| urgent need: QA Specialist || Location:Santa Monica, CA(local candidate) || Duration: 6 Months at Santa Monica, California, USA |
| Email: [email protected] |
| From: shashmita, VYZE INC [email protected] Reply to: [email protected] Hi, Hope you are doing well please find the requirement below and kindly let me know if you have good consultant for this. Role: QA Specialist Location: Santa Monica, CA(local candidate) Duration: 6 Months Visa: No H1b/CPT MOI: Skype Job Description: 5 years of experience in a GMP environment with BS degree in the biological sciences or related field 3 years of experience in a GMP environment with MS degree in the biological sciences or related field In-depth knowledge of and ability to apply GMP in conformance to US, EU and ROW standards Proficient in cGMP regulations, quality systems and regulatory requirements. Experience writing, evaluating and closing investigations, CAPAs and change control records. Experience with conducting and managing internal and external audits. In-depth understanding and application of qualification and validation principles, concepts, practices, and standards. Ability to effectively negotiate and build collaboration amongst individuals. Proficient in MS Word, Excel, Power Point and other applications. Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment. Willingness to think outside of the box and adapt best practices to a growing environment Must be able to work on multiple projects simultaneously and demonstrate organizational, prioritization, and time management proficiencies Comfortable in a fast-paced company environment with minimal direction and able to adjust workload based upon Changing priorities. Self-motivated, detail-oriented, and willing to accept temporary responsibilities outside of initial job description. Possess critical thinking skills when making sound quality decisions based on risk management and available data. Ability to recognize deviations from accepted practice and apply knowledge of current Good Manufacturing Practices CGMP) on a daily basis. Advanced technical writing and excel skills are highly desired for creating and presenting reports. Ability to work independently and effectively coach peers in a high-paced environment with tight timelines, while Maintaining accuracy and quality. Ability to effectively generate metrics, and present; data, findings, andimprovement initiatives/projects to QA and ross-functional leadership. A relevant background in Quality Control or Analytical Development with arole as a supervisor or manager is highly desired Best Regards, Shashmita Sen Das Technical Recruiter, Vyze Inc. (An E-Verified Company), 25179 Methley Plum Place, Aldie, VA 20105 Email: [email protected] Desk:(571)367-1411 www.vyzeinc.com Keywords: quality analyst computer associates |
| [email protected] View all |
| Mon Jan 02 18:42:00 UTC 2023 |