Production Technician I - Formulation 2nd Shift

Quva•Sugar Land, TX
•Onsite

About The Position

The Production Technician I – Formulation supports daily manufacturing activities for non-sterile and sterile bulk/CSP operations after completing required training. The role helps ensure pharmaceutical products meet safety, efficacy, and quality standards through precise procedures and attention to detail. It is a full-time, onsite position in Sugar Land, Texas, working the second shift Monday through Friday from 2:00 PM to 10:30 PM CST. The schedule is set and consistent, with minimum overtime requirements. This is a safety-sensitive position and may be subject to random drug testing in accordance with applicable laws. The position requires extensive training and qualification, including gown training, aseptic technique, competency assessments, direct observation, and media-fill qualification for each compounding process.

Requirements

  • High school diploma or equivalent.
  • Successfully complete a drug and background check.
  • Familiarity with and comfort using mobile devices such as smartphones, tablets, and handhelds.
  • Ability and willingness to walk, stoop, stand, bend, and lift throughout each shift, with or without accommodation.
  • Must be at least 18 years old.
  • Currently authorized to work in the United States on a full-time basis; the employer will not sponsor applicants for work visas.
  • Complete extensive training and qualification, including gown training, aseptic technique, competency assessments, direct observation, and media-fill qualification for each compounding process.
  • Strong math skills.
  • Approach others in a tactful manner, react well under pressure, follow through on commitments, carefully follow directions, pay attention to detail and take careful notes, and take initiative to identify problems and opportunities.

Nice To Haves

  • College degree with an emphasis in Chemistry, Biochemistry, or equivalent.
  • One year of pharmaceutical manufacturing experience.
  • Working knowledge of cGMPs, regulatory requirements, and applicable SOPs.

Responsibilities

  • Weigh chemicals to support product formulation.
  • Formulate bulk intermediate solutions.
  • Perform sterile filter integrity testing.
  • Clean and disinfect clean rooms.
  • Perform equipment calibration checks.
  • Submit the daily supply list for the respective area to receiving by the scheduled time.
  • Open and close Formulation pods and ILP in accordance with work instructions and daily task lists.

Benefits

  • Comprehensive health and wellness benefits, including medical, dental, and vision.
  • 401(k) retirement program with company match.
  • 17 paid days off plus 8 paid holidays per year.
  • Occasional weekend and overtime opportunities with advance notice.
  • Future career advancement opportunities.
  • Set, full-time, consistent work schedule.
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