Production Supervisor (3rd shift)

American Regent, Inc.; Hilliard (OH); Sur place; USD 65 000 - 90 000; Plein temps

Résumé du poste

American Regent, Inc. is seeking a Production Supervisor (3rd shift) in Hilliard, OH to oversee aseptic manufacturing processes, mentor junior staff, and ensure batch records compliance. The role requires ensuring proper use of documentation, materials, and equipment per SOPs and cGMP standards.

The supervisor will coordinate with Production Management to maintain schedules, troubleshoot processes, and support continuous improvement while training team members on safety and regulatory compliance.

Qualifications

• High School Diploma or GED required; Bachelor’s in Pharmaceutical Science, Chemistry, Engineering, or related field preferred.
• 1–3 years of leadership experience required, with ability to lead, coach or mentor a team.
• Experience in manufacturing, pharmaceutical industry, or GMP/FDA regulations is a plus.
• Must be able to read Standard Operating Procedures and operate/manipulate manufacturing equipment.
• Physical requirement: able to lift up to 50 pounds.

Responsabilités

• Supervises manufacturing activities for multiple products daily/weekly, delegating resources as needed.
• Trains and mentors staff in all aspects of 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 per production schedules.
• Ensures only approved materials and equipment are used and training records are current.
• Follows approved documentation and SOPs; attends mandatory trainings.
• Performs other duties as assigned by management.

Connaissances

Leadership

GMP/FDA knowledge

Reading SOPs

Troubleshooting

Documentation

Formation

High School Diploma or GED

Bachelor's in Pharmaceutical Science/ Chemistry/ Engineering or related field preferred

Outils

Manufacturing equipment maintenance

Description du poste

Production Supervisor (3rd shift)### Production Supervisor (3rd shift)Apply: Hilliard, OH: Full time: Posted Today: R-103520**Nature and Scope**This 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 Responsibilities**Nothing 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 Qualifications**To 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.pdf* Know Your Rights: Know Your Rights: Workplace discrimination is illegal (eeoc.gov)* Employee Polygraph Protection Act: https://www.dol.gov/whd/regs/compliance/posters/eppac.pdf**Alert: 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].