Associate Quality Control
Spectraforce
Prince George's County, Maryland
3 hours ago
Job Description
Location: Juncos, PR
Pay Rate: $21.01 / Hourly
Shifts: Must have full availability to work rotating shifts based on business needs. Work schedules are subject to change and may include, but are not limited to, the following shifts:
Under general supervision, responsible for one or more of the following activities in Quality Control including analytical testing, characterization, method development, and sample and data management.
Responsibilities:
At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $ 21.01/hr.
Pay Rate: $21.01 / Hourly
Shifts: Must have full availability to work rotating shifts based on business needs. Work schedules are subject to change and may include, but are not limited to, the following shifts:
- 1st shift: 5:30am - 1:30pm / 6:00am - 2:00pm
- 2nd shift: 1:30pm - 9:30pm / 2:00pm - 10:00pm
- 3rd shift: 9:00pm - 5:30am
Under general supervision, responsible for one or more of the following activities in Quality Control including analytical testing, characterization, method development, and sample and data management.
Responsibilities:
- Perform routine laboratory procedures.
- May perform aseptic aliquot ting, sampling and analysis for compendia and non-compendia methods.
- May perform non-routine lab procedures under close supervision.
- Perform or review one or more of the following: sample testing, standards preparation and testing procedures, compendia and non-compendia test. methods, environmental monitoring, reagents and solutions preparation, sample management and equipment maintenance.
- Prepare complete, accurate, concise laboratory documentation.
- Data entry, review, analysis, and communication of results.
- Perform general lab housekeeping.
- Maintain/operate specialized equipment.
- Participate in the document revision process.
- Comply with safety guidelines, cGMPs and other applicable regulatory requirements.
- May participate in lab investigations/ audits.
- Maintain training proficiency.
- May approve lab results.
- Knowledge of basic principles, methods, and practices of technical/ scientific field.
- Typically obtained through formal study.
- General knowledge of procedures and activities within own work area.
- Ability to relate day-to-day work to business priorities.
- General understanding of industry practice and standards.
- Applies broad-based research, information gathering and analytical skills to factual information.
- Selects appropriate alternatives from defined options.
- Collects required documentation/raw data; verifies conformance of documents.
- Assesses accuracy of detailed information.
- Tracks, maintains, and produces regular work products.
- Ability to identify roadblocks to task completion and effectively brings them to line managers for resolution.
- Works under general direction, seeks assistance as needed.
- Completes work in accordance with established procedures and practices within field of technical/scientific knowledge.
- Establishes approaches for completing assignments.
- Work requires consistent exercise of discretion and independent judgment.
- Works with team to support achievement of project milestones.
- Contributes to own work group/team through quality and accuracy of own output.
- Builds productive internal/external relationships.
- High school/GED + 2 years of directly related work experience OR Associate’s + 6 months of directly related work experience OR Bachelor’s in Chemistry or Biochemistry is preferable.
- Knowledge in CIMS, LMES, LIMS, CDOCS is preferable.
- Ability and willingness to work any shift in support of operations that may include 24/7.
- Availability to work non-standard shifts, holidays, weekends, as per business needs.
- Perform routine sampling and inspection of raw materials, components, devices, drug substance, drug product and printed materials.
- Ability to understand, apply, and evaluate basic chemistry, biology, physical principles, and mathematics.
- Ability to adhere to regulatory requirements, written procedures, and safety guidelines.
- Ability to evaluate documentation/data according to company and regulatory guidelines.
- Ability to organize work, handle multiple priorities and meet deadlines.
- Demonstrated written and oral communication skills.
- Technical writing capabilities.
- Presentation capabilities.
- Must be detail oriented.
- Must be flexible and adaptable to changing priorities and requirements.
- General understanding of company products and QAL operations.
- Ability to interact with inspectors (internal and external).
Applicant Notices & Disclaimers
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At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $ 21.01/hr.