Live opening · Posted 7 days ago
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About the role
Description supplied by the original job listing.
**Applicants MUST have authorization to work in the United States indefinitely without restriction or sponsorship**
Perform various type of testing using chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, various wet chemistry analyses, HPLC, IC, IR, ICP, AA, TGP, DSC, PDA, auto-titrators, TLC, and dissolution apparatus
Execute specialized analyses and method transfer and feasibility testing
Document work as required for GMP compliance
Perform tests accurately
Troubleshoot method and instrumentation problems
Use office and instrumentation specific computer software
Produce written reports (e.g., SOP, OMC, client reports)
Develop and execute validation plans
Carry out method transfers and feasibility studies
Train technical staff
Some travel to client sites for technical meetings could be required
Minimum Qualifications:
Bachelor's degree in chemistry, analytical chemistry, biochemistry, or other related degree concentration
2 years of related pharmaceutical experience in a cGMP environment
HPLC and validation experience
Authorization to work in the United States indefinitely without restriction or sponsorship
The Ideal Candidate Would Possess:
Strong computer, scientific, and organizational skills
Experience working with protein chromatography
Strong computer, scientific, and organizational skills
Excellent communication (oral and written) and attention to detail
Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
Employment type
Full-time
Work arrangement
No
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