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QC Senior Analyst

Portsmouth, NH

Posted: 08/13/2020 Job Number: JN -082020-11856

Job Description

QC Senior Analyst:

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.

Title: QC Senior Analyst
Location: Portsmouth, NH
Industry: Pharmaceutical
Shift Hours: 40 Hour work week - Mon - Fri
Salary: $34.00 Based on Experience
Employment Type: Long Term Contract (Benefits Available)

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.

Overview:
The QC Senior Analyst will act as a team member of the Quality Control department to support production of in-process and final product drug lots for customers. Also participate in quality testing for ongoing customer stability studies. Provide on-time, high quality results to meet Manufacturing demands. Applies job skills and company's policies and procedures to complete a variety of tasks. Works on assignments that are semi-routine in nature where ability to recognize deviation from accepted practice is required. Works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors.

Key Accountabilities and Duties:
Running test samples for In-Process, Lot Release and Stability studies
Reviewing assays
Training others
Writing- Quality Records (Deviations, CAPA, Change Control) and Test Methods
Projects such as method transfers, new instruments, method qualifications
Perform other duties as assigned.

Minimum Required Qualifications/Skills:
Bachelor or Associates Degree. Preferred area of study in Microbiology, Biochemistry or Related Science Fields.
5-8+ years industry experience, preferably in a cGMP environment.
Use of Microsoft Suites (Word, Excel, PowerPoint)
Use of Laboratory computer systems
Potential previous use of GMP Quality Systems such as: TrackWise, LIMS
Excellent ability to speak publicly. Able to maintain control of meetings as required. Holds group meetings as backup to Supervisor, delivering clear concise messages.
Excellent ability to interpret data. Makes more advanced quality decisions independently.
Perform assigned, complex and/or varied tasks. Organizes tasks for other analysts as required.
Mentors junior analysts.
Excellent ability to prioritize and problem solving.
Comprehend and follow instructions. Gives instructions to junior level analysts.
Direct, control and plan tasks/projects.
Excellent ability to communicate in both written and verbal format to Supervisor and QC Management.

EOE/ADA

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