competency and training for relevant processes and equipment.
  • Ensure that all work is accurate, precise, properly documented, within GMP requirements.
  • Organize multiple project responsibilities to ensure tasks are appropriately prioritized and executed on time.
  • Design, coordinate, and execute development and CTM activities, including formulation, data interpretation, equipment selection, generation of batch records and other appropriate documentation, and problem-solving exercises.
  • Ongoing communication with clients, internal support groups, resources, vendors and staff.
  • All other duties as assigned.

The Candidate
  • Bachelor's degree in pharmaceutical science, chemistry, engineering, or related science with at least three years of industrial pharmaceutical experience.
  • Master's degree in pharmaceutical science or chemistry or related science with at least two years of industrial pharmaceutical experience.
  • Ph.D. in Pharmaceutical Science or related field or Pharm.D. with at least one year of industrial pharmaceutical experience.
  • Some exposure to hazardous chemicals and other active chemical ingredients.
  • Position requires the capacity to handle and manipulate objects using hands and arms.
  • Requires ability to occasionally lift items in excess of 50 pounds.
  • This position requires that a respirator be worn for your safety, and as such, employment is contingent upon being able to complete a medical evaluation with satisfactory results. The medical evaluation is conducted via an external vendor assigned by Catalent.

Why you should Join Catalent:
  • Potential for career growth on an expanding team
  • Abundance of cross-functional exposure to other areas within the organization
  • 152 hours of paid time off annually + 8 paid holidays
  • Day one benefits! Medical, dental, vision and 401K benefit effective on your first day

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.
Visit Catalent Careers to explore career opportunities.
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.

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About Catalent

Sourced by ZipRecruiter

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.Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Somerset, NJ, US

Year founded

2007

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