Immediate need for a talented Quality Control Analyst. This is a 07+ months Contract opportunity with long-term potential and is located in Hayward, CA(Onsite). Please review the job description below and contact me ASAP if you are interested.
Job ID: 23-54367
Pay Range: $30 - $32.14/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:
- Conduct critical chemical and physical analysis such as raw materials, in-process and finished goods products samples at *** manufacturing facility.
- Use a variety of laboratory instrumentation (KF Titrator, DSC, HPLC, Particle Size, Tensile Tester, spectrophotometer) and computer systems to collect and record data.
- Perform assays requiring precise analytical skills and understanding of chemistry principles.
- Complete all testing, including special project / protocol testing in a timely and appropriate manner.
- Support laboratory equipment qualification
- Support test method validation
- Support laboratory investigation and conduct nonconformance investigation
- Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, GLP, QSR and cGMP regulations.
- Participate in functional efforts involving teams, which impact production, increase efficiency, solve problems, generate cost savings and improve quality.
- Perform laboratory preparation for internal/external audits as required.
- Perform equipment maintenance and calibrations as required.
- May perform other duties as assigned
- Weekend work may be required as needed to meet production timeline schedules.
- Ability to handle multiple tasks concurrently, and in a timely fashion.
- Computer literate. Must be detail oriented, conscientious and have high reading comprehension skills.
- Must understand laboratory instrumentation.
- Must be able to communicate effectively with supervisors and peers.
- Must be able to read, write, and converse in English.
- Must be able to navigate, conduct searches, and fill online forms on Personal Computer for the purposes of training, performance management, and self service applications.
- Must have the ability to navigate electronic mail systems and intranet for communication purposes.
- Good interpersonal skills and be able to work effectively and efficiently in a team environment.
- Knowledge of cGMP manufacturing and GDP.
- Knowledge of basic laboratory and pharmaceutical production equipment including but not limited to: HPLC, DSC, KF Titrator, etc.
- Knowledge of equipment qualification, test method validation
- Knowledge of basic chemical and biological safety procedures.
- Must be able to read and follow detailed written instructions and have good verbal/written communication skills.
- Must have the following personal attributes: integrity and trust, work ethic, sound judgment, intellectual honesty, pragmatism, courage and conviction.
- Must have passion to innovate and drive for solutions.
- Must display personal accountability for results and integrity.
- Must display eagerness to learn and continuously improve.
- Must have uncompromising dedication to quality
- Bachelor’s Degree in Chemistry or Biological Sciences with Analytical Chemistry or Laboratory coursework with 0-2 years’ experience.
- Regular attendance is necessary to perform the essential functions of the job.
- Light work, frequent lifting up to 10 lbs; frequent standing/walking.
- Minimal to moderate travel required.
- Normal office working conditions: computer, phone, files, fax, copier.
- Personal Protective Equipment: Gloves, Lab coat, Safety Glasses
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, color, 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.
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