Catalent Pharma Solutions Inc

QC - Lead Scientist I

Catalent Pharma Solutions Inc$85K — $110K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's, Master's, or Doctorate in Life Science or Physical Science with 5-11 years relevant experience.
  • Skilled in testing procedures per USP, EP, and JP using key analytical techniques like HPLC and GC.
  • Experience in peer reviewing laboratory documentation and ensuring regulatory compliance.
  • Physical capability to perform various tasks, including lifting up to 40 pounds and using a respirator if needed.
  • Ability to focus on detailed visual tasks and operate a computer.

Responsibilities

  • Plan and execute laboratory tests independently, aligning with customer timelines.
  • Conduct analytical testing on raw materials using various techniques.
  • Develop and verify testing methods and carry out method transfer activities.
  • Write and author technical documents including procedures and reports.
  • Review technical documentation for accuracy and compliance standards.
  • Act as a project lead, interfacing with customers and ensuring project outcomes.
  • Identify and recommend efficiency improvements and business opportunities.
  • Train laboratory associates on analytical methods.

Benefits

  • Cost-effective Kansas City location with access to local amenities.
  • Close proximity to the airport and train commuting options.
  • Generous paid time off and holidays totaling 152 hours plus 8 paid holidays.
  • Comprehensive medical, dental, and vision insurance options.
  • Strong 401(k) plan with a generous company match.
  • Opportunities for tuition reimbursement.
Full Job Description
Quality Control - Lead Scientist I

Position Summary

We have an opportunity for a QC - Lead Scientist I to join our team. In this role, you will use your technical expertise to lead complex projects and design experiments that support the department's goals. You will work independently, make decisions, and solve problems while ensuring compliance with site procedures and safety requirements. This position requires a detail-oriented and self-motivated individual who can also collaborate and assist team members as needed.

Shift: Monday - Friday, 8am-5pm
Location: Kansas City, MO
100% Onsite

The Role
  • Plan and execute laboratory testing independently, creating work plans and schedules based on customer timelines and site performance expectations.
  • Perform analytical testing on raw materials using techniques such as HPLC, GC, Karl Fischer, FTIR, UV-Vis, Polarimetry, and wet chemistry.
  • Write method development documents and carry out method verification and transfer activities.
  • Author technical documents, including protocols, test methods, reports, and standard operating procedures.
  • Review technical documents for accuracy, completeness, and compliance.
  • Act as a technical lead or subject matter expert on assigned projects, interacting with customers and taking responsibility for project outcomes.
  • Support efficiency improvement projects with guidance and identify potential business opportunities during project work.
  • Train other laboratory associates on analytical techniques.
  • Perform other laboratory-related duties as assigned.


The Candidate

Minimum Requirements
  • Bachelor's degree in a related Life Science or Physical Science field with 11+ years of related work experience, or a Master's degree in a related Life Science or Physical Science field with 9+ years of related work experience, or a Doctorate degree in a related Life Science or Physical Science field with 5+ years of related work experience.
  • Ability to execute testing procedures for the identification and characterization of raw materials per USP, EP, and JP using techniques such as HPLC, GC, UV/Vis, FTIR, conductivity, and wet chemistry.
  • Experience performing peer review of routine and complex laboratory documentation and reviewing technical documents for accuracy, thoroughness, and regulatory compliance.
  • On an average 8-hour day, ability to walk, sit, stand, use hands to handle or feel, reach at or above shoulder height and below waist height, climb or balance, stoop, kneel, crouch, or crawl; talk and hear, smell, and lift up to 40 pounds.
  • Specific vision requirements include reading written documents, visual inspection of materials, and frequent use of a computer monitor screen.
  • May require the use of a respirator.


Preferred Skills & Background
  • Ability to train, coach, or mentor others on technical material, personal development, business matters, and compliance topics.
  • Experience identifying, developing, and executing efficiency or compliance improvement projects within a team and recommending business opportunities on a project-specific basis.


Why You Should Join Catalent
  • The Kansas City site offers a cost-effective location with a strong talent pool, modern office spaces, and easy commuting options. It provides a collaborative work environment with a good quality of life and access to local amenities and cultural attractions.
  • Close to the airport and commutable by train with 24/7 operations.
  • 152 hours of paid time off plus 8 paid holidays.
  • Medical, dental, and vision coverage options.
  • Generous 401(k) match.
  • Tuition reimbursement.

About Catalent Pharma Solutions Inc

Catalent Pharma Solutions Inc is a global provider of advanced delivery technologies, development, and manufacturing solutions for drugs, biologics, gene therapies, and consumer health products. The company operates in four segments: Softgel and Oral Technologies, Biologics, Oral and Specialty Delivery, and Clinical Supply Services. Catalent Pharma Solutions serves customers in various industries, including pharmaceuticals, biotechnology, and consumer health. The company was founded in 2007 and is headquartered in Somerset, New Jersey.
Learn more about Catalent Pharma Solutions Inc
Size
14,000 employees
Industry
Founded
2007

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