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Manufacturing Operations Supervisor I

Avantor

Bakersfield, CAOnsitePosted 11 days ago$62,500.00 - $100,625.00
Full TimeMid LevelManufacturing & CMCLife Science Service & Supply
Original posting ↗

Summary

Avantor is seeking a Manufacturing Operations Supervisor (3rd Shift) to oversee the daily planning, implementation and maintenance of the manufacturing activities of a specific area. This person ensures the effective use of materials, equipment and personnel in producing quality products at minimum costs. They also select, develop, and evaluate personnel to ensure the efficient operation of the function and may assist a higher level supervisor. This is a full-time position based out of our Bakersfield, CA location. Work Schedule: 3rd Shift: Monday-Friday, 10pm-6:30am.

Job description

How you will thrive and create an impact:

  • Supervise the activities of the manufacturing employees. May supervise the activities of other departments (production, maintenance, shipping).
  • Plan, schedule, and coordinate departmental activities (including staffing) to fulfill sales orders, meet inventory requirements, and deliver manufactured products in accordance with established procedures and approved processes.
  • Responsible for site security, safety and proper shutdown of site at conclusion of shift.
  • Supervise and participate in the production operations.
  • Monitor and improve the efficiency, output and safety of manufacturing processes through observations and measurements as well as by collecting and interpreting data.
  • Ensures proper manufacturing processes are followed in accordance to written documentation (i.e., Batch Records, cGMPs, SOP’s, Work Instructions).
  • Maintains and revises procedures associated with production processes to ensure accuracy, consistency and product quality.
  • Create, edit, and maintain necessary documentation (SOP’s, Work Instructions).
  • Ensure all manufacturing safety policies and procedures are implemented and maintained at all times.
  • Investigates and eliminates departmental non-conformities in manufacturing processes by employing root cause analysis and implements corrective and preventative actions.
  • Analyze and design lean manufacturing cells using effective systems to optimize use of space, equipment, material, personnel and increase capacities.
  • Assist in developing plant layout in planning rearrangement of facilities, equipment and operations for better utilization of space and to increase capacities.
  • Supports process validations by defining process to quality parameters, executing protocols, collecting/interpreting data and supporting protocol summary where needed.
  • Monitors work for accuracy, neatness, and conformance to policies and procedures.
  • Trains, motivates, monitors and evaluates performance of manufacturing employees.
  • Develop and implement departmental cross training initiatives to allow for flexible resources and aid in improved capacities.
  • Actively participates with internal and/or customer audits.
  • Participates with activities directly related to ISO certification, and on-going conformance.
  • Works closely with internal departments to assure commitment to customer is met in a timely manner.
  • Performs other duties as assigned.

What we're looking for:

Education: High School diploma or GED; Bachelors degree preferred and/or equivalent experience. Experience: Minimum 3 years of progressive manufacturing experience and responsibilities, 1 of which must be in a supervisory capacity; or equivalent combination of education and experience. Life science, chemistry, chemical engineering or chemical production experience required. Experience in cGMP manufacturing a plus.

Additional Qualifications:

  • Familiarity with Chemical and/or Aseptic production processes and applications within similar industry preferred.
  • Highly organized and self-motivated individual who can work independently with little supervision.
  • Must have strong leadership skills and problem solving abilities.
  • Excellent oral and written communication skills.
  • Ability to perform risk assessment of products and processes and develop corrective measures.
  • Must be able to manage multiple tasks and priorities and easily adapt to changing situations.
  • Computer literacy applied to scheduling, procedure revisions and data management is required.
  • Ability to take initiative, meet deadlines, and lead people in a team environment essential.
  • Proven track record of reducing costs through process improvements and efficiencies.
  • Must be hands-on, team oriented and committed to business improvement processes.

Requirements

  • High School diploma or GED
  • Minimum 3 years of progressive manufacturing experience and responsibilities
  • 1 year of supervisory experience
  • Life science, chemistry, chemical engineering or chemical production experience required
  • Experience in cGMP manufacturing a plus
  • Familiarity with Chemical and/or Aseptic production processes and applications within similar industry preferred
  • Highly organized and self-motivated individual who can work independently with little supervision
  • Must have strong leadership skills and problem solving abilities
  • Excellent oral and written communication skills
  • Ability to perform risk assessment of products and processes and develop corrective measures
  • Must be able to manage multiple tasks and priorities and easily adapt to changing situations
  • Computer literacy applied to scheduling, procedure revisions and data management is required
  • Ability to take initiative, meet deadlines, and lead people in a team environment essential
  • Proven track record of reducing costs through process improvements and efficiencies
  • Must be hands-on, team oriented and committed to business improvement processes

Company overview

Avantor is a leading global provider of mission-critical products and services to customers in the life sciences and advanced technology industries. Founded in 1904 as J.T. Baker Chemical Company, the company has evolved into a Fortune 500 organization with operations in over 30 countries and serving more than 300,000 customer locations worldwide. Avantor's comprehensive portfolio supports virtually every stage of research, development, and production activities across biopharma, healthcare, education, government, and advanced technology sectors. The company specializes in providing high-purity chemicals, laboratory equipment, single-use bioprocessing systems, and specialized services that enable breakthroughs in medicine, healthcare, and technology. With approximately 14,500 employees globally, Avantor plays a crucial role in supporting scientific innovation, including significant contributions to COVID-19 vaccine manufacturing through its synthetic lipid production capabilities. The company went public in 2019 and is listed on the New York Stock Exchange under the symbol AVTR.

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