- Under direction, conduct critical chemical, physical, and biological analyses on finished product stability samples. May also support testing of raw materials, initial, in-process and final product samples from the manufacturing facility, as required.
- Work under minimum supervision.
- Use sophisticated laboratory instrumentation and computer systems to collect and record data. May be required to conduct validations.
- Complete all testing, including special project / protocol testing in a timely and appropriate manner to meet project schedules.
- Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, cGxP, and QSR regulations.
- Participate with management to investigate deviations and write exception documents.
- May perform advanced biological and chemical assays requiring precise analytical skills and understanding of chemistry principles.
- May perform review of test data, which includes overall documentation practices. May perform review functions in LIMS or other computerized systems.
- May participate in cross functional teams, which impact production, increase efficiency, solve problems, generate cost savings and improve quality and provide new product support.
- Maintain laboratory supplies and laboratory safety requirements to ensure audit readiness at all times.
- Perform equipment maintenance and calibrations as required. Troubleshoot and resolve instrument problems with some assistance.
- Proficient in advanced wet chemistry, volumetric preparation techniques and instrumental methods of analysis
- Must demonstrate effectiveness in attention to detail, organization, teamwork/interpersonal skills, results orientation, and task completion.
- Must be able to handle multiple tasks concurrently and in a timely fashion.
- Possess writing and computer skills.
- Must communicate effectively with managers and peers.
- Interpret available information and make recommendations to resolve technical challenges.
- Education and/or Experience. 0 N/A: Intern or Co-op
- Bachelor's degree in Chemistry or biological science with analytical chemistry laboratory coursework and 0-1 years' experience.
- Analytical chemistry instrumentation experience (e.g. HPLC, pH, KF, AA, GFAA, titrations, etc.) preferred.
- Pharmaceutical GMP/QC laboratory experience is desired.
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Quality Lab Associate - Round Lake, United States - Pyramid Consulting, Inc
Description
Immediate need for a talented Quality Lab Associate. This is a 06+ Months contract opportunity with long-term potential and is located in Round lake, IL (Onsite). Please review the job description below and contact me ASAP if you are interested.
Job ID:
Pay Range: $25/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).
Key Responsibilities:
Key Requirements and Technology Experience:
Our client is a leading Healthcare organization and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration.
Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, colour, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
