STAQ Pharma is currently hiring for a production supervisor to join our team here in the Columbus are
Strictly adheres to all regulatory requirements, health and safety (e.g., OSHA, EPA, RCRA) requirements, procedures, work instructions, and corporate policies.
Immediately stops any task that is determined to be an imminent hazard.
Promotes and demonstrates safe work practices and adhere to PPE requirements.
Safely handles chemicals, corrosives, solvents, and other pharmaceutical compounds.
Demonstrates physical ability to lift a minimum of 50 lbs. and push/pull pallets, product containers, etc., multiple times per shift.
PRIMARY RESPONSIBILITIES
Supervise employees who are responsible for formulation; aseptic filling; inspection and labeling; or facility sanitization.
Position may have dotted line supervision to other areas of operations.
Provide support to technicians who are responsible for product formulation, aseptic filling, inspection and labeling, or facility cleaning and disinfection.
Participate in production activities as required.
Coordinate training and education for employees in areas of good documentation practices, gowning, formulation, aseptic filling, and other applicable production processes. Ensure employees trainings are completed on time.
Assist in interviewing, hiring, and onboarding operations personnel.
Demonstrates and serves as an example to others safe work culture including PPE use, chemical and material handling.
Create and maintain production schedule with input from key leadership, and ensure daily tasks and resources are allocated to support schedule and achieve Production goals. Participate in the creation, review, and revision of batch records, procedures, policies, and other quality documents that pertain to Operations.
Identify and analyze production efficiencies, downtime, and waste.
Leads team to improve results and production output. Exercise discretion, judgment, and personal responsibility
Recognizes and initiates deviations when discovered.
Appropriately investigates and documents in a timely manner.
Implements corrective actions and CAPAs as required.
Supports technical teams such as engineering, R&D, facilities, etc. in their activities and goals.
Ensure all SOPs are current, training on SOPs and processes remains current and compliance with STAQ Quality Systems.
Analyze Production efficiencies, downtime, and waste.
Lead teams to improve results and production output.
Write or assist with writing non-conformances that occur in the department.
Work with Quality to quickly resolve any variance or document errors so that product may be released on time.
Supports technical teams such as engineering, facilities, etc. in their activities.
Assist in managing staffing levels and budget spending when necessary.
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
QC Microbiologist
STAQ is currently hiring for a microbiologist to join our team here in Denver.
Schedule:
Monday to Friday, 9 AM to 6 PM
Pay: $70,000-$75,000
At minimum, the role is responsible for reviewing environmental monitoring data, providing support for batch disposition, assist in maintaining facility control, generating appropriate reports, leading quality control deviations/investigations, organizing/implementing appropriate processes and conducting all environmental monitoring validations.
• Organize, monitor, and assist with all production/routine environmental monitoring performance.
• Provide quality control and microbiology support to operations .
• Provide guidance and changes in scheduled cleaning of facility based on shutdown activities and environmental monitoring trending.
• Organize, manage, review and trend all environmental monitoring data .
• Provide trending reports to upper management.
• Lead and draft investigations as they relate to environmental monitoring or quality control deviations.
• Implementing CAPA’s as they relate to routine and production environmental monitoring deviations.
• Solve process, procedural, equipment issues via experimentation or revision of procedures.
• Other duties as assigned .
Experience Required:
B.S. or B.A. in Microbiology or a closely related field / or equivalent experience
• Minimum three (3) years’ experience in a quality control environment
• Experience in a cGMP Environment
• Preferred previous pharmaceutical experience .
• Minimum three (3) years’ experience in a quality control environment
• Experience in a cGMP Environment
• Preferred previous pharmaceutical experience .
Experience with cGMP aseptic manufacturing environments