
R&D PDM Assistant (Wilson, NC, US, 27893) bei Reckitt
Reckitt · Wilson, Vereinigte Staaten Von Amerika · Onsite
- Professional
- Optionales Büro in Wilson
We are Reckitt
Research & Development
We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality.
The size of our organisation means you'll have the opportunity to learn and work in different functions within R&D, giving you exposure to different disciplines, teams and environments. You will also have access to our Research and Development Academy, designed to develop our team and allow you to grow in our great organisation.
About the role
We are seeking a detail-oriented individual to join our team as an Analytical Assistant with a minimum of 1-2 years’ experience in an analytical testing laboratory. This individual will be integral in the start-up and technology transfer for our R&D laboratory, supporting the launch of a new GMP manufacturing production site for Over-the-Counter (OTC) products and Vitamins, Minerals, and Supplements (VMS), based in Wilson, NC.
Your responsibilities
- Supporting analytical method transfer activities, including protocol execution and laboratory notebook second scientist review (SSR), for raw material, intermediate and finished product test methods
- Assist in method validation and USP verification studies in accordance with ICH and USP guidelines
- Conduct USP compendial testing (e.g., assay, dissolution, content uniformity, identification, etc.)
- Maintain accurate and complete laboratory records in compliance with GMP and GLP standards
- Participate in laboratory investigations and support root cause analysis
- Prepare and review technical documentation including equipment qualification protocols and reports, standard operating procedures (SOPs) etc.
- Support installation, qualification and maintenance activities of analytical laboratory equipment and utilities
- Support lab start-up activities, including establishment of foundational SOP’s, equipment/personnel flow assessments and Lab 5S
- Ensure adherence to safety and quality standards when conducting all laboratory activities
This role is not currently sponsoring visas or considering international movement at this time.
The experience we're looking for
- Bachelor's degree in relevant scientific discipline (e.g. Chemistry, Pharmaceutical Science, Chemical Engineering, Biology, Biochemistry)
- 1-2 years of related analytical experience in a regulated or technical industry (e.g. pharmaceuticals, manufacturing, healthcare)
- Must be familiar with Good Documentation Practices (GDP), Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP)
- Possess knowledge of United States Pharmacopeia (USP) standards and their application in laboratory settings
- Experience with analytical method transfer and validation is strongly preferred
- Excellent attention to detail and organizational skills
- Strong interpersonal and communication skills
- Proficient in Microsoft Word, Excel and PowerPoint
Strongly Preferred:
- Experience with chromatography and mass spectrometry instruments and analytical testing techniques (e.g. ICP/MS, HPLC, UPLC, GC)
- Experience with raw material testing (e.g. NIR, FTIR, Karl Fischer, general wet chemistry testing)
- Experience with LIMS, Empower CDS
- Knowledge of Lab 5S principles
The skills for success
What we offer
Salary Range
USD $68,000.00 - $102,000.00
Hiring Range: 68,000 - 85,000