Quality Control Analyst
The Staffing Resource Group, Inc
Quakertown, PA
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JOB DETAILS
SALARY
LOCATION
Quakertown, PA
POSTED
30 days ago
Title: Quality Control (QC) Analyst
Location: Quakertown, PA
Industry: Pharmaceutical
Salary: $25/hr. + 10% Shift Differential
Schedule: Training Hours will be 1:30pm-11:30pm, Mon-Thurs. After training period of 60-90 days, QC Analyst will then work from 4:30pm-2:30am, Mon-Thurs.
Employment Type: Direct Hire
Company Overview:
Operating from a 100,000 square foot, US-based, state-of-the-art, FDA inspected facility, this company has the experience and capabilities to rapidly develop, scale up, and process APIs and excipients ranging from grams to multi-metric tons, including highly potent compounds.
Job Overview:
The Quality Control Analyst is critical to the Company s success in providing a quality service to our customers in a timely fashion. This position carries out the practical work in the laboratory such as routine analytical testing. Performs required testing on raw materials, intermediates and finished products. May support Quality management to provide method technology transfer and project preparation. Follows GLP and cGMP procedures and documenting actions.
Job Description:
- Testing of raw materials, intermediates and finished products according to Standard Operating Procedures and Test Methods
- Records test results and maintains raw data and accurate laboratory records
- Maintain lab assets in accordance with written procedures and schedules as required by cGMP, GLP and ISO 9001 when applicable
- May write and revise Standard Operating Procedures
- Approve or reject finished product samples
- General lab support including housekeeping, equipment maintenance, inventory of supplies, etc.
- Evaluate existing analytical methods and develop new methods when appropriate
- Runs analytical method transfer and validation experiments.
- Method transfer, validation, experiment
- Assist on preparation work of projects
- Assist on the OOS investigations
- Provide technical support and answers during the analysis of production sample
- Follow safety protocols; ensure personal safety in the working area
- Assist with various duties when needed as instructed by a supervisor
- Associates degree or higher
- Prior GMP or Quality experience preferred but not required
- Prior HPLC experience highly preferred, Microtrac (Particle Size) preferred but not necessary
- Basic computer skills
- Strong communication skills both verbal and written required
- Must know and follow job safety procedures, attend required health and safety training, proactively promote safety at work, and promptly report actual and potential accidents and injuries.
- Must comply with safety policies of the company and site
- Adherence to cGMPs is required at all times.
- All personnel own the quality of what they deliver and are responsible for notifying responsible management in a timely manner of regulatory inspections, serious GMP deficiencies, process deviations, product defects and related actions
- Majority of role is laboratory based and must abide by good laboratory practices.
- Wear PPR on occasion as dictated by SOP s.
- Must accurately record process details.
- Ability to multi-task in a fast-paced manufacturing environment.
- Must be able to lift 30lbs
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 match professionals rapidly and precisely to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.
EOE/ADA
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About the Company
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