As a global leader in staffing and recruitment, we are dedicated to connecting you with opportunities that foster growth and advancement in the life sciences sector. Working with a recruiter gives you exclusive access to a vast network of top employers and valuable insights into a wide range of roles. One of our premier partnerships is with a world-renowned leader in eye care, committed to advancing vision health through innovative surgical and vision care solutions. With a strong legacy of groundbreaking developments, this company is making a meaningful impact on the lives of millions worldwide. If you're looking to contribute to cutting-edge advancements in eye care and be part of a team shaping the future of vision health, this could be the perfect opportunity for you!
location: Fort Worth, Texas
job type: Contract
salary: $33.64 - 38.45 per hour
work hours: 9 to 5
education: Bachelors
responsibilities:
- Perform analytical chemistry in collaboration with others to develop and validate analytical methodology, including stability-indicating HPLC methods, GC methods, Karl Fischer for new drug substances and products.
- Perform and verify compendia methods when appropriate.
- Generate analytical data for new and existing methods to trouble-shoot issues.
- Assists in the design and execution of clinical phase-appropriate method validation protocols.
- Executes stability studies to support the development of new drug substances or drug products.
- Compiles laboratory data.
- Assists laboratory investigations for aberrant and out-of-specification data.
- With assistance, author technical documents such as method development/validation reports, stability reports, and certificates of analysis.
- Able to maintain laboratory records and provide peer review and approval of quality critical data.
- Able to independently schedule work activities and maintain laboratory supplies and equipment.
- Authors and/or reviews standard operating procedures pertaining to analytical testing and reporting.
- Able to execute investigational studies in collaboration with others to address specific issues.
- Conducts work in compliance with cGMP, safety, and regulatory requirements.
- Provides analysis and evaluation of materials and products at all stages of development and for their area of focus.
qualifications:
- Bachelor's degree in Instructional Design, Education, Communication, or related field (Master's preferred)
- 3-5+ years of experience in instructional design, preferably in a regulated industry (medical devices, pharmaceuticals, healthcare)
skills: HPLC, Chemistry, GMP (Good Manufacturing Practice)
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact ....
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
This posting is open for thirty (30) days.
Job ID: 483486628
Originally Posted on: 7/1/2025
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