Supervisor Production Injectables (2nd Shift)

Tolmar; Windsor (CO); On-site; USD 83,000 - 88,000; Full time

Benefits offered by this job

Shift differential 8%

Bonus Eligible

Benefits information: https://www.tolm

Job summary

Tolmar in Windsor, CO is seeking an Injectable Production Supervisor to coordinate shift production activities and supervise hourly staff in the injectable manufacturing group. You will ensure quality, drive process improvements, and manage timesheets and training progress.

The role requires cGMP knowledge, strong communication, and the ability to operate on a fast-paced line with attention to documentation and SOPs. Typical hours are 2:00pm–10:30pm, with occasional overtime.

Qualifications

• Highschool diploma or GED required.
• Bachelor’s degree in scientific discipline preferred, not required.
• 3 or more years of experience in a GMP manufacturing environment.
• Specific training in cGMP is desired.

Responsibilities

• Supervise hourly manufacturing staff in the injectable group.
• Conduct interviews and hire hourly employees.
• Communicate daily production priorities to the team.
• Create, revise and implement SOPs and Production Batch Records.
• Review batch records and follow up on corrections and CAPA.
• Monitor training progress and readiness to work independently.
• Ensure adherence to quality standards and specifications.

Skills

Supervisory experience

GMP knowledge

Shift work

Communication skills

Problem solving

Microsoft Office

Education

High school diploma or GED

Bachelor’s degree in scientific discipline preferred

Job description

Purpose and Scope

The Injectable Production Supervisor coordinates and supervises shift production activities and related staffing, scheduling and planning in manufacturing, while ensuring that products are made with quality for our patients.

Core Hours

Monday - Friday 2:00pm - 10:30 pm

Training schedule may vary

Purpose and Scope

The Injectable Production Supervisor coordinates and supervises shift production activities and related staffing, scheduling and planning in manufacturing, while ensuring that products are made with quality for our patients.

Key Responsibilities

• Demonstrates a high degree of honesty, initiative, integrity, drive, reliability and trustworthiness.
• Actively models and fosters a positive, respectful, and harassment-free work environment for all employees.
• Actively supervises and manages the performance of hourly manufacturing employees in the injectable manufacturing group.
• Conducts interviews and makes hiring decisions on hourly employees.
• Ensures open and transparent communication to the hourly employees about company priorities, policies and general company announcements.
• Identifies, proposes and sees through process improvements and optimizations of injectable manufacturing processes.
• Conducts employee performance evaluations
• Reviews and approves direct report timesheets.
• Communicates and sets daily production priorities with Process Leads and hourly employees.
• The Manufacturing Supervisor oversees the work of the Process Lead who conducts or coordinates the on-process training, including line orientation and risk review, of all new team members or those transferring.
• The Supervisor is responsible for monitoring the training progress and readiness to work independently of all direct reports.
• Ensures production team’s adheres to all quality standards and specifications.
• Create, revise and implement Standard Operating Procedures (SOPs) and Production Batch Records.
• Performs Batch Record review, including prioritization, reviewing corrections, and following up to ensure timely completion.
• Perform Transactions in the Inventory Control Systems ERP (Enterprise Resource Planning) Systems on a timely basis.
• Performs Investigations, and CAPA implantations for non-conforming events.
• Pre-approves expiration dates on batch records prior to manufacturing.
• Performs other related duties as assigned.

Special Skills And Knowledge

• Mastered knowledge of current Good Manufacturing Procedures (cGMP) as they relate to production packaging activities.
• Ability to stand for extended periods of time (up to 8 hours or more).
• Proficient in Microsoft Office (Excel, Word, Outlook).
• Excellent verbal and written communication skills.
• Ability to adhere to written production records and validation protocols.
• Strong understanding of basic math and writing skills to document production activities in batch records and/or log books.
• Excellent attention to detail for documentation in production documents and to compare produced goods against specified requirements.
• Capability to operate on a fast-paced manual assembly line using basic production equipment.
• Ability to legibly complete required documentation.
• Technical ability to assemble and disassemble filling equipment.
• Strong analytical and problem solving skills.
• Supports management’s decisions and communicates change positively
• Maintains open and constructive dialogue with other leaders
• Take ownership for their responsibilities and their team’s performance
• Creates a cadence of accountability for their team
• Ability to analyze and make decisions within time and schedule constraints
• Proactively and effectively manages performance
• Ability to quickly make decisions and understand the impact on processes and employees.
• Ability to lead by example and have a proven record of excellence in attendance, dependability and safety.

Core Values

• Center on People: We commit to support the well‑being of our patients and treat our employees and those we serve as valued partners. By placing people at the heart of our actions, we actively engage, invigorate, acquire knowledge, and grow together with an enterprise‑wide mindset that lifts the whole organization.
• Are Proactive & Agile: We embody a culture of engagement and action. With a hands‑on approach, we fearlessly adapt to change. We anticipate, respond swiftly and efficiently to ignite a spirit that propels us towards extraordinary outcomes.
• Act Ethically: We are committed to consistently conducting our business in an ethical, compliant, and socially aware manner, in line with our purpose of positively impacting lives. We actively cultivate diversity, equity, inclusion & sustainability in our workplace.
• Constantly Improve: We are committed to a proactive, collaborative effort to enhance our products, systems, processes, and services by reducing waste, increasing efficiency, and improving quality. We strive to be innovative, embracing calculated risk‑taking that drives better ways of working.
• Are Accountable: We think, act, and communicate with honesty, transparency, and clarity in alignment with our core values. We don't compromise our values for near term gain. We take accountability & ownership of our work, actions, successes, and setbacks. We strive to deliver our best as we shape the future.

Communication

• Interact with peers and members of other departments in team settings in a professional manner.

Provide consistent coaching, guidance, development and mentorship to operators and technicians.

Education & Experience

• Highschool diploma or GED required
• Bachelor’s degree in scientific discipline or related field preferred, not required.
• 3 or more years of experience in a GMP manufacturing environment.
• Specific training in cGMP is desired

Additional Requirements

• Acceptable results on both a quantitative and verbal assessment test.
• Valid driver’s license and acceptable motor vehicle record may be required.
• Shift work in a manufacturing and warehouse environment.
• May require overtime.
• Successful completion of gowning qualification for sterile manufacturing.

Compensation And Benefits

• Annual pay range $83,000 - $88,000 depending on experience
• Shift differential 8%
• Bonus Eligible
• Benefits information: https://www.tolmar.com/careers/employee-benefits

Tolmar compensation programs are focused on equitable, fair pay practices including market-based base pay and a strong benefits package. The final compensation offered may vary from the posted range based on the selected candidates qualifications and experience.

Tolmar is an Equal Opportunity Employer. We do not discriminate on the basis age 40 and over, color, disability, gender identity, genetic information, military or veteran status, national origin, race, religion, sex, sexual orientation or any other applicable status protected by state or local law. It is our intention that all qualified applicants be given equal opportunity and that selection decisions are based on job-related factors.