QC Technical Scientist

Portsmouth, NH

Posted: 06/11/2020 Job Number: JN -062020-11683

Job Description

QC Technical Scientist

SRG offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services. SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to rapidly and precisely match professionals to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.

Environment: A global leader and trusted supplier in the pharma, biotech and specialty ingredients markets. Headquartered in Basel, Switzerland, the company is focused on advanced manufacturing, high-quality control systems, regulatory expertise, and research and development (R&D) capabilities. The company s products and services include active pharmaceutical ingredients (API), stem cell therapies, drinking water sanitizers, vitamin B compounds, organic personal care ingredients, industrial preservatives and microbial control solution to combat viruses, bacteria and other dangerous pathogens.

Title: QC Scientist
Location: Portsmouth, NH
Industry: Pharmaceutical
Hours: Monday-Friday, 8-5
Salary: $28.00 hr.
Employment Type: Long Term Contract (Benefits Available)

Environment: This client is one the world s leading suppliers to the pharmaceutical, biotech and specialty ingredients markets. We create products that support a healthier lifestyle and enhance ones quality of life. Isn t this a company you want to work for?

Summary
  • Act as a team member of the Quality Control department to support technology transfer, validation, deviation support, and investigation projects. Subject Matter Expert for all disciplines.
  • Work on extremely complex problems in which analysis of situations or data requires an evaluation of intangible variables.
  • Support the review of all regulatory documents including APRs and BLAs.
  • Direct contact with customers and project teams.
  • Act as advisor to junior staff to meet schedules and/or resolve technical problems.
  • Troubleshoot assay and instrumentation issues involving data mining, trending and analysis to identify problems.
  • Provide hands-on and theoretical training as appropriate for QC and other operational groups
Overview
  • Oversee assigned projects in group and ensure on track for on-time completion
  • Represent QC and Lonza in customer meetings to receive/deliver information, request and requirements.
  • Document writing/review for transfers/validations/investigations
  • Measures throughput, performance and other appropriate metrics and report them to management
    Other such as leading OE initiatives and improvements.
  • Perform other duties as assigned
Qualifications
  • Bachelor degree and/or Advanced Graduate degree (MS/PhD)
  • Preferred area of study: Microbiology, Biochemistry or equivalent Science Field
  • Experience in a GMP/Professional environment
  • Use of Microsoft Suites (Word, Excel, PowerPoint)
  • Expert in all applicable laboratory software and hardware systems including Empower 3 and SoftMax
  • Demonstrated expertise and proficiency in method transfer and method validation
  • Use of GMP Quality Systems such as: TrackWise, LIMS
  • Experience with HPLC Systems preferred
  • Able to communicate in both written and verbal format
  • Able to speak publicly
  • Makes quality decisions independently
EOE/ADA
Search words: GMP, FDA, HPLC, Microsoft, TrackWise, LIMS, PHD
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