Quality Control Inspector

VSSI Staffing Services; Town of Texas (WI); On-site; USD 28,000 - 32,000; Full time

Job summary

VSSI Staffing Services is hiring a QC Inspector in Wisconsin. The role focuses on testing, data review, and investigations in compliance with cGMPs and SOPs. The position executes product analyses, adheres to SOPs, and ensures proper documentation and equipment readiness for production.

The candidate will support calibration, sanitation verification, and sample management to sustain quality standards. The role requires a degree or equivalent experience, 2–4 years in pharma or related fields, and

Qualifications

• Bachelor’s degree in related field or equivalent experience.
• 2–4 years related experience or equivalent.
• Knowledge of pharmaceutical manufacturing processes, GMPs, and validation.
• Ability to develop clear, concise, timely reports (oral and written).
• Experience in laboratory environment, equipment, and safety procedures.
• Experience in R&D including statistics understanding.

Responsibilities

• Analyze products per cGMP and SOPs.
• Follow work instructions and SOPs.
• Inspect production areas, processes, and finished goods.
• Document data in forms, logs, and inventories.
• Calibrate and maintain equipment per GMP and SOPs.
• Monitor cleanliness and report issues.
• Read and follow SOPs and GMPs.
• Swab and verify equipment cleanliness with ATP testing.
• Prepare and drop off customer samples for shipment.
• Maintain retain samples in Excel workflow.
• Review BOM and production processes before production.
• Follow safety regulations.
• Perform other duties as assigned.

Skills

Analytical thinking

Attention to detail

Oral communication

Written communication

Teamwork

Education

Bachelor's degree or equivalent

Tools

Laboratory equipment

Job description

Job Description

Pay: $20.00 - $23.00 per hour

Pay: $20 - $23 an hours DOE

Job description

QC inspector

Schedule: 2:30pm - 11:30 pm + OT

SUMMARY

Performs testing, reviews test data, and writes investigations in compliance with cGMPs and SOPs.

RESPONSIBILITIES

• Analyzes products in compliance with cGMP regulations and SOPs.
• Follow work instructions and standard operating procedures.
• Inspect production areas, production processes, and finished goods produced.
• Completes and maintains appropriate documentation to support testing procedures and comply with GMPs including but not limited to data capture forms, equipment logbooks, and inventory forms.
• Calibrates and maintains laboratory equipment according to maintenance schedules, GMP requirements, and SOPs.
• Monitor cleanliness of production and if unacceptable, report to direct supervisor.
• Reads, understands, and follows SOPs; complies with current GMP as required by FDA.
• Swab all production equipment’s clean and sanitized by sanitation, with a ATP instrument to ensure they meet the pass threshold before use in production.
• Prepare and drop off customer samples for shipment.
• Document all retain samples pulled in excel workflow.
• Detail review of BOM and production process prior to production.
• Follows all safety regulations.
• Performs other related duties as assigned by management.

QUALIFICATIONS

• Bachelor’s degree (B.S.) in related field preferred or equivalent work experience.
• Two to four years related experience or equivalent
• Strong knowledge of pharmaceutical manufacturing processes, computer, and equipment validation, GMPs, and product/process validation.
• Ability to develop clear, concise, and timely oral and written reports.
• Experience with laboratory environment, equipment, and safety procedures.
• Experience in research and development, including understanding of statistical analysis.
• Commitment to excellence and high standards
• Excellent written and oral communication skills
• Strong organizational, problem-solving, and analytical skills
• Ability to manage priorities and workflow
• Versatility, flexibility, and a willingness to work within constantly changing priorities with enthusiasm
• Acute attention to detail
• Demonstrated ability to plan and organize projects
• Ability to work independently and as a member of various teams and committees
• Proven ability to handle multiple projects and meet deadlines
• Ability to work on complex projects with general direction and minimal guidance.
• Working knowledge of data collection, data analysis, evaluation, and scientific method.

COMPETENCIES

• Analytical--Synthesizes complex or diverse information; Collects and researches data; Uses intuition and experience to complement data; Design’s workflows and procedures.
• Technical Skills--Assesses own strengths and weaknesses; Pursues training and development opportunities; Strives to continuously build knowledge and skills; Shares expertise with others.
• Customer Service--Manages difficult or emotional customer situations; Responds promptly to customer needs; Solicits customer feedback to improve service; Responds to requests for service and assistance; Meets commitments.
• Interpersonal Skills--Focuses on solving conflict, not blaming; Maintains confidentiality; Listens to others without interrupting; Keeps emotions under control; Remains open to others' ideas and tries new things.
• Oral Communication--Speaks clearly and persuasively in positive or negative situations; Listens and gets clarification; Responds well to questions; Demonstrates group presentation skills; Participates in meetings.
• Written Communication--Writes clearly and informatively; Edits work for spelling and grammar; Varies writing style to meet needs; Presents numerical data effectively; Able to read and interpret written information.
• Teamwork--Balances team and individual responsibilities; Exhibits objectivity and openness to others' views; Gives and welcomes feedback; Contributes to building a positive team spirit; Puts success of team above own interests; Able to build morale and group commitments to goals and objectives; Supports everyone's efforts to succeed.
• Quality Management--Looks for ways to improve and