QC Sample Technician 3rd Shift
QC Sample Technician 3rd Shift
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1 Vacancy
Job Description
Our QC Sample Technician plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training your responsibilities will include providing support and subject matter expertise within areas of the Quality Management System (QMS). This position is responsible for collecting samples for testing to ensure they conform to all applicable laws and company quality standards. Operates within the legal and regulatory compliance producing a quality product. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety efficacy and quality providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US.
This is a fulltime role for our 3rd shift working Monday through Friday from 10:00 PM to 6:30 AM. This is a set consistent schedule with minimum overtime requirements and based on site in our Sugar Land TX location. This is a safety sensitive position that may be subject to random drug testing in accordance with applicable laws.
What the QC Sample Technician Does Each Day:
- The ability to learn and understand cGMP requirements
- Collect inspect and label QC Samples in accordance with procedures and production needs
- Review and verify critical batch record information related to the QC samples sections in the batch record
- Interact with other departments to assist in maintaining production flow following QC Sample collection and if supervision deemed necessary
- Assist in the submission and shipping of QC samples to internal and external laboratories on a daily basis
- Assist in the participation of process improvement projects within the company
Our Most Successful QC Sample Technicians:
- Are attentive to all aspects of the system while working to monitor and solve routine activities/issues
- Work effectively in a team environment with great organization skills
- Demonstrate initiative and accountability in a fastpaced environment
- Have excellent verbal and written communication skills
- Maintain a mature problemsolving attitude while dealing with interpersonal conflict complex environments or time demands
- Work independently and follow good documentation practices
- Demonstrate leadership skills through example
- Start and persist with specific courses of action while exhibiting high motivation and a sense of urgency to exceed internal customer satisfaction
Minimum Requirements for this Role:
- High school Diploma or GED required
- Able to successfully complete a drug and background check
- Familiarity with and comfortable using mobile devices such as smartphones tablets handhelds
- Able and willing to walk stoop stand bend and lift up to 50 lbs. throughout each shift with or without reasonable accommodation
- 18 years of age
- Proficient in the use of office applications such as MS Word Excel PowerPoint
- Must be currently authorized to work in the United States on a fulltime basis; QuVa will not sponsor applicants for work visas
Any of the Following Will Give You an Edge:
- Bachelors Degree in Business Engineering or related field
- Experience managing documents and records in a regulatory or controlled environment
- Knowledge in business computer applications (e.g. MasterControl Documentum SAP LIMS Track wise etc.
- 2 years experience in Quality Assurance / cGMP / FDA regulated industry
Benefits of Working at QuVa:
- Set fulltime consistent work schedule
- Comprehensive health and wellness benefits including medical dental and vision
- 401k retirement program with company match
- 17 paid days off plus 8 paid holidays per year
- Occasional weekend and overtime opportunities with advance notice
- National industryleading high growth company with future career advancement opportunities
About QuVa:
QuVa is a national industryleading provider of pharmacy services including readytoadminister sterile outsourcing and advanced AIgenerated insights providing clarity for revenue capture and inventory management. QuVa Pharma delivers essential medications in injectable formats critical for effective patient care. LogicStream a QuVa company partners with health systems to aggregate normalize and analyze large amounts of complex data through AI and machine learning tools that generate actionable insights supporting revenue optimization inventory management and inventoryrelated workflows. Through QuVas integrated solutions health systems can transform pharmacy management to achieve greater value by operating more efficiently and effectively as they deliver highquality patient care.
QuVa is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. QuVas Equal Opportunity Policy prohibits harassment or discrimination due to age ancestry color disability gender gender expression gender identity genetic information marital status medical condition military or veteran status national origin race religious creed sex (including pregnancy childbirth breastfeeding and any related medical conditions) sexual orientation and any other characteristic or classification protected by applicable laws. All employment with QuVa is at will.
Required Experience:
IC
Employment Type
Full-Time
