QC Analyst

Quality Control Technical Transfer Analyst III

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: Quality Control Technical Transfer Analyst III
Location: Portsmouth, NH
Industry: Pharmaceutical
Hours: M-F: 8AM-5PM (100% Onsite)
Salary: $33.00 hourly paid weekly (Benefits Available)
Employment Type: Long term contract (potential for extension or direct offer)

Job Summary:
The Quality Control Technical Transfer Analyst 3 will act as a team member of the Quality Control department to support production by contributing to the completion of the technical transfer activities. Also participate in quality testing for customer in-process, final product testing and stability studies when needed.
Applies job skills and company's policies and procedures to complete a variety of tasks of increased scope. 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.

Duties may include any of the following:
Applies job skills and company's policies and procedures to complete a variety of tasks.
Running test samples for In-Process, Lot Release and Stability studies.
Running test samples for (but not limited to) investigations, transfers and validations.
Reviewing assays
Training others
Writing- Quality Records (Deviations, CAPA, Change Control) and Test Methods
Projects such as method transfers, new instruments, method qualifications
Use of Microsoft Suites (Word, Excel, PowerPoint)
Use of Laboratory computer systems
Potential previous use of GMP Quality Systems such as: TrackWise, LIMS
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.
Apply Data Integrity principles in all aspects of work, in compliance with our policies, guidelines and procedures.
Perform other duties as assigned.

Job Requirements:

Strong ability to speak publicly.
Strong ability to interpret data both alone and with guidance.
Perform assigned, complex and/or varied tasks.
Prioritization and problem solving.
Comprehend and follow instructions.
Direct, control and plan tasks/projects.
Brainstorming
Strong ability to communicate in both written and verbal format.
Exercises judgment within defined procedures and practices to determine appropriate action.
Self-motivated team player
Completes assignments on-time and accurately
Displays commitment to quality and performs job functions to the best of his/her ability
Relate to others in a team setting.
Maintain positive attitude in a team environment.
Timeliness in completing assigned tasks.
Works entire assigned shift, including arriving on time

EOE/ADA