Production Supervisor

American Regent; Hilliard (OH); On-site; USD 65,000 - 90,000; Full time

Job summary

American Regent seeks a Production Supervisor to oversee aseptic manufacturing activities, ensuring safe, compliant operations and timely production of sterile liquids. You will mentor junior staff, review batch records, and coordinate resources to meet schedules.

The role requires 1–3 years of leadership experience, familiarity with GMP/FDA guidelines, and the ability to perform equipment maintenance tasks. Apply to join a focused manufacturing team in Ohio.

Qualifications

• High School Diploma or GED required; a Bachelor’s degree is preferred in Pharmaceutical Science, Chemistry, Microbiology, Engineering, or related field.
• 1–3 years of leadership experience; ability to coach or mentor a team.
• Experience in manufacturing/pharma or GMP/FDA regulations is a plus.
• Chemical handling, mathematical aptitude, and ability to assemble, troubleshoot and perform minor repairs on equipment.
• Experience writing, reviewing, and executing SOPs.
• Must read Standard English in SOPs, maintenance schedules and operating manuals.

Responsibilities

• Supervises manufacturing activities for multiple products and allocates resources.
• Trains and mentors team members across the manufacturing process.
• Reviews batch records and logbooks before final production review.
• Reallocates personnel based on production needs and creates weekly schedules.
• Maintains equipment and supply inventories and ensures only approved materials are used.
• Ensures training records and procedures are current and compliant.
• Attends training programs as required by SOPs and company policies.

Skills

Leadership

Mentoring

Training

Team supervision

Education

High School Diploma or GED

Bachelor’s degree in Pharmaceutical Science, Chemistry, Microbiology, Engineering, or related field

Job description

Nature and ScopeThis position is a member of the Manufacturing Team. The Manufacturing Team is responsible for activities associated with the manufacture of safe, effective, and sterile pharmaceuticals in accordance with company SOPs, policies and cGMPs. The Manufacturing Team ensures aseptic and sanitary conditions are maintained where required, appropriate manufacturing area and equipment records are neat and accurate and safe, effective, and professional behavior is displayed at all times. In conjunction with Production Management the Manufacturing Team provides input and assistance to other Departments as needed, playing a critical role in maintaining production schedules and meeting Company goals. The Production Supervisor will be able to oversee all aspects of the Manufacturing Process. The Manufacturing Process includes component prep, aseptic cleaning, compounding, filtration, and filling in accordance with established production records in a concerted effort to manufacture sterile liquid pharmaceuticals. The Production Supervisor will be able to perform, oversee and provide signatory approval for all activities associated with the manufacturing process. The Production Supervisor will be able to provide direction, training and mentorship to all junior team members as needed. The Production Supervisor will be the responsible person for the proper use of batch documentation. The Production Supervisor will be able to troubleshoot most of the manufacturing process and equipment and where necessary make adjustments and minor repairs during setup and during operations.Essential Duties and ResponsibilitiesNothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time.· Supervises manufacturing activities as defined by established operating procedures for multiple products on a daily and weekly basis by delegating resources as well as participating in the process.· Responsible for the training and mentoring in all facets of the manufacturing process.· Responsible for reviewing executed batch records and logbooks prior to submitting for final production review.· Responsible for reallocation of personnel based on production needs.· Responsible for creating weekly activity schedules to ensure production needs are met.· Ensures equipment and supply inventories are maintained and available for use in accordance with production schedules.· Ensures only approved materials and equipment are utilized at all times.· Ensures that personnel do not perform tasks for which they do not have accurate and approved training records.· Ensures that only approved documentation and procedures are utilized at all times.· Attends all training programs as required by Company SOPs, procedures and policies.· Perform any other tasks/duties as assigned by management.Education Requirements and QualificationsTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required.· High School Diploma or GED equivalent required. Bachelor’s in Pharmaceutical Science, Chemistry, [Micro] Biology, Engineering, or a related field is preferred.· 1 to 3-years of leadership experience required and/or has demonstrated the ability to lead, coach or mentor a team or group.· Experience in manufacturing, the pharmaceutical industry, or with GMP/FDA regulations is a plus.· Chemical handling, mathematical aptitude, and the ability to assemble, troubleshoot and perform minor repairs on manufacturing equipment is preferred.· Experience writing, reviewing, and executing standard operating procedures.· Must be able to read documents in Standard English such as Standard Operating Procedures, maintenance schedules and operating manuals. Physical Environment and Requirements· Physically able to wear cleanroom/protective gowning and equipment, including but not limited to gowning, goggles, face shields, respirators, and protective gloves. PPE and Respirators are essential for the health and safety of employees.· Employees must maintain a clean-shaven appearance each working shift to wear tight-fitting respirators properly.· Employee must be able to occasionally lift and/or move up to 50 pounds.American Regent celebrates diversity and we are committed to creating an inclusive environment for all employees. We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, or protected veteran status.Applicants have rights under Federal Employment Laws.FMLA poster: https://www.dol.gov/whd/regs/compliance/posters/fmlaen.pdfKnow Your Rights: Know Your Rights: Workplace discrimination is illegal (eeoc.gov)Employee Polygraph Protection Act: https://www.dol.gov/whd/regs/compliance/posters/eppac.pdfAlert: We’re aware of individuals impersonating our staff to target job seekers. Please note:· All legitimate communication will come directly from a verified ARI recruiter either by phone or via an americanregent.com email address.· Our recruiting process includes multiple in person and/or video interviews and assessments.· If you are unsure about the legitimacy of a message, contact John Rossini at [e-mail] before responding.· We never request payment, bank information, or personal financial details during our offer process.Your security is important to us, and we encourage you to stay vigilant when job searching.American Regent Inc. endeavors to make https://careers.americanregent.com/ accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please email [e-mail].