Job Description This is an entry-level role responsible for performing a variety of routine and non-routine tasks in a regulated laboratory environment to support and help develop pharmaceutical platforms. The Chemist will work in accordance with company policies and current Good Laboratory Practices (GLP), regulatory requirements, and standards to meet quality and accuracy requirements. The role involves conducting procedures for process analysis and assisting managers and peers with routine and non-routine Quality Control and Research procedures. Responsibilities
- Comply with all quality system requirements.
- Perform preparation, collection, measurement, and recordkeeping of samples.
- Document test and data analysis results.
- Participate in cross-functional teams for continuous improvement activities.
- Communicate with team members to ensure schedule requirements are met.
- Apply knowledge of performed tasks to elucidate test method failures.
- Analyze and deduce data and collate test results.
- Communicate priority and timeliness for completion of customer requests.
- Help drive the team to meet business goals.
- Support development area as needed for commercial QC release.
- Learn and understand the manufacturing organization that the lab supports.
- Degree in Chemistry or related science.
- 3+ months of experience in chromatography (HPLC, GC, UPLC), wet chemistry, analytical chemistry, FTIR, and pharmaceutical processes.
- 6+ months of experience with GMP/cGMP/GLP.
- Ability to maintain good time management.
- Excitement and desire to learn.
- 6+ months of industry wet chemistry experience.
- Experience with chromatography software such as Empower.
- Equipment troubleshooting experience.
- Working experience with UPLC, HPLC, dissolution GC-FID/MS, FT-IR, and UV-Vis.
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following: Medical, dental & vision
Critical Illness, Accident, and Hospital
401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
Life Insurance (Voluntary Life & AD&D for the employee and dependents)
Short and long-term disability
Health Spending Account (HSA)
Transportation benefits
Employee Assistance Program
Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Minneapolis,MN. Application Deadline This position is anticipated to close on Jul 4, 2025. About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email ... for other accommodation options.