Supervisor, Production Operations (3rd Shift)
Kindeva Drug Delivery, Brentwood, MO, United States
Our Work Matters
Kindeva is a leading global contract developer and manufacturer (CDMO) with delivery platform expertise in Autoinjector, Inhalation, Transdermal/Intradermal Patch Technologies. We partner with our customers to improve patient outcomes around the world. Together, as One Team, we will manufacture many more tomorrows.
The Impact You Will Make
Supervision of a production unit at the Sterile Production Manufacturing (SPM) facility, support services operations and (union) operators. Responsible for ensuring production and support services are performed in compliance with cGMP’s and following Standard Operating Procedures (SOPs).
ROLE RESPONSIBILITIES
Instructs the operations of (union) operators and staff in the daily duties and assures they are performed in a timely manner and in conformance with cGMP at SPM (Sterile Manufacturing Facility). Departmental duties include prep of sterile components/machine parts and/or sterile filling operations.
Supervises operations to ensure adherence with all Safety requirements when working with autoclaves, Water for Injection (WFI), machine parts and/or sterile fillers. Immediately addresses all safety events or concerns with Environmental, Health and Safety (EH&S) personnel.
Performs GMP audits of the aseptic processing area and/or supporting areas as required and investigates any process deviations; performs daily reviews of area documentation (including batch records) for accuracy and ensures compliance with Standard Operating Procedures and adherence to aseptic processing requirements.
Composes new or revises departmental SOPs as required.
Reports any significant shift activities to the Manager/TL; root cause analysis and ability to define effective corrective/preventative action.
Maintains inventory of materials and sterile items used in the SPM facility.
Sustains and improves labor standards.
Assists with the development and maintenance of the annual department overhead budget and orders supplies for area.
Schedules shift to maintain hands‑on support with operators; fills in for other supervisors as needed.
Maintains communications with supporting teams (i.e., Work Team Enablers/MRCs for documentation and SOP’s; Materials and Planning for scheduling of operations and ordering of materials; Manager/TL to report daily activities and receive information on activities for the area; and MQA for any quality issues/concerns).
Assists the Production Manager with special projects and other duties as assigned.
QUALIFICATIONS
Education: HS Diploma/AA degree required; Bachelor's degree in Engineering, Chemistry, Computer Science or other Technology or Life Science field preferred.
Experience: 3‑5 years previous supervisory experience required and/or combination of education and experience. Pharmaceutical or manufacturing experience highly desirable.
Language Skills: Effective written and oral communication skills required. Excellent written skills in English. Good verbal communication and ability to coach and provide guidance to others.
Computer Skills: Computer literate, with skills in managing Microsoft Applications, PLS, Trackwise.
Reasoning Ability: Demonstrated reading comprehension and writing proficiency at a level that meets ‘role’ and/or ‘test’ requirements. Ability to effectively communicate within a diverse group resulting in desired outcomes. Proven record of problem solving, decision‑making skills and application of process improvement tools.
Physical Demands: Ability to stand upright for several consecutive hours absent of any medical restrictions which could restrict completion of required duties. Additional requirements are line and product specific.
Work Environment: Use of eye protection, gloves and other PPE is required. Maintaining aseptic area certification may be required. Aseptic gowning procedures will be required. Aseptic gowning requires all body parts to be completely covered (gowned) for substantial periods of time. Practices and promotes a safe working environment at all times. Self‑starter, team player, with strong interpersonal and coaching skills.
PHYSICAL/MENTAL REQUIREMENTS
Job task may include bending, twisting, and lifting items up to 35 lbs at a frequency that meets position requirements. This position requires standing and frequent walking between production areas to supervise operations.
This position works around moving machines, is exposed to temperature changes and requires wearing personal protective equipment in certain areas and being aseptic gown qualified.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Position requires regular on-site attendance – this position cannot be performed on a remote or telecommute basis on a short‑term, long‑term, or temporary basis. Must have the ability to simultaneously multi‑task across multiple capabilities and functions and handle multiple competing priorities and requirements, including performing site and functional responsibilities, responding to email and phone communications and attending meetings. Note these activities may not be time bound to core hours or presence at the site.
Must have the ability to effectively manage strict production, time and performance deadlines.
Must be willing to work a variable and irregular shift beyond the hours typically defined as a ‘regular’ work day, which may or may not include we.
