Hourly – STAQ Pharma

Production Technician – Denver

STAQ Pharma is currently working hiring for production associates for our 1st and 2nd shift. Come join a team that offers exposure to work in the pharmaceutical manufacturing industry, and grow a career path with our team!
1st shift: Monday to Friday, 6 AM to 2:30 PM – $20/hour
2nd shift: Monday to Friday, 2 PM to 11 PM (or until done) – $22/hour

BENEFITS:
We provide medical, dental & vision insurance, as well as a 401K, Life insurance, voluntary life insurance, long term and short term disability, HSA & FSA, Aflac, LegalShield & IDShield, pet insurance, MetLife & SupportLinc Employee Assistance (mental health support)

This position functions primarily in a controlled-non-classified (CNC) environment and requires the individual to wear appropriate PPE. This position will perform labelling, visual inspection, and other duties, such as cleaning, restocking, and waste destruction, as required and/or assigned. All assigned tasks must be conducted in adherence with all applicable procedures, cGMPs, company policies and any other quality or regulatory (Ex: OSHA, DEA, FDA, etc.) requirements. Facility is a multiple shift operation where variable shifts, including weekends, may be required.

PRIMARY RESPONSIBILITIES:

Perform manual labeling and visual inspection operations in the CNC environment consistent with established protocols, procedures, and regulatory/cGMP requirements.

Responsible for acquiring and maintaining visual operator qualification status for syringes.
Complete and document required training to gain proficiency for all assigned job tasks.
Accurately and contemporaneously document all actions performed per GDP standards.
Assist with non-classified area cleaning and maintenance as required.
Perform waste destruction, material transfer, and additional support tasks as required.
Make recommendations for process improvements.
Possess the ability to master multiple processes across different areas.
Recognize and respond appropriately to equipment/documentation issues and deviations; obtain appropriate clarification and guidance from leadership before proceeding.
Must be able to read and write in English

Please apply using the link below to see all of our open roles
https://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=9acbf878-718b-4e5c-bdb5-7cbb9133c786&ccId=19000101_000001&lang=en_US

Quality Assurance Technician

STAQ is currently hiring for a Quality Assurance Technician for our 1st shift
Monday to Friday
6 AM to 2:30 PM
Pay: $20-$22/hour

Effectively encourage and motivate associates to be successful and remain focused on Quality, Transparency, Safety and Availability objectives compatible with the company’s mission and vision. Responsible for supporting maintenance of the Quality System and providing support on Quality management projects.

Print and maintain control of product labelsPerform sampling and inspection of in-process and finished productsAssist with investigations and develop and implement corrective and preventive actions geared toward continuous process improvementsPerform evaluations to determine effectiveness of corrective actionsReview GMP documents including master batch production records, room and equipment logs, etc.Support quality management system activities including document control and training program managementProvide supplier related support to production and receiving inspection teamOther duties and tasks, as assigned

1-3 years as a Quality TechnicianPharmaceutical or Medical Device industry or biotechnology experience, preferably in support of manufacturingAssociates degree in the sciences or equivalent experience preferred

Excellent independent judgement and interpersonal skillsStrong attention to detailExcellent mathematical, written communication, and verbal communication skills Familiarity with Good Manufacturing Practices and FDA RegulationsProficient in using Microsoft Word, Excel, PowerPoint, Outlook

This position will work closely with the Production team and report quality data to department management, as needed

Please apply below
https://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=9acbf878-718b-4e5c-bdb5-7cbb9133c786&ccId=19000101_000001&type=JS&lang=en_US&selectedMenuKey=CurrentOpenings

Engineering Intern

STAQ Pharma is currently looking for 2 Engineering Interns to join us for our summer 2025!

We are located in West Columbus, off of Phillipi Rd.

The Engineering Intern is responsible for various maintenance and cGMP system tasks. Will have the opportunity to work closely with experienced engineers and contribute to various aspects of engineering projects. Should have the willingness to take on special projects and be naturally inclined to take ownership of tasks.

