Production Technician I - Formulation 2nd Shift

QuVa - Advancing Healthcare Possibilities; Sugar Land (TX); On-site; USD 25,000 - 39,000; Full time

Benefits offered by this job

Healthcare benefits

401k with match

Paid time off

Overtime opportunities

Career growth

Job summary

QuVa Pharma is seeking a Production Technician I – Formulation for the 2nd shift at our Sugar Land, TX location. The role focuses on weighing chemicals, preparing bulk solutions, sterile testing, and clean room duties to ensure quality and compliance with cGMP standards.

The position is full-time, on-site, Monday–Friday, with a consistent schedule and potential overtime. Training includes gowning, aseptic technique, and competency assessments to support each compounding step.

Qualifications

• High School diploma or equivalent required.
• Must pass drug and background check.
• Familiar with mobile devices (smartphones/tablets/handhelds).
• Able to stand, walk, stoop, bend, and lift as needed on shift.
• Must be 18+ years old and authorized to work in the United States.

Responsibilities

• Weigh chemicals to support formulations.
• Formulate bulk intermediate solutions.
• Sterile filter integrity testing.
• Clean Room cleaning and disinfection per SOPs.
• Daily supply list submitted by scheduled time.
• Open/close Formulation pods and ILP per work instructions.

Skills

Attention to detail

Formulation

Aseptic technique

Education

High School diploma or equivalent

Chemistry degree preferred

Tools

Mobile devices familiarity

Job description

Production Technician I - Formulation 2nd Shift

Job Category: Site Operations

Requisition Number: PRODU006194

• Posted : October 29, 2026
• Full-Time
• On-site

Locations

Showing 1 location

TX - Sugar Land 1075

1075 W Park One Dr #100

Sugar Land, TX 77478, USA

Description

Our Production Technician I – Formulation plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical product. Once you complete our training, your responsibilities will include supporting daily manufacturing activities for non-sterile and sterile bulk/CSP operations. 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 2nd shift, working Monday through Friday from 2:00 PM to 10:30 PM CST. 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 Production Technician I – Formulation Does Each Day:

• Weighing of chemicals to support product formulation
• Formulation of bulk intermediate solutions
• Sterile filter integrity testing
• Clean Room cleaning and disinfection
• Daily Supply list for respective area turned into receiving by scheduled time
• Open/close Formulation pods and ILP in accordance with work instructions and daily task lists
• Approach others in a tactful manner
• React well under pressure
• Follow through on commitments
• Carefully follows clear directions to ensure safety and accuracy
• Are detail-oriented and take careful notes
• Take initiative to identify problems and opportunities

Minimum Requirements for this Role:

• A High School diploma or equivalent
• 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 throughout each shift, with or without accommodation
• 18+ years of age
• Must be currently authorized to work in the United States on a full-time basis; QuVa will not sponsor applicants for work visas
• Requires extensive training and qualification including but not limited to: gown training; aseptic technique; competency assessments; direct observation; and media fill qualification for each compounding process

Any of the Following Will Give You an Edge:

• College Degree with an emphasis in Chemistry, Biochemistry or equivalent
• 1 year of pharmaceutical manufacturing experience
• Working knowledge of cGMPs and regulatory requirements as well as all applicable SOPs

Benefits of Working at QuVa:

• 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.”

Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.For further information, please review the Know Your Rights notice from the Department of Labor.