QC Laboratory Technician Mid Shift

Our QC Laboratory 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 performing basic laboratory support functions related to the management of laboratory samples, materials, and testing supplies. 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 full-time role for our Mid shift, working Monday through Friday from 10:30 AM to 7:00 PM. This is a set, consistent schedule with minimum overtime requirements and based on site in our Sugar Land location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws.

What The QC Laboratory Technician Does Each Day

• Verifies information on incoming lab samples and enters sample information into the laboratory database
• Place orders and stock laboratory supplies
• Light housekeeping, including operation of glassware washer
• Ensures all work is performed and documented in a timely manner and according to approved standard operating procedures and in general compliance with cGMPs
  
  

Our Most Successful QC Laboratory Technicians

• Are accurate and well organized, with strong attention to detail
• Express energy, show accountability, can multi-task and work in a fast-paced, quality-rich environment
• Fulfill expectations, establish sustainable relationships with team members, maintain effective and meaningful communication channels
• Have good interpersonal skills and work effectively and efficiently in a team environment to accomplish goals
• Have strong verbal and written communications skills
  
  

Minimum Requirements For This Role

• A High School diploma or equivalent
• Able to successfully complete a drug and background check
• Proficient in Microsoft Office, Word and Excel
• Must be currently authorized to work in the United States on a full-time basis; QuVa will not sponsor applicants for work visas
  
  

Any Of The Following Will Give You An Edge

• Bachelor’s Degree in life science or related field
• 1 to 2 years’ experience in data entry/clerical, or related responsibilities
  
  

Benefits Of Working At QuVa

• Set, full-time, 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, industry-leading high growth company with future career advancement opportunities
  
  

About QuVa

QuVa Pharma is a national, industry-leading, FDA registered 503B outsourcing services company that provides hospitals with essential medications in ready-to-administer injectable formats that are critical for effective patient care. We are leading the way with unmatched expertise in current Good Manufacturing Practices and sterile pharmaceutical manufacturing, and the highest quality and safety standards so hospitals can more confidently and reliably focus on patient care nationwide. As a leader in sterile compounding, we continue to invest in automation and integrated technologies to improve our production processes, safety, consistency, and product quality.

As part of our team, you'll experience being at the forefront of groundbreaking solutions, collaborating with brilliant minds, and making a tangible impact in healthcare delivery.

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. QuVa's 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.”