Equal Opportunity Employer
Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.
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Kindeva is a leading global contract developer and manufacturer (CDMO) with delivery platform expertise in Autoinjector, Inhalation, Transdermal/Intradermal Patch Technologies. We partner with our customers to improve patient outcomes around the world. Together, as One Team, we will manufacture many more tomorrows.
The Impact You Will Make
Supervision of a production unit at the Sterile Production Manufacturing (SPM) facility, support services operations and (union) operators. Responsible for ensuring production and support services are performed in compliance with cGMP’s and following Standard Operating Procedures (SOPs).
ROLE RESPONSIBILITIES
Instructs the operations of (union) operators and staff in the daily duties and assures they are performed in a timely manner and in conformance with cGMP at SPM (Sterile Manufacturing Facility). Departmental duties include prep of sterile components/machine parts and/or sterile filling operations.
Supervises operations to ensure adherence with all Safety requirements when working with autoclaves, Water for Injection (WFI), machine parts and/or sterile fillers. Immediately addresses all safety events or concerns with Environmental, Health and Safety (EH&S) personnel.
Performs GMP audits of the aseptic processing area and/or supporting areas as required and investigates any process deviations; performs daily reviews of area documentation (including batch records) for accuracy and ensures compliance with Standard Operating Procedures and adherence to aseptic processing requirements.
Composes new or revises departmental SOPs as required.
Reports any significant shift activities to the Manager/TL; root cause analysis and ability to define effective corrective/preventative action.
Maintains inventory of materials and sterile items used in the SPM facility.
Sustains and improves labor standards.
Assists with the development and maintenance of the annual department overhead budget and orders supplies for area.
Schedules shift to maintain hands‑on support with operators; fills in for other supervisors as needed.
Maintains communications with supporting teams (i.e., Work Team Enablers/MRCs for documentation and SOP’s; Materials and Planning for scheduling of operations and ordering of materials; Manager/TL to report daily activities and receive information on activities for the area; and MQA for any quality issues/concerns).
Assists the Production Manager with special projects and other duties as assigned.
QUALIFICATIONS
Education: HS Diploma/AA degree required; Bachelor's degree in Engineering, Chemistry, Computer Science or other Technology or Life Science field preferred.
Experience: 3‑5 years previous supervisory experience required and/or combination of education and experience. Pharmaceutical or manufacturing experience highly desirable.
Language Skills: Effective written and oral communication skills required. Excellent written skills in English. Good verbal communication and ability to coach and provide guidance to others.
Computer Skills: Computer literate, with skills in managing Microsoft Applications, PLS, Trackwise.
Reasoning Ability: Demonstrated reading comprehension and writing proficiency at a level that meets ‘role’ and/or ‘test’ requirements. Ability to effectively communicate within a diverse group resulting in desired outcomes. Proven record of problem solving, decision‑making skills and application of process improvement tools.
Physical Demands: Ability to stand upright for several consecutive hours absent of any medical restrictions which could restrict completion of required duties. Additional requirements are line and product specific.
Work Environment: Use of eye protection, gloves and other PPE is required. Maintaining aseptic area certification may be required. Aseptic gowning procedures will be required. Aseptic gowning requires all body parts to be completely covered (gowned) for substantial periods of time. Practices and promotes a safe working environment at all times. Self‑starter, team player, with strong interpersonal and coaching skills.
PHYSICAL/MENTAL REQUIREMENTS
Job task may include bending, twisting, and lifting items up to 35 lbs at a frequency that meets position requirements. This position requires standing and frequent walking between production areas to supervise operations.
This position works around moving machines, is exposed to temperature changes and requires wearing personal protective equipment in certain areas and being aseptic gown qualified.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Position requires regular on-site attendance – this position cannot be performed on a remote or telecommute basis on a short‑term, long‑term, or temporary basis. Must have the ability to simultaneously multi‑task across multiple capabilities and functions and handle multiple competing priorities and requirements, including performing site and functional responsibilities, responding to email and phone communications and attending meetings. Note these activities may not be time bound to core hours or presence at the site.
Must have the ability to effectively manage strict production, time and performance deadlines.
Must be willing to work a variable and irregular shift beyond the hours typically defined as a ‘regular’ work day, which may or may not include we.
Equal Opportunity Employer
Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.
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