Duties/Responsibilities:

• Assist engineers in the application of principles, methods, and techniques of engineering.
• Serve as leader of assigned projects and manage a schedule and tracking daily progress
• Execute Validation activities on critical manufacturing equipment and utilities.
• Investigating and executing manufacturing process improvement projects
• Create and update asset management documents related to preventative maintenance and calibration requirements.
• Writing process, utilities, and validation procedures, evaluating test results, writing reports, and processing action to be taken with in the quality system.
• Driving practical knowledge of science and technology into all levels of the manufacturing organization for improved plant performance
• Lead cross functional teams to achieve improvement objectives, and monitor daily operations to find improvement opportunities
• Work with production operators, maintenance technicians and vendors staff on solving technical problems

Required Skills/Abilities:

• Must be a team player and effectively collaborate with internal departments.
• Excellent attention to detail.
• Experience in a regulated manufacturing industry.
• Demonstrates ability to handle multiple responsibilities at any given time.

Education and Experience:
• Current enrollment in an accredited Chemical, Mechanical, or Biomedical Engineering program. Other related Majors may be considered.
• Sophomore, Junior, Senior, or graduate level.
• Excellent oral communication and technical writing skills.
• Microsoft word and excel experience.
• AutoCAD Microsoft excel experience preferred. Current human resources and/or compensation

Physical Requirements:
Prolonged periods of sitting at a desk and working on a computer. Must be able to lift up to 50 pounds at times,

Filling Technician

STAQ Pharma is currently hiring for filling technicians for our 1st and 2nd shift

Schedule:
Monday to Friday
6 AM to 2:30 PM
Pay: $26/hour
Monday to Friday
2 PM to 10:30 PM
Pay: $28/hour

This position functions primarily in a classified ISO-7 environment and requires the individual to wear appropriate PPE. This position will support sterile filling operations and perform other duties, such as cleaning, restocking, visual inspection, and labeling, as required and/or assigned. All assigned tasks must be conducted in adherence with all applicable procedures, cGMPs, company policies and any other quality or regulatory (Ex: OSHA, DEA, FDA, etc.) requirements. Facility is a multiple shift operation where variable shifts, including weekends, may be required.

Hours of Work: 8-hour shift Monday through Friday. 0600-1430 or 1400-2230.

SAFETY Strictly adhere to all cGMP, health and safety requirements, procedures, and corporate policies.Authorized to immediately stop any task that is determined to be an imminent hazard.Always promote and demonstrate safe work practices and adhere to PPE requirements.Safely handle chemicals, corrosives, solvents, and other pharmaceutical compounds.Demonstrate physical ability to lift a minimum of 50 lbs. and push/pull pallets, product cans, etc. multiple times per shift.

PRIMARY RESPONSIBILITIES: Perform ISO-7 support functions for aseptic filling operations consistent with established protocols, procedures, and regulatory/cGMP requirements.Learn to utilize all relevant equipment/technology for filling operations.Responsible for acquiring and maintaining classified area gowning qualification.Complete and document required training to gain proficiency for all assigned job tasks.Accurately and contemporaneously document all actions performed per GDP standards.Assist with classified and non-classified area cleaning and maintenance as required.Perform visual inspection, labeling, and additional support tasks as required.Make recommendations for process improvements.Possess the ability to master multiple processes across different areas.Recognize and respond appropriately to equipment/documentation issues and deviations; obtain appropriate clarification and guidance from leadership before proceeding.Maintain a quality focused, “Right First Time”, attitude.

Arrive for work on-time, prepared to work in the classified environment for the majority of each shift.Operate with Integrity by maintaining high ethical standards. Treat all employees with trust, respect, and professionalism. Speak up and hold others accountable for high integrity by providing constructive feedback. Take accountability for individual and team mistakes and participate in related corrective actions.Ensure patient safety by understanding you and your team’s impact on product quality.Excel within a diverse and high performing team. Remain open to new ideas and perspectives, communicate across shifts as required, and comply with site process to create a safe work environment. Demonstrate a passion to perform by meeting personal and departmental goals. Self-driven and self-accountable, performs required tasks, and progresses on qualifications within reasonable timelines.Demonstrate innovation abilities by identifying and speaking up about viable options for improvements and exploring and creating a path for implementation.

High School Diploma or equivalent.Must pass a drug test.Must speak, write, and read English.Must be a team player.Must have excellent attention to detail.

Prior Sterile Compounding and Pharmaceutical Industry experience.Prior experience operating manufacturing equipment/machinery.Knowledge of FDA guidelines, cGMP, and GDP.Willingness to participate in training and gain other certifications as needed.Knowledge of basic arithmetic and chemistry calculations.Ability to work in a fast-paced environment with dynamic priorities and demands.Excellent written and verbal communication skills.Desire to expand knowledge and grow with the company.Leadership ability.